Abstract
The temperature dependence of the ESR spectra of the radical-cations of the N-derivatives of phenothiazine were studied in the range of 200-393 K (o-xylene). It was established that at temperatures of 323-333 K the nature of the HFS varies from doublet to quartet with approximate intensity ratios of 1:2:2:1, and this transformation is irreversible. A hypothesis explaining the results is proposed. IR spectroscopy was used to confirm the proposed mechanism of localization of the unpaired electron.
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Tomilin, O.B., Shchegolikhin, A.N., Sanaeva, E.P. et al. Synthesis and Properties of Phenothiazine Derivatives. 2. Spectral (ESR and IR) Characteristics of the Radical-cations of the Phenothiazine N-Derivatives. Chemistry of Heterocyclic Compounds 36, 1097–1102 (2000). https://doi.org/10.1023/A:1002746301863
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DOI: https://doi.org/10.1023/A:1002746301863