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Deconvoluting Substrates, Support, and Temperature Effects on Leaching and Deactivation of Pd Catalysts: An In Situ Study in Flow.
Newton, Oliver J; Takle, Matthew J; Richardson, Jeffery; Hellgardt, Klaus; Hii, King Kuok Mimi.
Afiliação
  • Newton OJ; Department of Chemistry, Imperial College London, Molecular Sciences Research Hub, 82, Wood Lane, London W12 0BZ, U.K.
  • Takle MJ; Department of Chemistry, Imperial College London, Molecular Sciences Research Hub, 82, Wood Lane, London W12 0BZ, U.K.
  • Richardson J; Discovery Chemistry Research and Technologies, Eli Lilly and Company, Windlesham, Surrey GU20 6PH, U.K.
  • Hellgardt K; Department of Chemical Engineering, Imperial College London, Exhibition Road, South Kensington, London SW7 2AZ, U.K.
  • Hii KKM; Department of Chemistry, Imperial College London, Molecular Sciences Research Hub, 82, Wood Lane, London W12 0BZ, U.K.
ACS Catal ; 14(13): 9678-9686, 2024 Jul 05.
Article em En | MEDLINE | ID: mdl-38988654
ABSTRACT
Leaching behavior of three different Pd heterogeneous catalysts (PdEnCat 30, FibreCat FC1001, and Pd/Al2O3) during the Heck reaction of iodobenzene and methyl acrylate, in the presence of triethylamine, was compared using a tandem flow reactor. While leaching was observed in all three cases, Pd/Al2O3 appeared to be the most robust, showing little/no leaching at ambient temperature. The leached Pd species also appear to display different catalytic activities. With a slight modification of the reactor, the leaching caused by individual components of the reaction mixture can be assessed separately. For the polymer-supported catalysts, triethylamine caused the largest amount of leaching, even at 30 °C. In contrast, the leaching from Pd/Al2O3 was observed only in the presence of iodobenzene at 90 °C. Variations in leaching behavior were ascribed to differences in Pd species and immobilization methods.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article