Hanusch Franziska, Groll Lisa, Inoue Shigeyoshi
Department of Chemistry, Catalysis Research Center and Institute of Silicon Chemistry, Technische Universität München Lichtenbergstrasse 4, Garching bei München 85748 Germany
Chem Sci. 2020 Aug 3;12(6):2001-2015. doi: 10.1039/d0sc03192e.
Since the first heavy alkene analogues of germanium and tin were isolated in 1976, followed by West's disilene in 1981, the chemistry of stable group 14 dimetallenes and dimetallynes has advanced immensely. Recent developments in this field veered the focus from the isolation of novel bonding motifs to mimicking transition metals in their ability to activate small molecules and perform catalysis. The potential of these homonuclear multiply bonded compounds has been demonstrated numerous times in the activation of H, NH, CO and other small molecules. Hereby, the strong relationship between structure and reactivity warrants close attention towards rational ligand design. This minireview provides an overview on recent developments in regard to bond activation with group 14 dimetallenes and dimetallynes with the perspective of potential catalytic applications of these compounds.
自1976年首次分离出锗和锡的重烯烃类似物,随后1981年分离出韦斯特的乙硅烯以来,稳定的14族双金属烯和双金属炔的化学取得了巨大进展。该领域的最新进展将重点从新型键合模式的分离转向模仿过渡金属激活小分子和进行催化的能力。这些同核多键化合物在激活H、NH、CO和其他小分子方面的潜力已得到多次证明。因此,结构与反应性之间的紧密关系值得在合理的配体设计方面给予密切关注。本综述从这些化合物潜在的催化应用角度,概述了14族双金属烯和双金属炔在键活化方面的最新进展。