On-Demand Access to Palladium Oxidative Addition Complexes (OACs) from a Stable Organopalladate Salt

Palladium oxidative addition complexes (OACs) are state-of-the-art catalysts for many C–C and C-heteroatom cross-coupling reactions, but altering the ancillary ligand identity (i.e., phosphine, N-heterocyclic carbene) often requires a bespoke synthesis. This has limited the modularity and accessibility of these ideal catalysts. We report a simple admixture approach combining a bench-stable organopalladate salt with a mono- or bidentate ligand to generate OACs within minutes at room temperature. High yields across a suite of canonical cross-coupling reactions demonstrate the “on-demand” Pd OAC strategy can function as a drop-in replacement for isolated OACs as well as several other contemporary Pd precatalysts. Characterization of a previously unknown OAC coordinated by a single NHC ligand also highlights how this approach can circumvent the decomposition of thermally sensitive OACs that are difficult to access directly from oxidation addition reactions.

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Publication Details

Journal
Organometallics
Published
2025-02-28
DOI
https://doi.org/10.1021/acs.organomet.5c00039
Citations
3
Primary Topic
Catalytic Cross-Coupling Reactions
Type
article
Field-Weighted Citation Impact
2.81

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article

On-Demand Access to Palladium Oxidative Addition Complexes (OACs) from a Stable Organopalladate Salt

Lalu Venigalla, Brad P. Carrow, Wenjun Hou, Hao Chen et al.
3 citations
Organometallics
Catalytic Cross-Coupling Reactions
2.81
article

On-Demand Access to Palladium Oxidative Addition Complexes (OACs) from a Stable Organopalladate Salt

Lalu Venigalla, Brad P. Carrow, Wenjun Hou, Hao Chen, Mengyuan Xiao, Yongqing Yang, Aidan P. Looby
article en
3 citations

Abstract

Palladium oxidative addition complexes (OACs) are state-of-the-art catalysts for many C–C and C-heteroatom cross-coupling reactions, but altering the ancillary ligand identity (i.e., phosphine, N-heterocyclic carbene) often requires a bespoke synthesis. This has limited the modularity and accessibility of these ideal catalysts. We report a simple admixture approach combining a bench-stable organopalladate salt with a mono- or bidentate ligand to generate OACs within minutes at room temperature. High yields across a suite of canonical cross-coupling reactions demonstrate the “on-demand” Pd OAC strategy can function as a drop-in replacement for isolated OACs as well as several other contemporary Pd precatalysts. Characterization of a previously unknown OAC coordinated by a single NHC ligand also highlights how this approach can circumvent the decomposition of thermally sensitive OACs that are difficult to access directly from oxidation addition reactions.

OrganometallicsVol. 44(5)
New Jersey Institute of Technology (US), University of Houston (US)
National Science Foundation, Welch Foundation, National Institute of General Medical Sciences
Openalex Percentile: Top 12%
Catalytic Cross-Coupling Reactions
2.81
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