Current Green Chemistry
Send Orders for Reprints to reprints@benthamscience.net
Current Green Chemistry, 2020, 7, 105-119
105
MINI REVIEW ARTICLE
Task-specific Ionic Liquids as a Green Catalysts and Solvents for Organic
Synthesis
Swapnil A. Padvi
1
and Dipak S. Dalal
2,*
1
Department of Chemistry, Jai Hind Educational Trust Z. B. Patil College, Dhule – 424 002 (M. S.), India;
2
School of
Chemical Sciences, Kavayitri Bahinabai Chaudhari North Maharashtra University, Jalgaon - 425 001 (M. S.), India
Abstract: Task-specific ionic liquids (TSILs) have received increased attention over the past few
years as a Green Catalysts and Solvents for a large number of organic transformations. The present re-
view article aims to provide an introduction, types of task-specific ionic liquids, preparation/synthesis,
physical properties, characterization, use of TSILs as solvent and catalyst in organic synthesis.
A R T I C L E H I S T O R Y
Received: June 29, 2019
Revised: December 11, 2019
Accepted: December 13, 2019
DOI:
10.2174/2213346107666200115153051
Keywords: Task-specific ionic liquids, green chemistry, organic synthesis, Ionic liquids (ILs), molten salts, typical cations.
1. INTRODUCTION
To date, molecular solvents were used for most of the
chemical processes [1, 2]. These molecular solvents can in-
duce environmental pollution due to the use of huge amounts
in the chemical industry and laboratory may cause environ-
mental problems and creates adverse effects on organisms
and human health because they are toxic, flammable, explo-
sive and volatile [3, 4]. Among the several important princi-
ples of green chemistry, the elimination of hazardous sol-
vents and catalyst has attracted significant attention world-
wide to avoid the generation of chemical wastes [5]. Re-
searchers both from academia and the industry have been
focused on reducing or eliminating the use of toxic solvents
to minimize damage to the environment [6] and search for a
safer solvent and catalyst alternative is thus holding a key
role in the green chemistry.
Ionic liquids have been recognized as a new green chem-
ical revolution which excited both the scientific community
from the academia and the chemical industries. This peculiar
class of molecular solvent can reduce the use of hazardous
and polluting organic solvents due to their useful properties
[7].
Ionic liquids are known as salts that are liquid consist-
ing of ions (organic cations and anions), but it is different
from molten salts [8-10]. Molten salts are usually defined
as a high melting, highly viscous and highly corrosive liq-
uid, while ionic liquids are defined as pure compounds,
*Address correspondence to this author at the School of Chemical Sciences,
Kavayitri Bahinabai Chaudhari North Maharashtra University, Jalgaon - 425
001 (M. S.), India; Tel: +91-2572257432; Fax: +91-257-2258403;
E-mail: dsdalal2007@gmail.com
entirely composed of ions which melt at or below 100°C
(212°F) [11].
Ionic liquids (ILs) have attracted great considerable at-
tention in the context of green chemistry. They have eco-
friendly alternatives to conventional and environmentally
detrimental molecular solvents for many chemical applica-
tions in the field of sciences due to their unique chemical and
physical properties [12-15] that are principally in accordance
to a green chemistry point of view, such properties include
chemical stability, thermal stability, non-flammability, non-
volatility, precise miscibility, and recyclability.
2. HISTORY
The first ionic liquid reported was ethyl ammonium ni-
trate [EtNH
3
][NO
3
] (m.p. 12°C) in 1914 by Paul Walden
[16]. In between the 1970s and 1980s, ionic liquids based on
alkyl-imidazolium and pyridinium cations, with halide or
tetra halogenoaluminate anions, were developed as potential
electrolytes in batteries [17]. Afterwards, the first generation
of ILs appeared and was widely described by Wilkes and co-
workers in 1982 as a Room-temperature ILs (RTILs) based
on typical cations i.e. 1-alkyl-3-methylimidazolium and
tetrachloroaluminates as an anion [18]. This salt is liquid at
room temperature and possesses favorable physical and elec-
trochemical properties but sensitive to moisture, usually con-
tains a small amount of water. The second generation of ILs
invented as an air and moisture stable ILs by replacing the
tetrafluoroborate ion and other anions instead of the mois-
ture-sensitive anion led in 1992 [19]. These ILs have suc-
cessfully been used as a reaction media for various kinds of
organic reactions. The third generation of ILs introduced by
Davis and co-workers in 2004 as a task-specific ionic liquids
(TSILs) to describe ILs in which a functional group is cova-
2213-347X/20 $65.00+.00 © 2020 Bentham Science Publishers