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Gold(III) Alkyne Complexes: Bonding and Reaction Pathways.
Rocchigiani, Luca; Fernandez-Cestau, Julio; Agonigi, Gabriele; Chambrier, Isabelle; Budzelaar, Peter H M; Bochmann, Manfred.
Afiliação
  • Rocchigiani L; School of Chemistry, University of East Anglia, Norwich Research Park, Norwich, NR4 7TJ, UK.
  • Fernandez-Cestau J; School of Chemistry, University of East Anglia, Norwich Research Park, Norwich, NR4 7TJ, UK.
  • Agonigi G; School of Chemistry, University of East Anglia, Norwich Research Park, Norwich, NR4 7TJ, UK.
  • Chambrier I; School of Chemistry, University of East Anglia, Norwich Research Park, Norwich, NR4 7TJ, UK.
  • Budzelaar PHM; Department of Chemistry, University of Naples Federico II, Via Cintia, 80126, Naples, Italy.
  • Bochmann M; School of Chemistry, University of East Anglia, Norwich Research Park, Norwich, NR4 7TJ, UK.
Angew Chem Int Ed Engl ; 56(44): 13861-13865, 2017 10 23.
Article em En | MEDLINE | ID: mdl-28892244
The synthesis and characterization of hitherto hypothetical AuIII π-alkyne complexes is reported. Bonding and stability depend strongly on the trans effect and steric factors. Bonding characteristics shed light on the reasons for the very different stabilities between the classical alkyne complexes of PtII and their drastically more reactive AuIII congeners. Lack of back-bonding facilitates alkyne slippage, which is energetically less costly for gold than for platinum and explains the propensity of gold to facilitate C-C bond formation. Cycloaddition followed by aryl migration and reductive deprotonation is presented as a new reaction sequence in gold chemistry.
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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: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2017 Tipo de documento: Article