Ligand exchange of tris(2,4-di- <i>tert</i> -butylphenyl) phosphite: a practical and efficient route to organo gold( <scp>i</scp> ) complexes

Tris(2,4-di-<i>tert</i>-butylphenyl)phosphite (2,6-<sup><i>t</i></sup>Bu<sub>2</sub>-PhO)<sub>3</sub>P is used as a stable, easily displaceable ancillary ligand in the preparation of organo Au(I) complexes. The phosphite gold(I) precursors are bench-stable and readily accessible. They undergo high-yielding ligand exchange with a variety of ligands such as phosphines, N-heterocyclic carbenes and bidentate ligands. This ligand exchange strategy overcomes the limitations associated with traditional gold halide-based synthetic routes and is compatible with different organogold fragments. The protocol is scalable, operationally simple and broadly applicable.

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Publication Details

Journal
Chemical Communications
Published
2025-01-01
DOI
https://doi.org/10.1039/d5cc05744b
Primary Topic
Catalytic Alkyne Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Ligand exchange of tris(2,4-di- tert -butylphenyl) phosphite: a practical and efficient route to organo gold( i ) complexes

David Vesseur, Sonia Mallet‐Ladeira, Didier Bourissou, Shuo Li
Chemical Communications
Catalytic Alkyne Reactions
article

Ligand exchange of tris(2,4-di- tert -butylphenyl) phosphite: a practical and efficient route to organo gold( i ) complexes

David Vesseur, Sonia Mallet‐Ladeira, Didier Bourissou, Shuo Li
article en

Abstract

Tris(2,4-di-<i>tert</i>-butylphenyl)phosphite (2,6-<sup><i>t</i></sup>Bu<sub>2</sub>-PhO)<sub>3</sub>P is used as a stable, easily displaceable ancillary ligand in the preparation of organo Au(I) complexes. The phosphite gold(I) precursors are bench-stable and readily accessible. They undergo high-yielding ligand exchange with a variety of ligands such as phosphines, N-heterocyclic carbenes and bidentate ligands. This ligand exchange strategy overcomes the limitations associated with traditional gold halide-based synthetic routes and is compatible with different organogold fragments. The protocol is scalable, operationally simple and broadly applicable.

Chemical CommunicationsVol. 61(94)
Centre National de la Recherche Scientifique (FR), Institut National Polytechnique de Toulouse (FR), Laboratoire de Chimie de Coordination (FR), Laboratoire Hétérochimie Fondamentale et Appliquée (FR)
Agence Nationale de la Recherche, Université de Toulouse, Centre National de la Recherche Scientifique
Openalex Percentile: Top 77%
Catalytic Alkyne Reactions
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