Sasamori Takahiro
Division of Chemistry, Faculty of Pure and Applied Sciences, Tsukuba Research Center for Energy Materials Science (TREMS), University of Tsukuba 1-1-1 Tennodai Tsukuba Ibaraki 305-8571 Japan
Chem Sci. 2021 Mar 26;12(19):6507-6517. doi: 10.1039/d1sc00130b.
Reactions of isolable disilynes and digermynes with alkynes can result in the formation of the corresponding disila- (DSBs) and digermabenzenes (DGBs), wherein two carbon atoms of the benzene ring are replaced by silicon or germanium atoms. Detailed structural and spectroscopic analyses of these DSBs and DGBs have revealed that they exhibit considerable aromaticity, comparable to that of benzene. However, in contrast to the all-carbon system benzene, these DSBs and DGBs are highly reactive toward small molecules such as oxygen, hydrogen, 1,3-dienes, and water. During the investigation of their reactivity, we discovered that a 1,2-DGB works as a catalyst for the cyclotrimerization of arylalkynes, which provides access to the corresponding 1,2,4-triarylbenzenes. In this perspective article, our recent progress in the area of DSB and DGB chemistry is summarized.
可分离的乙硅烯和乙锗烯与炔烃反应可生成相应的乙硅苯(DSBs)和乙锗苯(DGBs),其中苯环的两个碳原子被硅或锗原子取代。对这些DSBs和DGBs进行的详细结构和光谱分析表明,它们表现出相当程度的芳香性,与苯相当。然而,与全碳体系的苯不同,这些DSBs和DGBs对诸如氧气、氢气、1,3 - 二烯和水等小分子具有高反应活性。在研究它们的反应活性过程中,我们发现一种1,2 - DGB可作为芳基炔烃环三聚反应的催化剂,从而可得到相应的1,2,4 - 三芳基苯。在这篇综述文章中,我们总结了DSB和DGB化学领域的近期进展。