Deep Eutectic Solvents - Syntheses, Properties and Applications

View Online / Journal Homepage
Chem Soc Rev
Dynamic Article Links
Cite this: DOI: 10.1039/c2cs35178a

www.rsc.org/csr
CRITICAL REVIEW
Deep eutectic solvents: syntheses, properties and applications

Qinghua Zhang, Karine De Oliveira Vigier, Sebastien Royer and Francois Jerome*
Downloaded by UNIVERSITY OF SOUTH AUSTRALIA on 27 August 2012

Published on 17 July 2012 on http://pubs.rsc.org | doi:10.1039/C2CS35178A
Received 11th May 2012

DOI: 10.1039/c2cs35178a
Within the framework of green chemistry, solvents occupy a strategic place. To be qualied as a
green medium, these solvents have to meet dierent criteria such as availability, non-toxicity,
biodegradability, recyclability, ammability, and low price among others. Up to now, the number
of available green solvents are rather limited. Here we wish to discuss a new family of ionic uids,
so-called Deep Eutectic Solvents (DES), that are now rapidly emerging in the current literature.
A DES is a uid generally composed of two or three cheap and safe components that are capable
of self-association, often through hydrogen bond interactions, to form a eutectic mixture with a
melting point lower than that of each individual component. DESs are generally liquid at
temperatures lower than 100 1C. These DESs exhibit similar physico-chemical properties to the
traditionally used ionic liquids, while being much cheaper and environmentally friendlier. Owing
to these remarkable advantages, DESs are now of growing interest in many elds of research.
In this review, we report the major contributions of DESs in catalysis, organic synthesis,
dissolution and extraction processes, electrochemistry and material chemistry. All works discussed
in this review aim at demonstrating that DESs not only allow the design of eco-ecient processes
but also open a straightforward access to new chemicals and materials.
Universite de Poitiers/CNRS, UMR 7285, Institut de Chimie des

Milieux et Materiaux de Poitiers, ENSIP, 1 rue Marcel Dore,
86022 Poitiers, France. E-mail: [email protected];
Fax: +33 (0)5 49 45 33 49
catalysis, electrochemistry, material chemistry, and more recently

for the pre-treatment of biomass.13 At the early stages of these
research studies, scientists mainly focused on the formation of
ionic liquids by mixing metal salts, mostly zinc, aluminium, tin
and iron chlorides, with quaternary ammonium salts. Although
both salts have very high melting points, their proper mixing
leads to the formation of a liquid phase, the so-called eutectic
mixture. These eutectic mixtures are generally characterized by
Qinghua Zhang was born in

Shandong (China) in 1979,
and graduated from Shandong
Normal University with a BS
in chemistry in 2003. He
received his PhD degree in
2008 from the Lanzhou
Institute of Chemical Physics
(LICP), Chinese Academy of
Sciences, and worked as an
assistant researcher in the
LICP from 2009 to 2010. In
2010, he joined the group of
Francois Jerome as a CNRS
associate researcher at the
Qinghua Zhang
University of Poitiers. His
major research interests focus on the development of new green
solvents (ionic liquids, deep eutectic solvents, etc.) for the
biomass pretreatment, as well as their applications in biomass
conversion.
Karine De Oliveira Vigier

received her PhD in chemistry
(specialization in catalysis) in
2002 from the University of
Poitiers (France). Then she
moved to the University of
Sherbrooke (Canada) for
two years where she has a
postdoctoral position on catalysis reforming of ethanol. In
2004, she got a position of
Associated Professor at the
Laboratoire de Catalyse en
Chimie Organique (LACCO)
at the University of Poitiers.
Karine De Oliveira Vigier
Her actual research focuses on
carbohydrates chemistry (from cellulose to platform molecules)
and the valorization of fats and oils. She pays a particular
attention to the catalysis and the development of new reaction
media for the conversion of biomass.
1. Introduction
In the past 20 years, room temperature ionic liquids (RTILs)
have attracted considerable attention especially in the elds of
This journal is
The Royal Society of Chemistry 2012
Chem. Soc. Rev.

View Online
a very large depression of freezing point, generally higher

than 150 1C. With the introduction of the concept of green
chemistry in the early 1990s, the search for metal-free ionic
liquids (ILs) has become of growing interest.4 In this context, a
lot of works were dedicated to the design of ILs by combining
an organic cation (usually imidazolium-based cations) with a
large variety of anions, the most common ones being Cl,
BF4, PF6, NTf2. From that time, ILs have emerged as a
new class of promising solvents. The possibility to chemically
modify the cationic moiety almost innitely in combination
with a very large choice of anions oers chemists a broad
range of ILs exhibiting dierent physical properties such as
melting point, solubility, viscosity, density, conductivity, and
refractivity, among others. For instance, in 2009, Seddon and
co-workers have reported that 1018 dierent ILs can be
theoretically produced, 250 of them being already commercialized.5 Owing to their low vapour pressure and high boiling
point, which facilitates their recycling, ILs were qualied as
green solvents. However, the green aliation of these
neoteric solvents is now largely contested in the current
literature.6 Indeed, many reports pointed out the hazardous
toxicity and the very poor biodegradability of most ILs.7 ILs
with high purity are also required since impurities, even in
trace amounts, aect their physical properties. Additionally,
their synthesis is far to be environmentally friendly since it
generally requires a large amount of salts and solvents in order
to completely exchange the anions. These drawbacks together
with the high price of common ILs unfortunately hamper their
industrial emergence and new concepts are now strongly
needed in order to utilize these systems in a more rational way.
To overcome the high price and toxicity of ILs, a new
generation of solvent, named Deep Eutectic Solvents (DES),
has emerged at the beginning of this century. Formation of these
DESs can be obtained by simply mixing together two safe
components (cheap, renewable and biodegradable), which are
capable of forming a eutectic mixture. One of the most widespread components used for the formation of these DESs is
choline chloride (ChCl). ChCl is a very cheap, biodegradable
and non-toxic quaternary ammonium salt which can be either
extracted from biomass or readily synthesized from fossil reserves
(million metric tons) through a very high atom economy process.
In combination with safe hydrogen bond donors such as urea,
renewable carboxylic acids (e.g. oxalic, citric, succinic or amino
acids) or renewable polyols (e.g. glycerol, carbohydrates), ChCl is
capable of rapidly forming a DES. Although most of DESs are
made from ChCl as an ionic species, DESs cannot be considered
as ILs because (1) DESs are not entirely composed of ionic
species and (2) can also be obtained from non-ionic species.
As compared to the traditional ILs, DESs derived from ChCl
gather many advantages such as (1) low price, (2) chemical
inertness with water (i.e. easy storage), (3) easy to prepare since
DESs are obtained by simply mixing two components, thus
by-passing all problems of purication and waste disposal
generally encountered with ILs and (4) most of them are biodegradable,8 biocompatible9 and non-toxic,10 reinforcing the greenness of these media.11 Physico-chemical properties of DESs
(density, viscosity, refractive index, conductivity, surface tension,
chemical inertness, etc.) are very close to those of common ILs. For
this reason, DESs derived from ChCl are also familiarly named
biocompatible or biorenewable ionic liquids in a few studies.
Thanks to their low ecological footprint and attractive price, DESs
have now become of growing interest both at academic and
industrial levels and the number of publications dedicated to the
use of DESs is now rapidly increasing in the current literature,
further demonstrating the attractiveness of these media.
Sebastien Royer received his

PhD in Chemical Engineering
in 2004 from the Laval University, Quebec. His research
focuses on the catalytic properties
of
nanocrystalline
perovskites for oxidation
reactions. In 2006, he got
a position of Associated
Professor at LACCO Poitiers.
His actual research focuses on
the design of size- and shapedcontrolled active oxides for
applications in environment
and energy.
Francois Jerome received his

PhD degree in chemistry from
the University of Burgundy
(France) in 2000. Then, he
moved to the University of
California of Davis (USA)
as a postdoctoral researcher.
Then, he returned to France
for a second potdoctoral
position at the University of
Rennes 1 with Pr P. H.
Dixneuf, where he worked on
homogeneous catalysis. In
2002, he joined the CNRS as
a permanent researcher in the
Francois Jerome
Laboratoire de Catalyse en
Chimie Organique at the University of Poitiers. Recently he
was promoted as a CNRS research director at the Institut de
Chimie des Milieux et Materiaux de Poitiers. His scientic
research studies are focussing on the conversion of biomass with
a particular attention to catalysis and non-conventional media.
In 2010, his research studies have been awarded by the french
division of catalysis (SCF-DIVCAT).
Sebastien Royer
Chem. Soc. Rev.
2. Denition of DESs
A DES is generally composed of two or three cheap and safe
components which are capable of associating with each other,
This journal is
View Online

to handle and no purication is required, thus making their

large-scale use feasible.
In the following sections, we wish to present an overview of
the recent advances made in the eld of DESs. Through
selected examples, we will show that DESs are particularly
promising for the design of innovative catalytic processes,
the preparation of new materials and novel structures, the
dissolution of valuable substrates and also in the eld of
electrochemistry. In all these DES-based processes, we will
try to demonstrate that use of DESs not only allows the design
of safer processes but also provides a straightforward access to
new chemicals and materials.
3. Physicochemical properties of DESs
Scheme 1 Typical structures of the halide salts and hydrogen bond

donors used for DES syntheses.
through hydrogen bond interactions, to form a eutectic mixture.

The resulting DES is characterized by a melting point lower
than that of each individual component. Generally, DESs are
characterized by a very large depression of freezing point and
are liquid at temperatures lower than 150 1C. Note that most
of them are liquid between room temperature and 70 1C.
In most cases, a DES is obtained by mixing a quaternary
ammonium salt with metal salts or a hydrogen bond donor
(HBD) that has the ability to form a complex with the
halide anion of the quaternary ammonium salt. Scheme 1
summarizes the dierent quaternary ammonium salts that
are widely used in combination with various HBDs in the
formation of DESs.
In 2007, Abbott and co-workers dened DESs using the
general formula R1R2R3R4N+XY.12
Type I DES Y = MClx, M = Zn, Sn, Fe, Al, Ga
Type II DES Y = MClxyH2O, M = Cr, Co, Cu, Ni, Fe
Type III DES Y = R5Z with Z = CONH2, COOH, OH
Note that the same group also dened a fourth type of DES
which is composed of metal chlorides (e.g. ZnCl2) mixed with
dierent HBDs such as urea, ethylene glycol, acetamide or
hexanediol (type IV DES).
Owing to its low cost, biodegradability and low toxicity,
ChCl was widely used as an organic salt to produce eutectic
mixtures generally with cheap and safe HBDs such as urea,
glycerol, carbohydrate-derived polyols or renewably sourced
carboxylic acids. These DESs are attractive since they exhibit
similar physico-chemical properties to traditional imidazoliumbased ILs and thus can advantageously replace them in many
applications. As compared to traditional organic solvents,
DESs are not considered as volatile organic solvents and not
ammable, making their storage convenient. From the view
point of green chemistry, these DESs are even more attractive
since some of them have been proven to be biodegradable and
compatible with enzymes further increasing their interest.
Additionally, synthesis of DESs is 100% atom economic, easy
This journal is
Similar to ILs,13 DESs are chemically tailorable solvents since

they can be designed by properly combining various quaternary
ammonium salts (e.g. ChCl) with dierent hydrogen bond
donors (HBD). Hence, task-specic DESs with dierent
physicochemical properties such as freezing point, viscosity,
conductivity, and pH, among others, can be prepared. Owing
to their promising applications, many eorts have been
devoted to the physicochemical characterization of DESs. In
this section, the main physicochemical properties of DESs will
be described and discussed.
3.1 Freezing point (Tf)
As mentioned above, DESs are formed by mixing two solids
capable of generating a new liquid phase by self-association via
hydrogen bonds. This new phase is generally characterized by
a lower freezing point than that of individual constituents. For
instance, when ChCl and urea are mixed together in a molar
ratio of 1 : 2, the freezing point of the eutectic is 12 1C, which
is considerably lower than that of ChCl and urea (melting
point of ChCl and urea are 302 and 133 1C, respectively). The
signicant depression of the freezing point stems from an
interaction between the halide anion and the hydrogen bond
donor component, here urea. For all reported DESs, their
freezing points are below 150 1C. Generally, DESs with a
freezing point lower than 50 1C are more attractive since they
can be used as inexpensive and safe solvents in many elds.
Tables 1 and 2 list the freezing points of various DESs
described in the literature. Although a broad range of amides
have been employed in combination with ChCl to produce
DESs with a freezing point lower than 100 1C, it should be
pointed out that the number of DESs which are liquid at room
temperature is still very limited. Among them, urea and 2,2,2triuoroacetamide are capable of forming a liquid DES with
ChCl at room temperature, presumably due to their stronger
ability to form hydrogen bond interactions with ChCl. It
means that in the case of ChCl, the choice of HBDs is a
critical point in the formation of a DES with a low freezing
point. When carboxylic acids (e.g. levulinic acid, malonic acid,
phenylpropionic acid, etc.) or sugar-derived polyols (e.g. xylitol,
D-isosorbide, and D-sorbitol) are used as HBDs, room
temperature liquid DESs can also be obtained. Similar to the
HBDs, the nature of the organic salts (e.g. ammonium or
phosphonium salts) also aects the freezing points of the
corresponding DESs. For example, when urea is selected as
Chem. Soc. Rev.
View Online
Table 1
Freezing point (Tf) of the reported DESs. Tm : melting point of pure HBD; RT = room temperature
ChCl : HBD (molar ratio)
Tm /1C
Urea
1:2
134
12
15
Thiourea
1:2
175
69
15
1-Methyl urea
1:2
93
29
15
1,3-Dimethyl urea
1:2
102
70
15
1,1-Dimethyl urea
1:2
180
149
15
Acetamide
1:2
80
51
15
Benzamide
1:2
129
92
15
Ethylene glycol
1:2
12.9
66
16
Glycerol
1:2
17.8
40
17,27
2,2,2-Triuoroacetamide
1 : 2.5
72
45
16
Imidazole
3:7
89
56
18
Adipic acid
1:1
153
85
14
Benzoic acid
1:1
122
95
14
Citric acid
1:1
149
69
14
Malonic acid
1:1
135
10
14
Oxalic acid
1:1
190
34
14
Phenylacetic acid
1:1
77
25
14
Phenylpropionic acid
1:1
48
20
14
Succinic acid
1:1
185
71
14

Hydrogen bond donor (HBD)
Chem. Soc. Rev.
This journal is
Tf/1C
Ref.
View Online
Table 1
(continued )
ChCl : HBD (molar ratio)
Tm /1C
Tricarballylic acid
1:1
159
Levulinic acid
1:2
32
Itaconic acid
1:1
166
Xylitol
1:1
D-Sorbitol
1:1

Hydrogen bond donor (HBD)
L-(+)-Tartaric
acid
1 : 0.5
Ref.
90
14
Liquid at RT
19
57 3
19
96
Liquid at RT
19
99
Liquid at RT
19
47 3
19
Liquid at RT
19
171
D-Isosorbide
1:2
4-Hydroxybenzoic acid
1 : 0.5
215
87 3
19
Caeic acid
1 : 0.5
212
67 3
19
p-Coumaric acid
1 : 0.5
214
67 3
19
trans-Cinnamic acid
1:1
133
93 3
19
Suberic acid
1:1
142
93 3
19
Gallic acid
1 : 0.5
251
77 3
19
Resorcinol
1:4
110
87
20
the HBD and mixed with dierent ammonium salts in a molar

ratio of 2 : 1 (urea : salt), the obtained DESs exhibit very
dierent freezing points ranging from 38 1C to 113 1C
(Table 2). The anion of choline-derived salts also impacts
the freezing point of DESs. For instance, in combination with
urea, the freezing point of a choline salt-derived DES decreases
This journal is
Tf/1C
62
in the order F > NO3 > Cl > BF4, suggesting a

correlation with the hydrogen bond strength. The organic
salt/HBD molar ratio has also a signicant impact on the
freezing point of DESs. For example, when ChCl was mixed
with urea in a molar ratio of 1 : 1 and 1 : 2, the resulting DESs
exhibited a freezing point >50 1C and 12 1C, respectively.
Chem. Soc. Rev.
View Online
Table 2
Table 2 (continued )
Freezing point (Tf) of other DESs
Organic salts

Cation
Hydrogen
bond
Anion donor
(X) (HBD)
Salt :
HBD
(molar
ratio) Tf/1C Ref.
Urea
1:2
15
BF4
Urea
1:2
67
15
NO3
Urea
1:2
15
Cl
Urea
1:2
38
15
Br
Urea
1:2
113
15
Cl
1:2
14
Urea
1:2
33
15
Cl
Urea
1:2
15
15
Br
Urea
1:2
55
15
Br
Br
Cl
Br
Glycerol
Glycerol
Glycerol
Glycerol
Ethylene glycol
1:2
1:3
1:4
1:5
1:3
34
Cation
Hydrogen
bond
Anion donor
(X) (HBD)
Salt :
HBD
(molar
ratio) Tf/1C Ref.
Br
Ethylene glycol
1:4
50
21,27
Br
Ethylene glycol
1:5
48
21
Cl
Ethylene glycol
1:3
47.9
22
Br
Triethylene glycol 1 : 3
8
21
Br
19
21
Br
21
21
Cl
2,2,21:2
Triuoracetamide
91
22
Br
2,2,21:8
Triuoracetamide
69
22
Cl
Glycerol
1:2
1
26
Cl
Glycerol
1:3
1.7
26
Cl
Glycerol
1:4
26
Cl
Ethylene glycol
1:2
31
26
15
Cl
Br
Chem. Soc. Rev.
Urea
Organic salts
21
5.5 21
15.6
50
46
21
21
21
This journal is
View Online
Table 2
(continued )
Organic salts
Cation
Hydrogen
bond
Anion donor
(X) (HBD)
Salt :
HBD
(molar
ratio) Tf/1C Ref.
Cl
1:3

Cl
Ethylene glycol
Ethylene glycol
1:4
22
21
26
26
Fig. 1 shows the phase diagram for mixtures of ChCl with

ve carboxylic acids as a function of the molar composition.
For phenylpropionic acid and phenylacetic acid-based DESs,
the lowest freezing point was formed at a composition of
67 mol% of acid, which was similar to the case of the ChClurea
system (Fig. 1a). This also means that two carboxylic acid
molecules are required to complex each chloride anion of
choline in order to form the eutectic mixture. In the case of
diacids such as oxalic, malonic and succinic acid, the eutectic is
formed at 50 mol% of diacid, suggesting a 1 : 1 complex
between the HBD and chloride. This is in accordance with
the interaction of two carboxylic acid functions per chloride of
ChCl (Fig. 1b). Although these systems are also characterized
by a signicant decrease of the freezing point, no clear
correlation between the freezing point of DESs and the melting
points of the pure components (HBDs or ChCl) has been
established (Tables 1 and 2). When using acids as HBDs, it
seems that the acid with the lowest molecular weight shows the
largest depression of freezing point. Abbott et al.14 proposed
Fig. 1 Freezing points of choline chloride with ve carboxylic acids

as a function of composition.14 (Reproduced with permission from
ref. 14. Copyright (2004) American Chemical Society.)
This journal is
that the freezing point of HBD-salt eutectic mixtures should be

dependent on (1) the lattice energies of DESs, (2) the way how
the couple anionHBD interacts, and (3) the entropy changes
arising from the formation of a liquid phase. In a rst
approximation, the depression of freezing point might be a
measure of the entropy change.
3.2 Density
The density is one of the most important physical properties
for a solvent. Generally, densities of DESs are determined by
means of a specic gravity meter. Table 3 lists the density data
of common DESs. Most of DESs exhibit higher densities than
water. For instance, type IV ZnCl2HBD eutectic mixtures
have densities higher than 1.3 g cm3. Among them, density of
ZnCl2urea (1 : 3.5) and ZnCl2acetamide (1 : 4) are dierent
(1.63 and 1.36 g cm3, respectively). This notable dierence of
density might be attributed to a dierent molecular organization or packing of the DES. Note that densities of both DESs
are higher than those of pure HDBs (acetamide: 1.16 and urea:
1.32 g cm3). This phenomenon may be explained by the hole
theory. Similar to imidazolium-based ILs, DESs are composed
of holes or empty vacancies. When ZnCl2 was mixed with urea
for instance, the average hole radius was decreased, resulting
in a slight increase of the DES density as compared to that of
neat urea.12
The organic salt/HBD molar ratio also has an obvious
eect on the densities of DES. Fig. 2 shows the density of a
glycerol/ChCl DES as a function of the molar composition.
Table 3 Densities of common DESs at 25 1C
Salts
HBD
Salt : HBD
(mol : mol)
Density
(r, g cm3)
Ref.
EtNH3Cl
EtNH3Cl
EtNH3Cl
ChCl
AcChCl
ChCl
ZnCl2
ZnCl2
ZnCl2
ZnCl2
ChCl
ChCl
ChCl
ChCl
ChCl
ChCl
ChCl
Et2(EtOH)NCla
Et2(EtOH)NCla
Et2(EtOH)NCla
Et2(EtOH)NCla
Et2(EtOH)NCla
Et2(EtOH)NCla
Me(Ph)3PBrc
Me(Ph)3PBrc
Me(Ph)3PBrc
Me(Ph)3PBrc
Me(Ph)3PBrc
Me(Ph)3PBrc
CF3CONH2
Acetamide
Urea
CF3CONH2
Urea
Urea
Urea
Acetamide
EG
Hexanediol
Glycerol
Glycerol
Glycerol
Glycerol
EGb
EG
Malonic acid
Glycerol
Glycerol
Glycerol
EG
EG
EG
Glycerol
Glycerol
Glycerol
EG
EG
EG
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1.273
1.041
1.140
1.342
1.206
1.25
1.63
1.36
1.45
1.38
1.18
1.20
1.16
1.20
1.12
1.12
1.25
1.17
1.21
1.22
1.10
1.10
1.10
1.31
1.30
1.30
1.25
1.23
1.22
23
23
23
23
23
23,24
12
12
12
12
25,27
25
26
26
25,26
25,26
24
26
26
26
26
26
26
26
26
26
26
26
26
:
:
:
:
:
:
:
:
:
:
:
:
:
:
:
:
:
:
:
:
:
:
:
:
:
:
:
:
:
1.5
1.5
1.5
2
2
2
3.5
4
4
3
2
3
1
3
2
3
2
2
3
4
2
3
4
2
3
4
3
4
6
a
Et2(EtOH)NCl: N,N-diethylenethanol ammonium chloride. b EG is
ethylene glycol. c Me(Ph)3PBr:methyltriphenylphosphonium bromide.
Chem. Soc. Rev.
View Online

Table 4 Viscosities of selected DESs at dierent temperatures
Fig. 2 Densities of the glycerol/ChCl DES as a function of the molar

composition.27 (Reproduced with permission from ref. 27. Copyright
(2011) Royal Society of Chemistry.)
Addition of ChCl to glycerol results in a decrease of the DES

density, which may be explained in terms of free volume.26
Experimental measurements of DES densities as a function
of the temperature are sometimes dicult to be achieved.
Hence, particular attention was given to the development of
new methods capable of providing these data with a maximum
of accuracy. The Rackett equation modied by Spencer and
Danner was employed to predict the density of DES with an
error of 1.9%.28
3.3
Viscosity
Like most of the ILs, viscosity of DESs is an important issue

that needs to be addressed. Except for ChClethylene glycol
(EG) eutectic mixture, most of the DESs exhibit relatively high
viscosities (>100 cP) at room temperature. The high viscosity
of DESs is often attributed to the presence of an extensive
hydrogen bond network between each component, which
results in a lower mobility of free species within the DES.
The large ion size and very small void volume of most DESs
but also other forces such as electrostatic or van der Waals
interactions may contribute to the high viscosity of DES.
Owing to their potential applications as green media, the
development of DESs with low viscosities is highly desirable.
In general, viscosities of eutectic mixtures are mainly aected
by the chemical nature of the DES components (type of the
ammonium salts and HBDs, organic salt/HBD molar ratio,
etc.), the temperature, and the water content. As discussed
above, viscosity of DES is also dependent on the free volume.
Hence, the hole theory can also be used to design DESs with
low viscosities. For instance, use of small cations or uorinated hydrogen-bond donors can lead to the formation of
DES with low viscosity.23
Viscosity of binary eutectic mixtures is essentially governed
by hydrogen bonds, van der Waals and electrostatic interactions. Table 4 lists the viscosity data of common DESs at
dierent temperatures. It can be seen that the viscosity of
ChCl-based DESs is closely dependent on the nature of the
HBD. For instance, ChCl/EG (1 : 4) DES exhibits the lowest
viscosity (19 cP at 20 1C). In contrast, use of derived sugars
(e.g. xylitol, sorbitol) or carboxylic acids (e.g., malonic acid) as
HBDs led to DESs exhibiting high viscosities (e.g., 12 730 cP at
20 1C for ChCl/sorbitol) due to the presence of a more robust
3D intermolecular hydrogen-bond network.
Chem. Soc. Rev.
Organic
Salts
HBD
Salt : HBD molar

ratio
Viscosities
(cP)
Ref.
ChCl
ChCl
ChCl
ChCl
ChCl
ChCl
ChCl
ChCl
ChCl
ChCl
ChCl
ChCl
ChCl
ChCl
ChCl
ChCl
ChCl
ChCl
ChCl
ZnCl2
Bu4NBr
EtNH3Cl
EtNH3Cl
EtNH3Cl
AcChCl
Bu4NBr
Urea
Urea
EG
EG
EG
EG
Glucose
Glycerol
Glycerol
Glycerol
Glycerol
1,4-Butanediol
1,4-Butanediol
CF3CONH2
Imidazole
ZnCl2
Xylitol
Sorbitol
Malonic acid
Urea
Imidazole
CF3CONH2
Acetamide
Urea
Urea
Imidazole
1
1
1
1
1
1
1
1
1
1
1
1
1
1
3
1
1
1
1
1
3
1
1
1
1
3
750 (25 1C)

169 (40 1C)
36 (20 1C)
37 (25 1C)
19 (20 1C)
19 (20 1C)
34 400 (50 1C)
376 (20 1C)
259 (25 1C)
450 (20 1C)
503 (20 1C)
140 (20 1C)
88 (20 1C)
77 (40 1C)
15 (70 1C)
85 000 (25 1C)
5230 (30 1C)
12 730 (30 1C)
1124 (25 1C)
11 340 (25 1C)
810 (20 1C)
256 (40 1C)
64 (40 1C)
128 (40 1C)
2214 (40 1C)
810 (20 1C)
24
23
25
24
25
25
19
25
24
25
25
25
25
23
18
29
19
19
24
25
18
23
23
23
23
18
:
:
:
:
:
:
:
:
:
:
:
:
:
:
:
:
:
:
:
:
:
:
:
:
:
:
2
2
2
2
3
4
1
2
2
3
4
3
4
2
7
2
1
1
2
3.5
7
1.5
1.5
1.5
2
7
Interestingly, in the case of a ChCl/glycerol DES, an

increase of the ChCl/glycerol molar ratio results in a decrease
of the DES viscosity (Fig. 3). For example, at 20 1C, viscosities
of ChClglycerol mixtures with a molar ratio of 1 : 4, 1 : 3,
1 : 2 were 503, 450, and 376 cP, respectively. Glycerol has
a strong cohesive energy due to the presence of an important intermolecular hydrogen bond network. This drastic
decrease of the glycerol viscosity upon addition of ChCl was
attributed to the partial rupture of this hydrogen bond
network.27
Viscosity (Z) of most eutectic mixtures obviously changes
signicantly as a function of the temperature. Like ILs, the
viscositytemperature proles also follow an Arrheniuslike behaviour. As the temperature increases, the viscosity
decreases.
Fig. 3 Eect of ChCl on the viscosity, Z of glycerol as a function of

composition at 298 K.27 (Reproduced with permission from ref. 27.
Copyright (2011) Royal Society of Chemistry.)
This journal is
View Online
3.4
Polarity
Generally, polarity of a solvent can be evaluated by its polarity

scale, ET (30), which is the electronic transition energy of a
probe dye (e.g. Reichardts Dye 30) in a solvent. By means of
UV-vis technology and using Reichardts Dye 30, ET(30) can
be calculated according to eqn (1).
ET(30)(kcal mol1) = hCU
maxNA

= (2.8591 103)Umax(cm1) = 28591/lmax
(1)
In Table 5, the polarity data of various ChClglycerol eutectic

mixtures using the Reichardts Dye method are summarized.27
These results show that ChCl/glycerol DESs exhibit similar
polarity to those of RNH3+X and R2NH2+X ILs bearing
discrete anions.30 Clearly, an increase in the ChCl/glycerol
molar ratio results in an increase of the ET(30) of the DES.
Additionally, a roughly linear increase of ET(30) with the
ChCl concentration was observed.29
3.5
Ionic conductivity
Owing to their relatively high viscosities, most of DESs exhibit

poor ionic conductivities (lower than 2 mS cm1 at room
temperature). Table 6 lists the ionic conductivities of various
DESs at dierent temperatures. Conductivities of DESs generally
increase signicantly as the temperature increases due to a
decrease of the DES viscosity. Hence, Arrhenius-like equation
can also be used to predict the conductivity behavior of a
DES.
Considering that changes of the organic salt/HBD molar
ratio signicantly impact the viscosities of DES, it is clear that
this parameter also dramatically inuences the conductivities
of DESs.14 The conductivity of DES increases with increasing
the ChCl content.25 When the molar fraction of ChCl is
Table 5 Solvent polarity parameters of various ChClglycerol mixtures
Solvents
Molar ratio of
ChCl: Glycerol
ET(30)/kcal mol1
Glycerol
ChCl: Glycerol
ChCl: Glycerol
ChCl: Glycerol
ChCl: Glycerol
1:
1:
1:
1:
57.17
57.96
58.28
58.21
58.49
Table 6
3
2
1.5
1
increased to 25 mol%, the conductivity of the ChClglycerol

DES is 0.85 mS cm1. At higher salt concentrations, these
ChCl/glycerol-based DESs exhibit a viscosity (o400 cP) and
conductivity (>1 mS cm1) comparable to those of an IL.
3.6 Acidity or alkalinity
The Hammett function has been widely used to evaluate the
acidity and basicity of nonaqueous solvents by determining
the ionization ratio of indicators in a system. For a basic
solution, the Hammett function measures the tendency of the
solution to capture protons. When weak acids are chosen as
indicators, the Hammett function H_ is dened by the following
equation.
H_ = pK(HI) + log([I]/[HI])
(2)
where pK(HI) is the thermodynamic ionization constant of the

indicator in water, [I] and [HI] represent the molar concentrations of anionic and neutral forms of the indicator, respectively. A medium with large H_ value has strong basicity.
When 4-nitrobenzylcyanide was used as indicator, the
H_ value of the ChCl/urea (1 : 2) DES was 10.86, suggesting
that this DES is weakly basic.31 Note that when the system
contains 13 wt% of water, the H_ values decrease slightly
(from 10.77 to 10.65) due to a partial solvation of basic sites.
Owing to the weak alkalinity of the ChClurea eutectic
mixture, this DES is capable of absorbing a small amount of
acid gas such as CO2. In the presence of 1 atm of CO2, the
H_ value of ChCl/urea decreases from 10.86 to 6.25. After
bubbling of N2, the initial H_ value was recovered, suggesting
that the acidity or basicity of this DES can be switched reversibly
by bubbling CO2 and N2 through the solution alternately.
Obviously, the chemical nature of the HBDs has a strong
eect on the acid or basic strength of the corresponding DESs.
Fig. 4 shows the pH of several phosphonium-based DESs as a
function of the temperature.22 From these curves, it is clear
that the Me(Ph)3PBr/glycerol (1 : 1.75) DES has a neutral pH,
which did not vary signicantly with the temperature.
Conversely, the pH of the Me(Ph)3PBrCF3CONH2 (1 : 8)
eutectic mixture was very low (2.5 at 20 1C) and increased
when the temperature was raised. Note that when sugar-derived
Ionic conductivities of part DESs at dierent temperatures
Salts
HBD
Salt : HBD
(mol : mol)
Conductivity
(k, mS cm1)
Ref.
ChCl
ChCl
ChCl
ChCl
ChCl
ChCl
ChCl
ZnCl2
Bu4NBr
EtNH3Cl
EtNH3Cl
EtNH3Cl
AcChCl
Bu4NBr
Urea
EG
Glycerol
1,4-Butanediol
CF3CONH2
Imidazole
ZnCl2
Urea
Imidazole
CF3CONH2
Acetamide
Urea
Urea
Imidazole
1
1
1
1
1
3
1
1
3
1
1
1
1
3
0.199 (40 1C)

7.61 (20 1C)
1.05 (20 1C)
1.64 (20 1C)
0.286 (40 1C)
12 (60 1C)
0.06 (42 1C)
0.18 (42 1C)
0.24 (60 1C)
0.39 (40 1C)
0.688 (40 1C)
0.348 (40 1C)
0.017(40 1C)
0.24 (20 1C)
23
25
25
25
23
18
29
29
18
23
23
23
23
18
This journal is
:
:
:
:
:
:
:
:
:
:
:
:
:
:
2
2
2
3
2
7
2
3.5
7
1.5
1.5
1.5
2
7
Fig. 4 pH values for selected phosphonium-based DESs as a function

of temperature t in the range of 5 to 95 1C. (Reproduced with
permission from ref. 22. Copyright (2010) American Chemical Society.)
Chem. Soc. Rev.
View Online
polyols are used as HBDs in combination with ChCl, the

obtained DES always exhibits a neutral pH.19

3.7
Surface tension
Up to now, studies related to the surface tension of DESs have

been very scarce. Abbott et al. reported some data about the
surface tension of ChCl-based and ZnCl2-based DESs. Surface
tensions of ChCl/malonic acid (1 : 1) and ChCl/phenylacetic
acid (1 : 2) DESs were about 65.68 and 41.86 mN m1,
respectively.14 Additionally, surface tensions of ChClethylene
glycol (1 : 3), ChClglycerol (1 : 3) and ChCl1,4-butanediol
(1 : 3) eutectic mixtures were 45.4, 50.8, and 47.6 mN m1 at
20 1C, respectively.25 Surface tension of ZnCl2/urea (1 : 3.5)
DES was 72 mN m1, while the ZnCl2/acetamide (1 : 4) DES
has a smaller surface tension (53 mN m1 at 25 1C). The
ZnCl2/ethylene glycol (1 : 4) and ZnCl2/1,6-hexanediol (1 : 3)
DESs have surface tensions of 56.9 and 49 mN m1 at 25 1C,
respectively. All these values were larger than the surface
tensions of most of molecular solvents and comparable to
those of imidazolium-based ILs and high temperature molten salts,
e.g. 1-butyl-3-methylimidazolium tetrauoroborate ([BMIM]BF4,
38.4 mN m1 at 63 1C) and KBr (77.3 mN m1 at 900 1C).
Surface tension is also expected to follow a similar trend to
viscosity since it strictly depends on the strength of intermolecular interaction that governs the formation of DESs. In
particular, the surface tensions of various ChCl/glycerol DESs
showed a linear correlation with temperature.27 Additionally,
surface tension of the ChCl/glycerol DES decreases as the
ChCl concentration increases, supporting that addition of
ChCl to glycerol disrupts the extensive hydrogen bond network
of glycerol, as previously discussed for viscosity.
4. Dissolution and separation in DESs

4.1
CO2 solubility
It is now well established that many ILs have strong ability to

dissolve CO2. Similar to ILs, DESs consist predominantly of
ionic species, and thus also have interesting solvent properties
for high CO2 dissolution. Considering that combination of
CO2 with green DES systems has a great potential for a variety
of chemical processes (separation and purication of gas,
chemical xation of CO2, catalysis, etc.), studies on the CO2
solubility in DESs are of prime importance. Recently,
Han and co-workers determined the solubility of CO2 in a
ChCl/urea DES at dierent temperatures, pressures and with
dierent ChCl/urea molar ratio.32
The solubility of CO2 (x1) in ChCl/urea DES depends on
three factors: (1) x1 values increased with increase in the CO2
pressure (solubility of CO2 is more sensitive to the pressure in
the low-pressure range); (2) x1 values decreased with increase
in the temperature whatever the pressure and (3) the ChCl/
urea molar ratio also has a signicant eect on x1 values
(e.g. at the same temperature and pressure, the ChClurea
(1 : 2) eutectic mixture exhibits higher x1 values than DES
with a ChCl/urea molar ratio of 1 : 1.5 and 1 : 2.5).
Similar to the case of ILs, the gaseous phase can be assumed
to be pure CO2 due to the very low vapor pressure of DESs at
low temperatures (r60 1C). Thus, Henrys constants (kH) of
Chem. Soc. Rev.
CO2 in dierent DESs can be obtained. At 333.15 K, the

ChCl/urea (molar ratio 1 : 2.5) DES exhibited a kH value of
29.0 MPa. Because ChCl is hygroscopic, most of the ChClbased DESs always contain a small amount of water. Water
acts as an antisolvent that drives CO2 out from rich solutions,
thereby aecting the solubility of CO2. Recently, Wong and
co-workers studied the solubility of CO2 in ChCl/urea/H2O
DES at dierent temperatures (303, 308, and 313 K) and
Henrys constants and at a CO2 pressure of 0.1 MPa.33 Results
showed that the solubility of CO2 in the ChCl/urea (molar
ratio 1 : 2) DES decreased with increase in the water content.
Determination of the enthalpy of CO2 absorption demonstrated that at a DES/water molar fraction higher than 0.231,
the absorption of CO2 was endothermic. Below this molar
ratio, the CO2 absorption was exothermic. These data were
very helpful for the evaluation and development of a concentration swing absorptionstripping process for capturing CO2.
4.2 Dissolution of metal oxides
DESs are capable of donating or accepting electrons or
protons to form hydrogen bonds which confers them excellent
dissolution properties.34 For example, in a ChCl/urea
(1 : 2) DES at 50 1C, a large number of compounds can be
dissolved, including water-soluble inorganic salts (e.g. LiCl >
2.5 mol L1), salts that are sparingly soluble in water
(e.g. AgCl solubility = 0.66 mol L1), aromatic acids (e.g.
benzoic acid solubility = 0.82 mol L1) and amino acids
(e.g. D-alanine solubility = 0.38 mol L1).15 More interestingly,
DESs are also capable of dissolving various metal oxides,
thereby opening a green strategy for the separation and
recycling of metals, a key point in electrochemistry technology
(see Section 7). The dissolution and solubility of metal oxides
in DESs still remain poorly explored due to the lack of data in
comparable systems. In 2003, Abbott et al. rst demonstrated
the possibility of using DESs for the dissolution of metal
oxides.14 For instance, at 50 1C, the solubility of CuO in a
ChClurea eutectic mixture was 0.12 mol L1. Shortly after,
Abbott et al. investigated the solubility of three metal oxides
(ZnO, CuO, and Fe3O4) in dierent DESs. The employed
DESs were formed by mixing ChCl with dierent carboxylic
acids such as malonic, propionic and phenylpropionic acid. As
shown in Table 7, ZnO, CuO, and Fe3O4 are soluble to a
large extent in these DESs (0.0710.554 mol L1 at 50 1C).
However, notable dierences in solubilities were observed
according to the nature of DESs. For instance, Fe3O4 is highly
soluble in the ChCloxalic acid (1 : 1) eutectic mixture,
whereas it is nearly 20 times less soluble in the ChClphenylpropionic acid (1 : 2) DES. In contrast, CuO shows the opposite behavior, i.e. it is more soluble in ChClphenylpropionic
acid (1 : 2) than in the ChCloxalic acid (1 : 1) eutectic mixture.
Table 7 Solubility of ZnO, CuO, and Fe3O4 in three DESs at 50 1C
Solubility (mol L1)
DESs
CuO
Fe3O4
ZnO
ChCl/malonic acid
ChCl/oxalic acid
ChCl/phenylpropionic acid
0.246
0.071
0.473
0.071
0.341
0.014
0.554
0.491
>0.491
This journal is
View Online
Table 8
Metal oxides
mp/1C
Solubility /ppm
Al2O3
CaO
CuO
Cu2O
Fe2O3
Fe3O4
MnO2
NiO
PbO2
ZnO
2045
2580
1326
1235
1565
1538
535
1990
888
1975
o1
6
470
8725
49
40
493
325
9157
8466

Solubility of metal oxides in a ChCl/urea (1 : 2) at 60 1C
The metal solubility was determined using ICP-AES.
Oxides such as aluminates or silicates are, however, insoluble

in tested DESs. This dierence of solubility of metal oxides
in DESs can be used for the selective recovery of metals.
Note that metals such as copper can be recovered electrochemically from the DES with high current eciencies using
bulk electrolysis.
The solubility of metal oxides in a ChCl/urea (1 : 2) DES
was also explored. Solubility data at 60 1C were collected
and summarized in Table 8. Dissolution of metal oxides in
ChCl/urea DES is mainly governed by the complexation
abilities of urea and the chloride anion. The electrospray mass
spectrometry (MS) showed that a group of signals at m/z 174,
176, and 178, with an isotope pattern consistent with the
formation of the [ZnClOurea] anion, were observed when
ZnO was dissolved in a ChClurea system, pushing forwards
the coordination role of urea in the dissolution process.
Such phenomenon was also observed by UV-vis spectrometry
analysis in the case of CuO and CuCl2.
Abbott et al. also systematically studied solubilities of ZnO,
CuO, and Al2O3 in a DES formed between ChCl and thiourea.
Although ZnO and CuO were soluble in such DES, Al2O3
remained insoluble.35
This dierence of solubility of metal oxides in DES has been
successfully applied for the selective recovery of Zn and Pb
from a waste material produced by an electric arc furnace
(EAF). In particular, the ChClurea eutectic mixture was
capable of selectively extracting zinc oxide (solubility =
4288 ppm at 60 1C) and lead oxides versus iron and aluminium
oxides from waste of EAF. A similar result was reported using
less viscous (56 cP at 298 K) DES such as ChCl/ethylene
glycol/urea (molar ratio = 1 : 1.5 : 0.5).
A systematic study related to the solubility of transition
metal oxides of Period 4 of the periodic table in three dierent
DESs was reported by Abbott et al.36 In ChClmalonic acid
(1 : 1), ChClurea (1 : 2), and ChClethylene glycol (1 : 2)
eutectic mixtures, metal oxides with a high ionic nature such as
ZnO were highly soluble. Conversely, metal oxides with a
more pronounced covalent nature such as TiO2 were poorly
soluble in these DESs. As expected, the solubility of metal
oxides in DESs is strongly dependent on the temperature,
especially Cu2O and ZnO. FAB-MS spectrometry was also
used to identify the metal-containing species in the DES after
dissolution. In the cases of ChCl/malonic acid (1 : 1), CuO,
Cu2O, MnO, and ZnO gave predominantly chlorometalate
species of the form MClx.
This journal is
Owing to their ability to dissolve metal oxides, DESs have

become of great interest for surface cleaning, metallurgy, etc.
It has been discussed above that the dissolution process of
metal oxides in a ChClurea eutectic mixture involves the
formation of a metal complex with urea. Very recently, density
function theory (DFT) was employed to determine the extent
of molecular ionic character of urea in a DES and how urea in
its neutral and anion states binds with the surface of metal
oxides or metals.37 Quantum chemical calculations are proven
very ecient to determine the binding energy of neutral and
anionic urea with copper oxide and metallic copper, the main
complexes believed to participate in surface cleaning with
ChCl/urea (molar ratio 1 : 2) DES. These calculations
suggested that the hydrogen bond interactions between urea
and the chloride anion of choline maintain an open cluster
structure. Proton transfer can then occur with an increase of
the temperature or with metallic complex formation, leading
to more aggressive solvent action.
4.3 Drug solubilization
To date, explorations of the solubility properties of DESs were
mainly focusing on the dissolution of metal oxides. Studies on
the dissolution of organic macromolecules in DESs are very
scarce. Morrison et al. investigated the dissolution of several
poorly soluble drugs including benzoic acid, griseofulvin,
danazol, itraconazole and N-[4-[[6-[4-(triuoromethyl)phenyl]4-pyrimidinyl]oxy]-2-benzothiazolyl]acetamide (AMG517) in
ChCl/urea and ChCl/malonic acid DESs.38 Solubility was
measured in pure DESs, mixtures of DESs with water
(75 : 25 and 50 : 50 by weight), and pure water. Tested drugs
are 522 000 folds more soluble in pure DESs (i.e., ChCl/urea
and ChCl/malonic acid) than in pure water. For example,
the solubility of AMG517 in pure water was lower than
0.0001 mg mL1 vs. 0.01 mg mL1 and 0.4727 mg mL1 in
pure ChCl/urea and ChCl/malonic acid, respectively. In the
case of aqueous solution of DES, solubility of drugs was also
enhanced as compared to neat water. Note that a separate use
of aqueous solution of urea or ChCl or malonic acid did not
result in an increase of the solubility of drugs, highlighting the
particular behavior of eutectic mixtures for the dissolution of
drugs. Owing to their low toxicity, DESs are now emerging as
promising vehicles for oral dosing of rats during the early
development of pharmacokinetic investigations. Indeed, toxicity (oral lethal dose for rats) for urea, choline chloride and
malonic acid is 8471 mg kg1, 3400 mg kg1 and 1310 mg kg1,
respectively, while the toxicity prole for mice for urea, choline
chloride and malonic acid is 11 000 mg kg1, 3900 mg kg1
and 4000 mg kg1, respectively.
Moreover, it is noteworthy that recently the DESs have also
been proven to be promising anhydrous solvents for nucleic acids.
Hud and coworkers39 showed that the nucleic acids can form
several secondary structures that are reversibly denatured upon
heating in DESs. In our opinion, this work denitely provides a
new concept to widen the scope of DESs for life science.
4.4 Purication of biodiesel
Owing to their high polarity, DESs have also been used to
separate residual glycerol from raw biodiesel. Biodiesel is
Chem. Soc. Rev.

View Online
produced through a transesterication reaction of vegetable

oils either with methanol or ethanol. In this reaction, glycerol
is released as a side product. Conversely to biodiesel, glycerol
is highly polar. Hence, glycerol is commonly separated from
biodiesel by liquidliquid phase decantation. However, a nonnegligible amount of glycerol remains in the biodiesel phase,
thus requiring extra-treatments in order to reach the ASTM
specications prior to its use in vehicles. In this context,
Abbott et al.40 took benet of the ability of various quaternary
ammonium salts to form eutectic mixtures in the presence of
glycerol in order to extract residual glycerol from raw biodiesel.
Five quaternary ammonium salts including Pr4NBr, EtNH3Cl,
ClEtMe3NCl, ChCl, and AcChCl (acetylcholine chloride)
were employed and all of them were capable of forming
eutectic mixtures with glycerol. These DESs were miscible
with water and immiscible with biodiesel. Soy bean oil was
chosen as tested raw material because separation from glycerol
is known to be dicult in this case. Initially, pure quaternary
ammonium salts were directly added to raw biodiesel in order
to evaluate if a DES could be spontaneously formed with
residual glycerol contained in biodiesel. Unfortunately, this
approach failed.
Next, the authors decided to extract residual glycerol from
raw biodiesel with a quaternary ammonium saltglycerol
(1 : 1) eutectic mixture. In this case, the DES/biodiesel ratio
was adjusted in order to obtain, after extraction of residual
glycerol, an ammonium salt/glycerol molar ratio of 1 : 2
(sum of glycerol in the starting eutectic mixture with residual
glycerol contained in the biodiesel phase). By means of
1
H NMR analysis of the biodiesel recovered after treatment with
the ammonium salt/glycerol (1 : 1) DES, the authors observed a
signicant decrease of the content of glycerol in biodiesel,
showing that DES can be used for the purication of biodiesel.
Fig. 5 presents the evolution of the glycerol mole fraction in
an AcChCl (acetylcholine chloride)glycerol eutectic mixture
when mixed with raw biodiesel as a function of time.
Results showed that the eutectic mixture was saturated with
glycerol after 10 min of contact time, which corresponded to
the formation of an AcChClglycerol eutectic mixture in a
molar ratio of 1 : 2. At this stage, 99% of glycerol was
removed from biodiesel. According to the nature of the
Fig. 5 Glycerol mole fraction in an AcChClglycerol mixture in

contact with biodiesel containing glycerol as a function of time.
(Reproduced with permission from ref. 40. Copyright (2007) Royal
Society of Chemistry.)
Chem. Soc. Rev.
quaternary ammonium salts, the extraction eciency was

changed to some extent. For example, formation of glycerolbased DES with ammonium bromide such as Pr4NBr was
found to be less ecient than with ammonium chloride.
The higher extraction eciency observed with ammonium
chloride-based DES may be attributed to the higher electronegativity of the chloride anion. After extraction, quaternary
ammonium salts were partly separated from the saturated
DESs by recrystallisation from 1-butanol, although this
process was not very ecient. Similarly, Hayyan et al. showed
that ChCl/glycerol based DESs can also be used as a solvent
for extracting glycerol from palm oil-derived biodiesel in a
continuous mode.17 In such a process, a ChCl/glycerol molar
ratio of 1 : 1 was found to be the best composition for an
ecient extraction of residual glycerol.
Recently, other ChCl-based DESs have also been used for
the extraction of residual glycerol from biodiesel. For example,
ChCl/ethylene glycol and ChCl/2,2,2-triuracetamide DESs
were also found to be ecient.16 Best extraction eciency was
obtained using a ChClethylene glycol (1 : 2.5) or ChCl2,2,2triuracetamide (1 : 1.75) eutectic mixture together with a
DES/biodiesel ratio of 2.5 : 1 and 3/1, respectively. Phosphonium bromide based DESs were also used for the purication
of palm oil-derived biodiesel.21 DESs were obtained by mixing
methyl triphenyl phosphonium bromide with three dierent
HDBs such as glycerol, ethylene glycol, or triethylene glycol.
This study revealed that ethylene glycol and triethylene glycolbased DESs were very ecient for removing residual glycerol
from palm oil-derived biodiesel. Note that, in these cases, a
DES/biodiesel ratio of 0.75 : 1 was found to be optimum.
Interestingly, all tested DESs were also capable of reducing the
content of monoglycerides (MGs) and diglycerides (DGs)
contained in raw biodiesel, thus aording biodiesel with the
required ASTM specications.
5. Catalysis in DESs
In the eld of catalysis, the choice of the solvent is crucial. The
solvent not only allows a better contact between reactants and
catalysts but also determines the choice of work-up procedures
and recycling (including the catalyst) or disposal strategies. In
this context, the search of cheap and safe media for catalysis
has become a very important topic. Recently, ILs have
received considerable attention, especially for the stabilization
of nanoparticles, the immobilization of homogeneous catalysts, the catalytic conversion of renewable raw materials
(i.e. biomass, CO2), among others. Comprehensive reviews
covering this topic can be found in the current literature.41
Although fascinating results have been reported, ecological
and economical footprint of these ILs-based processes still
remains at an unacceptable level for an industrial application.
As mentioned earlier, DESs exhibit similar properties to ILs.
Hence, much eort is devoted to the use of DESs as cheap and
safe solvents for catalysis. In this section, advances reported in
the utilization of DESs for catalysis will be discussed.
5.1 Base-catalyzed reactions
In 2010, Shankarling and co-workers reported the electrophilic
substitution of 1-aminoanthra-9,10-quinone derivatives in the
This journal is
View Online

Scheme 2 Electrophilic substitution of 1-aminoanthra-9,10-quinone

derivatives in ChCl/urea (1 : 2). (Adapted from ref. 42.)
safe and cheap ChClurea (1 : 2) system.42 In particular, in the

presence of 2.5 eq. of bromine, dibrominated products
were obtained with a yield ranging from 84% to 95% at
80 1C (Scheme 2). As compared to traditionally-used organic
solvents such as methanol or chloroform, the reaction rate
was greatly improved in the ChClurea eutectic mixture.
Although no explanation was provided by the authors, one
may suspect that this rate enhancement might be attributed to
the basic nature of the DES and/or to the ability of urea to
stabilize transition states as previously observed for catalysis
in water.43
At the end of the reaction, products were selectively separated from the ChClurea (1 : 2) eutectic mixture by precipitation upon addition of water. Then, water was removed
under vacuum, thus allowing the ChClurea (1 : 2) system to
be recycled at least ve times without appreciable decrease of
reaction yields.
Later, the same group has reported the use of ChCl/urea
(1 : 2)-based DES for the synthesis of cinnamic acid via the
base-catalyzed Perkin reaction (Scheme 3).44 Owing to its
basic properties, the ChClurea (1 : 2) eutectic mixture was
found to be a solvent of choice for promoting this reaction.
From an equimolar mixture of benzaldehyde derivatives and
acetic anhydride heated at 30 1C in a ChCl/urea (1 : 2)-based
Scheme 3 Base-catalyzed synthesis of cinnamic acid derivatives in

ChCl/urea (1 : 2)-based DES. (Adapted from ref. 44.)
DES, a large library of cinnamic acids were obtained with

good to excellent yields (6292%).
As compared to the conventional route (benzaldehyde/
acetic anhydride/sodium acetate trihydrate in a molar ratio
of 1 : 2 : 3), the reaction proceeded at much lower temperature (30 1C vs. 140 1C) allowing saving 62% of energy
(estimated to 14.15 kJ g1 by calculation).
The basic nature of ChClurea (1 : 2) eutectic mixture
can also be used for catalyzing other reactions such as a
Knoevenagel reaction (Scheme 4). In this context, Sonawane
et al. have reported the synthesis of diphenylamine-based
chromophores in ChCl/urea (1 : 2) DES.45 In particular, they
have shown that a large library of valuable chromophores can
be synthesized with high yields (7595%) in ChCl/urea (1 : 2),
oering an attractive alternative route to lipases or imidazoliumbased ILs (Scheme 4). As mentioned earlier, this DES was
successfully recycled ve times thanks to the easy isolation of
the products of the reaction from the DES phase.
In 2009, B. Konig and co-workers reported that basecatalyzed DielsAlder reaction can be performed in L-carnitine
(obtained by fermentation from renewable bulk product)/urea
(2 : 3) melt in the presence of 5 mol% of proline as a basic
catalyst.46 After 4 hours of reaction at 80 1C, the DielsAlder
adduct was obtained with 93% yield, oering an alternative
to Sc(OTf)3 traditionally used as a Lewis acid catalyst or
imidazolium-based ILs, supercritical CO2 and water used as
solvent (Scheme 5).
Very recently, Coulembier and co-workers reported the
copolymerization of lactide (LA) and 1,3-dioxan-2-one (TMC)
in the presence of 1,8-diazabicyclo[5.4.0]undecec-7-ene (DBU)
as a basic catalyst.47 Although use of lactide is attractive for
the fabrication of safer and biodegradable polymers, assistance of potentially toxic organic solvents required for the
solubilization of lactide dramatically decreases the environmental benet of using this monomer. Within this context,
the authors have found that LA and TMC were capable of
forming a DES at 21.3 1C when mixed in a ratio of 1 : 1. At
room temperature and in the presence of benzyl alcohol as
initiator and DBU as catalyst, the resulting poly(lactide)
(PLLA) chain started to nucleate in the eutectic and to crystallize
out of the melt, limiting the growing of PLLA (15 500 g mol1).
Interestingly, when the medium was slightly heated (up to
60 1C) or rapidly solubilized in dichloromethane when the
Scheme 4 Base-catalyzed Knovenagel in the ChClurea (1 : 2) system. (Adapted from ref. 45.)
This journal is
Chem. Soc. Rev.
View Online

Scheme 5 Base-catalyzed DielsAlder reaction in the

urea melt. (Adapted from ref. 46.)
L-carnitine/
Scheme 6 Co-polymerization of the LATMC eutectic mixture in the

presence of DBU as catalyst. (Reproduced with permission from
ref. 47. Copyright (2007) Royal Society of Chemistry.)
Scheme 7 Mono-N-alkylation of aniline with hexyl bromide in ChClderived DES. (Adapted from ref. 48.)
PLLA chain started to crystallize out of the melt, incorporation of TMC occurred (Scheme 6).
In 2011, Shankarling and co-workers reported that ChCl/
urea and ChCl/glycerol DESs can be used as both catalyst and
solvent for the mono-N-alkylation of aromatic amines.48 In
particular, the ChClurea eutectic mixture was more ecient
than the ChClglycerol DES, presumably due to its higher
basicity (Scheme 7). This methodology was tolerant to a wide
range of substrates since various aromatic amines and alkyl
bromides were successfully reacted aording, at 50 1C, the
corresponding mono-N-alkylated amines with 7089% yield.
At the end of the reaction, products were selectively extracted
from the ChClurea eutectic mixture by liquidliquid phase
extraction using ethylacetate. Hence, the authors successfully
recycled the DES at least 5 times without noticeable decrease
of yield, thereby oering an alternative route to lipasecatalyzed reaction for which a deactivation of the enzyme
was observed cycle after cycle.
5.2
Acid-catalyzed reactions
Acid-catalyzed dehydration of hexoses to 5-hydroxymethylfurfural (HMF) has gained considerable attention in recent
years since HMF is a valuable molecule platform, especially
for the fabrication of safer polymers and fuel additives.49 In
most of the works, acid-catalyzed dehydration of hexoses to
HMF is achieved in imidazolium-based ILs for three reasons:
(1) imidazolium-based ILs can dissolve large amounts of
Chem. Soc. Rev.
hexoses, (2) imidazolium-based ILs can dilute released water,

thus limiting the side rehydration of HMF to levulinic and
formic acids and (3) HMF can be conveniently separated from
imidazolium-based ILs by liquidliquid phase extraction.
However, as mentioned earlier, the price and toxicity of
imidazolium-based ILs is a strong limitation for the commercialization of this process. To date, much eort has been paid
to dehydrate hexoses in a more rational way using cheap and
safe DESs.
In 2009, Konig and co-workers reported the acid-catalyzed
dehydration of fructose to HMF in choline chloride/urea
(1 : 2)-based DES.10 In this work, a high concentration of
carbohydrates (40 wt%) was used. In the presence of an acid
catalyst (10 mol% CrCl2, CrCl3, FeCl3, AlCl3 or Amberlyst 15),
HMF was unfortunately obtained with low yields (o30%)
due to side reaction between fructose and urea. When tetramethylurea was used instead of urea, side reactions were
suppressed and HMF was obtained with 89% yield in the
presence of 10 mol% of FeCl3. However, the toxicity and
problem of separation arising from the use of TMU represent
two serious limitations. These results are in accordance with a
previous work of Han and co-workers who have reported that
basic DES (ChCl/urea) and Lewis acid (ZnCl2, CrCl3) in ChCl/
metal chlorides-based DES were poorly ecient in the dehydration of fructose to HMF.50 In order to overcome these problems,
B. Konig and co-workers have next investigated the production
of HMF in a eutectic mixture composed of carbohydrates and
choline chloride. These high concentrated melts exhibit a low
melting point (o80 1C), a low viscosity and a low toxicity.
In Table 9 are summarized the yields of HMF obtained
from various melts. Except in the presence of ZnCl2, HMF
was obtained with 4060% yields from melts composed of
ChCl and fructose or inulin. Solid catalysts were also capable
of promoting the dehydration of fructose to HMF (4049%
yield). From inulin, one should mention that montmorillonite
is however less ecient than homogeneous catalysts. Conversion
of glucose to HMF is more challenging and requires rst an
isomerization step to fructose before dehydration to HMF. As
previously observed by Zhao et al. in imidazolium-based ILs,51
Table 9 Acid-catalyzed dehydration of carbohydrates to HMF in
various melts
Yield of HMF (%) obtained from
Catalyst
Fructose/
Inulin/
Glucose/
Sucrose/
ChCl (2 : 3), ChCl
ChCl (1 : 1), ChCl (1 : 1),
70 1C
(2 : 3) nd 80 1C
80 1C
FeCl3
ZnCl2
CrCl2
CrCl3
pTsOH
Sc(OTf)3
A15
Montmorillonite
59
8
40
60
67
55
40
49
55
3
36
46
57
44
54
7
15
6
45
31
15
9
9
7
27
6
62
43
25
28
27
35
10 mol% of homogeneous catalyst or 5 wt% for solid catalyst, 100 1C.
This journal is

View Online
chromium-based catalysts were found to be the most ecient

in concentrated carbohydrate-derived DESs aording HMF
with 3145% yield and 4362% yield from glucose and
sucrose, respectively.
Han and co-workers have reported that HMF can also be
produced in ChCl-derived DES without assistance of metal
chloride-based catalysts, thus oering an even more attractive
strategy from the view point of green chemistry.50 In particular, the authors have shown that more than 76% yield of
HMF (at 80 1C, 1 h, ratio DES/fructose = 5) can be obtained
by dehydration of fructose in Bronsted DES composed of
ChCl and citric acid, a cheap and renewable carboxylic acid
readily obtained in large scale by fermentation of agricultural
wastes. Note that other renewably sourced carboxylic acids
such as oxalic and malonic acids were also eligible. Owing to
the low solubility of HMF in ChCl/citric acid, the process can
be performed in a continuous mode (biphasic system) using
ethylacetate as an extraction solvent aording HMF with 91%
yield. It should be noted that a slight decrease of the HMF
yield was observed upon performing recycling experiments.
The authors ascribed this drop of yield to the accumulation of
water in the reaction media that aected the selectivity of the
process (presumably due to the dominant acid catalyzed
rehydration of HMF to levulinic and formic acid). After
drying the ChClcitric acid eutectic mixture, the initial yield
of HMF was recovered, further demonstrating the stability of
ChCl/citric acid-derived DES in such conditions.
Later, the same authors extended the scope of this process
to the tandem depolymerization/dehydration of inulin, a biopolymer of fructose, to HMF.52 In particular, in ChCloxalic
acid and ChCl/citric acid, HMF was produced with 56% and
51% yield, respectively (80 1C, 2 h, 16 mol% of fructose in
DES) (Scheme 8). In these systems, water plays a pivotal role
by governing the depolymerization of inulin to fructose. For
this reason, DESs were formed using hydrated oxalic and citric
acids. Note that yields of HMF can be slightly improved by
addition of water to the system. The authors dened R as the
molar ratio of the additional water to fructose units in inulin.
The HMF yield was optimal (nearly 60%) with R = 20 and
25 from ChCl/oxalic acid and ChCl/citric acid, respectively.
As described above, in a biphasic system (ChCloxalic acidethylacetate), the yield of HMF can be slightly improved up to
64%. After separation of the ethylacetate phase containing
HMF, the ChCl/oxalic acid was recycled at least 6 times
without appreciable loss of HMF yield.
In a similar way, De Oliveira Vigier et al. reported that
betaine hydrochloride (BHC), a side product of the sugar beet
industry, can be used as a renewably sourced Bronsted acid in
combination with ChCl and water for the production of HMF
from fructose and inulin.53 In a ternary mixture ChCl
BHCwater (10/0.5/2), HMF was produced with 63% yield
(at 130 1C from 40 wt% of fructose). As observed by Han and
co-workers, when the reaction was performed in a biphasic
system using methylisobutylketone (MIBK) as an extraction
solvent, HMF was recovered with a purity higher than 95%
and an isolated yield of 84% (from 10 wt% of fructose),
further demonstrating that these systems similarly behave like
traditional imidazolium-derived ILs (Scheme 8). Here also, the
ChClBHCwater system was successfully recycled 7 times. In
the same work, the authors have shown that the dehydration
of fructose to HMF can also conveniently take place in a
BHCglycerol (1 : 1) mixture. Although 51% yield of HMF
was obtained at 110 1C (from 10 wt% of fructose), extraction
of HMF from the BHC/glycerol medium remained very
dicult due to the very high solubility of HMF in this mixture.
One should comment that the recent progress reported in
the eld of ChCl-derived DESs now oers suitable ways for
the catalytic conversion of valuable renewable raw materials
such as starch, lignin and cellulose.54 It makes no doubt
that DESs will denitely contribute to the catalytic conversion of lignocellulosic biomass in a more rational way and
thus to the emergence of new bio-based chemicals in a close
future.55
Acid-catalyzed reactions in DESs have been also explored
to access higher value added chemicals. In 2009, Zou and
co-workers reported the a,a-dichlorination of acetophenone
derivatives in an acidic DES composed of ChCl and p-toluene
sulfonic acid (p-TsOH) mixed in a ratio of 1 : 1.56 When the
ratio DES/acetophenone was 2 : 1, the a,a-dichlorinated
adduct was obtained with 86% yield at room temperature
and in the presence of 1,3-dichloro-5,5-dimethylhydantoin as a
chlorinating agent (Scheme 9). At the end of the reaction, the
a,a-dichlorinated adduct was easily and selectively extracted
from the ChCl/pTsOH DES using methyltertiobutylether as
an extraction solvent, thereby allowing the authors to successfully recycle such DES at least 5 times.
In 2002, Davies and co-workers have reported the possible
DielsAlder reaction in ChCl/MCl2 (M = Zn or Sn).57 The
Lewis acid nature of these eutectic mixtures signicantly
enhanced the reaction rate. Various dienes and dienophiles
were reacted in ChCl/MCl2, aording the DielsAlder adduct
Scheme 8 Acid-catalyzed dehydration of inulin and fructose in

ChCl-derived DES.
Scheme 9 a,a-dichlorination of acetophenone in ChCl/pTsOH.

(Adapted from ref. 56.)
This journal is
Chem. Soc. Rev.
View Online

Table 10 DielsAlder reaction in various carbohydrate-derived melts
Scheme 10 DielsAlder reaction in Lewis acid ChCl/MCl2 (M = Zn

or Sn). (Adapted from ref. 57.)
with 8591% yield along with an endo/exo selectivity in the

range of 83 : 17 to 97 : 3 (Scheme 10).
As compared to imidazolium-based ILs, ChCl/MCl2 was
not sensitive to the presence of water. For instance, the same
reaction can be successfully performed in a mixture ZnCl2
ChClH2O (2 : 1 : 2), resulting in a decrease of the medium
viscosity. Products of the reaction were not soluble in the
ChClMCl2 eutectic mixture. Hence, products can be conveniently isolated by simple decantation allowing, the recycling
of the ChCl/MCl2 DES.
Very recently, Azizi and co-workers reported the acidcatalyzed synthesis of bis(indolylmethane) in a ChCl/SnCl2
(1 : 2) DES (Scheme 11).58 In such media a broad range of
indole and aldehydes derivatives were successfully converted
to the desired bis(indolyl)methane with moderate to excellent
yields. Note that other ChCl-derived DESs were also eligible
for this reaction.
In 2005, Imperato et al. investigated the DielsAlder reaction in various melts composed of renewably sourced carbohydrates (or derived polyols) such as fructose, maltose,
lactose, mannitol, glucose and sorbitol in combination with
either urea or N,N-dimethylurea (DMU).59 In a fructose/
DMU (7 : 3) melt, the reaction proceeded well and the Diels
Alder adduct was obtained with a quantitative yield after
8 h of reaction at 71 1C. As shown in Table 10, other
carbohydrate-derived melts were found to be very ecient
for promoting the DielsAlder reaction. In all cases, 72100%
yields were obtained while the endo/exo selectivity (2.7 : 1 to
5 : 1) was comparable to what was previously reported for
other green solvents such as supercritical solvent, water, or
imidazolium-based ILs. Addition of 10 mol% of a Lewis acid
such as Sc(OTf)3 to the sorbitol/DMU/NH4Cl melt increases
the endo/exo selectivity.
Scheme 11 Synthesis of bis(indolyl)methane in acid derived ChCl

DESs. (Adapted from ref. 58.)
Chem. Soc. Rev.
Melt
T/1C
Yield (%)
Endo/exo
ratio
Fructose/DMU (7 : 3)
Maltose/DMU/NH4Cl (5 : 4 : 1)
Lactose/DMU/NH4Cl (6 : 3 : 1)
Mannitol/DMU/NH4Cl (5 : 4 : 1)
Glucose/urea/CaCl2 (5 : 4 : 1)
Sorbitol/DMU/NH4Cl (7 : 2 : 1)
Sorbitol/DMU/NH4Cla (7 : 2 : 1)
71
83
88
89
75
67
67
Quant.
79
83
74
76
Quant.
Quant.
2.9
3.3
3.6
2.7
3.2
5.0
6.0
:
:
:
:
:
:
:
1
1
1
1
1
1
1
In the presence of 10 mol% of Sc(OTf)3.
Eciency of these carbohydrate-derived DESs was also

successfully demonstrated using butyl acrylate as another
dienophile.59 At the end of the reaction, products of the
reaction can be separated by decantation (upon addition of water)
or distillation, oering the possibility to reuse these carbohydratederived DESs.
In 2011, del Monte and co-workers reported a frontal
polymerization reaction using acid DES as a medium but also
as a reservoir of monomer.60 In particular, acrylic acid and
methacrylic acid form a DES when mixed with ChCl in a ratio
of 1 : 6 and 2 : 1, respectively. These DESs exhibit high
viscosities (115 cP and 193 cP), which are helpful to stabilize
the polymerization front. Upon addition of benzolyl chloride
(thermal initiator) and ethyleneglycol (crosslinker), the frontal
polymerization takes place. Under these conditions, conversion
of acrylate and methacrylate are 75% and 85%, respectively.
After dilution in water, the resulting poly(acrylic acid) was
easily recovered and the ChCl was recycled. Proceeding on
the same line, Serrano et al. have attempted the synthesis of
poly(octanediol-co-citrate) elastomers loaded with lidocaine,
an attractive anti-inammatory compound.61 In this work,
1,8-octanediol and lidocaine were used as components of the
DES. Here, the DES played multiple roles (1) as a reservoir
of monomer (1,8-octanediol), (2) as a reservoir of active
pharmaceutical ingredient (lidocaine) and (3) as a solvent for
the dissolution of citric acid used as an initiator in this
polymerization reaction.
5.3 Transition-metal-catalyzed reactions
5.3.1 Catalytic CC bond coupling. In 2006, Konig and
co-workers investigated the palladium-catalyzed Suzuki coupling
of phenyl boronic acid with aryl bromides in dierent carbohydratesureainorganic salts eutectic mixtures.62 In all tested
melts, quantitative conversion was observed and biarylated
products were isolated with 7898% yields (Scheme 12). At the
end of the reaction, products were isolated by liquidliquid
phase extraction with pentane (after dilution in water).
Next, the same group highlighted that palladium-catalyzed
Heck coupling can be successfully performed in low melt
composed of D-mannose and N,N-dimethylurea (DMU) in a
ratio of 3 : 7.46 In the presence of homogeneous catalysts such
as Pd(OAc)2 or PdCl2(PPh3)2, the cross-coupling was achieved
with good to excellent yields (7791%, Scheme 13). As compared
This journal is
View Online

Scheme 12 Palladium-catalyzed Suzuki coupling in various carbohydrateureainorganic salts eutectic mixtures. (Adapted from ref. 62.)
Scheme 15 Palladium-catalyzed Stille coupling of aryl bromide and

iodide with alkyl and aryl stannate in polyol/DMU/NH4Cl melts.
(Adapted from ref. 63.)
Scheme 13 Palladium-catalyzed Heck coupling in D-mannose/DMU

melts. (Adapted from ref. 46.)
to the traditionally used imidazolium-based ILs ([BMIM]PF6),

lower reaction temperature (80 1C vs. 120 1C) and higher
reaction rate were observed. In the presence of a heterogeneous catalyst such as Pd/C, the reaction rate was dramatically
lowered, which was attributed to an increase in the reaction
viscosity.
In such a case, the authors found that assistance of ultrasound allowed enhancing the reaction rate by a factor of 4.3.
Catalytic Heck coupling can also be conveniently performed
in low melting melt composed of L-carnitine and urea mixed in
a ratio of 2 : 3.46 The viscosity of such a melt, however, is
slightly higher than that of other melts based on renewable
feedstocks, which unfortunately lowers the reaction rate.
Sonogashira cross coupling is catalyzed by palladium but
assistance of copper is generally required. Interestingly, in the
presence of the PdCl2(PPh3)2 in a D-mannose/DMU melt,
the Sonogashira coupling takes place without assistance of
copper, aording the Sonogashira adduct with 6179% yield
(Scheme 14).
Imperato et al. have investigated the Stille cross-coupling
in various sugarureasalt melts.63 In a typical procedure,
iodobenzene was rst coupled at 90 1C with tetravinyltin,
tetramethyltin and tetrabutyltin in the presence of the tris(dibenzylideneacetone)dipalladium(0) chloroform complex as
palladium source and AsPh3 as ligand. Maltose/DMU/NH4Cl
was found to be the most promising eutectic mixture for the
catalytic transfer of butyl and vinyl groups from tin to
Scheme 14 Sonogashira coupling in D-mannose/DMU melts. (Adapted

from ref. 46.)
This journal is
iodobenzene, aording the targeted alkylaryl with 42% and

100% yield, respectively. From tetramethyltin, the highest
yield (90%) was obtained in the mannitol/DMU/NH4Cl melt
(Scheme 15). The authors highlighted that DMU can be
replaced by urea without signicant decrease of yields, thereby
oering an even cheaper and greener route. As compared to
imidazolium-based ILs, no biphenyl was produced in the melt.
However, formation of benzene was noticed.
Synthesis of biaryl by Stille coupling also smoothly proceeds
in polyol/DMU/NH4Cl (with polyol = lactose, maltose,
mannitol and sorbitol) from aryl bromide and tributylphenylstannate. After 6h of reaction at 90 1C in the presence of
1 mol% of tris(dibenzilideneacetone)dipalladium(0) and
4 mol% of AsPPh3 as ligand, desired biaryl derivatives were
produced with 85100% yield. The amount of catalyst can be
lowered up to 0.001 mol% without signicant alteration of the
reaction eciency (TON = 87 000). More importantly, the
recycling of the palladium-based catalyst is possible because
products can be conveniently and selectively isolated from
the catalytic phase by precipitation after addition of water,
thereby oering an environmentally friendly route as compared
to dimethylformamide or dioxane traditionally used as extraction solvents in such a coupling reaction.
5.3.2 Copper-catalyzed azide alkyne 1,3-dipolar cycloaddition.
The CuI-catalyzed Huisgen 1,3-dipolar cycloaddition is a very
useful synthetic tool in organic synthesis. In this context,
D-sorbitol (hydrogenated form of glucose)/urea/NH4Cl melt
(7 : 2 : 1) has been used as a solvent owing to its high stability
in the presence of a strong nucleophile such as sodium azide.46
After 5 h of reaction at 85 1C in the presence of 5 mol% of
CuI, the 1,4-substituted 1,2,3-triazoles were obtained with
93% yield (Scheme 16). More importantly, the azide formation
and cycloaddition can be performed in a one-pot process (from
alkyne, benzyl bromide and sodium azide) in D-sorbitol/urea/
NH4Cl without aecting the reaction yield and allowing
reduction of the number of synthetic steps (Scheme 16).
As described above for DielsAlder reaction, click chemistry
can also be successfully performed in L-carnitineurea eutectic
mixture.46 Under similar conditions, the reaction rate was
slightly enhanced in L-carnitine/urea (96% after 4 h of reaction
vs. 93% after 5 h of reaction in D-Sorbitol/urea/NH4Cl)
presumably due to the stabilization of CuI by L-Carnitine as
previously suggested by Ma and co-workers with proline.64
Chem. Soc. Rev.
View Online
Table 11 Yield of butylvalerate obtained by transesterication of
ethyl valerate by butanol at 60 1C in the presence of various enzymes

Scheme 16 Cu-catalyzed azide-alkyne 1,3-dipolar cycloaddition in

D-sorbitol/urea/NH4Cl or L-carnitine/urea melts. (Adapted from ref. 46.)
Scheme 17 Catalytic hydrogenation of methyl a-cinnamate in citric

acid/DMU (2 : 3). (Adapted from ref. 62.)
However, the one-pot reaction is more ecient in D-sorbitol/

urea/NH4Cl than in L-carnitine/urea due to the higher reactivity
of the latter melt (55% yield vs. 91% in D-sorbitol/urea/NH4Cl).
5.3.3 Hydrogenation reaction. In 2006, Konig and
co-workers have reported the hydrogenation of methyl
a-cinnamate in various carbohydrate/urea melts in the
presence of Wilkinsons catalyst.62 Among all tested melts,
the citric acid/DMU (2 : 3) was the most ecient eutectic
mixture aording the hydrogenated product in a quantitative
yield at 90 1C and under 1 atm of H2 (Scheme 17). Although
some of tested eutectic mixtures were chiral (sorbitol/DMU/
NH4Cl (7 : 2 : 1) or mannitol/DMU/NH4Cl (5 : 4 : 1)), no
asymmetric induction was observed.
5.4
Biocatalysis in DESs
Utilization of DES for biotransformations has not been

extensively investigated because strong hydrogen bond donors
such as urea are known to denature proteins.65 In 2008,
Kazlauskas and co-workers reported the rst example of
biocatalysis in various DESs.66 In this work, the authors have
investigated the activity of enzymes in the transesterication of
ethyl valerate with butanol. Although poorly stable in an
aqueous solution of ChCl (5 mol L1) and urea (10 mol L1),
enzymes were found to be stable in a ChCl/urea DES. This
remarkable stability was ascribed by the authors to the
hydrogen bond network of DES that lowered the chemical
reactivity of the DES components towards enzymes. As shown
in Table 11, activity of enzymes in selected DES was similar to
that observed in toluene. In particular, use of ChCl/glycerol or
ChCl/urea DESs in the presence of lyophilized Candida
antarctica lipase B (CLAB) or its immobilized form on acrylic
resin (iCLAB) was the most ecient combination leading to
more than 90% conversion of ethyl valerate to butyl valerate.
Note that activity of iCLAB in ChCl/urea (20 mmol h1 mg1)
or in ChCl/glycerol (50 mmol h1 mg1) was also found to be
comparable and even higher than those collected in imidazoliumbased ILs such as [BMIM]NTf2 (24 mmol h1 mg1) or
Chem. Soc. Rev.
Solvent
iCALBa
CALBb
CALAc
PCLd
ChCl/acetamide
ChCl/glycerol
ChCl/malonic acid
ChCl/urea
Toluene
23
96
30
93
92
96
96
58
99
92
0.5
70
0.7
1.6
76
0.0
22
0.0
0.8
5.0
Novozym 435 (Candida antarctica lipase B immobilized on acrylic resin).

Roche chirazyme L-2 (lyophilized Candida antarctica lipase B).
c
Roche chirazyme L-5 (lyophilized Candida antarctica lipase A).
d
Amano PS (lyophilized burkholderia (formerly pseudomonas) cepacia
lipase).
b
[BMIM]BF4 (7 mmol h1 mg1), further demonstrating the

potential of DESs for biotransformations.
Interestingly, in ChCl/glycerol DES, side transesterication
reaction between ethyl valerate and glycerol occurred to a very
low extent (o0.5% of glyceryl esters), further demonstrating
the lower reactivity of glycerol when involved in the formation
of a DES. Next, use of ChCl/urea and ChCl/glycerol was
successfully extended to the biocatalytic aminolysis of ethyl
valerate with butylamine and to the ring opening of styrene
oxide. Finally, the authors pointed out that ChCl/urea and
ChCl/glycerol DESs were also suitable co-solvents with water
for hydrolase-catalyzed reactions. In this case, DESs enhanced
the reaction rate up to 20 times.
Positive eect of a DES as a co-solvent on the hydrolasecatalyzed reaction rate was later conrmed by Widersten and
co-workers in the hydrolysis of 1S, 2S-2-methylstyrene epoxide.67
Among all tested DESs, the ChClglycerol eutectic mixture
was the most ecient medium. In this case, 50% of the relative
activity of a potato epoxide hydrolase was indeed retained in
the presence of 60% of ChCl/glycerol in an aqueous solution
of sodium phosphate (0.1 M). At higher concentration of
ChCl/glycerol DES, a loss of activity was observed. In the
presence of ChClglycerol eutectic mixture, the regioselectivity
was improved and the ring opening at the benzylic position
became dominant. More importantly, the ChClglycerol eutectic
mixture was capable of dissolving 1.5 times more epoxide than
the phosphate buer without aecting the optimal conversion
rate, further demonstrating the potential oered by such DES
for biocatalysis.
In 2011, Zhao and co-workers reported the use of DES
based on choline acetate (ChOAc) and glycerol as a renewable
hydrogen-bond donor for lipase-catalyzed transesterication
reaction.68 The main advantage of glycerol/choline-derived
DES stems from their reduced viscosity as compared to
the ChClurea system (80 mPa s vs. 120 mPa s at 50 1C).
Additionally, the ChOAcglycerol eutectic mixture is much
less hygroscopic than ChClurea. One should also comment
that viscosity and hygroscopicity of the ChOAcglycerol
eutectic mixture are, however, still higher than that of a
hydrophobic imidazolium-based ILs such as [BMIM]NTf2.
In a rst set of experiments, the authors have investigated
the transesterication of ethyl sorbitate with 1-propanol
This journal is
View Online

Table 12 Activity and selectivity of Novozyms 435 in the transesterication of ethylsorbate with 1-propanol
Solvent
Activity/mmol min1 g1
Selectivity (%)
t-Butanol
1-Propanol
Glycerol
ChCl/urea (1 : 2)
ChCl/glycerol (1 : 2)
ChOAc/glycerol (1 : 2)
ChOAc/EG (1 : 2)a
ChOAc/glycerol (1 : 2)
0.57
0.10
0.71
1.00
1.12
0.21
0.07
1.02
>99
>99
38
>99
45
40
12b
99
EG = ethylene glycol.
selectivity.
EG is reactive explaining the lower
catalyzed by Novozyms 435 (Candida antarctica lipase B

immobilized on acrylic resin) in various DESs. Among tested
DESs, the highest initial rate (B1 mmol min1 g1) and
selectivity (>99%) were obtained in ChCl/urea and ChOAc/
glycerol DESs. When the reaction was performed in neat
glycerol, t-butanol or 1-propanol, the activity of enzyme was
lower, indicating the superior performances of the ChOAc/
glycerol DES (Table 12).
A decrease of the ChCl/glycerol mass ratio from 1 : 2 to
1 : 1 resulted in a decrease of the lipase activity. This phenomenon was ascribed by the authors to the higher concentration
of the chloride anion in the melt resulting in the destabilization
of lipase. Remarkably, in a ChOAc/glycerol (1 : 1.5) DES, the
lipase was highly stable since Novozyms 435 maintained 92%
and 50% of its activity after 48 h and 168 h of pre-incubation,
respectively, showing the potential oered by this cheap and
biodegradable medium for biotransformations. Note that no side
transesterication reaction with the glycerol or cholinium cation
was observed in agreement with the work of Kazlauskas and
co-workers, who have showed that, in a ChCl/glycerol DES, the
reactivity of glycerol was 600 times lower than that of 1-butanol.66
In continuation of their eorts, the same group next
investigated the methanolysis of Miglyols oil 812, a mixture
of triglycerides of caprylic acid and capric acid. After 1 h of
reaction at 50 1C, 82% conversion was achieved in a ChOAc/
glycerol (1 : 1.5) DES containing 1.0 vol% of water and 20 vol%
of methanol. Nearly complete conversion was observed after
3 h of reaction whereas 24 to 96 h were required with
traditionally used imidazolium-based ILs, showing the highest
compatibility of ChOAc/glycerol DES for lipase.
Later, Zhao et al. reported that proteases, known to be less
stable in non-aqueous medium than lipases can also be
successfully used in choline acetate (ChOAc)/glycerol and
ChCl/glycerol DESs.69 Such DESs have been preferred to
ChCl/urea owing to their lower viscosity and because glycerol
is less denaturant than urea for proteases. In order to highlight
the potential of the cholineglycerol eutectic mixtures for
biotransformations, the protease-catalyzed transesterication
of N-acetyl-L-phenylalanine ethyl ester with 1-propanol has
been chosen as a representative model reaction. This reaction
involves two stages: (1) formation of an acyl-enzyme intermediate
This journal is
Table 13 Activities of subtilisin and a-chymotrypsin in glycerolderived DESs
Solvent
Proteasea
Water
Sel.
content Activity/
(v/v)% mmol min1 g1 (%)
t-Butanol
ChOAc/glycerol (1 : 1.5)
S/Chit
S/Chit
S/Chit
S/Chit
Free a-C
a-C/Chit
a-C/Chit
S/Chit
2
2
3
4
2
2
3
3
0.50
0.42
0.40
0.90
0.028
0.031
0.75
2.90
29
99
99
99
99
99
99
98
50 1C, S = subtilisin, a-C = a-chymotrypsin, Chit = chitosan.
followed by (2) a competition between transesterication and

hydrolysis. All reactions were performed at 50 1C either in
ChOAc/glycerol or ChCl/glycerol DESs in the presence of
cross-linked proteases (subtilisin and a-chymotrypsin), immobilized on chitosan. As shown in Table 13, the best results were
obtained in ChCl/glycerol (1 : 2) with 3 vol% of water using
subtilisin on chitosan. Under such conditions, activity of the
protease reached 2.9 mmol min1 g1 along with the formation
of the desired propyl ester with 98% selectivity, indicating that
glycerol-derived DESs were very attractive for biocatalytic
reactions involving more sensitive enzyme than lipase. As
compared to t-butanol used as a reference solvent, ChCl/
glycerol DES provided much better results in terms of activity
and selectivity. Interestingly, as observed above, glycerol seems
to be chemically inert. Although protease can be denatured by an
anion such as chloride or acetate, their eect is dramatically
lowered in a DES due to the presence of glycerol which tends to
form strong hydrogen bonds with these anions.
It is noteworthy that in 2010, Gutierrez et al. have reported
the use of a freeze-drying process for the ecient incorporation of enzymes in ChCl/glycerol (1 : 2) DES without altering
their integrity and viability.70 It is our opinion that this work
denitely opens a promising route to widen the scope of DESs
for biotransformations.
The remarkable stability of enzymes in DESs has been recently
highlighted by Verpoorte and co-workers in a scientic correspondence. In particular, the authors have hypothesized that
the formation of natural DESs from chemicals that are present
at high concentration in living cells may contribute to explain
(1) mechanisms and phenomena that are nowadays dicult to
understand and (2) the resistance of living organisms under
extreme conditions.71
6. Organic synthesis in DESs

In the eld of organic synthesis, the search for a green solvent is also
of great interest and aims at reducing the use of toxic chemicals.
Chem. Soc. Rev.
View Online

Scheme 18 Example of Biginelli reaction performed in acid L-(+)-tartaric

acid/DMU (3 : 7) DES. (Adapted from ref. 72.)
In this context, Gore et al. reported the multicomponent

synthesis of valuable biologically active dihydropyrimidinone
(DHPM) in acidic DESs.72 This work aims at by-passing the
traditional use of Bronsted and Lewis acids which dramatically impact the economical and ecological footprint of this
reaction. DHPM was synthesized from urea, aldehyde and
b-ketoesters (Biginelli reaction, Scheme 18). Hence, urea was
used in this example not only as a reactant but also as a
component of the DES. For instance, in a citric acid/DMU
(2 : 3) DES, p-4-nitrobenzaldehye, ethylacetoacetate and
DMU were selectively assembled at 65 1C to the desired
DHPM which was obtained with 90% yield. An even higher
yield (96%) was reported in a L-(+)-tartaric acid/DMU
(3 : 7) DES.
This methodology exhibits a very broad substrate scope and
many aldehydes and b-ketoesters were successfully assembled
in L-(+)-tartaric acid/DMU (3 : 7), aording DHPM with
good to excellent yields. Note that in L-(+)-tartaric acid/ChCl
(1 : 1), thiourea and 3-hydroxybenzaldehyde smoothly reacted
with ethylacetoacetate to produce an anticancer drug named
monastrol with 86% yield. Finally, the authors highlighted
that masked aldehydes can also be used in the L-(+)-tartaric
acid/DMU melt for the production of DHPM.
Multicomponent reaction can also take place in other
carbohydrate-derived melts. In this context, Zhang et al.
reported the synthesis of quinazoline derivatives via a one-pot
three component reaction of 2-aminoaryl ketones, aldehydes
and ammonium acetate in various carbohydrate-derived
melts.73 The best results were obtained in a maltose/DMU/
NH4Cl DES and the desired quinazoline was obtained with
92% yield (Table 14). This work exhibited a broad substrate
scope and products of the reaction were conveniently isolated
from the DES either by crystallization or by extraction with
ethyl acetate, allowing the DES to be recycled.
Table 14 Three component reactions of 2-amino-benzophenone,

4-nitrobenzaldehyde and ammonium acetate in various DESs
Melt
T/1C
Yield (%)
Citric acid/DMU (4 : 6)
Fructose/DMU (7 : 3)
Tartaric acid/DMU (3 : 7)
Tartaric acid/ChCl (5 : 5)
Mannose/DMU/NH4Cl (5 : 4 : 1)
Lactose/DMU/NH4Cl (5 : 4 : 1)
Maltose/DMU/NH4Cl (5 : 4 : 1)
65
71
70
90
89
88
84
85
75
82
89
82
86
92
Chem. Soc. Rev.
Scheme 19 Reduction of aldehydes and epoxides by NaBH4 in ChCl/

urea. (Adapted from ref. 75.)
Very recently, Zhang et al. extended this work and have

reported that synthesis of quinoline derivatives (from aniline
and ketones derivatives) can also be conveniently performed
via the Friedlander reaction in low melting tartaric acidurea
mixtures.74 This reaction exhibits a broad substrate scope in
such DES and the targeted quinoline derivatives were obtained
with fair to excellent yields.
Azizi and co-workers reported the chemoselective reduction
of functionalized carbonyl derivatives and epoxides in ChCl/
urea in the presence of sodium borohydride (NaBH4).75 At
room temperature and with 2 eq. of NaBH4, a wide range of
aldehydes and ketones were reduced in less than 5 min in
ChCl/urea, aording the corresponding alcohol with a yield in
the range of 7599% (Scheme 19). Additionally, a broad range
of epoxides were also reduced in the presence of NaBH4 in
ChCl/urea, aording the desired alcohols with 7595% yield.
7. Electrochemistry in DESs
The earliest research studies on ionic uids started with the
purpose of electrochemical application, viz. Humphrey Davys
pioneering works on the electrodeposition of simple molten
salts. Due to their unique properties, ILs found a wide range of
applications in various electrochemical devices including for
instance lithium ion batteries, fuel cells, super capacitors, dye
sensitized solar cells, etc. Similar to ILs, DESs were also used
in electrochemistry as electrolytes for electrodeposition of
metal, as solvents for electrochemistry reaction and for
electropolishing (metal dissolution), etc.
7.1 Electrodeposition
Electrodeposition is a process leading to the formation of solid
materials by electrochemical reactions in a liquid phase. The
setup is composed of a three-electrode electrochemical cell
(a reference electrode, a specially designed cathode, and an
anode or counter electrode). In a very simple way, the metal
(cationic form) contained in the electrolyte is reduced at the
cathode and deposited as metal as shown in Fig. 6.
Electrodeposition of metals is widely used to functionalize
surfaces for corrosion-resistance, electrocatalysis, magnetic
applications, photoactive semiconductors (photovoltaics) electrotypes in the printing industry and hardening of steel for
engineered components or in electronic industries for the
production of printed circuit boards.76 Electrodeposition of
metals can be performed in the presence of various solvents
but this process is obviously limited by the redox potential
windows of the considered solvent. Electrolytes should indeed
have a high resistance against electrochemical reduction and
This journal is

View Online
Fig. 6 Schematic view of the electrodeposition process.
oxidation. In aqueous solutions, electrodeposition of metals is

generally restricted to those exhibiting a redox potential higher
than that of water. Organic solvents are also attractive for
electrodeposition mainly because some of them exhibit a
potential window that is 1.52.5 times wider than that of
common aqueous acid electrolytes. In this context, DMF,
DMSO, THF, methylene chloride and propylene carbonate
are of particular interest for electrodeposition processes.77
In the past two decades ILs have received considerable
interest for electrodeposition.78 In particular, electrodeposition of metals and alloys, which is carried out with diculties
in aqueous solvents, was successfully achieved in ILs.79
Although promising results have been reported, syntheses of
ILs, their sensitivity to water and their possible degradation
under oxygen represent some major drawbacks. Thanks to
their similar properties with those of ILs, DESs have received
growing interest for their use as electrolytes. In particular,
their tolerance to water together with their low price and
biodegradability represent three major advantages over ILs.
In this section, we will describe the contribution of DESs for
electrodeposition of metals. In this eld of research, DESs
made of ChCl and either urea or ethylene glycol or glycerol
have been mostly investigated.
7.1.1 Electrodeposition in a ChCl/urea DES. Electrodeposition of SmCo has been successfully performed in a
ChCl/urea (1 : 2) DES by Gomez et al. using a cylindrical
three electrode cell of one single compartment.80 The working
electrode was a vitreous carbon and the counter electrode was
a platinum spiral. The reference electrode was an Ag/AgCl/
NaCl 3 M xed in a Luggin Capillary containing the DES. The
redox window of the DES (2.4 to 0.4 V) is compatible with
the use of vitreous carbon electrodes. The electrodeposition
was performed at 70 1C in order to decrease the viscosity of the
DES and to overcome the mass transfer problem. In a rst set
of experiments, cobalt alone was deposited on vitreous carbon
in the ChCl/urea (1 : 2) DES. These experiments have shown
that the nucleation and growth of metallic cobalt readily takes
place in ChCl/urea. When samarium was deposited instead of
cobalt, an unusual deposition process was observed. Two
reduction regions were indeed identied with Sm. At low
overpotential, the deposit of Sm formed was less conductive
than the vitreous carbon used as substrate. When the potential
becomes higher (i.e. 1.6 V), the deposition of samarium is
This journal is
more ecient. Note that at this high potential, the current

density increases with the stirring. Concomitant deposition of
cobalt and samarium can also be achieved in this DES.
Starting from a SmIII/CoII molar ratio of 4 : 1, SmCo was
deposited. The deposit contained up to 70 wt% of Sm when
the potential applied to vitreous carbon was suciently negative
(1.6 V) or when anodic metallic substrate (Ni/Cu/Au) was
used instead of vitreous carbon. Note that composition of the
Sm/Co deposit may be changed when the deposition process
was achieved at a potential higher than 0.85 V. Using such a
process, deposition of SmCo formed either lms or nanowires,
depending on the temperature.81
The electrodeposition of CuGa can also be performed in
ChCl/urea DES, yielding cheap thin lm with interesting
applications in solar cells. Shivagan et al. have shown that
electrodeposition of (CuIn5Ga)Se can be performed in
ChCl/urea DES, leading to 68% of incorporation of Ga into
CuInSe lm even when the concentration of GaCl3 was very
high (4080 mM).82 Later, Dale et al. have shown that, in a
ChCl/urea DES, Gd can also be deposited over a Mo electrode
in a reversible process without any interference of the solvent.83
In particular, an increase in the temperature induced an
increase in the redox window of the DES, owing to a decrease
in the DES viscosity.
Nickel was also successfully electrodeposited in a ChCl/urea
DES using a copper microelectrode. The potential window of
the ChCl/urea DES is between 1.35 and 0.24 V.84 Morphology,
microstructure and redox behaviour of Ni(II) deposited on Cu
was aected by the addition of nicotinic acid in the DES. In
particular, addition of nicotinic acid to the DES led to an
inhibition of the nickel deposition current explained by the
adsorption of nicotinic acid in the DES and the formation of a
Ni(II) complex with nicotinic acid. By controlling the amount
of nicotinic acid in DES, it was possible to control the nature
of the deposit. In a similar way, Abbott et al. have reported
that addition of ethylenediamine to the DES containing
0.2 M NiCl26H2O led to the formation of a deposit with
smaller particles size mainly due to the formation of a
[Ni(ethylenediamine)3]2+ complex.85 Eect of nicotinic acid
and ethylenediamine on the electrodeposition of Ni was
attributed to (i) the formation of a Ni complex and (ii) its
absorption on the electrode surface, which block the nucleation and the particle growth. Compact nickel-multiwalled
carbon nanotube composites were also deposited on a copper
substrate.86 Success of this reaction relied on the homogeneous
dispersion of microwall carbon nanotubes (MWCNTs) which
is a pre-requisite step for an ecient electrodeposition with the
nickel matrix. Remarkably, in ChCl/urea DES, the dispersion
of MWCNTs was very good (high stability of the suspension).
Addition of anhydrous nickel chloride to the suspension of
MWCNTs in DES did not drastically aect the dispersion
of MWCNTs. Morphology, roughness and crystallinity of
deposited Ni were obviously aected by the presence of
MWCNTs in the DES. Ni was also deposited on a Pt electrode
in a ChCl/EG DES.87 The deposition is quasi-reversible. Two
dierent morphologies of metal deposits, nanodeposits and
bulk metal, were observed.
Ethylenediamine (en) and sodium acetylacetonate (acac)
were also used as additives (brighteners) during the nickel
Chem. Soc. Rev.

View Online
deposition process. This experiment aimed at (i) producing

more stable Ni complex (ii) suppressing underpotential deposition and (iii) decreasing the ability of the metal to nucleate. In
the cathodic part, three moles of additives were necessary to
reduce free ethylenediamine and to form [Ni(en)3]2+. In the
anodic part only 1 mol equivalent is necessary to oxidize
nickel. Birbilis et al. have studied the electrodeposition of
NiZn alloys in a ChCl/urea DES using a cupper electrode.88
Electrodeposition was carried out at 70 1C in the presence of
anhydrous nickel and zinc chlorides. Composition, surface
morphology and phase structure of the NiZn alloys are
dependent on the current density and the working potential.
Although Ni was incorporated in a higher amount than Zn in
the NiZn alloy, the Ni content decreased when (i) the
deposition potential became more negative (decrease from
0.6 to 1.2 V) and (ii) the current density increased. Similar
alloy was obtained using a platinum electrode.89 The NiZn
alloy formed in this last case was made of cubic crystallites.
The electrochemical depositions were rather slow in ChCl/urea
DES due to its high viscosity that induces low diusion
coecients. Note that electrodeposition of neat zinc was also
possible by this method and led to the formation of small
crystallites.
Dale et al. have reported that CdS, CdSe and ZnS can be
electrodeposited in a ChCl/urea DES.90 In this study, the
working electrode was a glassy carbon or uorine doped with
tin oxide (FTO). In a rst set of experiments, the authors have
studied the stability of both electrodes and they have observed
that in the case of glassy carbon, the DES was partly contaminated by carbon residues. In the presence of FTO, the
reversible reduction of SnO2 to metallic Sn occurred. The
deposition of a lm of CdS on uorine doped tin oxide was
performed in a potential range of 0.6 to 0.8 V. During the
electrodeposition, a change of the CdS lm colour from pale
transparent yellow (0.6 V) to dark brown (0.8 V) was
observed due to the accumulation of Cd in the lm. The
recovered CdS lm exhibited a thickness lower than 50 mm.
Magnesium is a water-sensitive substrate (from the electrodeposition point of view), making technically dicult its
electrodeposition in aqueous solution. Hence, the ChCl/urea
DES was also investigated for the electrodeposition of Zn onto
several Mg alloys.91 The authors have compared the eciency
of several DESs such as ChCl/ethylene glycol (2/1), ChCl/
malonic acid (1/1), ChCl/glycerol (1/2) and ChCl/ZnCl2 (1/2).
From this study it appears that ChCl/urea and ChCl/glycerol
were the most ecient systems leading to the lowest corrosion
of magnesium. The use of ChCl/glycerol DES, however,
resulted in the pitting of the magnesium surface. Hence, the
ChClurea mixture was found to be the most appropriate DES
for the electrodeposition of Zn on Mg.
Ying et al. have studied the stability of the ChCl/urea DES
during the electrodeposition process. In particular, the authors
have observed the formation of gaseous chemicals at the
cathode (trimethylamine) and anode (chorine) during the
nucleation of metal (CoCr) suggesting a partial degradation
of the DES during the electrodeposition process.92
7.1.2 Electrodeposition in a ChCl/ethylene glycol DES.
Electrodeposition of Zn, Sn and ZnSn alloy has been carried
Chem. Soc. Rev.
out in ChCl/ethylene glycol by Abbott et al.93 They have

studied the deposition of Zn on a polished gold-coated quartz
crystal, by atomic force microscopy and quartz crystal microbalance. Zinc was deposited with a mean current of 92%. A
gradual formation and growth of crystallites, suggesting a
progressive nucleation mechanism, was observed. Later, the
same group has studied the eect of additives such as acetonitrile, ethylene diamine and ammonia on the zinc electrodeposition.94 Although viscosity of the DES was not modied,
the electrodeposition was aected by the presence of these
additives. Ammonia and ethylene diamine inhibited the
adsorption of chloride on the electrode surface. The presence
of these additives, however, acts as a brightener for zinc
deposition. It should be noted that, like in water, the presence
of these additives to the DES led to the formation of macrocrystalline deposits. Conversely to the ChCl/urea DES, the
same group has also shown that the concentration of ZnCl2
has no eect on the conductivity of the ChCl/ethylene glycol
DES.95 In ChCl/ethylene glycol DES, the mechanism is
dierent to what is observed in ChCl/urea DES. This dierence might be due to the specic adsorption of chloride on the
electrode surface, blocking the growth of few crystal faces
(Fig. 7). Another group has studied the electrodeposition of
ZnSn on carbon nanotubes.96 They have successfully performed the deposition with a high density and well distributed
ZnSn spherical NPs with an average diameter of 120 nm.
Electrodeposition of Cu is more dicult in such DES.
Abbott et al. have observed a progressive nucleation of Cu
that led to a bright nano-structured deposit. When the concentration of Cu in DES was lowered (less than 0.01 M), a
spontaneous nucleation of Cu was observed, leading to the
formation of a black deposit. For a copper concentration from
0.01 M and 0.1 M a bright deposit was obtained. The authors
have next demonstrated that composites of Cu and Al2O3 or
SiC can also be produced in such DES.97 Addition of Al2O3 or
SiC particles in the DES did not modify the morphology and
size of Cu particles. The composition of the composite material
was dependent on the amount of Al2O3 or SiC particles. They
have shown that the use of 5 wt% of Al2O3 yielded a
composite with 3.5 wt% of Al (1 mm particle) whereas from
10 wt% of Al2O3, the composite contained 23 wt% of Al
(1 mm particle). Llyod et al. have studied the kinetics of
electron transfer of the Cu(I)/Cu(II) redox couple at a platinum
electrode in a ChCl/ethylene glycol DES.98 They have shown
that the reaction was reversible and that a large amount of free
chloride was present in the DES due to the dissociation of ChCl.
Fig. 7 SEM images of Zn deposits obtained from 0.3 M ZnCl2 in

(a) 1 : 2 ChCl:U (b) 1 : 2 ChCl:EG at 50 1C, on mild steel at
I = 3 mA cm2. (Reproduced with permission from ref. 95. Copyright
This journal is

View Online
This leads to the formation of copper chloride-based complexes. The authors have demonstrated that in this system the
energy eciency of electrodeposition can be double because
(i) the cathodic eciency is very high and (ii) the low oxidation
state of metal complexes is stable.
Ag was also successfully electrodeposited on a Cu electrode
in ChCl/ethylene glycol DES.99 It was shown that silver can
not only oxidize copper but can also be deposited on the
copper surface at the same time. The deposit of silver was
nano-crystalline and gave a smooth shiny coating. Later, the
same team has studied the electrodeposition of silver using a
platinum working electrode.100 As mentioned earlier, AgCl
was found to be highly soluble in this DES (0.2 mol kg1).
When SiC was added to the solution of AgCl in ChCl/ethylene
glycol, the viscosity decreased due to microstirring eects.
Morphology of the Ag deposit was not aected by the
presence of SiC. A similar trend was observed in the case of
Al2O3. Note that the Ag particle size is however smaller in the
presence of SiC microparticles. The authors have also shown
that upon incorporation of SiC, the hardness of recovered Ag
in DES is higher than in aqueous solution. Note that the
hardness of metallic Ag did not depend on the SiC particles
size (from 50 nm to 2 mm). Incorporation of SiC or Al2O3 has,
however, an eect on the friction coecient and wear volume
of the Ag-based deposit. In particular, in the presence of
Al2O3, Ag particles are less abrasive. Since lithium salts are
known to modify the mechanism of metal nucleation and the
mechanical properties of the deposited lms, the addition of
LiF during the deposition of Ag was also investigated. The
hardness was greatly improved, but the structure of the
Ag/SiC lm was unchanged with the addition of 1 wt% of
LiF. Later, Tu et al. have performed the deposition of Ag on
copper alloys.101 They have shown that at 0 1C or at 50 1C a
self-assembled nanoporous network of Ag lms with ligament
or channel structure was obtained.
Saravanan and co-workers have shown that electrodeposition
of a CrCo alloy is also feasible in ChCl/ethylene glycol DES,
opening an interesting route for the replacement of common
noble metal alloys in dentistry.102 The authors have used an
anode made of graphite and a cathode composed of a brass
and mild-steel plates. Two electrodeposition methods were
developed (i) direct current deposition (DCD) and (ii) pulsed
electrodeposition (PED). In the DCD method, an alloy
composed of 80.04% of Co and 19.95% of Cr was obtained
with a nodular grain shape with sizes ranging from 24 mm.
From the PED method, the recovered alloy was composed
of 65.44% of Co and 34.56% of Cr with particle sizes ranging
from 12.5 mm.
The electrodeposition of nickel was also performed at 90 1C
in ChCl/ethylene glycol on polished brass foil (Cu0.64Zn0.36
alloy).103 A highly rough surface was obtained at 90 1C while it
is not the case at room temperature. Nickel is randomly
distributed on the lm. Nanosheets with a thickness of
1020 nm and grains with 1050 nm size were obtained.
Clearly, the authors have highlighted an increase in the Ni
deposit roughness with the temperature. This was explained by
a decrease of the DES viscosity, leading to an increase of ion
species mobility, favouring the nucleation and deposition
process of nickel. Moreover, the authors have shown that
This journal is
the nickel lms present a low corrosion potential. Abbott et al.

have also studied the deposition of nickel in ChCl/ethylene
glycol DES.87 A dark grey deposit was obtained and the
underpotential deposition of Ni was suppressed by the addition of ethylenediamine and acetylacetamide in the DES.
Polymers such as polypyrrole lms can also be electrodeposited in ChCl/ethylene glycol.104 As observed above for
the ChCl/urea DES, the ChCl/ethylene glycol DES was
unfortunately partly decomposed during the electrodeposition
process even in the presence of sacricial agents such as oxalic,
phthalic, formic or acetic acids.105
7.1.3 Electrodeposition in a ChCl/glycerol DES. Silva and
coworkers have investigated the interface properties between
ChCl/glycerol and either Au or Pt or glassy electrode.106 The
authors have shown that Au has the highest eect on the
capacitancepotential curves. Except for gold, an increase in
temperature led to an improvement of the capacitance in the
presence of Pt and glassy carbon electrodes.
This DES was also studied by Mason et al. In particular, the
authors have shown that mass transfer and cathodic current
increased in the presence of ultrasound during the electrodeposition of copper chloride on Pt electrodes.107 This property
resulted in an increase in the limited current density. Under
ultrasound, the anodic potential peak in cyclic voltammetry was
also increased 10 times and shifted to a more positive value as
compared to silent conditions. This phenomenon can be
ascribed to (i) an increase of mass transfer, (ii) a local increase
in temperature, (iii) a decrease in concentration over potential,
(iv) a cleaning eect by ultrasound, (v) a decrease in overpotential and (vi) formation of a hydroxyl radical. It should be
noted that after 30 seconds of ultrasound, the solution containing copper chloride and glycerol turned from bright yellow to a
turbid pale colour due to cavitational events occurring in such
highly viscous mixture. This change of colour can be due to the
decomposition of ChCl/glycerol under sonication.
7.1.4 Electrodeposition in others ChCl-derived DES. Lesuer
et al. have demonstrated that a ChCl/TFA (2,2,2-triuracetamide)
(1 : 2) DES can dissolve ferrocene.108 In particular, they have
studied electron-transfer reaction mechanisms in this DES.
It appears from this study that this DES behaved as a nonNewtonian uid.
Abbott et al. have reported that a ChCl/chromium chloride
DES with similar properties to ILs can be produced.109 In this
DES, electrodeposition of thick and adherent chromium lms
was achieved, oering an alternative to acid solutions commonly
used for chromium electrodeposition.
In conclusion, the above-described results clearly show that
electrodeposition of metals can be conveniently performed in
various DESs with similar eciency than methods based on
ILs (Fig. 8).109
However, instability of DESs during the electrodeposition
process still remains a major problem that needs to be solved
prior to a possible industrial transfer.
7.2 Other applications of DES in electrochemistry
DESs were also used in electrochemistry as electrolytes for
dye-sensitized solar cells.110 In this case, 3.88% of the sunlight
Chem. Soc. Rev.
View Online

Fig. 8 Metals electrodeposited in the three main DES used in this

process.
Fig. 9 Electropolishing process.
energy was converted in a ChCl/glycerol based electrolyte

which is comparable to most of IL-based electrolytes. The
photoanodes used were a double layer of TiO2 mesoporous
lms. The electrolyte was made by adding 0.2 M of I2 and
0.5 M of N-methylbenzimidazole to a mixture of 1-propyl-3methylimidazolium iodide and ChCl/Gly (v/v 13 : 7). This
study has shown that ChCl/glycerol is a promising candidate
for future electrolytes for dye-sensitized solar cells.
Electropolishing of metal (surface treatment that aims at
removing oxidized metal on surface) which corresponds to the
metal corrosion was also investigated in DES (Fig. 9).
A ChCl/ethylene glycol DES has been used for the electropolishing (anodic dissolution) of stainless steel, aording an
alternative to phosphoric and sulfuric acid solution commonly
used for such treatment. This electropolishing process was not
corrosive and tolerant to the presence of air and moisture.
Additionally, it is anisotropic and has micro roughness.111 The
authors have also shown that the metal surface oxidation was
rapid under aerobic conditions. Moreover, the anodic dissolution of metal ions was faster when the oxide layer was
continuously removed.112
Metal separation was also studied in DESs. The idea is to
use the ability of the chloride anion of DES electrolytes to
stabilize metal ions. In the process, chemical oxidation of
metals by I2 led to iodide and soluble metal species. The iodide
formed was oxidized at the anode, regenerating iodine.
Conversely, at the cathode, puried metal was obtained by
reduction reaction.113
DESs were also used to obtain natural polymer-based
electrolytes such as cellulose acetate114 or corn starch based
polymers,115,116 or p-doped polypyrrole116 with high conductivities.
8. Preparation of materials in DESs

Conventional preparation of inorganic materials often takes
place in water or organic solvents, using in many cases the
thermal step for crystallization and structure formation. The
Chem. Soc. Rev.
solvothermal synthesis then consists in growing single

crystals from a non-aqueous solution, by thermal treatment
under pressure. Recently, the ionothermal synthesis, a new
synthetic strategy involving predominantly ILs or deepeutectic solvents (DESs) as solvent, has been developed. In
these syntheses, ILs or DESs can be used as both solvent and
template (also called structure-directing agents). In solvothermal reactions where solvents are predominantly volatile
molecules, the high temperature required for crystallization
or pore structure formation needs the use of autoclaves.
Contrarily, ionothermal synthesis can be readily conducted
in a low-pressure environment (e.g. under ambient pressure)
due to the low volatility of ILs or DESs. The use of such
solvents thereby reduces all security risks arising from the use
of low boiling point solvents and simplies the synthesis
process. More importantly, the possibility to tune the ionic
nature of DESs provides modulating reaction environments
under which novel materials with useful structures (surface
properties and porosity) may be produced.
Nowadays, the ionothermal synthesis is gaining considerable attention. In this context, a newly emerging trend of this
eld consists in the replacement of ILs by cheap and safe
DESs. For example, DESs based on ChCl/urea or ChCl/
renewable carboxylic acids have been used as an alternative
medium to ILs in the ionothermal strategy. As mentioned
above, compared to ILs, DESs have notable advantages
including low toxicity, biodegradability and low cost.
Additionally, the presence of neutral components with high
boiling point such as urea, carbohydrates or carboxylic acids
also provide new and complementary environments to ILs
that are completely ionic. In addition, DESs can play multiple
roles during synthesis, including the classical role of solvent,
templating agent, reactant, etc. Thanks to these properties, DESs
are now receiving considerable attentions for the ionothermal
synthesis of materials and the design of novel structures.
Up to now, many inorganic materials with valuable properties
and structures, including zeolite-type materials, metalorganic
frameworks (MOFs), metal oxides, nano-materials, carbon
materials, among others, have been synthesized using the
ionothermal synthesis strategy. Although a few reviews focusing
on the preparation of inorganic materials using ILs can be
found in the recent literature,117,118 a comprehensive review
dedicated to the use of DESs in the ionothermal synthesis of
materials has not been covered yet in the current literature. In
this section we describe the promising materials prepared
in DESs for various applications including gas separation,
hydrogen storage, catalysis, etc. This review also highlights the
versatile role played by DESs during the material synthesis.
8.1 Metal phosphates and phosphites with open-framework
structures
8.1.1 Aluminophosphates. Zeolites or zeolite-like materials
are of great importance owing to their applications in dierent
areas of modern science. These zeolite-analogous framework
materials are often synthesized in water or organic solvents by
a traditional solvothermal approach and using structure
directing agents. In 2004, the DES-mediated ionothermal
procedure was rstly introduced for the preparation of
This journal is

View Online
Fig. 10 The synthesis of zeotypes by using ionic liquids and eutectic

mixtures. (a) Ball-and-stick diagrams of aluminophosphate materials
SIZ-1, SIZ-3, SIZ-4, and SIZ-5 synthesized ionothermally using
[EMIm]Br; (b) SIZ-2 and AlPO-CJ2 synthesized using a ChClurea
mixture. The structure-directing agents have been omitted for clarity.
Orange, cyan and red spheres correspond to phosphorus, aluminium
and oxygen atoms respectively.119 (Reproduced with permission from
ref. 119. Copyright (2004) Nature Publishing Group.)
microporous crystalline zeolite analogues by Morris and

co-workers.119 DESs based on ChCl/urea or IL ([EMIm]Br)
were used as alternative solvents for the synthesis of zeotypes.
In the presence of [EMIm]Br, four dierent aluminophosphate
zeotypes, SIZ-1, SIZ-3, SIZ-4, and SIZ-5 (Fig. 10), were
prepared under dierent experimental conditions, in which
the imidazolium-based IL acted as both the solvent and
template. For example, at 150 1C, SIZ-1, with a framework
structure composed of hexagonal prismatic units joined
together to form a three-dimensional framework, was
obtained. The framework is however interrupted by an
unusual hydrogen bond. Fully condensed structures can also
be achieved using a mineralizing agent (uoride) to promote
oxygen bond formation. Dierent from IL, the use of ChCl/
urea led to another type of framework, viz. SIZ-2. The AlOP
alternation is maintained and the chemical formula
(NH4)3[Al2(PO4)3] shows that SIZ-2 is also an interrupted
structure. Compared to the synthesis in IL, the addition of
uoride to the ChClurea eutectic mixture led to the formation
of a non-zeolitic aluminophosphate known as AlPO-CJ2
(Fig. 10). During the ionothermal synthesis in DES, ammonium
ions released by partial decomposition of urea play an
This journal is
important role in the formation of the inorganic framework

by templating and balancing charges generated by the terminal
PO bonds in the framework. The pore architecture consists in
three intersecting channels of small size. Even with this size
limitation, the authors succeeded in the subsequent and partial
exchange of ammonium by copper cation. Due to the low
volatility of ILs or DESs, the synthesis takes place at ambient
pressure.
Similarly, other SIZ-n type materials with zeolitic frameworks, i.e. SIZ-6, SIZ-7, SIZ-8, SIZ-9, have been synthesized
by means of ionothermal synthesis using [EMIm]Br.120,121
However, these syntheses without the involvement of DESs
fall out the scope of this section and therefore will not be
particularly discussed here.
As compared to traditional solvents (e.g. water), use of ILs
or DESs can also modify the way how material precursors are
assembled. Novel types of inorganic materials can then be
synthesized. The absence of competition between templateframework and solvent-framework interactions encountered
in classical hydrothermal preparations is then completely
depressed when using DES. As rightly notied by Copper
et al., this is an important specicity of these syntheses.119
Based on the successful preparation of SIZ-n type materials,
Morris and co-workers reported the ionothermal synthesis of
materials using various unstable DESs as template-delivery
agents.122 1,3-Dimethyl urea (DMU), 2-imidazolindone (ethylene
urea or e-urea) and tetrahydro-2-pyrimidione (THP, N,N 0 trimethylene urea) derivatives were investigated as eutectic
mixtures in combination with quaternary ammonium halides
(choline chloride or tetraethylammonium bromide). Aluminum phosphate-based materials with new structures have been
prepared using this strategy. For example, the use of ChCl/
e-urea led to the formation of two similar related aluminophosphate materials (Fig. 11, materials 4 and 5). In this case,
materials were templated by ethylene diammonium cations
plus some ammonium issued from DES decomposition when
temperature exceeded 200 1C. The use of ChCl/DMP, which
decomposes into propylene diammonium or ammonium
(conditions: high temperature and large excess of water),
induced the crystallization of four other types of solids
(Fig. 11). The obtained structures support the mechanistic
pathways previously proposed for the crystallization of aluminophosphates (through hydrolytic assembly of the parent chain).123
Indeed, the mild hydrolytic conditions of the ionothermal
synthesis (as compared to the classical hydrothermal/
solvothermal routes) allowed the isolation of an aluminophosphate structure close to the parent chain structure (suggested
to form before condensation in classical synthesis). Some
mechanistic studies also suggested that the nucleation and
crystallization of the structures take place at relatively low
levels of DES degradation, when concentration of the template
(propylene diammonium or ammonium) remains low.
Although the ionothermal synthesis was thought to take
place in a relatively dry and predominantly ionic environment, the presence of water cannot be ruled out. Interestingly,
when present in trace amounts, water did not have a detrimental eect on the DES-mediated ionothermal synthesis of
some materials.124 The low reactivity of water (in trace
amounts) was attributed to its strong interaction with the
Chem. Soc. Rev.

View Online
Fig. 12 The layered structure of SIZ-13 viewed parallel to the a axis

(top; hydrogen atoms are omitted), and a single [Al3CoClP4O16]2
layer viewed parallel to the c axis (bottom; choline template molecules
are omitted).126 (Reproduced with permission from ref. 126. Copyright
(2007) Wiley-VCH.)
Fig. 11 The synthesis of aluminophosphate materials from DESs.
(a) Materials 45 prepared from ChCl/IMI. (b) Four materials prepared
from ChCl/DMP. In compounds 68 the template is a propylene
diammonium cation while in compound 9, prepared at higher temperature, the template is ammonium. For clarity the location of the
templates in 6 and 8 is not shown.122 (Reproduced with permission
from ref. 122. Copyright (2006) Wiley-VCH.)
anion of the DES that drastically limits its reactivity.125 In

other words, it means that new inorganic materials that are
sensitive to water can be theoretically prepared by the
ionothermal synthesis in DESs. In this context, three dierent
ChCl/carboxylic acid-derived DESs were recently used for the
synthesis of unusual aluminophosphate layered materials with
chemical compositions that are unlikely to be accessible using
traditional hydrothermal methods. The possibility to achieve
new structures was then clearly exemplied by Morris et al.126
The use of ChCl/carboxylic acid (succinic, glutaric or citric
acid) DESs allowed the production of dense aluminophosphate phases. When bases are used to control solvent
properties (cyclam or pyridine), new CoAlPO structures,
SIZ-13, are obtained, independently of the base used.
The structure of SIZ-13 consists in [Al3CoClP4O16]2 layers
templated by choline cations lling the interlayer (Fig. 12).
The specicity of the structure is that cobalt ions are located in
only one crystallographic position, at the corner of the building
unit. Note that formation of CoCl bonds present in the
SIZ-13 structure is not possible using traditional routes due
to their high sensitivity to hydrolysis. As mentioned
previously, the strong interaction of water with the anion of
the DESs (at low content of water) provides media with very
Chem. Soc. Rev.
limited hydrolyzing properties.125 Like mentioned above in the

biocatalysis part, inhibition of the water reactivity in DES is
then proposed as the reason for the CoCl stabilization in
SIZ-13. Raising the temperature of the synthesis increases the
reactivity of water contained in DES, and thereby promotes
the formation of a fully connected zeolite framework, SIZ-14.
The authors highlighted that the presence of accessible relatively
large cages in the structure of SIZ-14 (3.6 4.8 A2) is of great
importance, especially for catalytic and adsorption applications.
8.1.2 Zinc phosphates. The above described results clearly
show that the material structure obtained by ionothermal
synthesis is inuenced by the chemical composition of the
DES (e.g. template species, mineralizers, charge balance, etc.).
DESs can play a multiple role such as template and solvent.
Zinc phosphates are an important subset of the large
phosphate family. More than 20 zinc phosphate structures,
exhibiting 1D, 2D or 3D framework structures have already
been synthesized, with the possibility to obtain large pore
structures.127 Inspired by the methodology reported for the
preparation of aluminophosphate-based materials, Liao and
co-workers reported in 2005 the ionothermal synthesis of a
[Zn(O3PCH2CO2)]NH4 structure using a ChClurea eutectic
mixture as the reaction medium.128 Deep investigations
showed that NH4+, generated in situ from the partial decomposition of urea at high temperature, played a pivotal role in
the formation of the targeted material. Ammonium acted as a
structure-directing agent which lled the voids of the structure,
and interacted with the CQO groups present on the surface of
This journal is

View Online
the helix-like tunnels through a hydrogen bond (3D framework).

Similarly, Harrison also obtained zincophosphite type
structure [with Zn2+ cation, HPO32 anion, and chloride ion
incorporated into the structure by a ZnCl covalent bond].
In this system, choline from the DES was incorporated into
the hybrid structure. Cholinium cations interacted with
[ZnCl(HPO3)] macroanionic layers by means of OH O
hydrogen bonds.129 Later, Dong and co-workers have
described the synthesis of a three-dimensional zinc phosphate
material (designated ZnPO4-EU1). In situ generation of
the structure directing agent (from imidazolidone) using an
unstable ChCl/imidazolidone DES (in a molar ratio of 1 : 2)
as the reaction medium at 150200 1C allows the material
formation.130 The obtained zinc phosphate material belongs to
the DFT topology framework structure, which is similar to
that of the previously reported (ZnPO4)2(NH3CH2CH2NH3)
material (DAF-3).131 Then, the expected decomposition
product of the DES based on choline chloride and imidazolidone
is ethylenediamine, which is progressively delivered in the
reaction media at a temperature higher than 150 1C. The
progressive ethylenediamine delivery allows the crystallization
of the 3D ZnPO4-EU1 structure.
In the synthesis of metal phosphate-based materials,
quaternary ammonium salts, such as TMABr, TEABr,
TPABr, and ChCl, have been extensively used. Quaternary
ammonium cations are capable of templating a wide variety
of frameworks. Thus, addition of these quartenary ammonium salts to oxalic acid leads to DESs that are able to
template such zincophosphate structures. Lin and co-workers
reported a new 2D crystalline layered zinc phosphate,
[N2C6H12]2[Zn7H3(HPO4x)5(PO4)3]H2O (denoted ZnPODES1).132 Structure of this material consists in 10-memberedring ellipsoidal channels perpendicular to the ladder-shaped
layers. This material was prepared by ionothermal synthesis
from a TPABr/oxalic acid DES, zinc acetate, H3PO4, and
triethanolamine (TEA) at 150180 1C for 3 days. During the
reaction, 1,4-diazabicyclo[2.2.2]octane (DABCO) is supposed
to be generated by TEA conversion and is suggested to
template the ZnPO-DES1 structure. Indeed, DABCO is
classically used to template zincophosphate structure.
Next, two new zincophosphate materials, i.e. ZnPO4-EU2
(Thomsonite-type framework) and ZnPO4-EU3 (JBW zeolitetype structure), have been ionothermally synthesized by Dong
et al.133 In this example, two DESs composed of 1,3-dimethylurea (DMU) mixed with either tetraethylammonium bromide
(TEABr) or N,N-dimethyl piperidinium chloride have been
used. The thermal decomposition of the DMU/TEABr DES
produced intermediates that exhibited strong structuredirecting abilities for zincophosphate framework formations,
yielding the ZnPO4-EU2 material. The negative charge of
the framework is compensated by protonated methylamine
(from DMU decomposition) and water. Protonated methylamine molecules are then located in the 8-rings pore channels
of the structure. The presence of H3O+ in the channels also
conrms the necessity to have a small amount of residual
water in the DES in order to successfully perform this synthesis.
SEM analysis shows that crystallites have a brick-like
morphology with a maximum edge length of about 100 mm.
However, crystal structure determination showed some small
This journal is
dierences from the classical Thomsonite structure, e.g. unit

cell and space group. ZnPO4-EU3 is templated by methylammonium cations issued from the DMU decomposition,
with Na+ added for the phase formation. As mentioned by
the authors, this is the rst DES mediated synthesis of a metal
phosphate analogue of Na-J JBW-type zeolitic material.
Morphology slightly diers from that of ZnPO4-EU2 (rodlike structure).
Although decomposition of urea derivatives from the DES
has been widely used to produce ionic templates, the same
strategy was employed using the cationic component of DES.
Very recently, Wang and co-workers have synthesized the rst
metal-activator-free orange phosphorus material NTHU-9 by
using a ChCloxalic acid dihydrate (1 : 1) eutectic mixture as a
synthesis medium. The material exhibits a layered structure of
zinc chlorophosphate with occluded organic templates
(Fig. 13).134 This zincophosphate material is the rst metal
phosphate exhibiting dual properties of photoluminescence
and photochromism. During the ionothermal synthesis, the
authors proposed that the hydrolysis of the choline cation
(the water content of the DES originates from oxalic acid
dihydrate) led to ethylene glycol (EG) and trimethylamine
which can react with CH3+ (from demethylation of choline) to
form tetramethylammonium ions (TMA). CH3+ is also
proposed to react with amines derivatives to form N,N 0 dimethylamine derivatives. All these intermediates play an
important role in the formation of the layered structure of
NTHU-9. The particular properties of the obtained materials
are attributed to these two concurrent reaction pathways:
(1) methylenium cations and N,N 0 -dimethylamine derivatives entrapped in the structure are responsible for the
photochromism;
(2) EG in the layered structure is at the origin of the
photoluminescence properties.
Fig. 13 Polyhedral plots of the inorganic layers in NTHU-9.

(a) Layers with disordered sites for choline ions (only N atom found)
in 9-tmdp (top) and dimethylated bpy molecules in 9-MV (bottom).
(b) Three types of tetrahedral Zn centers with dierent connectivity.
Blue, green, and red balls represent N, Cl, and water O atoms,
respectively.134 (Reproduced with permission from ref. 134. Copyright
(2010) Wiley-VCH.)
Chem. Soc. Rev.

View Online
8.1.3 Zirconium phosphates. As previously observed,

the use of DESs with dierent ionic compositions provides
notable advantages not only in terms of green solvent but also
for the rational design of new materials with open structures.
Like the aluminophosphate and zincophosphate, zirconium
phosphates with one-, two-, and three-dimensional connectivities are usually prepared using a solvothermal approach in
water or organic solvents. Recently, Dong and co-workers135
reported the synthesis of three dierent zirconium phosphate
frameworks using zirconium(IV) oxychloride, H3PO4 and HF
in DESs composed of tetramethylammonium chloride (TMA)/
urea and TMA/oxalic acid dehydrate. Among the reported
materials, two are new and exhibit chain or layered framework
structures which are unfortunately unstable upon calcination
(elimination step of the template). Using the TMA/urea DES,
ZrPO4-DES1 [(NH4)4[Zr(PO4)2F2], at an F/Zr ratio of 2.8]
and ZrPO4-DES2 [(NH4)3[Zr(PO4)2F], at an F/Zr ratio of 0.61]
were obtained. ZrPO4-DES1 is a chain framework structure
composed of {ZrO4F2} octahedra linked each to four {PO4}
tetrahedra to form innite macroanionic [ZrP2O8F2]n4n
chains. The NH4+ cations originating from the DES decomposition are located along the chains and act as template and
balance of the framework charge. ZrPO4-DES2 is a 2D
layered structure in which {ZrO5F} octahedra are linked to
{PO4} tetrahedra. The inorganic sheet consists in the alternation of {ZrO5F} octahedra and {PO4} tetrahedra to form
8- and 4-membered rings. Another material, ZrPO4-DES3, has
also been obtained when urea was replaced by oxalic acid. This
substitution aimed at avoiding the templating competition
between NH4+ (from urea decomposition evidenced to
template the two previous structures) and TMA+. ZrPO4DES3 exhibits a tridimensional framework with 10-ring and
8-ring channels. Structural characteristics are close to
the known structure [Zr12P16O60(OH)4F8] (C5H6N)4 (H2O)2
(ZrPOF-pyr).136 However, in this example, the material composition slightly diered since only the TMA cation templated
the structure. Thermal stability was also evaluated, and
logically the 3D structure (ZrPO4-DES3) presented satisfying
stability up to 450 1C while the two other 1D and 2D
structures collapsed. Catalytic properties of these newly prepared materials were evaluated in the selective oxidation of
cyclohexane, an industrially relevant reaction. Results showed
that tridimensional ZrPO4-DES3 exhibited good catalytic
performance, with a cyclohexane conversion of 32% and up
to 83% of selectivity to cyclohexanone. In contrast, the chain
and layered materials are relatively poor catalysts for this
catalytic reaction. The dierence of catalytic performances
between these catalysts was attributed to their dierent framework structures that aected the adsorption of reactants.
To further investigate the eects of the quaternary ammonium cation in ionothermal syntheses, a TPABr/oxalic acid
DES was used for the preparation of novel zirconium phosphate materials. Dong and co-workers described the possibility to form the known zirconium phosphate layered structure
a-Zr(HPO4)23H2O (a-ZrP) in pure TPABr/urea. In this case,
contrary to what was observed above with the TMA cation,135
the TPA cation cannot template the framework structure.137
However, when 1,4-dimethylpiperazine (DMP) was added
to the eutectic mixture, a new layered zirconium phosphate
Chem. Soc. Rev.
[C6H16N2]0.5Zr(H0.5PO4)2H2O denoted ZrPO4-DES8 was

successfully obtained. The layered structure of this material
is similar to that found in a-ZrP and can be regarded as a
DMP pillared a-ZrP structure. The DMP molecules are in
chair conformation and form an organic monolayer. However,
the direct DMP intercalation in classical a-ZrP structure does
not provide material with ZrPO4-DS8 structural properties.
Monitoring the in situ crystallization by XRD analyses showed
that, before crystallization of ZrPO4-DS8, an unknown phase
was formed after a short period of time. It should be noted
that layered zirconium phosphate materials, a-ZrP and
ZrPO4-DES8, are used as additives in a liquid lubricant.
Excellent friction behaviors with higher load-carrying and
antiwear capacities are obtained.
Very recently, Dong and co-workers138 also synthesized
a novel open-framework zirconium phosphate with small
7- and 8-ring channels. ZrPOF-EA, [(C2H7NH)8(H2O)8][Zr32P48O176F8(OH)16] formulae by ionothermal synthesis in
ethylammonium chlorideoxalic acid eutectic mixture. The
structure of ZrPOF-EA consists in units arranged in a rectangular array connected by ZrO6, ZrO5F, and PO4 linkages
(Fig. 14ac). One-dimensional channels parallel to the c (7-ring)
and a (8-ring) axes form due to the 3-, 4-, 5-, 6-, 7-, and 8-ring
units present in the structure.
Entrapped water and organic species in the structure can be
removed by calcination to produce a material with permanent
channel-like porosity. Elimination can be done under relatively mild conditions (410 1C for 9 h). SEM images have
showed that crystallites had a at needle-like morphology with
Fig. 14 ZrPOF-EA framework structure showing (a) the characteristic [41482] unit, (b) the projection along the c-axis with the [41482]
units highlighted, and (c) the projection along the a axis. Bridging O
atoms have been omitted for clarity. Terminal O atoms and bridging F
atoms are shown as balls, Zr gray, and P black.138 (Reproduced with
permission from ref. 138. Copyright (2011) Wiley-VCH.)
This journal is
View Online

dimensions of about 10 2 0.2 mm3. More interestingly, due

to the 8-ring dimensional channel, this porous material
showed a CO2 adsorption capacity largely higher than for
CH4. CO2 adsorption capacity is also signicantly higher
than that observed over conventional 8-ring pore materials
[adsorption performed at 25 1C and low pressure (01 bar)].
The selective adsorption of CO2 may be here the result of the
pore architecture and the presence of polar hydroxyl groups
located into the pore channels. Nevertheless, the selective
adsorption of CO2 vs. CH4 decreases by increasing the adsorption pressure, due to the exibility of the framework.
8.1.4 Borophosphates. Like aluminophosphate and zeolites, borate compounds have found a wide variety of applications, especially in the eld of nonlinear optics. Synthesis
of metal borate materials remains, however, dicult. The
volatility of boron oxide limits the potential of solid state
reaction syntheses. In addition, the presence of multiple borate
species in equilibrium in solution makes the hydrothermal
synthesis very complex. Recently, the use of choline chloride
1,3-dimethyl urea eutectic mixture has been reported as an
ecient medium for the preparation of cobalt phosphate
borate material that incorporates the [B5O6(OH)4] anion
between cobalt phosphate layers.139 The structure of this
material is composed of two-dimensional cobalt phosphate
layers pillared by polyborate building units, i.e. [B5O6(OH)4].
The inorganic layer is formed by corner-sharing cobalt oxide
and phosphate tetrahedrons. Oxygens from [PO4]3 tetrahedra
are localized on the surface of the layers, and are in interaction
with the polyborate unit by H-bond interaction. Unlike the
vast majority of metalloborophosphates, there is no direct
covalent bonding between phosphate and borate moieties. In
this ionothermal synthesis, two dierent alkyl ammonium
cations derived from the ionic media have distinct template
eects on the formation of cobalt phosphate layers and
hydrophobic borate channels. Indeed, the terminal NH3+
from methylammonium, issued from dimethyl-urea decomposition, is involved in H-bond interaction with oxygen atoms
from phosphate tetrahedrons. This interaction directs the
orientation of Co- and P- tetrahedrons, while the methyl
groups are located on the channel surface. Space between
the methyl groups as well as their hydrophobic nature allows
the incorporation of the tetramethyl ammonium ions derived
from the choline cation to compensate the framework charge
structure.
8.1.5 Iron oxalatophosphates. Although the ionothermal
synthesis in DESs has been widely used for the synthesis of
phosphates with open-framework structures, preparation of
metal oxalatophosphates in DESs has been reported only once
to our knowledge.140 Two new iron(III) oxalatophosphates,
Cs2Fe(C2O4)0.5(HPO4)2 (1) and CsFe(C2O4)0.5(H2PO4)(HPO4)
(2), have been synthesized in an eutectic mixture of ChCl and
malonic acid. While classical hydrothermal synthesis generally
leads to the formation of bi-valence [Fe(II) and Fe(III)] oxalatophosphate, only Fe(III) was found in these novel structures.
The structure of compound 1, obtained by reaction between
FeCl36H2O, H3PO4, H2C2O42H2O and 1,4-bis(3-aminopropyl)piperazine (APPIP) in DES, is presented in Fig. 15.
This journal is
Fig. 15 Polyhedral plot of the structure of 1 along the axis. The

yellow and green polyhedra represent FeO6 octahedra and phosphate
tetrahedra, respectively. Blue circles: Cs atoms. Black circles: C atoms.
Red circles: O atoms.140 (Reproduced with permission from ref. 140.
Copyright (2006) American Chemical Society.)
It comprises FeIIIO6 octahedra connected by HPO42 tetrahedra and bisbidentate oxalate (C2O42) anions to form a 3D
framework. Fig. 15 shows that the tunnels parallel to the [100]
direction have a window formed by six FeO6 octahedra and six
phosphate tetrahedra. The second kind of tunnel is formed by
six octahedra, four tetrahedra and two oxalate units. The
intersecting 12-ring channels form the 3D open structure,
with the framework charge-compensating Cs+ cations being
located at the intersections of these channels (Fig. 15).
Another structure (not shown), is obtained from the same
reactants but without 1,4-bis(3-aminopropyl)piperazine (APPIP),
resulting in a higher pH of the solution during the preparation
of the material. This material FeIIIO6 octahedra coordinate to
C2O42, H2PO4 and HPO42 anions to form macroanionic
layers, with Cs+ cations located between the layers. Four
FeO6 octahedra, connected to three HPO42 tetrahedra and
one oxalate unit form eight-membered windows in the layers.
The H2PO4 tetrahedra, positioned between the chains, stabilize
the 2D-layer structure.
For information, these materials cannot be prepared by a
hydrothermal method under similar reaction conditions pushing
forward the contribution of DESs for the ionothermal synthesis of new materials (even if no template eect is evidenced
in this study).
8.1.6 Metal oxalatophosphites. In line with their previous
research on photoluminescence properties of open framework
metallophosphate, i.e. NTHU-4 and NTHU-6,141 Wang et al.
demonstrated the successful synthesis of another luminescent
gallium oxalatophosphite in ChCl/oxalic acid dihydrate DES
(NTHU-7) (Fig. 16). The nanosized channel structure emits
Chem. Soc. Rev.

View Online
intense yellow light under excitation in near-ultraviolet (NUV)

and blue light.142 This material was prepared by reaction
between 4,40 -trimethylenedipiperidine (TMDPP), GaO, H3PO4,
and residual water contained in DES. Similar structures were
prepared by substituting the TMDPP by either 4,4 0 -trimethylenedipyridine (TMDP) or KOH, NaOH, RbOH, CsOH. The
NTHU-7 structure exhibits an organicinorganic hybrid nanotubular structure composed of GaO6 octahedra, bis(bidentate
oxalate) groups and HPO3 tetrahedra. Chemical composition
of the hybrid structure is [Ga2(HPO3)2(C2O4)(OH)(H2O)],
where the negative charge can be balanced by dierent cations
depending on the base used during the synthesis. However, the
counter cation always contains the choline ion, base and lattice
water molecule. The oxalate group incorporation into the
structure highlights that the tubular structure assembles with
DES contribution. Then all DES components, including
residual water, participated in the structure formation. The
role of DES is then multiple with a contribution as a solvent,
template, reactant, charge balancer and space ller. As
described in Fig. 16b, [Ga2(HPO3)2] units and oxalate groups
form a 16-ring aperture window at the tubule opening.
Five analogues of NTHU-7 (not presented) were also prepared in the same water-containing DES by changing the base
used during the synthesis.142 However, only 4,4 0 -trimethylenedipiperidine containing NTHU-7 nanotubules are able to
luminesce brightly under exposure to long-wavelength UV
light (365 nm). This indicates that they could be potentially
used as a yellow-green phosphor for blue LEDs as well as a
green phosphor for UV LEDs. Then, the photoluminescence
properties are not only related to the defect sites in the
structure, but also to the template occluded in the structure
(as a sensitizer) and to the host properties (nanoporous
structure).
Fig. 16 Structure plots of NTHU-7. (a) A perspective view of the

square-packing nanotubules. Ga centers cyan, P yellow, oxalate
groups white and red; (b) topological representation of one nanotubule showing the 16-ring aperture window surrounded by four strips
of [Ga2(HPO3)2] ribbons and four oxalate groups (gray balls);
(c) section of the single layer sheet of the layer polymorph NTHU-7L,
which may be viewed as the two-dimensional counterpart of NTHU-7.
The red arrows indicate folding to form a nanotubule and (d) a
NTHU-7 nanotubule with template tmdp. The green arrow indicates that emission can occur as the sensitizer is encapsulated.142
(Reproduced with permission from ref. 142. Copyright (2009) Wiley-VCH.)
Chem. Soc. Rev.
8.2 Metalorganic frameworks (MOFs)

Recently, the synthesis of metalorganic frameworks (MOFs)
has received great interest due to their potential applications in
many elds such as hydrogen storage, gas separation,
etc.143,144 Through the rational assembly of organic ligands
and metals or metal clusters, a huge variety of MOFs have
been obtained by means of solvothermal synthesis using
organic solvents such as N,N-dimethylformamide (DMF).
Taking advantage of the physico-chemical, economical and
ecological advantages of DESs in the ionothermal synthesis of
materials, eutectic mixtures are now regarded as promising
and particularly attractive media for large-scale synthesis of
new MOF structures. Dierent from ILs (two-component
systems with anions and cations), which were also used for
the MOF synthesis, DESs also contain neutral ligands such as
urea that can induce structure-directing eects making DES a
solvent of choice for the preparation of MOFs. To date, eorts
have been made toward the ionothermal synthesis of new
porous MOFs in DESs, due to the multiple roles that they
can play in such synthesis (Fig. 17).145
Bu and co-workers synthesized new MOF structures in
dierent urea-derived solvents (urothermal synthesis).146
More than 40 structures were obtained by assembly between:
a nitrate precursor of trivalent lanthanide or transition
metal or alkali and alkaline-earth metals (amongst In, Y, Nd,
Sm, Gd, Dy, Ho, Yb, Ce, Pr, Er, Cd, Mg, Cu, Co, Zn and Li)
1,4-benzenedicarboxylic acid (ligand bdc), 1,2,4-benzenetricarboxylic acid (ligand btc), naphtalene-1,4-dicarboxylic acid
(ligand ndc), thiophene-1,4-dicarboxylic acid, 1,3,5-benzenetribenzoic acid
ethylene urea hemihydrate (e-urea), propyleneurea (p-urea),
1,3-dimethyl-propyleneurea (p-murea), tetramethylurea (tm-urea)
diethylformamide (DEF), dimethylformamide (DMF),
2-pyrrolidinone (pyrol) (amide as solvent)
In these syntheses, urea derivatives (e-urea and others) can
act as a template for the formation of porous frameworks, but
also as a ligand and mixed pendant ligand. This is the case for
the URO-44 material, [Co3(bdc)3] (tm-urea)x, assembled
from H2bdc, cobalt nitrate and tm-urea, in which tm-urea
Fig. 17 (a) The structures of dierent DESs and (b) their multiple
roles in the ionothermal synthesis of MOFs (M = metal).145 (Reproduced
with permission from ref. 145. Copyright (2009) Wiley-VCH.)
This journal is

View Online
acts as a template. In opposition, in [Y2(bdc)3(e-urea)4],

assembled from H2bdc, yttrium nitrate and e-urea hemihydrate,
e-urea acts as a pendant ligand. Sometimes, urea-derivative is
also found to play a dual role [case of URO-162,
[Cd(thb)(en)1/2(e-urea)](e-urea)] or can be the reactant for
in situ ligand formation. However, these syntheses are beyond
the scope of DESs and therefore will not be particularly
discussed here. Some of these materials have a microporous
structure and thus exhibit promising gas-storage capabilities
for CO2 and H2 ([Sm(bdc)3/2(e-urea)], viz. the CO2 adsorption
is 26.8 cm3 g1 at approximately 1 atm and an H2 uptake of
74.9 cm3 g1 (0.66 wt%) at 77 K and 1 atm).
In 2009, Bus research group highlighted the versatile role of
the DES in the generation of porosity and open metal sites in
MOF structures for gas storage application.145 They then rst
reported the synthesis of a series of MOFs in DES, composed
of trivalent metal (In, Y, Nd, Sm), 1,4-benzenedicarboxylate
(bdc) and one or two components from the DES. Six dierent
topologies were obtained, and DES, in addition to its role of
solvent, acted as a structure directing agent. In the In-containing
structure, the extraframework choline ion was retained with
Cl bounded to the polymeric layers. In addition to the
external choline ion, neutral urea molecules can also be
bonded to the framework (example of the material (choline)
[Sm(bdc)2(urea)]). Choline can also be bounded to the MOF
framework through its OH groups, and neutral urea molecules
can serve as an external structure directing agent (the case of
[Nd(bdc)2(choline)](m-urea)). The last role of DES highlighted by the authors consists in the direct bonding of neutral
m-urea and e-urea to the polymeric framework (the case of
[Yb2(bdc)3(e-urea)4] material). All the novel structures have
clearly evidenced that DES not only acts as a solvent but also
as template and/or ligand supplier. Summary of the main
characteristics of the structures are given below:
2D anionic layer-type structure {[InCl(bdc)3/2(H2O)2]n}n.
Charge is compensated by guest extraframework choline
cations.
3D anionic framework (three isostructural compounds,
[MIII(bdc)2(urea)] with M = Y, Yb, Sm), lled with guest
choline cations.
Structures having neutral framework (when urea is substituted by larger urea derivatives, i.e. e-urea and m-urea). In
[Nd(bdc)2(choline)](m-urea), choline ion acts as a ligand
bound to the metal sites while m-urea acts as an extraframework template. In the other structures ([Gd2(bdc)3(m-urea)4],
[MIII2(bdc)3(e-urea)4] with M = Yb, Dy, Ho, and
[Sm(bdc)3/2(e-urea)]), urea-derived molecules act as bounded
ligands to the framework.
[Sm(bdc)3/2(e-urea)], which displays an excellent thermal
stability, was used to exemplify the potential of such structures
for gas storage application. After elimination of the neutral
e-urea ligand from the structure, a porosity was generated in
the obtained structure: [Sm(bdc)3/2]n, as conrmed by XRD.
In a similar way, the authors next prepared a series of
porous anionic C3N4-type ([In3(btc)4]n3n, btc = 1,3,5-benzenetricarboxylate) MOFs that contain size-tunable and ionexchangeable extraframework organic charge-compensating
cations. Synthesis was performed in dierent solvent including
molecular solvents, ILs and DESs.147 In ChCl/e-urea media, a
This journal is
C3N4-type ([In3(btc)4]n3n) framework was formed. The

choline cation compensated the framework charge, while
e-urea was also incorporated into the structure. The ionic
nature of DES may be particularly helpful in the formation of
the anionic [In3(btc)4]n3n framework. While similar framework compositions and topologies were obtained in DESs, six
dierent organic charge-compensating cations, having dierent
sizes, were entrapped in the structure. These new MOFs
exhibited dierent gas sorption capacity (N2, H2, CO2) due to
the dierent degrees of pore blockage by entrapment occluded
organic cations having dierent sizes. When pores are lled with
choline cation, high CO2 uptake capacity is obtained. The
authors suggest that strong interaction between the hydroxyl
group of the choline cation and CO2 is at the origin of the high
uptake capacity in this DES mediated structure.
Morris and co-workers148 also reported the ionothermal
synthesis of three new lanthanide/organic-derived MOFs in a
ChCl/dimethylurea DES. The use of hydrated mineral lanthanide
precursors unavoidably leads to the contamination of DES
with water. As observed above, the strong binding of isolated
molecules of water in DES through the hydrogen bond
network drastically limited its reactivity, aording a direct
access to materials that are hardly obtained with common
methods. The three obtained MOF structures are isostructural
materials of Ln(TMA)(DMU)2, with Ln among La-Nd-Eu,
TMA is trimesate (C9O6H3) and DMU is dimethylurea
[(CH3NH)2CO]. The ionothermal synthesis is performed
by reaction between the lanthanide salt (nitrate hydrate or
chloride hydrate) and trimesic acid in a ChCl/dimethylurea
DES. For the Nd-structure, HF in water was also used as a
mineralizing agent. Structures crystallized in the triclinic space
group P1% (Z = 2). The asymmetric unit of Ln(TMA)(DMU)2
was composed of the trivalent lanthanide atom, TMA and
DMU molecules, with eight-coordination of the lanthanide. In
the structure, TMA (through the COO group) acts as a
linking agent between neighboring lanthanide atoms to form
dimers. The 3D framework formation is ensured by H-bond
interaction between DMU and the carboxyl groups of Lanthanide dimers. In opposition to the classical decomposition of
DESs during ionothermal synthesis, DMU was not degraded
and was recovered in its initial form in the structure. This
shows that DMU acts as a ligand for the structure assembly.
Very recently, eight unique three dimensional lanthanidethiophene-2,5-dicarboxylate (TCD) materials were synthesized
in ChCl/e-urea DESs.149 Among them, six compounds are
isostructural, crystallizing in the P21/c space group of monoclinic symmetry, i.e. [Ln(TDC)2](choline) with Ln = Gd, Nd,
Eu, Er, Tb, Dy. In these structures, choline cation compensates the charge of the anionic frameworks. A similar material
was already obtained using 1-methyl-3-ethylimidazolium
bromide IL, showing that the guest cation (choline in the case
of the DES) did not play a template role. In the structure, four
carboxylate groups bridge two Gd3+ ions to generate
dinuclear units. These latter are bridged by TCD ligands to
form layers which thereafter interconnect with TCD ligands to
generate the 3D framework. The Yb-containing compound,
prepared under similar conditions, displays a dierent
structure. In [Yb(TCD)2(e-urea)](choline)(H2O), Yb3+ has
an additional coordination with a second ligand, e-urea.
Chem. Soc. Rev.

View Online
Fig. 18 (a) Coordination environment in [Nd2(TCD)3(e-urea)4]

3(e-urea); (b) distorted dicapped trigonal prism coordination polyhedron of the Nd(III) ion; (c) view of the framework along the b axis;
(d) two left- and two right-handed helices alternatively along the b axis;
(e) uninodal 6-connected nodes represented by {Nd2} units; (f) the rob
topology of [Nd2(TCD)3(e-urea)4]3(e-urea).149 (Reproduced with
permission from ref. 149. Copyright (2012) American Chemical Society.)
Two Yb3+ are bridged by two carboxyl groups to give a

dinuclear unit. TCD ligands bridge these dinuclear units to
form layers, which thereafter interconnect together to generate
the 3D framework. Finally, the [Nd2(TCD)3(e-urea)4]3(e-urea)
material presents a neutral framework with neutral e-urea
guest molecules. The structure characteristics are presented
in Fig. 18. A neutral 6-connected rob-type framework
(Fig. 18ef) with neutral guest e-urea molecules was obtained.
In this last structure, the dinuclear units are composed of two
Nd3+ ions, three TCD ligands, four terminal e-urea ligands
and the three guest e-urea molecules.
These materials are characterized by the presence of helical
substructures, as observed for [Yb(TCD)2(e-urea)](choline)(H2O)
material, due to the dierent coordination modes of the TCD
ligands (Fig. 18d).
Interestingly, with this material, single-crystal-to-singlecrystal guest exchange between e-urea (the guest molecule)
and ethanol can be achieved.
Bu et al.150 also reported the synthesis of zinc(II)-boron(III)imidazole framework with unusual pentagonal channels by
synthesis in ChCl/m-urea media. In Zn2(im)Cl2[B(im)4],
neither cation nor neutral ligand incorporates the material
structure, but DES helps to stabilize the metalhalogen bonds.
Then, the DES media allow the synthesis of a material which
integrates two distinct imidazolate frameworks, with Znim
linkage and B(im)4 complex.
8.3
Organicinorganic hybrids
The recent literature on crystalline porous materials such as

zeotypes has highlighted the great potential of DESs for the
Chem. Soc. Rev.
Fig. 19 The three-dimensional hydrogen-bonded supramolecular

framework of (1) material 1, and (2) material 2.151 (Reproduced with
permission from ref. 151. Copyright (2010) Elsevier.)
ionothermal synthesis of new materials. Besides metal phosphates with open-framework structures and MOFs, hybrid
polyoxometalate materials were also successfully synthesized
in DESs. Wang and co-workers151 rst reported the use of
DESs to prepare polyoxometalate (POM)-based hybrids.
By using the ChCl/urea DES as the reaction solvent,
two new compounds, [(CH3)3N(CH2)2OH]4[b-Mo8O26] (1)
and {(N2H5CO)[(CH3)3N(CH2)2OH]2}[Cr-Mo6O24H6]4H2O
(2), were successfully obtained at 30 1C starting from
Na2MoO4 2H2O and Cr(NO3)39H2O as precursors for
materials 1 and 2, respectively. Owing to an important hydrogen
bond network between organic cations and polyoxoanions, both
compounds exhibit a 3D supramolecular framework (Fig. 19).
For material 1, b-octamolybdate isopolyanion [b-Mo8O26]4
and four choline cations constitute the structural unit. The
polyoxoanion consists in eight {MoO6} edge-shared. The structural unit of material 2 is composed of one [CrMo6O24H6]3
Anderson-type anion, two choline cations, one protonated
urea molecule and four molecules of water. Subsequently,
three new polyoxometalate (POM)-based hybrids were
successfully synthesized in the DES ChCl/urea by the same
group.152 During the material syntheses, the decomposition
of urea was avoided thanks to the mild reaction conditions
(e.g. room temperature).
Consequently, the urea molecule was preserved in two
POM-based hybrid materials. The choline cations not only
act as the counter cation, but can also enter into the nal
structure of the material. In the basic structural unit of the rst
material, the [IMo6O24]5 Anderson type anion links with
one [Na2(H2O)6]2+ cation, two choline cations, one
protonated water molecule and one lattice water molecule: {[(CH3)3N(CH2)2OH]2(H3O)}[Na2(H2O)6][IMo6O24]H2O.
This journal is

View Online
For the second structure, {Na2[(CH3)(N(CH2)2OH]4}[Al(OH)6Mo6O18]28NH2CONH24H2O, two Anderson anions

are present. The two Anderson anions link with Na+, four
choline cations, eight urea molecules, and four water molecules to form the basic structural unit. Finally, in the
last structure, {Na6(H2O)18[(CH3)3N(CH2)2OH]2(CON2H5)2}
[NaMo7O24]24NH2CONH2H2O, two heptamolybdate cations
[Na2Mo7O24]4 are linked to {Na6(H2O)18[(CH3)3N(CH2)2OH]2(CON2H5)2}, four dissociated urea molecules, and lattice water
to form the structural unit. Some of these Mo-based POM
structures present interesting photocatalytic activity for the
rhodamine B elimination.
In line with their pioneer works on the use of DESs and ILs
for the synthesis of novel structures, Morriss research
group153 studied the synthesis of vanadium (oxy)uoride
materials by an ionothermal procedure in DESs or ILs media.
Among the 10 presented materials, six are new materials.
From a ChCl/1,3-dimethylurea DES, V2O5 (or (C5H8O2)3V)
and HF, three novel structures were obtained:
the monomeric (HNH2CH3)2VOF4(H2O)
the dimer (HNH2CH3)4V2O2F8(H2O)
the 1D chain (HNH2CH3)2VF5(V3)
Using the ChCl/2-imidazolidinone DES, V2O5 (or VOF3)
and HF, two novel structures are reported:
a-(H2NH2(CH2)2 NH2)VOF4
b-(H2NH2(CH2)2 NH2)VOF4
Due to the mild reaction temperature (110150 1C), DESs
have been proved to play a template role in the formation of
the nal structure. In ChCl/1,3-dimethylurea, dimethylurea
decomposed and provided a methylammonium cation to
produce the monomeric structure after only 2 days of reaction.
After ageing for 3 days, the dimeric structure is formed by
removal of one molecule of water.
8.4
Nanoparticles
Compared to their bulk counterparts, nano-materials have

unique properties including magnetic, electrochemical, and
photonic properties. Hence, nano-materials found a wide
variety of applications in dierent elds such as catalysis,
electronics, optical devices, magnetism, life science, etc.154 It
is well established that the control of the morphology of these
nanoparticles (NPs) is of considerable interest since it leads
to materials with dierent physicochemical properties and
functions. Therefore, the large-scale manufacture of nanoparticles
with well-dened size and functionality is a great challenge in
contemporary nanoscopic research.
In 2008, Sun and co-workers155 reported a simple route for
the shape-controlled synthesis of gold NPs. ChCl/urea DES
was used in replacement of the traditional surfactants,
HAuCl44H2O as the gold precursor, and L-ascorbic acid as
an anisotropic growth promoter. Synthesis was performed at
30 1C, with dierent water contents to orientate particle shape.
At intermediate water content (5000 ppm), star-shaped Au
nanoparticles with (331) and vicinal high-index facets were
successfully synthesized (Fig. 20(1)). More than 40% of the Au
NPs present a regular pentagonal symmetry (Fig. 20(2b)), even
if NPs with three, four and multiple branches were also
observed (also observed in Fig. 20(1)). The size of these at
This journal is
Fig. 20 (1) SEM images of the star-shaped Au nanoparticles;

(2) HRTEM images of Au nanoparticles recorded along [110] (bf)
and the SAED pattern (a).155 (Reproduced with permission from
ref. 155. Copyright (2008) Wiley-VCH.)
nanoparticles is about 300 nm. Au nanoparticles with dierent

shapes and surface structures including snowake-like
(without water) and nanothorns (with 10 000 ppm of water)
can be obtained simply by adjusting the water content in
the DES.
DES also presumably played the role of a stabilizer since the
NPs did not evolve with time in DES media. The obtained
star-shaped Au nanoparticles are reported to exhibit high
catalytic activity towards H2O2 electrocatalytic reduction,
due to the high density of step atoms on high index facets.
Lower catalytic activities were measured for the snowake-like
and nanothorns type NPs. However, for all the morphologies,
measured activities are higher than over the polycrystalline Au
electrode.
Very recently, another simple and ecient method was
developed by Chirea et al. for the synthesis of gold nanowire
from direct reduction of HAuCl4 by NaBH4 in DES.156 In
these syntheses, two dierent DESs, i.e. ChCl/ethylene glycol
(1 : 2) or ChCl/urea (1 : 2), were employed in the absence of a
surfactant. The length and average width of the nanowires
formed are aected by the nature of the DES and by the
NaBH4/HAuCl4 molar ratio. In particular, thinner and longer
nanowire networks (NWNs) were obtained in ChCl/ethylene
glycol. Dierent morphologies of NPs (from large plate,
spherical, tripods, tetrapods) can be obtained by only changing
the NaBH4/HAuCl4 ratio. FT-IR characterization of the
Chem. Soc. Rev.

View Online
AuNWNs evidenced the stabilizing role of the DES. Urea acts

as a stabilizing ligand on the AuNWN surface when synthesis
was performed in ChCl/urea DES while ethylene glycol stabilized the AuNWN synthesized in ChCl/ethylene glycol. The
obtained nanowire networks were used as catalysts for the
chemical reduction of p-nitroaniline (4-NA) with sodium
borohydride in aqueous solution. Catalytic investigations
showed that gold nanowires synthesized in ChCl/urea
(AuNWN2) were more active than those prepared in ChCl/
ethylene glycol (AuNWN1). For instance, under similar conditions, AuNWN2 led to a complete reduction of p-nitroaniline,
whereas AuNWN1 led to only 81% conversion. This dierence
in the catalytic activity is mainly attributed to the increased
number of low coordinated gold atoms on the surface of
AuNWN2.
Besides metal nanoparticles, nanostructured metal oxides
with controllable morphology have also been prepared in
DESs. Wong and co-workers developed an environmentally
friendly antisolvent approach, which involved the use of
DESs for the dissolution of metal oxides with the aim of
synthesizing various ZnO nanostructures including twin-cones
and nanorods with controllable dimensions.157 In the synthesis,
commercially available ZnO powders were rst dissolved in a
ChCl/urea DES. Then, various ZnO nanostructures were
obtained by precipitation after introduction of an antisolvent
(water/ethanol) into the DES. By closely controlling the
dierent reaction parameters, ZnO nanostructures, including
twin cones and nanorods, with controllable dimensions can be
readily prepared (Fig. 21). The ratio between water and
ethanol used for the precipitation of ZnO nanoparticles
strongly aects their size and morphology. While rice-grain
like micrometric particles are obtained when pure water is
used as antisolvent (Fig. 21(1a)), an increase of the ethanol
content in the antisolvent led to a decrease in ZnO crystal size.
Fig. 21 (1) SEM images of ZnO twin-cone nanostructures prepared

with the antisolvent of (a) pure water, (b) 50% ethanol and 50% water,
and (c) 90% ethanol and 10% water (injection time = 5 s). The inset
of (c) is a TEM image of a single twin-cone particle; (2) SEM images
of ZnO nanorods prepared with the antisolvent of (a) pure water,
(b) 50% ethanol and 50% water, and (c) 90% ethanol and 10% water
(injection time = 5 h).157 (Reproduced with permission from ref. 157.
Copyright (2010) American Chemical Society.)
Chem. Soc. Rev.
The injection rate of the ZnO-containing DES in the antisolvent solution also has a strong impact on the nal
morphology (compare Fig. 21 (1) injection time = 5 s and
(2) injection time = 5 h). Under slow injection conditions,
nanorods and ower-assembled nanorods of dierent sizes can
be obtained.
Additionally, monoclinic structured spindly bismuth vanadate
microtubes were prepared on a large scale by a simple ionothermal treatment in a ChClurea eutectic mixture, starting
from ammonium metavanadate, bismuth nitrate hydrate and
water.158 The obtained BiVO4 microtubes exhibited spindle
shape and saw-toothed structure. The authors studied the
time-dependant structure growth. For the spindle shaped
BiVO4, the growth mechanism was ascribed to a reactioncrystallization process controlled by the BiOCl concentration
and to a nucleation-growth process of nanosheets induced by
adsorbed solvent molecules on the microtube surfaces.
The obtained spindly microtubes exhibited much higher
visible-light photocatalytic activity for the rhodamine B
decolorization than that of bulk BiVO4 prepared by classical
solid-state reaction (thermal crystallization at 700 1C between
Bi(NO3)35H2O and NH4VO3). Dierence is attributed to the
larger surface and improved crystallinity of the DES-derived
mixed oxide.
8.5 Carbon materials
Porous carbon materials are extensively used for various
applications, including catalyst supports, electrochemical
devices, gas storage and separation, etc. Ionothermal synthesis
has been proven to be an ecient route for the preparation of
crystalline porous materials. Within this context, ILs have also
been recently demonstrated to be versatile precursors for the
preparation of porous carbon materials.159,160 In a similar
way, synthesis of porous carbon materials can be achieved in
DESs as reported by the group of del Monte. For example, the
resorcinol-formaldehyde (RF) polycondensation in DESs for
the preparation of carbons and carboncarbon nanotube
composites has been recently documented.161 During the
polycondensation of resorcinol and formaldehyde, hydroxymethyl species are formed. These hydroxymethyl species react
to form methylene and methylene ether bridged compounds. A
well-documented study is then given by these authors where
eects of water, catalyst, and the role of the DES (by comparison
with classical aqueous conditions) was systematically investigated. During the material preparation, the RF polycondensation rstly occurred in a ChCl/ethylene glycol DES. Then, the
resulting RF gels were carbonized to form monolithic carbons.
Conversely to the use of water, all RF gels prepared in DESs
exhibit similar textures, which is an interesting property of
DESs. Conversion rate and carbon content in the nal material are similar to those obtained using the classical route. After
the thermal treatment of these gels, surface areas of carbon
materials were largely improved. Another interesting point
concerns the ability of DES to disperse carbon nanotubes,
resulting in the formation of homogeneous carboncarbon
nanotube RF gels. Such a high composite homogeneity cannot
be obtained in water due to the poor dispersibility of nanotubes in such a medium.
This journal is

View Online
Next, the same group reported the synthesis of hierarchical

porous (bimodal, with micropores and mesopores) carbon
monoliths via formaldehyde polycondensation and subsequent
carbonization in DES.162 In these syntheses, both the bimolecular RC-DES (made from resorcinol and ChCl by varying the
ratio ChCl/resorcinol) and the ternary RUC-DES (made from
resorcinol, urea and ChCl, also by varying the resorcinol
concentration) were employed both as carbonaceous precursors and structure directing agents. Synthesis was only
performed in basic media, since the authors previously
evidenced that these conditions led to higher RF polycondensation. In these RU-DES and RUC-DES derived materials,
the ChCl molecule was evidenced to play a template role.
When the ternary RUC-DES was used, urea also participated
in the condensation reactions, and was incorporated into the
RF network. Carbonization of the obtained gels leads to the
production of high surface area carbons (455612 m2 g1),
with an important part of the surface developed in the
generated microporosity. In addition, narrow mesopores, with
size mainly depending on the nature of the DES, were formed.
As a consequence, larger mesopores were formed when ternary
RUC-DES is used, due to the incorporation of urea in the RF gel
(ca. 23 nm for urea-derived DES vs. 10 nm for urea-free DES).
Finally, Monte and co-workers163 reported the use of
ternary DESs composed of resorcinol, 3-hydroxypyridine
and ChCl (RHC-DES) as both precursors and structuredirecting agents in the synthesis of nitrogen-doped hierarchical
carbon monoliths. Like in their previous works, aqueous
solution of formaldehyde is added to the RHC-DES for the
condensation step in the presence of Na2CO3, prior to calcination. The morphology of the resulting carbons always consists
in a bicontinuous porous network made of highly cross-linked

clusters aggregated and assembled into interconnected structure, as observed in Fig. 22.
The DES is then described to play dierent roles:
a solvent that ensures reactants homogeneity,
the delivery of a structure-directing agent which governs
the formation of the hierarchical pore structure,
the source of carbon and nitrogen (retained in the nal
structure after carbonization).
While the increase in the carbonization temperature results
in a decrease in N-content, all carbonaceous materials always
retain a high nitrogen content showing the crucial participation of 3-hydroxypyridine during condensation reactions.
These nitrogen doped carbon materials are found to exhibit
high microporous surface area, in the range B540 m2 g1
(carbonized at 600 1C) to B680 m2 g1 (carbonized at 800 1C)
and narrow micropore size centered at B0.5 nm. The combination in these materials of a microporosity at size below
0.6 nm together with the presence of nitrogen makes these
carbon materials very promising for CO2 capture (CO2 adsorption capacities up to 3.3 mmol g1 were measured). Although
other microporous carbons are also known to exhibit even
higher adsorption capacities, carbon materials prepared in DES
were found to be highly stable, allowing their recycling.
Finally, the group of del Monte also demonstrated that
ecient synthesis of hierarchical porous multiwalled carbon
nanotube (MWCNT) composites can be achieved in DESs.164
Synthesis was performed through furfuryl alcohol (FA) condensation using a p-toluene sulfonic acid (pTsOH)/ChCl DES.
Again, the DES is an ideal medium to achieve a homogeneous
dispersion of the carbon nanotubes. Analysis of the porosity
of the carbonMWCNT composites obtained shows that high
surface areas are achieved (400550 m2 g1). Microporosity
and macroporosity are evidenced, with more of 60% of the
surface developed in the micropores. Large dierences in
porosity are induced upon addition of MWCNT in the DES.
Then, the morphology is progressively going to a bicontinuous
porous network, which resembles a skeleton of interconnected
MWCNTs, on the surface of which a carbon porous shell is
formed. This particular morphology, a carbon shell that
is entirely coating the MWCNT surface, leads to a high
conductivity, which is suitable for a use as an electrode for
supercapacitors. Finally, the authors rightly highlighted the
remarkable green character of the proposed process since all
the DES can be reused, due to its full recovery after condensation reaction.
9. Conclusions and outlook
Fig. 22 SEM micrographs of CRHC221-DES and CRHC111-DES obtained

after thermal treatments at 600 and 800 1C. Insets show pictures of the
CRHC221-DES and CRHC111-DES monoliths after thermal treatment at
800 1C.163 (Reproduced with permission from ref. 163. Copyright
This journal is
From the above described results, it clearly appears that DESs

exhibit close physico-chemical properties (viscosity, density,
conductivity, among others) to those of traditional ILs.
Additionally, like ILs, the physico-chemicals properties of
DESs can be tuned almost innitely by changing the nature
of the quaternary ammonium salt and the hydrogen-bond
donor, making possible the preparation of task-specic DESs.
As compared to ILs, DESs have however notable advantages
stemming from (1) their convenient synthesis (100% atom
economy), (2) their very low price since most of DESs can be
Chem. Soc. Rev.

View Online
prepared from readily accessible chemicals and (3) their low

toxicity, especially DESs derived from ChCl and renewable
chemicals. Clearly, these notable ecological and economical
advantages of DESs now open alternative routes for the
emergence of ionic uids at a larger scale. It should also be
noted that although components of DESs are potentially
reactive chemicals, their auto-association by a hydrogen bond
drastically limits their reactivity, allowing their use in many
elds of research.
In the eld of catalysis and organic synthesis, it is clear that
DESs will denitely contribute to the design of eco-ecient
processes. In particular, the possibility to (1) selectively and
conveniently extract products of the reaction from the DESs
phase, (2) adjust the pH of DESs, (3) dissolve not only organic
and inorganic salts but also transition metal-derived complexes
or nanoparticles and (4) recycle these media is among the
most promising advantages of DESs. It is our opinion that
development of DESs in the eld of catalysis will also be
drastically boosted by the need to urgently design innovative
processes for the catalytic conversion of biomass. Indeed,
imidazolium-based ILs have the unique ability to dissolve
large amounts of cellulose and more largely lignocelluloses
opening promising routes for the saccharication of biomass.
However, it is also clear that the price and toxicity of ILs
represent two serious drawbacks that hamper the scale-up
of these processes. We are fully convinced that the recent
progress made in the eld of DESs for the catalytic conversion
of carbohydrates will denitely open soon new methodologies
for converting lignocellulosic biomass in a more rational way.
In the eld of material chemistry, it is also apparent that ILs
can be advantageously replaced by cheap and safe DESs for
the ionothermal synthesis of a wide range of inorganic materials
with dierent textures and structures. Although a proper
selection of the exactly required DESs still remains a big
challenge, the above described works have clearly demonstrated that very important materials, from microporous
zeotypes to carbon materials, can be synthesized in DESs.
The very recent use of DESs for material synthesis demonstrates the exceptional potential of these media for the
generation of novel structures and engineered materials. In
these syntheses DESs may play dierent roles such as solvent,
structure-directing agent, water inhibitor, reactant for structure crystallization, etc.
Besides excellent dissolution properties for CO2, inorganic
salts, and organic molecules, many DESs can also selectively
dissolve dierent metal oxides, which thus provide great
potential for the selective recovery of pure metals, especially
in electrochemistry. In the particular eld of metal electrodeposition, similar results to those reported in conventional
ILs were obtained in DESs.
Despite all these promising applications, much eort is still
needed in order to widen the utilization of DESs in chemistry.
For instance, the instability of DESs during electrochemical
processes still represents an important issue that needs to be
addressed in the future. Viscosity of DESs can also be regarded
as a serious problem, especially for heterogeneously-catalyzed
processes. In this context, it makes no doubt that future
research will particularly focus on DESs with low viscosity.
Finally, a particular attention should also be given to the
Chem. Soc. Rev.
reactivity of DESs that can, in some cases, lead to formation

of undesirable side-products.
More than a green medium, DESs can also be regarded as a
poorly toxic and biocompatible lipotropic agent, thus opening
a new strategy for the vectorisation of pharmaceutical ingredients in the human body. This is motivated by the fact that
many DESs are suspected to be formed in living cells and
responsible for unexpected mechanisms.
Clearly, although DESs cannot replace ILs in all elds of
chemistry, we are fully convinced that their low ecological
footprint and attractive price will denitely contribute to the
industrial emergence of this new medium in a close future.
The authors are grateful to the French Ministry of Research
and the CNRS for their nancial support. The authors would
also like to thank Prof. A. P. Abbott and his co-workers for
their pioneering works in this eld of research and their
signicant contribution to the emergence of DESs in chemistry
and biology.
Notes and references

1 (a) J. P. Hallett and T. Welton, Chem. Rev., 2011, 111, 35083576;
P. Wasserscheid and W. Keim, Angew. Chem., Int. Ed., 2000, 39,
37723789; (b) H. Wang, G. Gurau and R. D. Rogers, Chem. Soc.
Rev., 2012, 41, 15191537.
2 D. A. Walsh, K. R. J. Lovelock and P. Licence, Chem. Soc. Rev.,
2010, 39, 41854194; Electrodeposition from Ionic Liquids,
ed. F. Endres, D. MacFarlane and A. Abbott, Wiley-VCH,
2008.
3 (a) J. Dupont and J. D. Scholten, Chem. Soc. Rev., 2010, 39,
17801804; (b) J. L. Bideau, L. Viau and A. Vioux, Chem. Soc.
Rev., 2011, 40, 907925.
4 Green Industrial Applications of Ionic Liquids, ed. R. Rogers,
K. Seddon and S. Volkov, Springer, 2003.
5 (a) M. J. Earle, S. P. Katdare and K. R. Seddon, Org. Lett., 2004,
6, 707710; (b) Q. Zhang, S. Zhang and Y. Deng, Green Chem.,
2011, 13, 26192637.
6 M. Deetlefs and K. R. Seddon, Green Chem., 2010, 12, 1730.
7 (a) A. Romero, A. Santos, J. Tojo and A. Rodr guez, J. Hazard.
Mater., 2008, 151, 268273; (b) N. V. Plechkova and
K. R. Seddon, Chem. Soc. Rev., 2008, 37, 123150.
8 Y. Yu, X. Lu, Q. Zhou, K. Dong, H. Yao and S. Zhang,
Chem.Eur. J., 2008, 14, 1117411182.
9 K. D. Weaver, H. J. Kim, J. Sun, D. R. MacFarlane and
G. D. Elliott, Green Chem., 2010, 12, 507513.
10 F. Ilgen, D. Ott, D. Kralish, C. Reil, A. Palmberger and B. Konig,
Green Chem., 2009, 11, 19481954.
11 D. Reinhardt, F. Ilgen, D. Kralisch, B. Konig and G. Kreisel,
Green Chem., 2008, 10, 11701181.
12 A. P. Abbott, J. C. Barron, K. S. Ryder and D. Wilson,
Chem.Eur. J., 2007, 13, 64956501.
13 S. Tang, A. Gary, Baker and H. Zhao, Chem. Soc. Rev., 2012, 41,
40304066.
14 A. P. Abbott, D. Boothby, G. Capper, D. L. Davies and
R. K. Rasheed, J. Am. Chem. Soc., 2004, 126, 91429147.
15 A. P. Abbott, G. Capper, D. L. Davies, R. K. Rasheed and
V. Tambyrajah, Chem. Commun., 2003, 7071.
16 K. A. Shahbaz, F. S. Mjalli, M. A. Hashim and I. M. AlNashef,
J. Appl. Sci., 2010, 10, 33493354.
17 M. Hayyan, F. S. Mjalli, M. A. Hashim and I. M. AlNashef, Fuel
Process. Technol., 2010, 91, 116120.
18 Y. Hou, Y. Gu, S. Zhang, F. Yang, H. Ding and Y. Shan, J. Mol.
Liq., 2008, 143, 154159.
19 Z. Maugeri and P. Dom nguez de Mar a, RSC Adv., 2012, 2,
421425.
20 D. Carriazo, M. C. Gutierrez, M. Luisa Ferrer and F. del Monte,
Chem. Mater., 2010, 22, 61466152.
21 K. Shahbaz, F. S. Mjalli, M. A. Hashim and I. M. AlNashef,
Energy Fuels, 2011, 25, 26712678.
This journal is

View Online
22 M. A. Kareem, F. S. Mjalli, M. A. Hashim and I. M. AlNashef,
J. Chem. Eng. Data, 2010, 55, 46324637.
23 A. P. Abbott, G. Capper and S. Gray, ChemPhysChem, 2006, 7,
803806.
24 C. DAgostino, R. C. Harris, A. P. Abbott, L. F. Gladden and
M. D. Mantle, Phys. Chem. Chem. Phys., 2011, 13, 2138321391.
25 A. P. Abbott, R. C. Harris and K. S. Ryder, J. Phys. Chem. B,
2007, 111, 49104913.
26 K. Shahbaz, S. Baroutian, F. S. Mjalli, M. A. Hashim and
I. M. AlNashef, Thermochim. Acta, 2012, 527, 5966.
27 A. P. Abbott, R. C. Harris, k. S. Ryder, C. DAgostino,
L. F. Gladden and M. D. Mantle, Green Chem., 2011, 13, 8290.
28 K. Shahbaz, F. S. Mjalli, M. A. Hashim and I. M. AlNashef,
Thermochim. Acta, 2011, 515, 6772.
29 A. P. Abbott, G. Capper, D. L. Davies and R. Rasheed, Inorg.
Chem., 2004, 43, 34473452.
30 M. G. D. Popolo, J. Kohano and R. M. Lynden-Bell, J. Phys.
Chem. B, 2006, 110, 87988803.
31 W. Li, Z. Zhang, B. Han, S. Hu, J. Song, Y. Xie and X. Zhou,
Green Chem., 2008, 10, 11421145.
32 X. Li, M. Hou, B. Han, X. Wang and L. Zou, J. Chem. Eng. Data,
2008, 53, 548550.
33 W. C. Su, D. S. H. Wong and M. H. Li, J. Chem. Eng. Data, 2009,
54, 19511955.
34 A. P. Abbott, G. Frisch, J. Hartley and K. S. Ryder, Green Chem.,
2011, 13, 471481.
35 A. P. Abbott, G. Capper and P. Shikotra, Trans. Inst. Min.
Metall., Sect. C, 2006, 115, 1518.
36 A. P. Abbott, G. Capper, D. L. Davies, K. J. McKenzie and
Stephen U. Obi, J. Chem. Eng. Data, 2006, 51, 12801282.
37 J. M. Rimsza and L. R. Corrales, Comput. Theor. Chem., 2012,
987(1), 5761.
38 H. G. Morrison, C. C. Sun and S. Neervannan, Int. J. Pharm.,
2009, 378, 136139.
39 I. Mamajanov, A. E. Engelhart, H. D. Bean and N. V. Hud,
Angew. Chem., Int. Ed., 2010, 49, 63106314.
40 A. P. Abbott, P. M. Cullis, M. J. Gibson, R. C. Harris and
E. Raven, Green Chem., 2007, 9, 868872.
41 (a) F. Jutz, J. Andanson and A. Baiker, Chem. Rev., 2011, 111,
322353; (b) V. I. Parvulescu and C. Hardacre, Chem. Rev., 2007,
107, 26152665; (c) F. Rantwijk and R. A. Sheldon, Chem. Rev.,
2007, 107, 27572785.
42 S. B. Phadtare and G. S. Shankarling, Green Chem., 2010, 12,
458462.
43 (a) Y. Jung and R. A. Marcus, J. Am. Chem. Soc., 2007, 129,
54925502; (b) R. Breslow, Acc. Chem. Res., 1991, 24, 159164;
(c) A. Lubineau, J. Auge and Y. Queneau, Synthesis, 1994,
741760.
44 P. M. Pawar, K. J. Jarag and G. S. Shankarling, Green Chem.,
2011, 13, 21302134.
45 Y. A. Sonawane, S. B. Phadtare, B. N. Borse, A. R. Jagtap and
G. S. Shankarling, Org. Lett., 2010, 12, 14561459.
46 F. Ilgen and B. Konig, Green Chem., 2009, 11, 848854.
47 O. Coulembier, V. Lemaur, T. Josse, A. Minoia, J. Cornil and
P. Dubois, Chem. Sci., 2012, 3, 723726.
48 B. Singh, H. Lobo and G. Shankarling, Catal. Lett., 2011, 141,
178182.
49 (a) E. Zakrzewska Malgorzata, E. Bogel-Lukasik and R. BogelLukasik, Chem. Rev., 2011, 111(2), 397417; (b) R. Karinen,
K. Vilonen and M. Niemela, ChemSusChem, 2011, 4(8), 10021016.
50 S. Hu, Z. Zhang, Y. Zhou, B. Han, H. Fan, W. Li, J. Song and
Y. Xie, Green Chem., 2008, 10, 12801283.
51 H. Zhao, J. E. Holladay, H. Brown and Z. C. Zhang, Science,
2007, 316, 15971600.
52 S. Hu, Z. Zhang, Y. Zhou, J. Song, H. Fan and B. Han, Green
Chem., 2009, 11, 873877.
53 K. de Oliveira Vigier, A. Benguerba, J. Barrault and F. Jerome,
Green Chem., 2012, 14, 285289.
54 (a) A. Biswas, R. L. Shogren, D. G. Stevenson, J. L. Willett and
P. K. Bhowmik, Carbohydr. Polym., 2006, 66, 546550;
(b) A. P. Abbott, T. J. Bell, S. Handa and B. Stoddart, Green
Chem., 2005, 7, 705707.
55 As a recent example please see A. P. Abbott, A. D. Ballantyne,
J. Palenzuela Conde, K. S. Ryder and W. R. Wise, Green Chem.,
2012, 14, 13021037.
This journal is
56 Z. Chen, B. Zhou, H. Cai and X. Zou, Green Chem., 2009, 11,

275278.
57 A. P. Abott, G. Capper, D. L. Davies, R. K. Rasheed and
V. Tambyrajah, Green Chem., 2002, 4, 2426.
58 N. Azizi and Z. Manocheri, Res. Chem. Intermed., 2012, DOI:
10.1007/s11164-011-0479-4.
59 G. Imperato, E. Eibler, J. Niedermaier and B. Konig, Chem.
Commun., 2005, 11701172.
60 J. D. mota-Morales, M. C. Gutierrez, I. C. Sanchez, G. Luna-Barcenas
and F. del monte, Chem. Commun., 2011, 47, 53285330.
61 M. C. Serrano, M. C. Gutierez, R. Jimenez, M. L. Ferrer and
F. del Monte, Chem. Commun., 2012, 48, 579581.
62 G. Imperato, S. Hoger, D. Lenoir and B. Konig, Green Chem.,
2006, 8, 10511055.
63 G. Imperato, R. Vasold and B. Konig, Adv. Synth. Catal., 2006,
348, 22432247.
64 H. Zhang, Q. Cai and D. Ma, J. Org. Chem., 2005, 70, 51645173.
65 (a) P. Dominguez de Maria and Z. Maugeri, Curr. Opin. Chem.
Biol., 2011, 15, 220225; (b) J. Gorke, F. Srienc and
R. Kazlauskas, Biotechnol. Bioprocess Eng., 2010, 15, 4053.
66 J. T. Gorke, F. Srienc and R. J. Kazlauskas, Chem. Commun.,
2008, 12351237.
67 D. Linberg, M. de la Fuente Revenga and M. Widersten,
J. Biotechnol., 2010, 147, 169171.
68 H. Zhao, G. A. Baker and S. Holmes, Org. Bio. Chem., 2011, 9,
19081916.
69 H. Zhao, G. A. baker and S. Holmes, J. Mol. Cat. B: Enzymatic,
2011, 72, 163167.
70 M. C. Gutierrez, M. L. Ferrer, L. Yuste, F. Rojo and F. del Monte,
Angew. Chem., Int. Ed., 2010, 49, 21582162.
71 Y. H. Choi, J. van Spronsen, Y. Dai, M. Verbene, F. hollmann,
I. W. C. E. Arends, G. J. Witkamp and R. Verpoorte, Plant
Physiol., 2011, 156, 17011705.
72 S. Gore, S. Baskaran and B. Konig, Green Chem., 2011, 13, 10091013.
73 Z.-H. Zhang, X.-N. Zhang, L.-P. Mo, Y.-X. Li and F. P. Ma,
Green Chem., 2012, 14, 15021506.
74 F.-P. Ma, G.-T. Cheng, Z.-G. He and Z.-H. Zhang, Aust. J.
Chem., 2012, 65(4), 409416.
75 N. Azizi, E. Batebi, S. Bagherpour and H. Ghafuri, RSC Adv.,
2012, 2, 22892293.
76 (a) P. C. Andricacos, C. Uzoh, J. O. Dukovic, J. Horkans and
H. Deligianni, Electrochem. Microfabr., 1998, 42, 5;
(b) P. C. Andricacos, Interface, 1998, 7, 23; (c) G. Pattanaik,
D. M. Kirkwood, X. Xu and G. Zangari, Electrochim. Acta, 2007,
52, 27552764; (d) R. Hasegawa, Physica B, 2001, 299, 199.
77 (a) D. Wei and M. Okido, Curr. Top. Electrochem., 1997, 5,
2126; (b) A. Etenko, T. McKechine, A. Shchetkovsiy and
A. Smirnov, ECS Trans., 2007, 3, 151157; (c) M. Gibilaro,
L. Massot, P. Chamelot and P. Taxil, Electrochim. Acta, 2009,
54, 53005306; (d) D. J. Fray and G. Z. Chen, Master. Sci.
Technol., 2004, 20, 295.
78 (a) T. Welton, Chem. Rev., 1999, 99, 2071; (b) P. Wassershied
and T. Welton, Ionic liquids in Synthesis, Wiley-VCH Verlag,
Weinheim, Germany 2003; (c) R. Wang, T. Okajima, F. kitamura
and T. Oshaka, Electroanalysis, 2004, 16, 6672; (d) R. T. Carlin,
H. C. De Long, J. Fuller and P. C. Truelove, J. Electrochem. Soc.,
1994, 141, L73; (e) A. B. Mc Ewen, S. F. McDevitt and V. Koch,
J. Electrochem. Soc., 1997, 144, L84; (f) M. C. Buzzeo, R. G.
Evans and R. G. Compton, ChemPhysChem., 2004, 5, 1106;
(g) F. Endres, Z. Phys. Chem. 2004, 218, 255; (h) M. Galinski,
A. Lewandowski and I. Stepniak, Electrochem. Acta, 2006,
51, 5567; (i) A. P. Abbott and K. J. McKenzie, Phys. Chem.
Chem. Phys., 2006, 8, 42654279.
79 (a) J. S. Wilkes and M. J. awototko, Chem. Commun., 1992, 965;
(b) J. Fuller, R. T. Carli and R. A. Osteryoung, J. Electrochem.
Soc., 1999, 144, 3881; (c) A. P. Abbott, G. Capper, D. L. Davies,
H. Munro and R. Rashreed, Inorg. Chem., 2004, 43, 3447;
(d) J. Z. Yang, W. G. Xu, P. Tian and L. L. He, Fluid Phase
Equilib., 2003, 204, 295.
80 E. Gomez, P. Cojocaru, L. Magagnin and E. Valles,
J. Electroanalytical Chem., 2011, 658, 1824.
81 P. Cojocaru, L. Magagnin, E. Gomez and E. Valles, Mater. Lett.,
2011, 65, 35973600.
82 D. D. Shivagan, P. J. Dale, A. P. Samantilleke and L. M. Peter,
Thin Solid Films, 2007, 515, 58995903.
Chem. Soc. Rev.

View Online
83 M. Steichen, M. Thomassey, S. Siebentritt and P. J. Dale, Phys.
Chem. Chem. Phys., 2011, 13, 4292.
84 H. Yang, X. Guo, N. Birbilis, G. Wu and W. Ding, Appl. Surf.
Sci., 2011, 257, 90949102.
85 A. P. Abbott, G. Capper, D. L. Davies, K. J. McKenzie and
S. U. Obi, J. Chem. Eng. Data, 2006, 51, 12801282.
86 P. Martis, V. S. Dilimon, J. Delhalle and Z. Mekhalif, Electrochim.
Acta, 2010, 55, 54075410.
87 A. P. Abbott, K. El Ttaib, K. S. Ryder and E. L. Smith, Trans.
Inst. Met. Finish., 2008, 86, 234240.
88 H. Y. Yang, W. Guo, X. B. Chen, S. H. Wang, G. H. Wu,
W. J. Ding and N. Birbilis, Electrochim. Acta, 2012, 63, 131138.
89 A. P. Abbott, G. Capper, K. J. McKenzie and K. S. Ryder,
J. Electroanal. Chem., 2007, 599, 288294.
90 P. Dale, A. P. Samantilleke, D. D. Shivagan and L. M. Peter, Thin
Solid Films, 2007, 515, 57515754.
91 A. Bakkar and V. Neubert, Electrochem. Commun., 2007, 9,
24282435.
92 D. Yue, Y. Jia, Y. Yao, J. Sun and Y. Jing, Electrochim. Acta,
2012, 65, 3036.
93 E. L. Smith, J. C. Barron, A. P. Abbott and K. S. Ryder, Anal.
Chem., 2009, 81, 84668471.
94 A. P. Abbott, J. C. Barron, G. Frisch, K. S. Ryder and
A. Fernando Silva, Electrochim. Acta, 2011, 56, 52725279.
95 A. P. Abbott, J. C. Barron, G. Frisch, S. Gurman, K. S. Ryder
and A. Fernando Silva, Phys. Chem. Chem. Phys., 2011, 13,
1022410231.
96 A. Sun, H. Zhao and J. Zheng, Talanta, 2012, 88, 259264.
97 A. P. Abbott, K. ElTtaib, G. Frisch and K. J. McKenzie, Phys.
Chem. Chem. Phys., 2009, 11, 42694277.
98 D. Lloyd, T. Vainikka, L. Murtomaki, K. Kontturi and
E. Ahlberg, Electrochim. Acta, 2011, 56, 49424948.
99 A. P. Abbott, S. Nandhra, S. Postlethwark, E. Smith and
K. S. Ryder, Phys. Chem. Chem. Phys., 2007, 9, 37353743.
100 A. P. Abbott, K. El Ttaib, G. Frisch, K. S. Ryder and D. Weston,
Phys. Chem. Chem. Phys., 2012, 14, 24432449.
101 C. D. Gu, X. J. Xu and J. P. Tu, J. Phys. Chem., 2010, 114,
1361413619.
102 G. Saravanan and S. Mohan, J. Alloys Compounds, 2012, 522,
162166.
103 C. Gu and J. Tu, Langmuir, 2011, 27, 1013210140.
104 M. A. Skopek, M. A. Mohamoud, K. S. Ryder and
A. R. Hillman, Chem. Commun., 2009, 935937.
105 K. Haerens, E. Matthijs, K. Binnemans and B. Ven Der Bruggen,
Green Chem., 2009, 11, 13571365.
106 M. Figueiredo, C. Gomes, E. Costa, A. Martins, C. M. Pereira
and F. Silva, Electrochim. Acta, 2009, 54, 26302634.
107 B. G. Pollet, J. Y. Hihn and T. J. Mason, Electrochim. Acta, 2008,
53, 42484256.
108 C. A. Nkuku and R. J. LeSuer, J. Phys. Chem. B, 2007, 111,
1327113277.
109 A. P. Abbott, G. Capper, D. L. Davies and R. K. Rasheed,
Chem.Eur. J., 2004, 10, 37693774.
110 H.-R. Jhong, D. Shan-Hill Wog, C.-C. Wan, Y.-Y. Wang and
T.-C. Wei, Electrochem. Commun., 2009, 11, 209211.
111 A. P. Abbott, G. Capper, K. J. McKenzie and K. S. Ryder,
Electrochim. Acta, 2006, 51, 44204425.
112 A. P. Abbott, G. Capper, K. J. McKenzie, A. Glidle and
K. S. Ryder, Phys. Chem. Chem. Phys., 2006, 8, 42144221.
113 A. P. Abbott, G. Frisch, S. J. Gurma, A. R. Hillman, J. Hartley,
F. Holyoak and K. S. Ryder, Chem. Commun., 2011, 47,
1003110033.
114 S. Ramesh, R. Shanti and E. Morris, J. Mater. Sci., 2012, 47,
17871793.
115 S. Ramesh, R. Shanti and E. Morris, Carbohydr. Polym., 2012,
87, 701706.
116 S. Ramesh, R. Shanti and E. Morris, J. Mol. Liq., 2012, 166, 4043.
117 (a) D. Freudenmann, S. Wolf, M. Wol and C. Feldmann,
Angew. Chem., Int. Ed., 2011, 50, 1105011060; (b) Z. Ma,
J. Yu and S. Dai, Adv. Mater., 2010, 22, 261285.
118 (a) E. R. Parnham and R. E. Morris, Acc. Chem. Res., 2007, 40,
10051013; (b) R. E. Morris, Chem. Commun., 2009, 29902998;
A. Taubert, Acta Chim. Slov., 2005, 52, 183186.
119 E. R. Cooper, C. D. Andrews, P. S. Wheatley, P. B. Webb,
P. Wormald and R. E. Morris, Nature, 2004, 430, 10121016.
Chem. Soc. Rev.
120 E. R. Parnham, P. S. Wheatley and R. E. Morris, Chem. Commun.,

2006, 380382.
121 (a) E. R. Parnham and R. E. Morris, J. Am. Chem. Soc., 2006,
128, 22042205; (b) E. R. Parnham and R. E. Morris, Chem.
Mater., 2006, 18, 48824887.
122 E. R. Parnham, E. A. Drylie, P. S. Wheatley, A. M. Z. Slawin and
R. E. Morris, Angew. Chem., Int. Ed., 2006, 45, 49624966.
123 L. Vidal, C. Marichal, V. Gramlich, J. Patarin and Z. Gabelica,
Chem. Mater., 1999, 11, 27282736.
124 H. J. Ma, Z. J. Tian, R. S. Xu, B. C. Wang, Y. Wei, L. Wang,
Y. P. Xu, W. P. Zhang and L. W. Lin, J. Am. Chem. Soc., 2008,
130, 81208120.
125 (a) L. Cammarata, S. G. Kazarian, P. A. Salter and T. Welton,
Phys. Chem. Chem. Phys., 2001, 3, 51925200; (b) C. G. Hanke
and R. M. Lynden-Bell, J. Phys. Chem. B, 2003, 107,
1087310878.
126 E. A. Drylie, D. S. Wragg, E. R. Parnham, P. S. Wheatley,
A. M. Z. Slawin, J. E. Warren and R. E. Morris, Angew. Chem.,
Int. Ed., 2007, 46, 78397843.
127 G. Y. Yang and S. C. Sevov, J. Am. Chem. Soc., 1999, 121,
83898390.
128 J. H. Liao, P. C. Wu and Y. H. Bai, Inorg. Chem. Commun., 2005,
8, 390392.
129 W. T. A. Harrison, Inorg. Chem. Commun., 2007, 10, 833838.
130 L. Liu, Y. Kong, H. Xu, J. P. Li, J. X. Dong and Z. Lin,
Microporous Mesoporous Mater., 2008, 115, 624628.
131 R. H. Jones, J. Chen, G. Sankar and J. M. Thomas, Stud. Surf.
Sci. Catal., 1994, 84, 22292236.
132 L. Liu, S. Ferdov, C. Coelho, Y. Kong, L. Mafra, J. P. Li,
J. X. Dong, U. Kolitsch, R. A. S. Ferreira, E. Tillmanns, J. Rocha
and Z. Lin, Inorg. Chem., 2009, 48, 45984600.
133 L. Liu, D. S. Wragg, H. Zhang, Y. Kong, P. J. Byrne, T. J. Prior,
J. E. Warren, Z. Lin, J. Dong and R. E. Morris, Dalton Trans.,
2009, 67156718.
134 P. Jhang, N. Chuang and S. Wang, Angew. Chem., Int. Ed., 2010,
49, 42004204.
135 L. Liu, Y. Li, H. Wei, M. Dong, J. Wang, A. M. Z. Slawin, J. Li,
J. Dong and R. E. Morris, Angew. Chem., Int. Ed., 2009, 48,
22062209.
136 J. X. Dong, L. Liu, J. Li, Y. Li, C. Baerlocher and
L. B. McCusker, Microporous Mesoporous Mater., 2007, 104,
185191.
137 L. Liu, Z. F. Chen, H. B. Wei, Y. Li, Y. C. Fu, H. Xu, J. P. Li,
A. M. Z. Slawin and J. X. Dong, Inorg. Chem., 2010, 49, 82708275.
138 L. Liu, J. Yang, J. Li, J. Dong, D. Sis ak, M. Luzzatto and
L. McCusker, Angew. Chem., Int. Ed., 2011, 50, 81398142.
139 Z. Lin, D. S. Wragg, P. Lightfoot and R. E. Morris, Dalton
Trans., 2009, 52875289.
140 C. Y. Sheu, S. F. Lee and K. H. Lii, Inorg. Chem., 2006, 45,
18911893.
141 (a) Y. C. Liao, C. H. Lin and S. L. Wang, J. Am. Chem. Soc.,
2005, 127, 9986; (b) Y. C. Yang and S. L. Wang, J. Am. Chem.
Soc., 2008, 130, 11461147.
142 P. C. Jhang, Y. C. Yang, Y. C. Lai, W. R. Liu and S. L. Wang,
Angew. Chem., Int. Ed., 2009, 48, 742745.
143 N. A. Ramsahye, G. Maurin, S. Bourrelly, P. L. Llewellyn,
C. Serre, T. Loiseau, T. Devic and G. Ferey, J. Phys. Chem. C,
2008, 112, 514520.
144 (a) T. K. Trung, P. Trens, N. Tanchoux, S. Bourrelly,
P. L. Llewellyn, S. Loera-Serna, C. Serre, T. Loiseau, F. Fajula
and G. Ferey, J. Am. Chem. Soc., 2008, 130, 1692616932;
(b) G. Ferey, Chem. Soc. Rev., 2008, 37, 191241.
145 J. Zhang, T. Wu, S. Chen, P. Feng and X. Bu, Angew. Chem., Int.
Ed., 2009, 48, 34863490.
146 J. Zhang, J. T. Bu, S. Chen, T. Wu, S. Zheng, Y. Chen,
R. A. Nieto, P. Feng and X. Bu, Angew. Chem., Int. Ed., 2010,
49, 88768879.
147 S. Chen, J. Zhang, T. Wu, P. Feng and X. Bu, J. Am. Chem. Soc.,
2009, 131, 1602716029.
148 F. Himeur, I. Stein, D. S. Wragg, A. M. Z. Slawin, P. Lightfoot
and R. E. Morris, Solid State Sci., 2010, 12, 418421.
149 C. H. Zhan, F. Wang, Y. Kang and J. Zhang, Inorg. Chem., 2012,
51, 523530.
150 S. Chen, J. Zhang, T. Wu, P. Feng and X. Bu, Dalton Trans.,
2010, 39, 697699.
This journal is
View Online

151 S. M. Wang, Y. W. Li, X. J. Feng, Y. G. Li and E. B. Wang,

Inorg. Chim. Acta, 2010, 363, 15561560.
152 S. M. Wang, W. L. Chen, E. B. Wang, Y. G. Li, X. J. Feng and
L. Liu, Inorg. Chem. Commun., 2010, 13, 972975.
153 F. H. Aidoudi, P. J. Byrne, P. K. Allan, S. J. Teat, P. Lightfoot
and R. E. Morris, Dalton Trans., 2011, 40, 43244331.
154 G. A. Ozin, A. C. Arsenault and L. Cademartiri, in Nanochemistry A Chemical Approach to Nanomaterials, The Royal
Society of Chemistry, 2nd edn, 2009.
155 H. G. Liao, Y. X. Jiang, Z. Y. Zhou, S. P. Chen and S. G. Sun,
Angew. Chem., Int. Ed., 2008, 47, 91009103.
156 M. Chirea, A. Freitas, B. S. Vasile, C. Ghitulica, C. M. Pereira
and F. Silva, Langmuir, 2011, 27, 39063913.
157 J. Y. Dong, Y. J. Hsu, D. S. H. Wong and S. Y. Lu, J. Phys.
Chem. C, 2010, 114, 88678872.
This journal is
158 W. Liu, Y. Yu, L. Cao, G. Su, X. Liu, L. Zhang and Y. Wang,

J. Hazard. Mater., 2010, 181, 11021108.
159 (a) J. P. Paraknowitsch, J. Zhang, D. S. Su, A. Thomas and
M. Antonietti, Adv. Mater., 2010, 22, 8792; (b) J. S. Lee, X. Q.
Wang, H. M. Luo and S. Dai, Adv. Mater., 2010, 22, 10041007.
160 J. S. Lee, X. Q. Wang, H. M. Luo, G. A. Baker and S. Dai, J. Am.
Chem. Soc., 2009, 131, 45964597.
161 M. C. Gutierrez, F. Rubio and F. Monte, Chem. Mater., 2010, 22,
27112719.
162 D. Carriazo, M. C. Gutierrez, M. L. Ferrer and F. Monte, Chem.
Mater., 2010, 22, 61466152.
163 M. C. Gutierrez, D. Carriazo, C. O. Ania, J. B. Parra, M. L.
Ferrer and F. Monte, Energy Environ. Sci., 2011, 4, 35353544.
164 M. C. Gutierrez, D. Carriazo, A. Tamayo, R. Jimenez, F. Pico,
J. M. Rojo, M. L. Ferrer and F. Monte, Chem.Eur. J., 2011, 17,
1053310537.
Chem. Soc. Rev.

Deep Eutectic Solvents - Syntheses, Properties and Applications

Uploaded by

Copyright:

Available Formats

Deep Eutectic Solvents - Syntheses, Properties and Applications

Uploaded by

Document Information

Original Title

Copyright

Available Formats

Share this document

Share or Embed Document

Sharing Options

Did you find this document useful?

Is this content inappropriate?

Copyright:

Available Formats

Deep Eutectic Solvents - Syntheses, Properties and Applications

Uploaded by

Copyright:

Available Formats

View Online / Journal Homepage

Chem Soc Rev

Dynamic Article Links

Cite this: DOI: 10.1039/c2cs35178a

Deep eutectic solvents: syntheses, properties and applications

Downloaded by UNIVERSITY OF SOUTH AUSTRALIA on 27 August 2012

Received 11th May 2012

Universite de Poitiers/CNRS, UMR 7285, Institut de Chimie des

catalysis, electrochemistry, material chemistry, and more recently

Qinghua Zhang was born in

Karine De Oliveira Vigier

The Royal Society of Chemistry 2012

Chem. Soc. Rev.

Downloaded by UNIVERSITY OF SOUTH AUSTRALIA on 27 August 2012

a very large depression of freezing point, generally higher

Sebastien Royer received his

Francois Jerome received his

Chem. Soc. Rev.

The Royal Society of Chemistry 2012

Downloaded by UNIVERSITY OF SOUTH AUSTRALIA on 27 August 2012

to handle and no purication is required, thus making their

3. Physicochemical properties of DESs

Scheme 1 Typical structures of the halide salts and hydrogen bond

through hydrogen bond interactions, to form a eutectic mixture.

The Royal Society of Chemistry 2012

Similar to ILs,13 DESs are chemically tailorable solvents since

Downloaded by UNIVERSITY OF SOUTH AUSTRALIA on 27 August 2012

Hydrogen bond donor (HBD)

Chem. Soc. Rev.

The Royal Society of Chemistry 2012

Downloaded by UNIVERSITY OF SOUTH AUSTRALIA on 27 August 2012

Hydrogen bond donor (HBD)

the HBD and mixed with dierent ammonium salts in a molar

The Royal Society of Chemistry 2012

in the order F > NO3 > Cl > BF4, suggesting a

Freezing point (Tf) of other DESs

Downloaded by UNIVERSITY OF SOUTH AUSTRALIA on 27 August 2012

Chem. Soc. Rev.

The Royal Society of Chemistry 2012

Downloaded by UNIVERSITY OF SOUTH AUSTRALIA on 27 August 2012

Fig. 1 shows the phase diagram for mixtures of ChCl with

Fig. 1 Freezing points of choline chloride with ve carboxylic acids

The Royal Society of Chemistry 2012

that the freezing point of HBD-salt eutectic mixtures should be

Chem. Soc. Rev.

Downloaded by UNIVERSITY OF SOUTH AUSTRALIA on 27 August 2012

Table 4 Viscosities of selected DESs at dierent temperatures

Fig. 2 Densities of the glycerol/ChCl DES as a function of the molar

Addition of ChCl to glycerol results in a decrease of the DES

Like most of the ILs, viscosity of DESs is an important issue

Salt : HBD molar

750 (25 1C)

Interestingly, in the case of a ChCl/glycerol DES, an

Fig. 3 Eect of ChCl on the viscosity, Z of glycerol as a function of

The Royal Society of Chemistry 2012

Generally, polarity of a solvent can be evaluated by its polarity

Downloaded by UNIVERSITY OF SOUTH AUSTRALIA on 27 August 2012

= (2.8591  103)Umax(cm1) = 28591/lmax

In Table 5, the polarity data of various ChClglycerol eutectic

= (2.8591 103)Umax(cm1) = 28591/lmax