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Photoactive preorganized subphthalocyanine-based molecular tweezers for selective complexation of fullerenes
The development of new chromophoric receptors capable of binding curved carbon nanostructures is central to the quest for improved fullerene-based organic photovoltaics. We herein report the synthesis and characterization of a subphthalocyanine-based multicomponent ensemble consisting of two electro...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8515455/ https://www.ncbi.nlm.nih.gov/pubmed/34745517 http://dx.doi.org/10.1039/d0sc00059k |
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author | Zango, Germán Krug, Marcel Krishna, Swathi Mariñas, Víctor Clark, Timothy Martinez-Diaz, M. Victoria Guldi, Dirk M. Torres, Tomás |
author_facet | Zango, Germán Krug, Marcel Krishna, Swathi Mariñas, Víctor Clark, Timothy Martinez-Diaz, M. Victoria Guldi, Dirk M. Torres, Tomás |
author_sort | Zango, Germán |
collection | PubMed |
description | The development of new chromophoric receptors capable of binding curved carbon nanostructures is central to the quest for improved fullerene-based organic photovoltaics. We herein report the synthesis and characterization of a subphthalocyanine-based multicomponent ensemble consisting of two electron-rich SubPc-monomers rigidly attached to the convex surface of an electron-poor SubPc-dimer. Such a unique configuration, especially in terms of the two SubPc-monomers, together with the overall stiffness of the linker, endows the multicomponent system with a well-defined tweezer-like topology to efficiently embrace a fullerene in its inner cavity. The formation of a 1 : 1 complex was demonstrated in a variety of titration studies with either C60 or C70. In solution, the underlying association constants were of the order of 10(5) M(−1). Detailed physicochemical experiments revealed a complex scenario of energy- and electron-transfer processes upon photoexcitation in the absence and presence of fullerenes. The close proximity of the fullerenes to the electron-rich SubPcs enables a charge shift from the initially formed reduced SubPc-dimer to either C60 to C70. |
format | Online Article Text |
id | pubmed-8515455 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-85154552021-11-04 Photoactive preorganized subphthalocyanine-based molecular tweezers for selective complexation of fullerenes Zango, Germán Krug, Marcel Krishna, Swathi Mariñas, Víctor Clark, Timothy Martinez-Diaz, M. Victoria Guldi, Dirk M. Torres, Tomás Chem Sci Chemistry The development of new chromophoric receptors capable of binding curved carbon nanostructures is central to the quest for improved fullerene-based organic photovoltaics. We herein report the synthesis and characterization of a subphthalocyanine-based multicomponent ensemble consisting of two electron-rich SubPc-monomers rigidly attached to the convex surface of an electron-poor SubPc-dimer. Such a unique configuration, especially in terms of the two SubPc-monomers, together with the overall stiffness of the linker, endows the multicomponent system with a well-defined tweezer-like topology to efficiently embrace a fullerene in its inner cavity. The formation of a 1 : 1 complex was demonstrated in a variety of titration studies with either C60 or C70. In solution, the underlying association constants were of the order of 10(5) M(−1). Detailed physicochemical experiments revealed a complex scenario of energy- and electron-transfer processes upon photoexcitation in the absence and presence of fullerenes. The close proximity of the fullerenes to the electron-rich SubPcs enables a charge shift from the initially formed reduced SubPc-dimer to either C60 to C70. The Royal Society of Chemistry 2020-02-28 /pmc/articles/PMC8515455/ /pubmed/34745517 http://dx.doi.org/10.1039/d0sc00059k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Zango, Germán Krug, Marcel Krishna, Swathi Mariñas, Víctor Clark, Timothy Martinez-Diaz, M. Victoria Guldi, Dirk M. Torres, Tomás Photoactive preorganized subphthalocyanine-based molecular tweezers for selective complexation of fullerenes |
title | Photoactive preorganized subphthalocyanine-based molecular tweezers for selective complexation of fullerenes |
title_full | Photoactive preorganized subphthalocyanine-based molecular tweezers for selective complexation of fullerenes |
title_fullStr | Photoactive preorganized subphthalocyanine-based molecular tweezers for selective complexation of fullerenes |
title_full_unstemmed | Photoactive preorganized subphthalocyanine-based molecular tweezers for selective complexation of fullerenes |
title_short | Photoactive preorganized subphthalocyanine-based molecular tweezers for selective complexation of fullerenes |
title_sort | photoactive preorganized subphthalocyanine-based molecular tweezers for selective complexation of fullerenes |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8515455/ https://www.ncbi.nlm.nih.gov/pubmed/34745517 http://dx.doi.org/10.1039/d0sc00059k |
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