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A retrievable fluorescence “TURN ON” sensor for sulfide anions

Paper ID Volume ID Publish Year Pages File Format Full-Text
26165 43937 2013 6 PDF Available
A retrievable fluorescence “TURN ON” sensor for sulfide anions

A benzimidazole based tripodal fluorescence derivative (L1) is synthesized and characterized. Combining L1 with Cu2+ shows excellent selectivity toward sulfide anions. The binding stoichiometry of L1 with Cu2+ is established by jobs plot analysis and mass spectral evidence and the binding mode is established by synthesis of a control compound L2. The initial fluorescence of L1 is lost on complexation with Cu2+ and is regained in presence of sulfide. The “OFF-ON” behavior of L1 is studied by Fluorescence, UV/vis and mass spectroscopic methods.

Graphical abstract.Figure optionsDownload full-size imageDownload as PowerPoint slideHighlights► The manuscript reports a tripodal flourogenic compound L1 which can selectively sense biologically and environmentally important Sulfide anions. ► The system is completely free from interference of other anions. ► The binding and sensing capability of L1 is studied by detailed emission, absorption and mass spectroscopic techniques.

Sulfide sensing; Fluorescence spectroscopy; UV/vis spectroscopy; Mass spectroscopy
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A retrievable fluorescence “TURN ON” sensor for sulfide anions
Database: Elsevier - ScienceDirect
Journal: Journal of Photochemistry and Photobiology A: Chemistry - Volume 251, 1 January 2013, Pages 128–133
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Physical Sciences and Engineering Chemical Engineering Bioengineering