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Chemosensors 2016, 4(1), 5;

Turn on Fluorescent Probes for Selective Targeting of Aldehydes

Istanbul Kemerburgaz University, School of Medicine, Department of Medical Biochemistry, Bagcilar, Istanbul 34217, Turkey
Department of Chemistry, State University of New York at Binghamton, Binghamton, NY 13902, USA
Author to whom correspondence should be addressed.
Academic Editor: Igor Medintz
Received: 25 November 2015 / Revised: 24 February 2016 / Accepted: 26 February 2016 / Published: 11 March 2016
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Two different classes of fluorescent dyes were prepared as a turn off/on sensor system for aldehydes. Amino derivatives of a boron dipyrromethene (BDP) fluorophore and a xanthene-derived fluorophore (rosamine) were prepared. Model compounds of their product with an aldehyde were prepared using salicylaldehyde. Both amino boron dipyrromethene and rosamine derivatives are almost non-fluorescent in polar and apolar solvent. However, imine formation with salicylaldehyde on each fluorophore increases the fluorescence quantum yield by almost a factor of 10 (from 0.05 to 0.4). These fluorophores are therefore suitable candidates for development of fluorescence-based sensors for aldehydes. View Full-Text
Keywords: fluorescence; amine; imine; aldehyde; fluorescent probes fluorescence; amine; imine; aldehyde; fluorescent probes

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Dilek, O.; Bane, S.L. Turn on Fluorescent Probes for Selective Targeting of Aldehydes. Chemosensors 2016, 4, 5.

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