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Phosphine-Scavenging Cationic Gold(I) Complexes: Alternative Applications of Gold Cocatalysis in Fundamental Palladium-Catalyzed Cross-Couplings

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posted on 2024-11-16, 03:35 authored by Curtis Ho, Alireza Ariafard, Christopher HylandChristopher Hyland, Alex C Bissember
We have demonstrated that air-stable cationic gold(I) cocatalysts have the capacity to enhance the efficiency of palladium-catalyzed cross-couplings. Specifically, we determined that a 1:1 [Pd{P(t-Bu)3}2]/[Au{P(t-Bu)3}(NTf2)] system provides superior reactivity relative to [Pd{P(t-Bu)3}2], across Suzuki-Miyaura, Stille, and Mizoroki-Heck reactions performed under mild conditions. Our results are consistent with cationic gold(I) species serving primarily as phosphine scavengers in this chemistry, as recently predicted by density functional theory (DFT).

Funding

A Midas touch for electrophiles in new reaction development

Australian Research Council

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History

Citation

Ho, C. C., Ariafard, A., Hyland, C. J.T. & Bissember, A. C. (2019). Phosphine-Scavenging Cationic Gold(I) Complexes: Alternative Applications of Gold Cocatalysis in Fundamental Palladium-Catalyzed Cross-Couplings. Organometallics, 38 (13), 2683-2688.

Journal title

Organometallics

Volume

38

Issue

13

Pagination

2683-2688

Language

English

RIS ID

136905

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