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

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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Publication Details

Journal
Journal of the American Chemical Society
Published
2026-04-13
DOI
https://doi.org/10.1021/jacs.6c04797
Primary Topic
Boron Compounds in Chemistry
Type
article
Field-Weighted Citation Impact
0.00

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article

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

Zheng Wang, Xuran Pan, Xinyao Li, Xiaohai Wang et al.
Journal of the American Chemical Society
Boron Compounds in Chemistry
article

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

Zheng Wang, Xuran Pan, Xinyao Li, Xiaohai Wang, Meitian Fu, Jiaxin Xi
article en

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.

Journal of the American Chemical SocietyVol. 148(16)
Shanghai University (CN), College of Medical Sciences (NP), Universidad del Noreste (MX), Tsinghua University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 21%
Boron Compounds in Chemistry
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