Abstract

A displacement assay based on the interaction of Brooker’s merocyanine ( BM), a merocyanine dye, with an excess of phenylboronic acid ( BA) was studied in acetonitrile. BM is colored in solution, but its reaction with BA yields a colorless covalently linked BA– BM species. This strategy was studied in the presence of different anions (F −, Cl −, Br −, I −, H 2 PO 4 - , HSO 4 - , CH 3COO −, and NO 3 - ), but only fluoride, a strongly nucleophilic anion, and to a much lesser extent acetate, reacted with BA– BM, displacing BM through a bimolecular nucleophilic substitution mechanism, and coloring the solution. Experimental data were collected and are shown here in order to gain a better understanding of this chromogenic sensor.

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