Koike Taichi, Sakurata Naoki, Ishida Shintaro, Iwamoto Takeaki
Department of Chemistry, Graduate School of Science, Tohoku University Aoba-ku, Sendai, 980-8578, Japan.
Angew Chem Int Ed Engl. 2024 Nov 18;63(47):e202411283. doi: 10.1002/anie.202411283. Epub 2024 Oct 14.
Compared to the outstanding development in the synthesis of Si-B single bonded species, borylsilanes and their application to organic synthesis, the chemistry of Si=B double bonded species, borasilenes and boratasilenes have only made little progress, first of all, due to the difficulties in accessing such double bonds. Herein we report the synthesis of the first Si=B analogue of a vinyl halide, a bromoboratasilene, via formal borylene insertion to the coordination sphere of a monoatomic Si(0) complex, using a dihaloborane as the borylene source. The treatment of bromoboratasilene toward neutral or anionic Lewis bases gives access to new boratasilenes, all of which were proved to possess significant Si=B double bond character by XRD analysis and DFT calculations. These results demonstrate exciting strategies to synthesize new types of Si=B double bonded species which should further progress the chemistry of boron, silicon-containing molecules.
与硅-硼单键物种、硼硅烷的合成及其在有机合成中的应用方面的显著进展相比,硅=硼双键物种、硼硅烯和硼杂硅烯的化学进展甚微,首先是由于获得此类双键存在困难。在此,我们报告了通过使用二卤硼烷作为硼烯源,将硼烯正式插入单原子硅(0)配合物的配位球中,首次合成了卤乙烯的硅=硼类似物——溴代硼杂硅烯。用溴代硼杂硅烯处理中性或阴离子型路易斯碱可得到新的硼杂硅烯,通过X射线衍射分析和密度泛函理论计算证明,所有这些硼杂硅烯都具有显著的硅=硼双键特征。这些结果展示了合成新型硅=硼双键物种的令人兴奋的策略,这将进一步推动含硼、硅分子的化学发展。