Conclusions
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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.
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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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N. N. Makarova, B. D. Lavrukhin, T. V. Timofeeva, and V. N. Zelencheva, Izv. Akad. Nauk SSSR, Ser. Khim., No. 5, 114 (1985).
N. N. Makarova and B. D. Lavrukhin, Izv. Akad. Nauk SSSR, Ser. Khim., No. 3, 652 (1986).
V. E. Shklover, Yu. T. Struchkov, N. N. Makarova, and A. A. Zhdanov, Cryst. Struct. Commun.,9, 1 (1980).
V. E. Shklover, Yu. T. Struchkov, I. V. Karpova, et al., Zh. Strukt. Khim.,35, 125 (1985).
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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