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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Published in: | Journal of luminescence Vol. 154; pp. 515 - 519 |
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Main Authors: | , , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Amsterdam
Elsevier B.V
01-10-2014
Elsevier |
Subjects: | |
Online Access: | Get full text |
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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−. |
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ISSN: | 0022-2313 1872-7883 |
DOI: | 10.1016/j.jlumin.2014.05.041 |