Conclusions
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1.
Thermolysis of doubly substituted aliphatic-aromatic triazenes proceeds through the formation of\(\overline {C_6 H_5 NH..R} S\) radical pairs (RP) in the initial stages of the reaction (R is an alkyl radical). C6H5NH.R
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2.
It is suggested mat thermolysis of methyl- and ethylphenyltriazenes leads to the formation of 1-methyl-2-imino-3,5-cyclohexadiene and 1-ethyl-2-imino-3,5-cylcohexadiene, unusual compounds resulting from the recombination of ethyl and methyl radicals with anil radicals.
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3.
Interference of1H and13C CPN effects in the\(\overline {C_6 H_5 NH..R} S,\overline {C_6 H_5 NH..R} F\) and\(\overline {R..R} FRP's\) was observed in the thermolysis of benzyl- and tert-butylphenyltriazenes.
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4.
A value has been obtained for the anil radical g factor.
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 3, pp. 553–558, March, 1977.
The authors would like to thank Yu. N. Molin for a discussion of this work.
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Dushkin, A.V., Sycheva, I.M., Leshina, T.V. et al. Chemical polarization of nuclei in reactions of azo compounds. Russ Chem Bull 26, 496–501 (1977). https://doi.org/10.1007/BF01179452
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DOI: https://doi.org/10.1007/BF01179452