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Disulfide-Driven Pore Functionalization of Metal-Organic Frameworks.
Moore, Jennifer M; Crom, Audrey B; Feldblyum, Jeremy I; Genna, Douglas T.
Afiliación
  • Moore JM; Department of Chemical and Biological Sciences, Youngstown State University, One University Plaza, Youngstown, OH 44555, USA.
  • Crom AB; Department of Chemistry, The University at Albany, State University of New York, 1400 Washington Avenue, Albany, NY, 12222, USA.
  • Feldblyum JI; Department of Chemistry, The University at Albany, State University of New York, 1400 Washington Avenue, Albany, NY, 12222, USA.
  • Genna DT; Department of Chemical and Biological Sciences, Youngstown State University, One University Plaza, Youngstown, OH 44555, USA.
Chemistry ; 29(61): e202302144, 2023 Nov 02.
Article en En | MEDLINE | ID: mdl-37486291
Post-synthetic modification (PSM) imparts additional functionality to metal-organic frameworks (MOFs) that is often difficult to access using solvothermal synthesis. As such, expanding the repertory of PSM reactions available to the practitioner is of increased importance for the generation of materials tailored for desired applications. Herein, a method is described for the protecting group-free installation of diverse functional groups within the pores of a MIL-53(Al) analogue via disulfide bond formation. The majority of the reactions proceed with thiol-to-disulfide conversions ranging from high to nearly quantitative. The disulfide bonds are stable in various solvents and can be cleaved in the presence of a reducing agent.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Chemistry Asunto de la revista: QUIMICA Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Chemistry Asunto de la revista: QUIMICA Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos