TL;DR: Ionic liquids have attracted a great deal of attention as possible replacement for conventional molecular solvents for catalytic and organic reactions as discussed by the authors, including acid catalyzed reactions and transition metal catalyzed transformations.
Abstract: Ionic liquids are attracting a great deal of attention as possible replacement for conventional molecular solvents for catalytic and organic reactions. They complete the use of environmentally friendly water, supercritical fluids or perfluorinated solvents. Features that make ionic liquids attractive include their lack of vapor pressure and the great versatility of their chemical and physical properties. By a judicious combination of cations and anions, it is possible to adjust the solvent properties to the requirement of the reactions, thus creating an almost indefinitely set of “designer solvents”. Besides the possibility of recycling the catalytic system, one main potential interest in using ionic liquids results in the unique interactions of these media with the active species and in the possibility to modify the reaction activity and selectivity. Their successful use as solvents has been demonstrated for a wide range of organic reactions including acid catalyzed reactions and transition metal catalyzed transformations.
TL;DR: A series of novel hexafluorophosphate salts, based on N,N′-dialkylimidazolium and substituted N-alkylpyridinium cations, display liquid crystalline behaviour at temperatures above their melting point as discussed by the authors.
Abstract: A series of novel hexafluorophosphate salts, based on N,N′-dialkylimidazolium and substituted N-alkylpyridinium cations, display liquid crystalline behaviour at temperatures above their melting point. The temperature range over which liquid crystalline behaviour is observed increases markedly with increasing alkyl chain length. Alkyl substitution at the 3- and 4-positions on the pyridinium ring results in a decrease in the melting point compared with the equivalent unsubstituted salt, but also leads to a large decrease in the tendency towards liquid crystalline behaviour (or mesogenicity). The salts prepared are fully characterised using a wide variety of techniques, including NMR and IR spectroscopy, DSC, and single crystal X-ray diffraction in the case of 1-dodecyl-3-methylimidazolium hexafluorophosphate. The effect of preparing mixtures containing different proportions of two cations is also reported.
TL;DR: The Rohrschneider-McReynolds constants were determined for both ionic liquids and a popular commercial polysiloxane stationary phase, and it appears that the unusual properties of ions could make them beneficial in many areas of separation science.
Abstract: Stable room-temperature ionic liquids (RTILs) have been used as novel reaction solvents. They can solubilize complex polar molecules such as cyclodextrins and glycopeptides. Their wetting ability and viscosity allow them to be coated onto fused silica capillaries. Thus, 1-butyl-3-methylimidazolium hexafluorophosphate and the analogous chloride salt can be used as stationary phases for gas chromatography (GC). Using inverse GC, one can examine the nature of these ionic liquids via their interactions with a variety of compounds. The Rohrschneider-McReynolds constants were determined for both ionic liquids and a popular commercial polysiloxane stationary phase. Ionic liquid stationary phases seem to have a dual nature. They appear to act as a low-polarity stationary phase to nonpolar compounds. However, molecules with strong proton donor groups, in particular, are tenaciously retained. The nature of the anion can have a significant effect on both the solubilizing ability and the selectivity of ionic liquid s...
TL;DR: In the last few years, it has been shown that ionic liquids can be advantageously used also for polymer synthesis and the increase of kp/kt ratio for polymerizations conducted in ionic liquid has been observed as discussed by the authors.
TL;DR: In this article, the feasibility of using supercritical carbon dioxide, another environmentally benign solvent, for the separation of organic solutes from an ionic liquid was investigated, and the results showed that supercritical fluid extraction is a viable separation technique with the additional benefits of environmental sustainability and pure product recovery.
Abstract: Ionic liquids (ILs) hold great potential as replacements for traditional volatile organic solvents and have been shown to be a viable medium for numerous types of reactions. This work investigates the feasibility of using supercritical carbon dioxide, another environmentally benign solvent, for the separation of organic solutes from an ionic liquid. Recovery rates of aromatic and aliphatic solutes from 1-n-butyl-3-methylimidazolium hexafluorophosphate ([bmim][PF6]) are given. Supercritical fluid extraction is shown to be a viable separation technique with the additional benefits of environmental sustainability and pure product recovery.