摘要
Here we report a nickel/photo co-catalyzed direct radical Si–H arylation of hydrosilanes with aryl halides. Tetrabutylammonium decatungstate (TBADT) serves as a robust hydrogen-atom-transfer (HAT) photocatalyst, working synergistically with a nickel catalyst through a cross-coupling pathway that proceeds via a silyl–nickel intermediate derived from the in situ-generated silyl radicals. This protocol features a broad substrate scope, mild photochemical conditions, and excellent functional group tolerance, offering a versatile and sustainable approach for accessing synthetically valuable arylsilanes directly from simple hydrosilanes.
| 源语言 | 英语 |
|---|---|
| 页(从-至) | 1125-1130 |
| 页数 | 6 |
| 期刊 | Organic Chemistry Frontiers |
| 卷 | 13 |
| 期 | 4 |
| DOI | |
| 出版状态 | 已出版 - 17 2月 2026 |
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