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Supramolecular Subphthalocyanine Cage as Catalytic Container for the Functionalization of Fullerenes in Water.
Salazar, Ainhoa; Moreno-Simoni, Marta; Kumar, Sunit; Labella, Jorge; Torres, Tomás; de la Torre, Gema.
Afiliação
  • Salazar A; Department of Organic Chemistry, Universidad Autónoma de Madrid, Campus de Cantoblanco C/Francisco Tomás y Valiente 7, 28049, Madrid, Spain.
  • Moreno-Simoni M; Department of Organic Chemistry, Universidad Autónoma de Madrid, Campus de Cantoblanco C/Francisco Tomás y Valiente 7, 28049, Madrid, Spain.
  • Kumar S; Department of Organic Chemistry, Universidad Autónoma de Madrid, Campus de Cantoblanco C/Francisco Tomás y Valiente 7, 28049, Madrid, Spain.
  • Labella J; Department of Organic Chemistry, Universidad Autónoma de Madrid, Campus de Cantoblanco C/Francisco Tomás y Valiente 7, 28049, Madrid, Spain.
  • Torres T; Department of Organic Chemistry, Universidad Autónoma de Madrid, Campus de Cantoblanco C/Francisco Tomás y Valiente 7, 28049, Madrid, Spain.
  • de la Torre G; Institute for Advanced Research in Chemical Sciences (IAdChem), Universidad Autónoma de Madrid Campus de Cantoblanco, 28049, Madrid, Spain.
Angew Chem Int Ed Engl ; 62(44): e202311255, 2023 Oct 26.
Article em En | MEDLINE | ID: mdl-37695637
Herein we report the first example of a supramolecular cage that works as a catalytic molecular reactor to perform transformations over fullerenes in aqueous medium. Taking advantage of the ability of metallo-organic Pd(II)-subphthalocyanine (SubPc) capsules to form stable host:guest complexes with C60 , we have prepared a water-soluble cage that provides a hydrophobic environment for conducting cycloadditions over encapsulated C60 , namely, Diels-Alder reactions with anthracene. Indeed, the presence of catalytic amounts of SubPc cage dissolved in water promotes co-encapsulation of insoluble C60 and anthracene substrates, allowing the reaction to occur inside the cavity under mild conditions. The lower stability of the host:guest complex with the resulting C60 cycloadduct facilitates its displacement by pristine C60 , which grants catalytic turnover. Moreover, bis-addition compounds are regioselectively formed inside the cage when using excess anthracene.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Espanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Espanha