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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Beilstein-Institut
2019
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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. |
format | Online Article Text |
id | pubmed-6604742 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
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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