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Organoboron compounds 376. Mass-spectrometric study of derivatives of 1,2-azaborqlidine and 1,2-oxaborolane

  • 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.

    Upon exposure to electron impact the decomposition of the molecular ions of 1,2-azaborolidines with an alkyl group at the boron atom involves mainly the formation of a [M-R]+ ion by the splitting off of an alkyl group and elimination of a R-CH3 group under formation of a [M-(R-CH3)]+ ion.

  2. 3.

    For derivatives of 1,2-oxaborolane the processes of ring destruction are much more distinctly developed than for 1,2-azaborolidines.

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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 7, pp. 1566–1570, July, 1980.

We thank N. A. Klyuev, who measured the high-resolution mass spectra of some samples.

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Bleshinskaya, A.S., Zolotarev, B.M., Chizhov, O.S. et al. Organoboron compounds 376. Mass-spectrometric study of derivatives of 1,2-azaborqlidine and 1,2-oxaborolane. Russ Chem Bull 29, 1111–1115 (1980). https://doi.org/10.1007/BF00949164

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  • DOI: https://doi.org/10.1007/BF00949164

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