Literature DB >> 24704596

Anion induced azo-hydrazone tautomerism for the selective colorimetric sensing of fluoride ion.

A Satheshkumar1, E H El-Mossalamy2, R Manivannan1, C Parthiban1, L M Al-Harbi3, S Kosa3, Kuppanagounder P Elango4.   

Abstract

The design, synthesis, characterization and their anion sensing properties of two receptors capable of exhibiting azo-hydrazone tautomerism are reported. The anion sensing properties have been investigated using electronic, fluorescence and nuclear magnetic spectral studies in addition to electrochemical and visual detection experiments. Both the receptors selectively bind fluoride ion with >100 nm red-shift in the electronic spectrum and the color changes from yellow to red. The results of the spectral studies revealed that the sensing mechanism involves fluoride ion induced change of chromophore from C=N (hydrazone form) to N=N (azo form) in these receptors leading to the visible color change. Density Functional Theory calculations were conducted to rationalize the optical response of the receptors.
Copyright © 2014 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Acenaphthenequinone; Chromophore; DFT calculation; Fluoride ion; Sensors; Tautomerism

Mesh:

Substances:

Year:  2014        PMID: 24704596     DOI: 10.1016/j.saa.2014.02.200

Source DB:  PubMed          Journal:  Spectrochim Acta A Mol Biomol Spectrosc        ISSN: 1386-1425            Impact factor:   4.098


  3 in total

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  3 in total

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