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ABAB Phthalocyanines: Scaffolds for Building Unprecedented Donor–π–Acceptor Chromophores
Unique donor–π–acceptor phthalocyanines have been synthesized through the asymmetric functionalization of an ABAB phthalocyanine, crosswise functionalized with two iodine atoms through Pd‐catalyzed cross‐coupling reactions with adequate electron‐donor and electron‐acceptor moieties. These push–pull...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5288760/ https://www.ncbi.nlm.nih.gov/pubmed/28168157 http://dx.doi.org/10.1002/open.201600113 |
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author | Fazio, Ettore Jaramillo‐García, Javier Medel, María Urbani, Maxence Grätzel, Michael Nazeerudin, Mohammad K. de la Torre, Gema Torres, Tomas |
author_facet | Fazio, Ettore Jaramillo‐García, Javier Medel, María Urbani, Maxence Grätzel, Michael Nazeerudin, Mohammad K. de la Torre, Gema Torres, Tomas |
author_sort | Fazio, Ettore |
collection | PubMed |
description | Unique donor–π–acceptor phthalocyanines have been synthesized through the asymmetric functionalization of an ABAB phthalocyanine, crosswise functionalized with two iodine atoms through Pd‐catalyzed cross‐coupling reactions with adequate electron‐donor and electron‐acceptor moieties. These push–pull molecules have been optically and electrochemically characterized, and their ability to perform as chromophores for dye‐sensitized solar cells has been tested. |
format | Online Article Text |
id | pubmed-5288760 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-52887602017-02-06 ABAB Phthalocyanines: Scaffolds for Building Unprecedented Donor–π–Acceptor Chromophores Fazio, Ettore Jaramillo‐García, Javier Medel, María Urbani, Maxence Grätzel, Michael Nazeerudin, Mohammad K. de la Torre, Gema Torres, Tomas ChemistryOpen Full Papers Unique donor–π–acceptor phthalocyanines have been synthesized through the asymmetric functionalization of an ABAB phthalocyanine, crosswise functionalized with two iodine atoms through Pd‐catalyzed cross‐coupling reactions with adequate electron‐donor and electron‐acceptor moieties. These push–pull molecules have been optically and electrochemically characterized, and their ability to perform as chromophores for dye‐sensitized solar cells has been tested. John Wiley and Sons Inc. 2016-12-27 /pmc/articles/PMC5288760/ /pubmed/28168157 http://dx.doi.org/10.1002/open.201600113 Text en © 2016 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Full Papers Fazio, Ettore Jaramillo‐García, Javier Medel, María Urbani, Maxence Grätzel, Michael Nazeerudin, Mohammad K. de la Torre, Gema Torres, Tomas ABAB Phthalocyanines: Scaffolds for Building Unprecedented Donor–π–Acceptor Chromophores |
title | ABAB Phthalocyanines: Scaffolds for Building Unprecedented Donor–π–Acceptor Chromophores |
title_full | ABAB Phthalocyanines: Scaffolds for Building Unprecedented Donor–π–Acceptor Chromophores |
title_fullStr | ABAB Phthalocyanines: Scaffolds for Building Unprecedented Donor–π–Acceptor Chromophores |
title_full_unstemmed | ABAB Phthalocyanines: Scaffolds for Building Unprecedented Donor–π–Acceptor Chromophores |
title_short | ABAB Phthalocyanines: Scaffolds for Building Unprecedented Donor–π–Acceptor Chromophores |
title_sort | abab phthalocyanines: scaffolds for building unprecedented donor–π–acceptor chromophores |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5288760/ https://www.ncbi.nlm.nih.gov/pubmed/28168157 http://dx.doi.org/10.1002/open.201600113 |
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