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Gold(I) α-Trifluoromethyl Carbenes: Synthesis, Characterization and Reactivity Studies.
Rigoulet, Mathilde; Vesseur, David; Miqueu, Karinne; Bourissou, Didier.
Afiliação
  • Rigoulet M; CNRS/Université Paul Sabatier, Laboratoire Hétérochimie, Fondamentale et Appliquée (LHFA, UMR 5069), 118 Route de Narbonne, 31062, Toulouse Cedex 09, France.
  • Vesseur D; CNRS/Université Paul Sabatier, Laboratoire Hétérochimie, Fondamentale et Appliquée (LHFA, UMR 5069), 118 Route de Narbonne, 31062, Toulouse Cedex 09, France.
  • Miqueu K; CNRS/Université de Pau et des Pays de l'Adour, E2S-UPPA, Institut des Sciences Analytiques et de Physico-Chimie pour l'Environnement et les Matériaux (IPREM, UMR 5254), Hélioparc, 2 Avenue du Président Angot, 64053, Pau Cedex 09, France.
  • Bourissou D; CNRS/Université Paul Sabatier, Laboratoire Hétérochimie, Fondamentale et Appliquée (LHFA, UMR 5069), 118 Route de Narbonne, 31062, Toulouse Cedex 09, France.
Angew Chem Int Ed Engl ; 61(25): e202204781, 2022 Jun 20.
Article em En | MEDLINE | ID: mdl-35466483
ABSTRACT
Aryl trifluoromethyl diazomethanes 2-R (R=Ph, OMe, CF3 ) are readily decomposed by the (o-carboranyl)diphosphine gold(I) complex 1. The resulting α-CF3 substituted carbene complexes 3-R have been characterized by multi-nuclear NMR spectroscopy as well as X-ray crystallography (for 3-Ph). The bonding situation was thoroughly assessed by computational means, showing stabilization of the electrophilic carbene center by π-donation from the aryl substituent and backdonation from Au, as enhanced by the chelating P^P ligand. Reactivity studies under stoichiometric and catalytic conditions substantiate typical carbene-type behavior for 3-Ph.
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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: 2022 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2022 Tipo de documento: Article País de afiliação: França