Conclusions
-
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.
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.
Similar content being viewed by others
Literature cited
V. I. Kadentsev, A. Ya. Podel'ko, O. S. Chizhov, S. M. Shostakovskii, T. K. Voropaeva, and N. M. Kuznetsova, Izv. Akad. Nauk SSSR, Ser. Khim., 2015 (1978).
V. I. Kadentsev, A. Ya. Podel'ko, O. S. Chizhov, S. M. Shostakovskii, and N. S. Nikol'skii, Izv. Akad. Nauk SSSR, Ser. Khim., 532 (1979).
V. I. Kadentsev, A. V. Krokhin, O. S. Chizhov, and V. V. Ershov, Izv. Akad. Nauk SSSR, Ser. Khim., 2532 (1978).
D. Chamot and W. Pirkle, J. Am. Chem. Soc.,91, 1569 (1969).
V. V. Ershov, G. A. Nikiforov, and A. A. Volod'kin, Sterically Hindered Phenols [in Russian], Khimiya (1972), p. 202.
A. A. Solov'ev, V. I. Kadentsev, O. S. Chizhov, D. I. Bel'kind, and A. G. Savel'ev, Prib. Tekh. Eksp., No. 2, 223 (1976).
Author information
Authors and Affiliations
Additional information
Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 3, pp. 540–544, March, 1979.
Rights and permissions
About this article
Cite this article
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
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF00924820