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Synthesis and some properties of functional linear and cyclic polyethylsiloxanes

  • Organic Chemistry
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Bulletin of the Academy of Sciences of the USSR, Division of chemical science Aims and scope

Conclusions

  1. 1.

    The stepwise condensation of ethylchlorosilane with diethylsilanediol and 1,3-dihy-droxytetraethyldisiloxane was used to obtain 2,6- and 2,8-dichloroethylcyclotetra (penta, hexa) siloxanes. It was established that the reaction is accompanied by intramolecular cyclization in the reaction with 1,3-dihydroxytetraethyldisiloxane: in the first step with the formation of chloropentaethylcyclotrisiloxane and in the second step with the formation of 2,8-dichlorodecaethylcyclohexasiloxane and its structural isomer.

  2. 2.

    An increased tendency to form ethylbicyclo [3.5.1]penta- and ethylbicyclo[5.5.1]-hexasiloxane was observed in the hydrolysis of 2,6-dichlorooctaethylcyclopenta- and 2,8-dichlorodecaethylcyclohexasiloxanes.

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Literature cited

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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 6, pp. 1351–1357, June, 1989.

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Makarova, N.N., Lavrukhin, B.D., Turkel'taub, G.N. et al. Synthesis and some properties of functional linear and cyclic polyethylsiloxanes. Russ Chem Bull 38, 1234–1240 (1989). https://doi.org/10.1007/BF00957159

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  • DOI: https://doi.org/10.1007/BF00957159

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