One-pot synthesis of symmetric imidazolium ionic liquids N,N-disubstituted with long alkyl chains |
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Authors: | Giacomo Damilano,Demian Kalebić ,Koen Binnemans,Wim Dehaen |
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Affiliation: | KU Leuven, Department of Chemistry, Celestijnenlaan 200F – P.O. Box 2404, B-3001 Leuven Belgium, |
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Abstract: | The Debus–Radziszewski imidazole synthesis was adapted to directly yield long-chain imidazolium ionic liquids. Imidazolium acetate ionic liquids with side-chains up to sixteen carbon atoms were synthesised in excellent yields via an on-water, one-pot reaction. The imidazolium acetate ILs acted as surfactants when dissolved in various solvents. The imidazolium acetate ionic liquids were also derivatised via an acid metathesis to the chloride, nitrate, and hydrogen oxalate derivatives. The thermal behaviour of all the ionic liquids was determined via thermogravimetric and calorimetric analysis.The modified Debus–Radziszewski reaction was used as a one-pot on-water reaction to allow a greener synthesis of long-chain 1,3-dialkylimidazolium acetate ionic liquids in high yield from long-chain linear amines. |
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