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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...

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Autores principales: Zango, Germán, Krug, Marcel, Krishna, Swathi, Mariñas, Víctor, Clark, Timothy, Martinez-Diaz, M. Victoria, Guldi, Dirk M., Torres, Tomás
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
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.
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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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