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Spectroscopic study of reaction of ethyldichlorosilane with organic solvents

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

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Conclusions

  1. 1.

    The reaction of ethyldichlorosilane with organic solvents is expressed more weakly than in the case of methyldichlorosilane, which is due to the steric effect of the C2H5 group.

  2. 2.

    Ethyldichlorosilane when dissolved in nitrobenzene exists as the trans conformer.

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Literature cited

  1. M. G. Vornokov and G. I. Lebedeva, Third International Symposium on Organosilicon Chemistry, Madison, 1972, Abstract of Paper, p. 57.

  2. M. G. Voronkov and G. I. Lebedeva, Izv. Akad. Nauk SSSR, Ser. Khim., 1973, 2473.

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  6. M. G. Voronkov and A. Ya. Deich, Dokl. Akad. Nauk SSSR,163, 337 (1966).

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Author information

Authors and Affiliations

  1. Irkutsk Institute of Organic Chemistry, Siberian Branch of Academy of Sciences of the USSR, USSR

    G. I. Lebedeva & M. G. Voronkov

Authors
  1. G. I. Lebedeva
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  2. M. G. Voronkov
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Additional information

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 11, pp. 2597–2600, November, 1973.

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Lebedeva, G.I., Voronkov, M.G. Spectroscopic study of reaction of ethyldichlorosilane with organic solvents. Russ Chem Bull 22, 2531–2533 (1973). https://doi.org/10.1007/BF00926412

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  • DOI: https://doi.org/10.1007/BF00926412

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