Bonsignore, Riccardo ![]() ![]() ![]() |
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Abstract
With the aim of exploiting new organometallic species for cross‐coupling reactions, we report here on the Au(III)‐mediated Caryl–P bond formation occurring upon reaction of C^N cyclometalated Au(III) complexes with phosphines. The [Au(C^N)Cl2] complex 1 featuring the bidentate 2‐benzoylpyridine (CCON) scaffold was found to react with PTA (1,3,5‐triaza‐7‐phosphaadamantane) under mild conditions, including in water, to afford the corresponding phosphonium 5 via C–P reductive elimination. A mechanism is proposed for the title reaction based on in situ 31P{1H} NMR and HR‐ESI‐MS analyses combined with DFT calculations. The C–P coupling has been generalized to other C^N cyclometalated Au(III) complexes and other tertiary phosphines. Overall, this work provides new insights into the reactivity of cyclometalated Au(III) compounds and establishes initial structure‐activity relationships to develop Au(III)‐mediated C–P cross‐coupling reactions.
Item Type: | Article |
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Date Type: | Publication |
Status: | Published |
Schools: | Chemistry |
Publisher: | Wiley |
ISSN: | 0947-6539 |
Funders: | European Union�s Horizon 2020 and EPSRC |
Date of First Compliant Deposit: | 3 February 2020 |
Date of Acceptance: | 22 January 2020 |
Last Modified: | 05 Jan 2024 07:43 |
URI: | https://orca.cardiff.ac.uk/id/eprint/129275 |
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