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A simple quinoline-based fluorescent “turn on” probe with high selectivity for Ag+ in aqueous media
A simple quinoline-based fluorescent probe L has been developed and shows fluorescence enhancement (turn on) response towards Ag+ with high selectivity in aqueous media based on a combinational effect of the inhibition of intermolecular photoinduced proton transfer and chelation-enhanced fluorescenc...
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Published in: | Inorganica Chimica Acta 2015-08, Vol.435, p.137-141 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | A simple quinoline-based fluorescent probe L has been developed and shows fluorescence enhancement (turn on) response towards Ag+ with high selectivity in aqueous media based on a combinational effect of the inhibition of intermolecular photoinduced proton transfer and chelation-enhanced fluorescence. [Display omitted]
•A simple quinoline-based fluorescent probe L has been developed.•Probe L exhibits a significant fluorescent enhancement toward Ag+ with high selectivity in aqueous media.•Probe L shows good fluorescence sensing ability to Ag+ over a wide pH range (from 6.0 to 12.0).•The response of the probe L toward Ag+ is fast.•The 1:1 binding mode between L and Ag+ was demonstrated by X-ray crystal diffraction.
A simple quinoline-based fluorescent probe L for Ag+ has been developed. Probe L shows fluorescence enhancement (turn on) response towards Ag+ with high selectivity in aqueous media (methanol–water, v/v=3:7, pH 7.2, 20mM Tris–HCl) based on a combinational effect of the inhibition of intermolecular photoinduced proton transfer and chelation-enhanced fluorescence. And an obvious fluorescent color change could be observed by naked eyes under the light of 365nm. The binding mode between L and Ag+ has been found to be 1:1 based on the fluorescence/absorption titration, ESI-MS and further confirmed by X-ray crystallography. |
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ISSN: | 0020-1693 1873-3255 |
DOI: | 10.1016/j.ica.2015.06.014 |