Photophysical behaviour of BODIPY-phenylacetylene macrocyclic dyads for light-harvesting applications

The synthesis and study of a family of BODIPY-phenylacetylene macrocycles where donor groups have been added to the macrocycle in order to tune the physicochemical properties and absorption profile is reported. Energy transfer is observed between this phenylacetylene antennae and BODIPY core and flu...

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Autores principales: Yousaf, Muhammad, Zarate, Ximena, Schott, Eduardo, Lough, Alan J., Koivisto, Bryan D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Chemistry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9083918/
https://www.ncbi.nlm.nih.gov/pubmed/35542483
http://dx.doi.org/10.1039/c8ra03384f
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author Yousaf, Muhammad
Zarate, Ximena
Schott, Eduardo
Lough, Alan J.
Koivisto, Bryan D.
author_facet Yousaf, Muhammad
Zarate, Ximena
Schott, Eduardo
Lough, Alan J.
Koivisto, Bryan D.
author_sort Yousaf, Muhammad
collection PubMed
description The synthesis and study of a family of BODIPY-phenylacetylene macrocycles where donor groups have been added to the macrocycle in order to tune the physicochemical properties and absorption profile is reported. Energy transfer is observed between this phenylacetylene antennae and BODIPY core and fluorescence emission from the BODIPY, at any excitation wavelength, is consistent with energy transfer from the macrocycle.
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spelling pubmed-90839182022-05-09 Photophysical behaviour of BODIPY-phenylacetylene macrocyclic dyads for light-harvesting applications Yousaf, Muhammad Zarate, Ximena Schott, Eduardo Lough, Alan J. Koivisto, Bryan D. RSC Adv Chemistry The synthesis and study of a family of BODIPY-phenylacetylene macrocycles where donor groups have been added to the macrocycle in order to tune the physicochemical properties and absorption profile is reported. Energy transfer is observed between this phenylacetylene antennae and BODIPY core and fluorescence emission from the BODIPY, at any excitation wavelength, is consistent with energy transfer from the macrocycle. The Royal Society of Chemistry 2018-08-10 /pmc/articles/PMC9083918/ /pubmed/35542483 http://dx.doi.org/10.1039/c8ra03384f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Yousaf, Muhammad
Zarate, Ximena
Schott, Eduardo
Lough, Alan J.
Koivisto, Bryan D.
Photophysical behaviour of BODIPY-phenylacetylene macrocyclic dyads for light-harvesting applications
title Photophysical behaviour of BODIPY-phenylacetylene macrocyclic dyads for light-harvesting applications
title_full Photophysical behaviour of BODIPY-phenylacetylene macrocyclic dyads for light-harvesting applications
title_fullStr Photophysical behaviour of BODIPY-phenylacetylene macrocyclic dyads for light-harvesting applications
title_full_unstemmed Photophysical behaviour of BODIPY-phenylacetylene macrocyclic dyads for light-harvesting applications
title_short Photophysical behaviour of BODIPY-phenylacetylene macrocyclic dyads for light-harvesting applications
title_sort photophysical behaviour of bodipy-phenylacetylene macrocyclic dyads for light-harvesting applications
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9083918/
https://www.ncbi.nlm.nih.gov/pubmed/35542483
http://dx.doi.org/10.1039/c8ra03384f
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