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Gas Phase Reaction of Tetrachlorogermane with Conjugated Dienes in the Presence of Hexachlorodisilane Initiator

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Abstract

Studies of the reaction of GeCl4 with acyclic conjugated dienes (1,3-butadiene, 2-methyl-1,3- butadiene, 2,3-dimethyl-1,3-butadiene) and cyclopentadiene in the presence of Si2Cl6 initiator were carried out. With acyclic dienes, corresponding 1,1-dichloro-1-germacyclo-3-pentenes and 1,1-dichloro-1-silacyclo-3- pentenes are preferrably formed. With cyclopentadiene the main reaction products are cyclopentenyltrichlorogermanes and cyclopentenyltrichlorosilanes formed respectively by hydrogermylation and hydrosilylation of the starting diene. The explanation of the established rule is offered.

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Chernyshev, E.A., Komalenkova, N.G., Yakovleva, G.N. et al. Gas Phase Reaction of Tetrachlorogermane with Conjugated Dienes in the Presence of Hexachlorodisilane Initiator. Russian Journal of General Chemistry 71, 1438–1442 (2001). https://doi.org/10.1023/A:1013914221503

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