Issue 3, 2000

Synthesis and anion coordination chemistry of new calix[4]arene pyridinium receptors

Abstract

New lower rim substituted calix[4]arene bis-pyridinium receptors L1, L2 and a novel lower rim bridged calix[4]arene pyridinium receptor L3 have been prepared and shown to bind a variety of anionic guest species. Proton NMR titration studies in deuteriated DMSO solutions reveal L1 and L2 to complex H2PO4, Cl, Br, HSO4 anions with L∶2X stoichiometry with L1 exhibiting a selectivity preference for H2PO4. L3 forms 1∶1 stoichiometric complexes with Cl and Br of similar stability. Cyclic voltammetric investigations have demonstrated L1 to electrochemically recognise H2PO4 and Cl anions.

Supplementary files

Article information

Article type
Paper
Submitted
08 Oct 1999
Accepted
03 Dec 1999
First published
21 Feb 2000

J. Chem. Soc., Perkin Trans. 2, 2000, 511-519

Synthesis and anion coordination chemistry of new calix[4]arene pyridinium receptors

P. D. Beer, M. G. B. Drew and K. Gradwell, J. Chem. Soc., Perkin Trans. 2, 2000, 511 DOI: 10.1039/A908106B

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