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Synthesis of thioether-containing carbosilane dendrimers with sterically shielded sulfur atoms

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Abstract

Carbosilane thiols were synthesized as the first- and second-generation (in silicon) dendrons. It was demonstrated that the resulting bulky thiols successfully undergo the thiol—ene addition to third-generation polyallyl carbosilane dendrimer as a photoinitiated radical reaction to give the corresponding thioether-containing derivatives with sterically shielded sulfur atoms.

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Correspondence to А. N. Tarasenkov.

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Dedicated to Academician of the Russian Academy of Sciences G. A. Abakumov on the occasion of his 80th birthday.

Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 9, pp. 1675—1685, September, 2017.

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Tarasenkov, А.N., Getmanova, E.V., Tatarinova, E.A. et al. Synthesis of thioether-containing carbosilane dendrimers with sterically shielded sulfur atoms. Russ Chem Bull 66, 1675–1685 (2017). https://doi.org/10.1007/s11172-017-1940-3

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  • DOI: https://doi.org/10.1007/s11172-017-1940-3

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