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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...

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Autores principales: Hwang, Jun Yeon, Lee, Jung-Yean, Cho, Chang-Woo, Choi, Wonjun, Lee, Yejin, Shim, Sangdeok, Hwang, Gil Tae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
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.
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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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