Abstract
A new four-membered ring compound having a Si2Ge2 skeleton, octaisopropyl-1,2-disiladigermacyclobutane (1), was synthesized by the reductive coupling of tetraisopropyl-1,2-dichlorosilagermane with sodium in toluene. The structure of 1, which has one Ge-Ge bond, one Si-Si bond, and two Ge-Si bonds in a ring; was confirmed by chemical derivatization; the reactions of 1 with m-chloroperoxy-benzoic acid and PCl5 led to the selective cleavage of the Ge-Ge bond in 1. The selective extrusion of a germylene from 1 was observed at the initial stage of the photolysis using 254 nm light.
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CITATION STYLE
Hashimoto, H., Yagihashi, Y., Ignatovich, L., & Kira, M. (2001). Synthesis, characterization, and photoreactions of 1,2-disiladigermacyclobutane. Heteroatom Chemistry, 12(5), 398–405. https://doi.org/10.1002/hc.1060
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