Issue 6, 2007

Synthesis and properties of chiral imidazolium ionic liquids with a (1R,2S,5R)-(−)-menthoxymethyl substituent

Abstract

A series of 1-[(1R,2S,5R)-(−)-menthoxymethyl]-3-alkylimidazolium salts have been synthesized, producing both hydrophilic and hydrophobic chiral imidazolium ionic liquids. Their physicochemical properties, single-crystal X-ray structures, antimicrobial activities, and antielectrostatic effects were determined and these compounds have proven to represent not only potential new solvents in asymmetric synthesis, but also effective, disinfectants with antielectrostatic activity. Given the number and diversities of the possible conformations and interionic interactions, coupled with the chiral nature of the cations, it should come as no surprise that these salts exhibit ionic liquid behavior and are so difficult to crystallize.

Graphical abstract: Synthesis and properties of chiral imidazolium ionic liquids with a (1R,2S,5R)-(−)-menthoxymethyl substituent

Supplementary files

Additions and corrections

Article information

Article type
Paper
Submitted
07 Dec 2006
Accepted
24 Jan 2007
First published
21 Feb 2007

New J. Chem., 2007,31, 879-892

Synthesis and properties of chiral imidazolium ionic liquids with a (1R,2S,5R)-(−)-menthoxymethyl substituent

J. Pernak, J. Feder-Kubis, A. Cieniecka-Rosłonkiewicz, C. Fischmeister, S. T. Griffin and R. D. Rogers, New J. Chem., 2007, 31, 879 DOI: 10.1039/B616215K

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