open access

https://hdl.handle.net/2115/97931

Introducing Steric Bulk Into Silylboranes: Enhanced Bench Stability and Novel Chemical Reactivity

英語

Silylboranes

2025-08-18

Wiley-Blackwell

Angewandte chemie-international edition

64(34)

e202506194

Silylboranes are versatile intermediates in organic synthesis, and a wide range of structural variants of silylboranes have already been synthesized. However, the stability of silylboranes varies significantly, and their decomposition mechanism remains to be fully understood. Moreover, some silylborane motifs have not yet been applied as synthetic reagents due to their instability. To address this issue, we first investigated the decomposition mechanism of silylboranes in air and moisture using experimental and theoretical methods. We discovered that oxygenation by atmospheric oxygen is the major decomposition pathway, resulting in the formation of a borylsilylether, and that the introduction of a bulky silyl group suppresses this decomposition. Based on these results, we synthesized triisopropylsilyldimesitylborane (i-Pr3Si-BMes2), which exhibits high bench stability. Moreover, i-Pr3Si-BMes2 reacts with carbon monoxide (CO), which is the first example of a reaction between a silylborane and CO. Further computational studies revealed that electronic effects, including hyperconjugation between the Si & horbar;B sigma-bond and C & horbar;O pi*-bond, are crucial for CO activation. Furthermore, we prepared a bench-stable bissilylaminoborane by introducing triisopropylsilyl groups, providing a bissilylchloroborane upon hydrogen chloride treatment. These findings provide valuable insights into how steric and electronic effects can be used to optimize the balance between stability and reactivity in silylboranes.

学術雑誌論文

Accepted Manuscript

This is the peer reviewed version of the following article: R. Takahashi, J. Jiang, S. Maeda, H. Ito, Angew. Chem. Int. Ed. 2025, 64, e202506194, which has been published in final form at https://doi.org/10.1002/anie.202506194. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. This article may not be enhanced, enriched or otherwise transformed into a derivative work, without express permission from Wiley or by statutory rights under applicable legislation. Copyright notices must not be removed, obscured or modified. The article must be linked to Wiley’s version of record on Wiley Online Library and any embedding, framing or otherwise making available the article or pages thereof by third parties from platforms, services and websites other than Wiley Online Library must be prohibited.