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1,10a-Dihydro-1-aza-10a-boraphenanthrene and 6a,7-Dihydro-7-aza-6a-boratetraphene: Two New Fluorescent BN-PAHs
[Image: see text] Previously unknown 1,10a-dihydro-1-aza-10a-boraphenanthrene and 6a,7-dihydro-7-aza-6a-boratetraphene have been efficiently synthesized. Bromination of these BN-PAHs proceeds with complete regioselectivity, resulting in the formation of different substituted derivatives via cross-co...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8650019/ https://www.ncbi.nlm.nih.gov/pubmed/34806882 http://dx.doi.org/10.1021/acs.joc.1c01095 |
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author | Valencia, Isabel García-García, Patricia Sucunza, David Mendicuti, Francisco Vaquero, Juan J. |
author_facet | Valencia, Isabel García-García, Patricia Sucunza, David Mendicuti, Francisco Vaquero, Juan J. |
author_sort | Valencia, Isabel |
collection | PubMed |
description | [Image: see text] Previously unknown 1,10a-dihydro-1-aza-10a-boraphenanthrene and 6a,7-dihydro-7-aza-6a-boratetraphene have been efficiently synthesized. Bromination of these BN-PAHs proceeds with complete regioselectivity, resulting in the formation of different substituted derivatives via cross-coupling reactions. These compounds exhibit rather high fluorescence quantum yields (up to ϕ(F) = 0.80). |
format | Online Article Text |
id | pubmed-8650019 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-86500192021-12-08 1,10a-Dihydro-1-aza-10a-boraphenanthrene and 6a,7-Dihydro-7-aza-6a-boratetraphene: Two New Fluorescent BN-PAHs Valencia, Isabel García-García, Patricia Sucunza, David Mendicuti, Francisco Vaquero, Juan J. J Org Chem [Image: see text] Previously unknown 1,10a-dihydro-1-aza-10a-boraphenanthrene and 6a,7-dihydro-7-aza-6a-boratetraphene have been efficiently synthesized. Bromination of these BN-PAHs proceeds with complete regioselectivity, resulting in the formation of different substituted derivatives via cross-coupling reactions. These compounds exhibit rather high fluorescence quantum yields (up to ϕ(F) = 0.80). American Chemical Society 2021-11-22 2021-12-03 /pmc/articles/PMC8650019/ /pubmed/34806882 http://dx.doi.org/10.1021/acs.joc.1c01095 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Valencia, Isabel García-García, Patricia Sucunza, David Mendicuti, Francisco Vaquero, Juan J. 1,10a-Dihydro-1-aza-10a-boraphenanthrene and 6a,7-Dihydro-7-aza-6a-boratetraphene: Two New Fluorescent BN-PAHs |
title | 1,10a-Dihydro-1-aza-10a-boraphenanthrene
and 6a,7-Dihydro-7-aza-6a-boratetraphene:
Two New Fluorescent BN-PAHs |
title_full | 1,10a-Dihydro-1-aza-10a-boraphenanthrene
and 6a,7-Dihydro-7-aza-6a-boratetraphene:
Two New Fluorescent BN-PAHs |
title_fullStr | 1,10a-Dihydro-1-aza-10a-boraphenanthrene
and 6a,7-Dihydro-7-aza-6a-boratetraphene:
Two New Fluorescent BN-PAHs |
title_full_unstemmed | 1,10a-Dihydro-1-aza-10a-boraphenanthrene
and 6a,7-Dihydro-7-aza-6a-boratetraphene:
Two New Fluorescent BN-PAHs |
title_short | 1,10a-Dihydro-1-aza-10a-boraphenanthrene
and 6a,7-Dihydro-7-aza-6a-boratetraphene:
Two New Fluorescent BN-PAHs |
title_sort | 1,10a-dihydro-1-aza-10a-boraphenanthrene
and 6a,7-dihydro-7-aza-6a-boratetraphene:
two new fluorescent bn-pahs |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8650019/ https://www.ncbi.nlm.nih.gov/pubmed/34806882 http://dx.doi.org/10.1021/acs.joc.1c01095 |
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