Inside Back Cover

gem ‐Bis(silanes) are valuable organosilicon compounds owing to their distinctive reactivity and broad synthetic potential. A highly efficient Co/Ni‐catalyzed dehydrogenative silylation/hydrosilylation of alkenes was developed for the construction of gem ‐bis(silanes), in which unanticipated nickel impurities were found to efficiently promote the key hydrosilylation step with a turnover number of up to 24000. Mechanistic studies further revealed a silicon‐based directing effect and nickel–hydride‐species‐dependent regiodivergent selectivity, enabling controlled access to geminal and vicinal bis(silanes). More details are discussed in the article by Lu et al. on pages 3349—3355. image

Publication Details

Journal
Chinese Journal of Chemistry
Published
2026-09-15
DOI
https://doi.org/10.1002/cjoc.70797
Primary Topic
Organoboron and organosilicon chemistry
Type
article
Field-Weighted Citation Impact
0.00
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Inside Back Cover

Chinese Journal of Chemistry
Organoboron and organosilicon chemistry
article

Inside Back Cover

article en

Abstract

gem ‐Bis(silanes) are valuable organosilicon compounds owing to their distinctive reactivity and broad synthetic potential. A highly efficient Co/Ni‐catalyzed dehydrogenative silylation/hydrosilylation of alkenes was developed for the construction of gem ‐bis(silanes), in which unanticipated nickel impurities were found to efficiently promote the key hydrosilylation step with a turnover number of up to 24000. Mechanistic studies further revealed a silicon‐based directing effect and nickel–hydride‐species‐dependent regiodivergent selectivity, enabling controlled access to geminal and vicinal bis(silanes). More details are discussed in the article by Lu et al. on pages 3349—3355. image

Chinese Journal of ChemistryVol. 44(20)
Openalex Percentile: Top 20%
Organoboron and organosilicon chemistry
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Inside Back Cover · Chinese Journal of Chemistry (2026) | TGRS Research Map | TGRS