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Gold(iii)-arene complexes by insertion of olefins into gold-aryl bonds.


ABSTRACT: The synthesis and characterization of the first gold(iii)-arene complexes are described. Well-defined (P,C)-cyclometalated gold(iii)-aryl complexes were prepared and characterized by NMR spectroscopy. These complexes swiftly and cleanly reacted with norbornene and ethylene to provide cationic gold(iii)-alkyl complexes, in which the remote phenyl ring was ?2-coordinated to gold. The interaction between the aromatic ring and the gold(iii) center was thoroughly analyzed by NMR spectroscopy, X-ray diffraction, and DFT calculations. The ?-arene coordination was found to significantly influence the stability and reactivity of low coordinated gold(iii) alkyl species.

SUBMITTER: Rekhroukh F 

PROVIDER: S-EPMC5472032 | biostudies-literature | 2017 Jun

REPOSITORIES: biostudies-literature

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Gold(iii)-arene complexes by insertion of olefins into gold-aryl bonds.

Rekhroukh Feriel F   Blons Charlie C   Estévez Laura L   Mallet-Ladeira Sonia S   Miqueu Karinne K   Amgoune Abderrahmane A   Bourissou Didier D  

Chemical science 20170419 6


The synthesis and characterization of the first gold(iii)-arene complexes are described. Well-defined (P,C)-cyclometalated gold(iii)-aryl complexes were prepared and characterized by NMR spectroscopy. These complexes swiftly and cleanly reacted with norbornene and ethylene to provide cationic gold(iii)-alkyl complexes, in which the remote phenyl ring was η<sup>2</sup>-coordinated to gold. The interaction between the aromatic ring and the gold(iii) center was thoroughly analyzed by NMR spectrosco  ...[more]

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