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Remarkable effect of alkynyl substituents on the fluorescence properties of a BN-phenanthrene

A series of BN-phenanthrenes with substituents of a diverse nature have been synthesized by palladium-catalyzed cross-coupling reactions of a common chloro-substituted precursor, which was made from readily available materials in only four steps. Evaluation of the photophysical properties of the pre...

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Autores principales: Abengózar, Alberto, Sucunza, David, García-García, Patricia, Vaquero, Juan J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6604742/
https://www.ncbi.nlm.nih.gov/pubmed/31293672
http://dx.doi.org/10.3762/bjoc.15.122
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author Abengózar, Alberto
Sucunza, David
García-García, Patricia
Vaquero, Juan J
author_facet Abengózar, Alberto
Sucunza, David
García-García, Patricia
Vaquero, Juan J
author_sort Abengózar, Alberto
collection PubMed
description A series of BN-phenanthrenes with substituents of a diverse nature have been synthesized by palladium-catalyzed cross-coupling reactions of a common chloro-substituted precursor, which was made from readily available materials in only four steps. Evaluation of the photophysical properties of the prepared compounds unveiled an impressive effect of the presence of alkynyl substituents on the fluorescence quantum yield, which improved from 0.01 in the parent compound to up to 0.65 in derivatives containing a triple bond.
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spelling pubmed-66047422019-07-10 Remarkable effect of alkynyl substituents on the fluorescence properties of a BN-phenanthrene Abengózar, Alberto Sucunza, David García-García, Patricia Vaquero, Juan J Beilstein J Org Chem Full Research Paper A series of BN-phenanthrenes with substituents of a diverse nature have been synthesized by palladium-catalyzed cross-coupling reactions of a common chloro-substituted precursor, which was made from readily available materials in only four steps. Evaluation of the photophysical properties of the prepared compounds unveiled an impressive effect of the presence of alkynyl substituents on the fluorescence quantum yield, which improved from 0.01 in the parent compound to up to 0.65 in derivatives containing a triple bond. Beilstein-Institut 2019-06-06 /pmc/articles/PMC6604742/ /pubmed/31293672 http://dx.doi.org/10.3762/bjoc.15.122 Text en Copyright © 2019, Abengózar et al. https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Abengózar, Alberto
Sucunza, David
García-García, Patricia
Vaquero, Juan J
Remarkable effect of alkynyl substituents on the fluorescence properties of a BN-phenanthrene
title Remarkable effect of alkynyl substituents on the fluorescence properties of a BN-phenanthrene
title_full Remarkable effect of alkynyl substituents on the fluorescence properties of a BN-phenanthrene
title_fullStr Remarkable effect of alkynyl substituents on the fluorescence properties of a BN-phenanthrene
title_full_unstemmed Remarkable effect of alkynyl substituents on the fluorescence properties of a BN-phenanthrene
title_short Remarkable effect of alkynyl substituents on the fluorescence properties of a BN-phenanthrene
title_sort remarkable effect of alkynyl substituents on the fluorescence properties of a bn-phenanthrene
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6604742/
https://www.ncbi.nlm.nih.gov/pubmed/31293672
http://dx.doi.org/10.3762/bjoc.15.122
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