Anion recognition ability of a novel azo dye derived from 4-hydroxycoumarin

The anion recognition ability of a novel azo dye derived from 4-hydroxycuomarin (L) was investigated by experimental (UV–vis, fluorescence and 1H NMR) and theoretical [(B3LYP/6-31G(d,p)] methods. Among the surveyed anions, the receptor L showed both naked-eye detectable color and spectral changes in...

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Bibliographic Details
Published in:Journal of luminescence Vol. 154; pp. 515 - 519
Main Authors: Chandel, Madhurya, Roy, Sutapa Mondal, Sharma, Darshna, Sahoo, Suban K., Patel, Amit, Kumari, Premlata, Dhale, Ranu S., Ashok, Kumar S.K., Nandre, Jitendra P., Patil, Umesh D.
Format: Journal Article
Language:English
Published: Amsterdam Elsevier B.V 01-10-2014
Elsevier
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Summary:The anion recognition ability of a novel azo dye derived from 4-hydroxycuomarin (L) was investigated by experimental (UV–vis, fluorescence and 1H NMR) and theoretical [(B3LYP/6-31G(d,p)] methods. Among the surveyed anions, the receptor L showed both naked-eye detectable color and spectral changes in the presence of F−, AcO− and H2PO4− due to the formation of hydrogen bonding complexes followed by deprotonation between these anions and L. •Anion recognition ability of an easy-to-prepare coumarin derivative L was reported.•L showed both naked-eye and spectral responses towards AcO−, F− and H2PO4−.•Deprotonation mechanism was proposed for the observed spectral responses.•L showed selective ratiometric fluorescence ‘turn-on’ responses towards AcO− and F−.
ISSN:0022-2313
1872-7883
DOI:10.1016/j.jlumin.2014.05.041