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5-Bromo-4′,5′-bis(dimethylamino)fluorescein: Synthesis and Photophysical Studies
In this study, three new fluorescein derivatives—5-bromo-4′,5′-dinitrofluorescein (BDNF), 5-bromo-4′,5′-diaminofluorescein (BDAF), and 5-bromo-4′,5′-bis(dimethylamino)fluorescein (BBDMAF)—were synthesized and their pH-dependent protolytic equilibria were investigated. In particular, BBDMAF exhibited...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017165/ https://www.ncbi.nlm.nih.gov/pubmed/29361711 http://dx.doi.org/10.3390/molecules23010219 |
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author | Hwang, Jun Yeon Lee, Jung-Yean Cho, Chang-Woo Choi, Wonjun Lee, Yejin Shim, Sangdeok Hwang, Gil Tae |
author_facet | Hwang, Jun Yeon Lee, Jung-Yean Cho, Chang-Woo Choi, Wonjun Lee, Yejin Shim, Sangdeok Hwang, Gil Tae |
author_sort | Hwang, Jun Yeon |
collection | PubMed |
description | In this study, three new fluorescein derivatives—5-bromo-4′,5′-dinitrofluorescein (BDNF), 5-bromo-4′,5′-diaminofluorescein (BDAF), and 5-bromo-4′,5′-bis(dimethylamino)fluorescein (BBDMAF)—were synthesized and their pH-dependent protolytic equilibria were investigated. In particular, BBDMAF exhibited pH-dependent fluorescence, showing strong emission only at pH 3–6. BBDMAF bears a bromine moiety and thus, can be used in various cross-coupling reactions to prepare derivatives and take advantage of its unique emission properties. To confirm this, the Suzuki and Sonogashira reactions of BBDMAF with phenylboronic acid and phenylacetylene, respectively, were performed, and the desired products were successfully obtained. |
format | Online Article Text |
id | pubmed-6017165 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-60171652018-11-13 5-Bromo-4′,5′-bis(dimethylamino)fluorescein: Synthesis and Photophysical Studies Hwang, Jun Yeon Lee, Jung-Yean Cho, Chang-Woo Choi, Wonjun Lee, Yejin Shim, Sangdeok Hwang, Gil Tae Molecules Communication In this study, three new fluorescein derivatives—5-bromo-4′,5′-dinitrofluorescein (BDNF), 5-bromo-4′,5′-diaminofluorescein (BDAF), and 5-bromo-4′,5′-bis(dimethylamino)fluorescein (BBDMAF)—were synthesized and their pH-dependent protolytic equilibria were investigated. In particular, BBDMAF exhibited pH-dependent fluorescence, showing strong emission only at pH 3–6. BBDMAF bears a bromine moiety and thus, can be used in various cross-coupling reactions to prepare derivatives and take advantage of its unique emission properties. To confirm this, the Suzuki and Sonogashira reactions of BBDMAF with phenylboronic acid and phenylacetylene, respectively, were performed, and the desired products were successfully obtained. MDPI 2018-01-20 /pmc/articles/PMC6017165/ /pubmed/29361711 http://dx.doi.org/10.3390/molecules23010219 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication Hwang, Jun Yeon Lee, Jung-Yean Cho, Chang-Woo Choi, Wonjun Lee, Yejin Shim, Sangdeok Hwang, Gil Tae 5-Bromo-4′,5′-bis(dimethylamino)fluorescein: Synthesis and Photophysical Studies |
title | 5-Bromo-4′,5′-bis(dimethylamino)fluorescein: Synthesis and Photophysical Studies |
title_full | 5-Bromo-4′,5′-bis(dimethylamino)fluorescein: Synthesis and Photophysical Studies |
title_fullStr | 5-Bromo-4′,5′-bis(dimethylamino)fluorescein: Synthesis and Photophysical Studies |
title_full_unstemmed | 5-Bromo-4′,5′-bis(dimethylamino)fluorescein: Synthesis and Photophysical Studies |
title_short | 5-Bromo-4′,5′-bis(dimethylamino)fluorescein: Synthesis and Photophysical Studies |
title_sort | 5-bromo-4′,5′-bis(dimethylamino)fluorescein: synthesis and photophysical studies |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017165/ https://www.ncbi.nlm.nih.gov/pubmed/29361711 http://dx.doi.org/10.3390/molecules23010219 |
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