Issue 19, 2015

Application of optically active chiral bis(imidazolium) salts as potential receptors of chiral dicarboxylate salts of biological relevance

Abstract

A family of chiral bis(imidazolium) salts derived from natural amino acids has been synthesized by a simple synthetic approach and the corresponding bis(trifluoromethylsulfonyl)imide salts have been shown to be room temperature chiral ionic liquids (RTCILs). The structures and self-assembling properties of the resulting salts have been studied by 1HNMR, ATR-FTIR, DSC, SEM and theoretical calculations. Moreover, these receptors have been applied to the enantiomeric recognition of dicarboxylic amino acids. The supramolecular complexes formed have been studied by 1HNMR titration experiments, ATR-FTIR and DSC.

Graphical abstract: Application of optically active chiral bis(imidazolium) salts as potential receptors of chiral dicarboxylate salts of biological relevance

Supplementary files

Article information

Article type
Paper
Submitted
19 Feb 2015
Accepted
01 Apr 2015
First published
02 Apr 2015

Org. Biomol. Chem., 2015,13, 5450-5459

Author version available

Application of optically active chiral bis(imidazolium) salts as potential receptors of chiral dicarboxylate salts of biological relevance

L. González-Mendoza, J. Escorihuela, B. Altava, M. I. Burguete and S. V. Luis, Org. Biomol. Chem., 2015, 13, 5450 DOI: 10.1039/C5OB00348B

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