An efficient organocatalytic system was developed for the synthesis of cyclic carbonates from epoxides and CO₂ (25–45 °C, 1 atm) in high-to-excellent yields (85–97%). Moreover, the 2,6-pyridinedimethanol system could be recycled several times without significant loss of activity.

We present a new series of polymer–ionic liquid solutions exhibiting LCST-type liquid–liquid phase separation behaviour, and reveal their phase behaviour and intermolecular interactions based on phase diagrams and NMR analysis.

The solubility and phase behavior of five polyethers (poly(ethylene oxide), poly(glycidyl methyl ether), poly(ethyl glycidyl ether), poly(ethoxyethyl glycidyl ether) and poly(propylene oxide)) in 14 different room-temperature ionic liquids (ILs) were studied by changing the structures of polyethers and the cations and anions in the ILs. Certain combinations of a polyether and an IL binary mixture exhibited lower critical solution temperature (LCST) phase behavior. For ILs containing the same anions, the polyethers were highly soluble in imidazolium- or pyridinium-based ILs, whereas they were insoluble in ammonium- or phosphonium-based ILs. An increase in length of the alkyl chain in the imidazolium cation and an increase in polarity of the polyethers resulted in a higher LCST phase separation temperature, whereas substitution of the hydrogen atoms on the imidazolium ring by methyl groups resulted in a lower LCST phase separation temperature. The hydrogen bonding interaction between the oxygen atoms in the polyethers and the aromatic hydrogen atoms on the cations in the ILs had an important role in the LCST phase behavior of the mixtures. Miscibility of the mixtures was also affected by the Lewis basicity of the anions in the ILs.