4.7 Article

Direct formation of Au(III) acetyl, alkoxyl and alkynyl functionalities via halide free tricationic Au(III) precursors

Journal

DALTON TRANSACTIONS
Volume 47, Issue 12, Pages 4228-4235

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c7dt04675h

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Funding

  1. La Trobe University
  2. La Trobe Institute of Molecular Sciences
  3. ARC [FT16010007]

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A novel synthetic approach for the synthesis of gold(iii) acetato, alkoxolato and alkynyl complexes was developed via the reactivity of gold(iii) trications containing the N,N-chelating ligand 2,2-bipyridine and N,N,N-chelating ligand terpyridine through direct reactions with the protic precursors. This protocol avoids the gold(iii) chloride bond activation pathway commonly employed to access these functionalities. For example exposure of [LAu(iii)L]OTf3 (L = N,N,N-terpyridine, L = 4-DMAP) to RH (R = OCH3, OAc, Ph-?) results in the facile formation of the corresponding functionalised gold(iii) complexes [LAu(iii)R]OTf2.

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