期刊
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 60, 期 46, 页码 24650-24658出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202110619
关键词
arylation; NMR spectroscopy; phosphine; photoredox catalysis; white phosphorus
资金
- European Research Council [ERC CoG 772299]
- Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) [TRR 325 - 444632635]
- Alexander von Humboldt Foundation
- Projekt DEAL
Detailed P-31{H-1} NMR spectroscopic investigations provide deeper insight into the mechanisms involved in the photocatalytic arylation of white phosphorus, revealing previously unrecognized side products and the unexpected behavior of the terminal reductant Et3N. The different rate of formation of these products explains the performance discrepancies of two effective catalysts, while the observation of PH3 as a minor intermediate led to the development of a new catalytic procedure for the arylation of white phosphorus. This method yields valuable triarylphosphines or tetraarylphosphonium salts depending on aryl substituents' steric profiles.
Detailed P-31{H-1} NMR spectroscopic investigations provide deeper insight into the complex, multi-step mechanisms involved in the recently reported photocatalytic arylation of white phosphorus (P-4). Specifically, these studies have identified a number of previously unrecognized side products, which arise from an unexpected non-innocent behavior of the commonly employed terminal reductant Et3N. The different rate of formation of these products explains discrepancies in the performance of the two most effective catalysts, [Ir(dtbbpy)(ppy)(2)][PF6] (dtbbpy=4,4 '-di-tert-butyl-2,2 '-bipyridine) and 3DPAFIPN. Inspired by the observation of PH3 as a minor intermediate, we have developed the first catalytic procedure for the arylation of this key industrial compound. Similar to P-4 arylation, this method affords valuable triarylphosphines or tetraarylphosphonium salts depending on the steric profile of the aryl substituents.
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