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Isolation of a Reactive Tricoordinate α‐Oxo Gold Carbene Complex
Authors:Abdallah Zeineddine  Dr. Feriel Rekhroukh  Dr. E. Daiann Sosa Carrizo  Sonia Mallet‐Ladeira  Dr. Karinne Miqueu  Dr. Abderrahmane Amgoune  Dr. Didier Bourissou
Affiliation:1. http://hfa.ups‐tlse.fr/LBPB/index lbpb.htm;2. CNRS/ Université Paul Sabatier, Laboratoire Hétérochimie Fondamentale et Appliquée (LHFA, UMR 5069), Toulouse Cedex 09, France;3. CNRS/UNIV PAU & PAYS ADOUR, Institut des Sciences Analytiques et de Physico-Chimie pour l'Environnement et les Matériaux (IPREM, UMR 5254). Hélioparc, Pau Cedex 09, France;4. Institut de Chimie de Toulouse (FR 2599), Toulouse Cedex 09, France
Abstract:The [(P,P)Au=C(Ph)CO2Et]+ complex 3 [where (P,P) is an o‐carboranyl diphosphine ligand] was prepared by diazo decomposition at ?40 °C. It is the first α‐oxo gold carbene complex to be characterized. Its crystallographic structure was determined and DFT calculations have been performed, unraveling the key influence of the chelating (P,P) ligand. The gold center is tricoordinate and the electrophilicity of the carbene center is decreased. Complex 3 mimics transient α‐oxo gold carbenes in a series of catalytic transformations, and provides support for the critical role of electrophilicity in the chemoselectivity of phenol functionalization (O?H vs. C?H insertion).
Keywords:bidentate ligand  carbene complexes  homogeneous catalysis  diazo compounds  gold
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