Conclusions
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1.
It has been shown that the intermediates (IP) formed in the oxidation of sterically hindered amines by singlet oxygen (1O2) can be converted into nitroxyl radicals (NR), either through photochemical reaction with1O2 or through thermal breakdown, in the liquid phase or as a result of heating.
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2.
Thermal conversion of the IP to NR follows a stepwise mechanism.
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3.
The probability of NR formation in the reaction of1O2 with an amine molecule increases as the amine concentration rises.
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 10, pp. 2263–2268, October, 1978.
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Anisimova, O.M., Invanov, V.B., Anisimov, V.M. et al. The kinetics of the formation of stable nitroxyl radicals in the oxidation of sterically hindered amines by singlet oxygen in a solid polymeric matrix. Russ Chem Bull 27, 2001–2006 (1978). https://doi.org/10.1007/BF00946514
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DOI: https://doi.org/10.1007/BF00946514