Issue 1, 2015

A dihydrogen phosphate selective anion receptor based on acylhydrazone and pyrazole

Abstract

A novel chromogenic anion receptor 1 based on acylhydrazone and pyrazole has been designed and synthesized. Chromogenic anion receptor 1 forms stable 1 : 1 complexes with dihydrogen phosphate (H2PO4) and other halide (Cl, Br) anions in DMSO solution, as shown by UV-vis, fluorescence and 1H NMR spectroscopic experiments. The pyrazole containing host 1 in the optimized geometry of the complex has been noted as planar. The planarity of the host with the H2PO4 anion resulted from four strong N–H⋯O and two weak C–H⋯O types of H-bonding. In total six H-bonding and the planarity of the host in the complex are responsible for the high binding energy. The addition of an excess of more basic anions (F and CH3COO) induces stepwise deprotonation, an event signalled by the appearance of a bright yellow color. The intensity of the fluorescence spectrum increases when hydrogen bonding occurs and decreases when deprotonation occurs, which is evidenced by fluorescence titrations.

Graphical abstract: A dihydrogen phosphate selective anion receptor based on acylhydrazone and pyrazole

Supplementary files

Article information

Article type
Paper
Submitted
27 Jun 2014
Accepted
03 Nov 2014
First published
03 Nov 2014

New J. Chem., 2015,39, 650-658

Author version available

A dihydrogen phosphate selective anion receptor based on acylhydrazone and pyrazole

T. S. Pandian, Y. Choi, V. Srinivasadesikan, M. Lin and J. Kang, New J. Chem., 2015, 39, 650 DOI: 10.1039/C4NJ01063A

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