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Mass-spectrometric study of compounds from the cyclopropane series 8. The behavior of the functional derivatives of the spirooctadienones under chemical ionization

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

Conclusions

  1. 1.

    The interaction of the spirooctadienones with CH4 plasmas gives rise to (M + C3H5)+, (M + C2H5)+, (M + H)+, (M + H − H2)+, (M + H − CH4)+, (M + H − C4H8)+, (M + H − 2C4H8)+, and (M + C2H5 − C4H8)+ ions; in turn, the appearance of these ions in the mass spectra gives information of the molecular weights of these compounds and the presence of the t-C4H9 groups in their molecules.

  2. 2.

    The presence of the cyclopropane ring in the molecule determines the breakdown of the protonated ions of spirooctadienones with functional groups in the CPR, (M + H − CHX)+ and (M + H − CH2CHX)+ ions being formed.

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Literature cited

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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 3, pp. 540–544, March, 1979.

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Kadentsev, V.I., Krokhin, A.V., Chizhov, O.S. et al. Mass-spectrometric study of compounds from the cyclopropane series 8. The behavior of the functional derivatives of the spirooctadienones under chemical ionization. Russ Chem Bull 28, 498–501 (1979). https://doi.org/10.1007/BF00924820

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  • DOI: https://doi.org/10.1007/BF00924820

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