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April 15, 2026Journal of the American Chemical Society4 citations

Visible-Light-Promoted Nickel-Catalyzed Cross-Coupling of Iodocarboranes with Triarylarsanes and Triphenylstibanes

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XWXiaohai WangMFMeitian FuXPXuran Pan

Key Points

  • The research aims to develop a mild strategy for forming stable B-As and B-Sb bonds using visible light and nickel catalysis.
  • Utilized visible-light promotion for nickel-catalyzed reactions.
  • Conducted reactions at room temperature with iodocarboranes, triarylarsanes, and triphenylstibanes.
  • Characterized products using X-ray crystallography.
  • Successfully synthesized stable boron-arsanylated and boron-stibanylated carboranes.
  • Produced compounds were air and thermally stable.
  • Demonstrated the efficiency of the radical cross-coupling strategy.

Abstract

The construction of stable B-As and B-Sb bonds has long been a formidable challenge. Herein, we present a mild visible-light-promoted nickel-catalyzed radical cross-coupling strategy that directly forges B-As and B-Sb bonds on carborane cages. This protocol efficiently converts iodocarboranes and triarylarsanes/stibanes into a series of previously inaccessible, well-characterized boron-arsanylated and boron-stibanylated carboranes at room temperature. The unique carborane framework stabilizes these typically labile bonds, yielding air- and thermally stable compounds, as confirmed by X-ray crystallography. This work provides a general radical-based platform for exploring boron-heavier pnictogen chemistry.

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Cite This Study

Wang et al. (2026) studied this question.

synapsesocial.com/papers/69df2a4be4eeef8a2a6af84chttps://doi.org/10.1021/jacs.6c04797
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