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Carbazole Substituted BODIPYs
Difluoroboron-dipyrromethenes (BODIPYs) are highly popular fluorescent dyes with applications as NIR probes for bioimaging, fluorescent tags/sensors and as photosensitizers in cancer therapy and organic photovoltaics. This review concentrates on the synthesis and spectral properties of BODIPY dyes c...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6914821/ https://www.ncbi.nlm.nih.gov/pubmed/31921766 http://dx.doi.org/10.3389/fchem.2019.00841 |
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author | Gupta, Iti Kesavan, Praseetha E. |
author_facet | Gupta, Iti Kesavan, Praseetha E. |
author_sort | Gupta, Iti |
collection | PubMed |
description | Difluoroboron-dipyrromethenes (BODIPYs) are highly popular fluorescent dyes with applications as NIR probes for bioimaging, fluorescent tags/sensors and as photosensitizers in cancer therapy and organic photovoltaics. This review concentrates on the synthesis and spectral properties of BODIPY dyes conjugated with carbazole heterocycle. The carbazole is an electron rich tricyclic compound and due to its excellent electronic properties, it is extensively used in the production of electroluminescent materials and polymers. This review highlights the recent progress made on the series of BODIPY derivatives containing carbazole ring at alpha, beta, and meso-positions of the BODIPY skeleton. Carbazole based hybrid BODIPYs, carbazole linked aza-BODIPYs and carbazole-fused BODIPYs are also discussed. |
format | Online Article Text |
id | pubmed-6914821 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-69148212020-01-09 Carbazole Substituted BODIPYs Gupta, Iti Kesavan, Praseetha E. Front Chem Chemistry Difluoroboron-dipyrromethenes (BODIPYs) are highly popular fluorescent dyes with applications as NIR probes for bioimaging, fluorescent tags/sensors and as photosensitizers in cancer therapy and organic photovoltaics. This review concentrates on the synthesis and spectral properties of BODIPY dyes conjugated with carbazole heterocycle. The carbazole is an electron rich tricyclic compound and due to its excellent electronic properties, it is extensively used in the production of electroluminescent materials and polymers. This review highlights the recent progress made on the series of BODIPY derivatives containing carbazole ring at alpha, beta, and meso-positions of the BODIPY skeleton. Carbazole based hybrid BODIPYs, carbazole linked aza-BODIPYs and carbazole-fused BODIPYs are also discussed. Frontiers Media S.A. 2019-12-10 /pmc/articles/PMC6914821/ /pubmed/31921766 http://dx.doi.org/10.3389/fchem.2019.00841 Text en Copyright © 2019 Gupta and Kesavan. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Chemistry Gupta, Iti Kesavan, Praseetha E. Carbazole Substituted BODIPYs |
title | Carbazole Substituted BODIPYs |
title_full | Carbazole Substituted BODIPYs |
title_fullStr | Carbazole Substituted BODIPYs |
title_full_unstemmed | Carbazole Substituted BODIPYs |
title_short | Carbazole Substituted BODIPYs |
title_sort | carbazole substituted bodipys |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6914821/ https://www.ncbi.nlm.nih.gov/pubmed/31921766 http://dx.doi.org/10.3389/fchem.2019.00841 |
work_keys_str_mv | AT guptaiti carbazolesubstitutedbodipys AT kesavanpraseethae carbazolesubstitutedbodipys |