Classical Gold Carbonyl Complexes in Tetrahedral and Trigonal‐Planar Settings

Author:

Vanga Mukundam1ORCID,Muñoz‐Castro Alvaro2,Dias H. V. Rasika1ORCID

Affiliation:

1. Department of Chemistry and Biochemistry The University of Texas at Arlington Arlington TX 76019 United States

2. Facultad de Ingeniería Arquitectura y Diseño Universidad San Sebastián Bellavista 7 Santiago 8420524 Chile

Abstract

AbstractA 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.

Funder

Directorate for Mathematical and Physical Sciences

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

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