New room temperature ionic liquids based on the tetra-alkyl-dimethylguanidinium cation present high stability under thermal, basic, acid, nucleophilic and oxidative conditions, low temperature glass transition phases and peculiar solubility properties in common solvents.

We present a new concept for the design of a polymeric conducting material that combines the chemical versatility of an organic salt (ionic liquid) with the morphological versatility of a biopolymer (gelatin); the resulting ‘ion jelly’ can be applied in electrochemical devices, such as batteries, fuel cells, electrochromic windows or photovoltaic cells.

Several specific synthetic protocols were developed for the preparation from cyanuric chloride of a range of symmetric and non-symmetric di- and tri-substituted 1,3,5-triazines containing alkyl, aromatic, hindered, chiral and achiral hydroxyalkyl, ester and imidazole groups via sequential nucleophilic substitution of the C-Cl bond by C-O, C-N and C-S bonds.

The catalytic activities of cutinase immobilized on zeolite NaY and Candida antarctica lipase B immobilized on an acrylic resin (Novozym 453) were measured in a model transesterification reaction in three imidazolium cation-based ionic liquids (RTILs), supercritical ethane (sc-ethane), sc-CO₂ and n-hexane, at a water activity (a_W) of 0.2 and 0.7. The transesterification activity of cutinase was highest and similar in 1-n-butyl-3-methylimidazolium hexafluorophosphate ([C₄mim][PF₆]), sc-ethane and n-hexane, more than one order of magnitude lower in sc-CO₂, and increased with an increase in a_W. Hydrolysis was not detected in sc-fluids and n-hexane, and was observed in RTILs at a_W 0.7 only. Both initial rates of transesterification and of hydrolysis of Novozym decreased with an increase in a_W. sc-CO₂ did not have a deleterious effect on Novozym activity, which was as high as in sc-ethane and n-hexane. The low reaction rates obtained in this case in RTILs suggested the existence of internal diffusion limitations absent in the cutinase preparation where the enzyme is only adsorbed at the surface of the support. sc-CO₂ did not adversely affect the catalytic activity of cutinase suspended in [C₄mim][PF₆], suggesting a protective effect of the RTIL. In the case of Novozym, a marked increase in the rate of transesterification was obtained in the [C₄mim][PF₆]/sc-CO₂ system, compared to the RTIL alone. This may reflect improved mass transfer of solutes to the pores of the immobilization matrix due to a high concentration of dissolved CO₂ and a reduction in viscosity of the RTIL.

New chiral ionic liquids can be prepared simply by combining the tetra-n-hexyl-dimethylguanidinium cation with readily available chiral anions and used as an asymmetric inducing agent as demonstrated for catalytic Rh(II) carbenoid C–H insertion and Sharpless dihydroxylation.