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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2016
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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. |
format | Online Article Text |
id | pubmed-7299146 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
record_format | MEDLINE/PubMed |
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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