Conclusions
In the ESR spectra of 6-triphenylmethyl-4-tert-butyl-2-hydroxyphenoxyl and 6-triphenylmethyl-4-phenyl-2-hydroxyphenoxyl and their deuterated analogs, temperature-dependent dynamic effects have been found; these are explained from the standpoint of a reversible intramolecular transition between different conformations of the radicals, differing in the spin density distribution, owing to direct interaction of the unpaired electron with the π orbitals of the phenyl rings of the triphenylmethyl substituent.
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 7, pp. 1513–1517, July, 1985.
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Tumanskii, B.L., Malysheva, N.A., Prokof'ev, A.I. et al. Dynamic effects in ESR spectra of 4-triphenylmethyl-6-tert-butyl-2-hydroxyphenoxyl and 4-triphenylmethyl-6-phenyl-2-hydroxyphenoxyl. Russ Chem Bull 34, 1383–1388 (1985). https://doi.org/10.1007/BF00950135
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DOI: https://doi.org/10.1007/BF00950135