Chemistry of Heterocyclic Compounds

, Volume 14, Issue 2, pp 135–140 | Cite as

Mass spectrometric study of monoalkyl-substituted thiacyclanes

  • V. G. Zaikin
  • E. A. Trusova
  • L. P. Shcherbakova
Article

Abstract

Monosubstituted α- and β-alkylthiophans and α-, β-, and γ-alkylthiacyclohexanes were subjected to a comparative mass spectrometric study. The stability of the M+ ion increases on passing from α- to β-alkylthiophans and from α- to β- and γ-alkylthiacyclohexanes. In the case of α-alkylthiophans and α- and β-alkylthia-cyclohexanes the principal process is associated with ejection of the substituent as a whole, whereas a portion of the alkyl substituent, with retention of one CH2 group in the composition of the charged fragment, is eliminated from the molecular ions of β-alkylthiophans and γ-alkylthiacyclohexanes.

Keywords

Organic Chemistry Alkyl Substituent Mass Spectrometric Study Spectrometric Study Comparative Mass 

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Copyright information

© Plenum Publishing Corporation 1978

Authors and Affiliations

  • V. G. Zaikin
    • 1
  • E. A. Trusova
    • 1
  • L. P. Shcherbakova
    • 1
  1. 1.A. V. Topchiev Institute of Petrochemical SynthesisMoscow

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