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Turn on Fluorescent Probes for Selective Targeting of Aldehydes

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 salic...

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Autores principales: Dilek, Ozlem, Bane, Susan L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7299146/
https://www.ncbi.nlm.nih.gov/pubmed/32550149
http://dx.doi.org/10.3390/chemosensors4010005
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author Dilek, Ozlem
Bane, Susan L.
author_facet Dilek, Ozlem
Bane, Susan L.
author_sort Dilek, Ozlem
collection PubMed
description 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.
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spelling pubmed-72991462020-06-17 Turn on Fluorescent Probes for Selective Targeting of Aldehydes Dilek, Ozlem Bane, Susan L. Chemosensors (Basel) Article 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. 2016-03-11 2016-03 /pmc/articles/PMC7299146/ /pubmed/32550149 http://dx.doi.org/10.3390/chemosensors4010005 Text en licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons by Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Dilek, Ozlem
Bane, Susan L.
Turn on Fluorescent Probes for Selective Targeting of Aldehydes
title Turn on Fluorescent Probes for Selective Targeting of Aldehydes
title_full Turn on Fluorescent Probes for Selective Targeting of Aldehydes
title_fullStr Turn on Fluorescent Probes for Selective Targeting of Aldehydes
title_full_unstemmed Turn on Fluorescent Probes for Selective Targeting of Aldehydes
title_short Turn on Fluorescent Probes for Selective Targeting of Aldehydes
title_sort turn on fluorescent probes for selective targeting of aldehydes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7299146/
https://www.ncbi.nlm.nih.gov/pubmed/32550149
http://dx.doi.org/10.3390/chemosensors4010005
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