Issue 23, 2005

Tetrakis(imidazolium) macrocyclic receptors for anion binding

Abstract

New (tetrakis)imidazolium macrocyclic receptor systems of variable cavity size have been synthesised by stepwise alkylation reactions of bis(imidazolium) precursor compounds. Proton NMR titration studies reveal the macrocycles to strongly bind halide and benzoate anions, with two receptor systems displaying notable selectivity for fluoride in competitive acetonitrile–water (9 : 1) solvent media.

Graphical abstract: Tetrakis(imidazolium) macrocyclic receptors for anion binding

Supplementary files

Article information

Article type
Paper
Submitted
15 Jul 2005
Accepted
10 Oct 2005
First published
31 Oct 2005

Org. Biomol. Chem., 2005,3, 4201-4208

Tetrakis(imidazolium) macrocyclic receptors for anion binding

W. W. H. Wong, M. S. Vickers, A. R. Cowley, R. L. Paul and P. D. Beer, Org. Biomol. Chem., 2005, 3, 4201 DOI: 10.1039/B510068B

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