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1-aryl-3-tert-butyl-3-hydroxytrlazenes

Communication 1. Synthesis and oxidative decomposition

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

Conclusions

  1. 1.

    We synthesized a number of p-substituted 1-aryl-3-tert-butyl-3-hydroxytriazenes. Their oxidation with lead peroxide leads to cleavage, with the formation of aryl radicals, nitrogen and 2-nitroso-2-methylpropane.

  2. 2.

    The EPR spectrum of p-nitrophenyl-tert-butyl nitroxide was obtained, which differs from that described previously in the literature. An interpretation of the spectrum is given.

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Authors and Affiliations

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

    G. A. Razuvaev, G. A. Abakumov, É. P. Sanaeva & L. G. Abakumova

Authors
  1. G. A. Razuvaev
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  2. G. A. Abakumov
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  3. É. P. Sanaeva
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  4. L. G. Abakumova
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Additional information

Translated from Izvestiya Akademiya Nauk SSSR, Seriya Khimicheskaya, No. 1, pp. 68–71, January, 1973.

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Razuvaev, G.A., Abakumov, G.A., Sanaeva, É.P. et al. 1-aryl-3-tert-butyl-3-hydroxytrlazenes. Russ Chem Bull 22, 61–63 (1973). https://doi.org/10.1007/BF00854115

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  • DOI: https://doi.org/10.1007/BF00854115

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