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A mesoporous metal–organic framework used to sustainably release copper(ii) into reducing aqueous media to promote the CuAAC click reaction

The mesoporous metal–organic framework Cr-MIL-101-NH(2) (MOF1) has been used to encapsulate, by a simple impregnation method, large amounts of copper sulfate. The resulting loaded material, Cu@MOF1, was successfully employed to slowly release copper(ii) into an appropriate reaction medium in which t...

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Autores principales: Hoffmann, Pascal, Lherbet, Christian, Fabing, Isabelle, Barthélémy, Marie-Claire, Borjon-Piron, Yann, Laurent, Christophe, Vigroux, Alain
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9494208/
https://www.ncbi.nlm.nih.gov/pubmed/36320833
http://dx.doi.org/10.1039/d2ra04298c
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author Hoffmann, Pascal
Lherbet, Christian
Fabing, Isabelle
Barthélémy, Marie-Claire
Borjon-Piron, Yann
Laurent, Christophe
Vigroux, Alain
author_facet Hoffmann, Pascal
Lherbet, Christian
Fabing, Isabelle
Barthélémy, Marie-Claire
Borjon-Piron, Yann
Laurent, Christophe
Vigroux, Alain
author_sort Hoffmann, Pascal
collection PubMed
description The mesoporous metal–organic framework Cr-MIL-101-NH(2) (MOF1) has been used to encapsulate, by a simple impregnation method, large amounts of copper sulfate. The resulting loaded material, Cu@MOF1, was successfully employed to slowly release copper(ii) into an appropriate reaction medium in which the reducing agent sodium ascorbate reduces copper(ii) to copper(i), thus allowing the well-known copper(i)-catalyzed alkyne–azide cycloaddition (CuAAC) “click” reaction to proceed in the absence of potentially high local copper(i) concentrations. The use of a MOF-based controlled copper release system such as Cu@MOF1 may be relevant for copper(i)-catalyzed reactions having substrates that could be degraded by potentially high local concentrations of copper(i). The copper chelating ligand TBTA (tris(benzyltriazolylmethyl)amine), a very useful ligand for click chemistry, has been successfully attached to the pores of MOF1. The resulting TBTA-functionalized MOF (MOF3) was compared with its non-functionalized version (MOF1). At copper loadings of ca. 3 mmol g(−1), the results revealed that the performances of the two materials are strikingly similar. Upon immersion in methanol/water (95/5) containing sodium ascorbate, both materials slowly released copper encapsulated in their pores and could be recovered and reused efficiently for up to five reaction cycles without reloading with metal ion, while allowing the CuAAC reaction to proceed with excellent conversion rates and yields.
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spelling pubmed-94942082022-10-31 A mesoporous metal–organic framework used to sustainably release copper(ii) into reducing aqueous media to promote the CuAAC click reaction Hoffmann, Pascal Lherbet, Christian Fabing, Isabelle Barthélémy, Marie-Claire Borjon-Piron, Yann Laurent, Christophe Vigroux, Alain RSC Adv Chemistry The mesoporous metal–organic framework Cr-MIL-101-NH(2) (MOF1) has been used to encapsulate, by a simple impregnation method, large amounts of copper sulfate. The resulting loaded material, Cu@MOF1, was successfully employed to slowly release copper(ii) into an appropriate reaction medium in which the reducing agent sodium ascorbate reduces copper(ii) to copper(i), thus allowing the well-known copper(i)-catalyzed alkyne–azide cycloaddition (CuAAC) “click” reaction to proceed in the absence of potentially high local copper(i) concentrations. The use of a MOF-based controlled copper release system such as Cu@MOF1 may be relevant for copper(i)-catalyzed reactions having substrates that could be degraded by potentially high local concentrations of copper(i). The copper chelating ligand TBTA (tris(benzyltriazolylmethyl)amine), a very useful ligand for click chemistry, has been successfully attached to the pores of MOF1. The resulting TBTA-functionalized MOF (MOF3) was compared with its non-functionalized version (MOF1). At copper loadings of ca. 3 mmol g(−1), the results revealed that the performances of the two materials are strikingly similar. Upon immersion in methanol/water (95/5) containing sodium ascorbate, both materials slowly released copper encapsulated in their pores and could be recovered and reused efficiently for up to five reaction cycles without reloading with metal ion, while allowing the CuAAC reaction to proceed with excellent conversion rates and yields. The Royal Society of Chemistry 2022-09-22 /pmc/articles/PMC9494208/ /pubmed/36320833 http://dx.doi.org/10.1039/d2ra04298c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Hoffmann, Pascal
Lherbet, Christian
Fabing, Isabelle
Barthélémy, Marie-Claire
Borjon-Piron, Yann
Laurent, Christophe
Vigroux, Alain
A mesoporous metal–organic framework used to sustainably release copper(ii) into reducing aqueous media to promote the CuAAC click reaction
title A mesoporous metal–organic framework used to sustainably release copper(ii) into reducing aqueous media to promote the CuAAC click reaction
title_full A mesoporous metal–organic framework used to sustainably release copper(ii) into reducing aqueous media to promote the CuAAC click reaction
title_fullStr A mesoporous metal–organic framework used to sustainably release copper(ii) into reducing aqueous media to promote the CuAAC click reaction
title_full_unstemmed A mesoporous metal–organic framework used to sustainably release copper(ii) into reducing aqueous media to promote the CuAAC click reaction
title_short A mesoporous metal–organic framework used to sustainably release copper(ii) into reducing aqueous media to promote the CuAAC click reaction
title_sort mesoporous metal–organic framework used to sustainably release copper(ii) into reducing aqueous media to promote the cuaac click reaction
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9494208/
https://www.ncbi.nlm.nih.gov/pubmed/36320833
http://dx.doi.org/10.1039/d2ra04298c
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