Abstract
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.
| Original language | English |
|---|---|
| Pages (from-to) | 1125-1130 |
| Number of pages | 6 |
| Journal | Organic Chemistry Frontiers |
| Volume | 13 |
| Issue number | 4 |
| DOIs | |
| State | Published - 17 Feb 2026 |
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