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PtII -N-Heterocyclic Carbene Complexes in Solvent-Free Alkene Hydrosilylation.
Maliszewski, Benon P; Bayrakdar, Tahani A C A; Lambert, Perrine; Hamdouna, Lama; Trivelli, Xavier; Cavallo, Luigi; Poater, Albert; Belis, Marek; Lafon, Olivier; Van Hecke, Kristof; Ormerod, Dominic; Cazin, Catherine S J; Nahra, Fady; Nolan, Steven P.
Afiliación
  • Maliszewski BP; Department of Chemistry and Centre for Sustainable Chemistry, Ghent University, Krijgslaan 281 (S3), 9000, Ghent, Belgium.
  • Bayrakdar TACA; Separation and Conversion Technology, VITO (Flemish Institute for Technological Research), Boeretang 200, 2400, Mol, Belgium.
  • Lambert P; Department of Chemistry and Centre for Sustainable Chemistry, Ghent University, Krijgslaan 281 (S3), 9000, Ghent, Belgium.
  • Hamdouna L; Separation and Conversion Technology, VITO (Flemish Institute for Technological Research), Boeretang 200, 2400, Mol, Belgium.
  • Trivelli X; Department of Chemistry and Centre for Sustainable Chemistry, Ghent University, Krijgslaan 281 (S3), 9000, Ghent, Belgium.
  • Cavallo L; Department of Chemistry and Centre for Sustainable Chemistry, Ghent University, Krijgslaan 281 (S3), 9000, Ghent, Belgium.
  • Poater A; CNRS, Centrale Lille, Univ. Artois, UMR 8181 - UCCS - Unité de Catalyse et Chimie du Solide, Université de Lille, 59000, Lille, France.
  • Belis M; CNRS, INRAE, Centrale Lille, Univ. Artois, FR 2638 - IMEC - Institut Michel-Eugène Chevreul, Université de Lille, 59000, Lille, France.
  • Lafon O; KAUST Catalysis Center, Physical Sciences and Engineering Division, King Abdullah University of Science and Technology, Thuwal, 23955-6900, Saudi Arabia.
  • Van Hecke K; Institut de Química Computacional i Catàlisi and Departament de Química, Universitat de Girona, c/Maria Aurèlia Capmany 69, 17003, Girona, Catalonia, Spain.
  • Ormerod D; Department of Chemistry and Centre for Sustainable Chemistry, Ghent University, Krijgslaan 281 (S3), 9000, Ghent, Belgium.
  • Cazin CSJ; CNRS, Centrale Lille, Univ. Artois, UMR 8181 - UCCS - Unité de Catalyse et Chimie du Solide, Université de Lille, 59000, Lille, France.
  • Nahra F; Department of Chemistry and Centre for Sustainable Chemistry, Ghent University, Krijgslaan 281 (S3), 9000, Ghent, Belgium.
  • Nolan SP; Separation and Conversion Technology, VITO (Flemish Institute for Technological Research), Boeretang 200, 2400, Mol, Belgium.
Chemistry ; 29(40): e202301259, 2023 Jul 14.
Article en En | MEDLINE | ID: mdl-37196153
ABSTRACT
Herein, we report the catalytic activity of a series of platinum(II) pre-catalysts, bearing N-heterocyclic carbene (NHC) ligands, in the alkene hydrosilylation reaction. Their structural and electronic properties are fully investigated using X-ray diffraction analysis and nuclear magnetic resonance spectroscopy (NMR). Next, our study presents a structure-activity relationship within this group of pre-catalysts and gives mechanistic insights into the catalyst activation step. An exceptional catalytic performance of one of the complexes is observed, reaching a turnover number (TON) of 970 000 and a turnover frequency (TOF) of 40 417 h-1 at 1 ppm catalyst loading. Finally, an attractive solvent-free and open-to-air alkene hydrosilylation protocol, featuring efficient platinum removal (reduction of residual Pt from 582 ppm to 5.8 ppm), is disclosed.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Chemistry Asunto de la revista: QUIMICA Año: 2023 Tipo del documento: Article País de afiliación: Bélgica

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