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Principal directions of primary fragmentation of the cyanoethylated amines under electron impact

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

Conclusions

  1. 1.

    A study has been made of the effect of the nature of the substituent at the nitrogen atom of cyanoethylated amines on the result of competition between the various primary paths for molecular in breakdown.

  2. 2.

    The data obtained here have been interpreted in terms of the enthalpies of formation of the eliminated radicals.

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Authors and Affiliations

  1. Institute of Physical Chemistry, Academy of Sciences of the USSR, Moscow

    N. S. Ovchinnikova, V. M. Brusnikina, A. A. Lyashenko, L. T. Zuravlev, M. P. Glazunov & I. L. Rozenfel'd

Authors
  1. N. S. Ovchinnikova
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  2. V. M. Brusnikina
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  3. A. A. Lyashenko
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  4. L. T. Zuravlev
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  5. M. P. Glazunov
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  6. I. L. Rozenfel'd
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Additional information

Deceased.

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 12, pp. 2703–2708, December, 1981.

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Ovchinnikova, N.S., Brusnikina, V.M., Lyashenko, A.A. et al. Principal directions of primary fragmentation of the cyanoethylated amines under electron impact. Russ Chem Bull 30, 2248–2252 (1981). https://doi.org/10.1007/BF00963680

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  • DOI: https://doi.org/10.1007/BF00963680

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