Harnessing Supported Gold Nanoparticle as a Single‐Electron Transfer Catalyst for Decarboxylative Cross‐Coupling

Author:

Miura Hiroki123ORCID,Ameyama Kaede1,Shishido Tetsuya123ORCID

Affiliation:

1. Department of Applied Chemistry for Environment Graduate School of Urban Environmental Sciences Tokyo Metropolitan University 1-1 Minami-Osawa Hachioji Tokyo 192-0397 Japan

2. Research Center for Hydrogen Energy-based Society Tokyo Metropolitan University 1-1 Minami-Osawa Hachioji Tokyo 192-0397 Japan

3. Elements Strategy Initiative for Catalysts & Batteries Kyoto University Katsura, Nishikyo-ku Kyoto 615-8520 Japan

Abstract

AbstractWe found that gold nanoparticles function as single‐electron transfer catalysts to promote decarboxylative cross‐coupling between N‐hydroxy phthalimide esters and disilanes or diborons. A variety of disilanes coupled with alkyl radicals could be generated from N‐hydroxy phthalimide esters via single‐electron reduction by active carbon‐supported gold nanoparticle catalysts to afford diverse alkylsilanes without the need for external bases. Furthermore, the present gold catalytic system was also effective for decarboxylative carbon‐boron coupling to afford alkyl boronates. A detailed mechanistic investigation revealed that single‐electron transfer mediated by supported gold nanoparticles enabled the generation of alkyl radical and silyl radical, thereby enabling radical cross‐coupling. The reusability and environmentally‐friendly nature of supported gold catalyst as well as the scalability of the reaction system enable the practical transformation of carboxylic acid derivatives into value‐added organosilicon and organoboron compounds.

Funder

Tokyo Metropolitan University

Publisher

Wiley

Subject

General Chemistry

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