The electron spin resonance spectra of eight mono- and di-substituted 1,4-naphthosemiquinones reflect steric properties of the substituents which were alkoxy, hydroxy and phenoxy groups. The radical anions were produced by electrolytic reduction at a mercury pool cathode in acetonitrile.
J. H. Binks, A. T. Bullock and D. J. Hopkin, J. Chem. Soc., Faraday Trans. 2, 1972, 68, 814 DOI: 10.1039/F29726800814
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