Fluoride ion receptors based on dipyrrolyl derivatives bearing electron-withdrawing groups: synthesis, optical and electrochemical sensing, and computational studies

Ghosh, Tamal ; Maiya, Bhaskar G. ; Wong, Ming Wah (2004) Fluoride ion receptors based on dipyrrolyl derivatives bearing electron-withdrawing groups: synthesis, optical and electrochemical sensing, and computational studies The Journal of Physical Chemistry A, 108 (51). pp. 11249-11259. ISSN 1089-5639

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Official URL: http://pubs.acs.org/doi/abs/10.1021/jp0464223

Related URL: http://dx.doi.org/10.1021/jp0464223

Abstract

Two dipyrrolyl derivatives, 2,3-di(1H-2-pyrrolyl)-7,12-dihydronaphtho[2,3-f]quinoxaline-7,12-dione (1) and 5,6-di(1H-2-pyrrolyl)-2,3-pyrazine-dicarbonitrile (2), bearing electron-withdrawing quinone or dicyano subunits, have been synthesized and fully characterized by various spectroscopic and electrochemical methods. Both 1 and 2 are specific binders of F- in organic solvents and show dramatic, binding-induced changes in their color (observable in the naked-eye experiments) and also optical and electrochemical signatures. These F--induced color changes remain the same even in the presence of a large excess of Cl-, Br-, I-, or ClO4-, thus rendering 1 and 2 to be efficient fluoride ion sensors. While Ka for F- binding by receptor 1 is ~1.6 × 104 M-1, that for receptor 2 is an order of magnitude higher. 1H NMR titrations were carried out to monitor the binding of 1/2 with F-. These experiments not only provide evidence for the hydrogen-bonding interaction between the pyrrolic NH groups of these receptors and F-, but also offer some key insights into the structures of the receptor-anion complexes. Further insights into the structures of the receptor-anion complexes and the observed binding discrimination have been obtained by density functional calculations. Both receptors 1 and 2 interact with a halide ion by forming two NH···X- hydrogen bonds with the pyrrolic NH protons in a bidentate fashion. The predicted order of halide binding affinity for receptors is F» Cl > Br. The high selectivity for F- among the halides is attributed mainly to the strength of the hydrogen bond and partly to the complementarity of the geometries between the receptor and anion. The higher F- binding ability of 2 over 1 has been interpreted in terms of the greater electron deficiency and enhanced hydrogen-bond-donating character of the former derivative. Calculations of the NMR and UV-visible spectra support the experimental characterization of the receptor-anion complexes.

Item Type:Article
Keywords:Copyright of this article belongs to American Chemical Society.
ID Code:31953
Deposited On:31 Mar 2011 10:34
Last Modified:09 Jun 2011 09:46

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