Classical Gold Carbonyl Complexes in Tetrahedral and Trigonal-Planar Settings

Mukundam Vanga, Alvaro Muñoz-Castro*, H. V.Rasika Dias*

*Autor correspondiente de este trabajo

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

2 Citas (Scopus)

Resumen

A unique four-coordinate, classical gold(I)-carbonyl complex with substantial backdonation from gold has been isolated by using a B-methylated and fluorinated tris(pyridyl)borate chelator. Its lighter silver(I) and copper(I) analogs enabled a study of trends in the coinage-metal family. The B-arylated ligand version also afforded a gold–carbon monoxide complex that displays a notably low C−O stretch value, but with trigonal planar geometry at the gold. A computational analysis shows that the AuI−CO bonds of these tris(pyridyl)borate ligand-supported molecules consist of electrostatic attraction, OC→Au σ-donation, and very significant Au→CO π-back-bonding components. The latter is responsible for the observed C−O stretching frequencies, which are lower than in free CO.

Idioma originalInglés
Número de artículoe202303339
PublicaciónChemistry - A European Journal
Volumen30
N.º5
DOI
EstadoPublicada - 2024

Nota bibliográfica

Publisher Copyright:
© 2023 Wiley-VCH GmbH.

Áreas temáticas de ASJC Scopus

  • Catálisis
  • Química General
  • Química orgánica

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