Issue 11, 2004

Calix[4]arenes containing thiourea and amide moieties: neutral receptors towards α,ω-dicarboxylate anions

Abstract

Two-armed neutral anion receptors (4, 5), were prepared and examined for their anion-binding ability using UV-vis, fluorescence and 1H NMR spectra in DMSO. The results of non-linear curve fitting indicate that 4 or 5 form 1 : 1 stoichiometric complexes with dicarboxylate anions by multiple hydrogen bonding interactions and the sensitivity for recognition of dicarboxylate depends on the chain length of these dicarboxylate anions. Receptors 4 and 5 have no binding ability with acetate, dihydrogen phosphate and the halogen (Cl, Br, I) anions. This demonstrates that receptors 4 or 5 could be used as chemical sensors for some special dicarboxylate anions.

Graphical abstract: Calix[4]arenes containing thiourea and amide moieties: neutral receptors towards α,ω-dicarboxylate anions

Article information

Article type
Paper
Submitted
08 Jan 2004
Accepted
24 Mar 2004
First published
06 May 2004

Org. Biomol. Chem., 2004,2, 1582-1586

Calix[4]arenes containing thiourea and amide moieties: neutral receptors towards α,ω-dicarboxylate anions

S. Liu, Y. He, J. Wu, L. Wei, H. Qin, L. Meng and L. Hu, Org. Biomol. Chem., 2004, 2, 1582 DOI: 10.1039/B400140K

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