Substituent and solvent perturbations for h.f.s. constants in 1,4-semiquinones. The additivity principle
Author:
Affiliation:
1. a Department of Chemistry , University of York , Heslington , York , YO1 5DD , England
Publisher
Informa UK Limited
Subject
Physical and Theoretical Chemistry,Condensed Matter Physics,Molecular Biology,Biophysics
Link
https://www.tandfonline.com/doi/pdf/10.1080/00268977500101961
Reference8 articles.
1. Assignment of h.f.s. constants of 1,4-benzosemiquinones by additivity rules. The free rotation oft-butyl groups
2. Electron spin resonance in tert-butyl-substituted semiquinones. The hyperfine structure of tert-butyl protons
3. 42. Spin densities in substituted 1,4-benzosemiquinones
4. Secondary radicals in the autoxidation of hydroquinones and quinones
5. Electron nuclear double resonance and electron spin resonance study of semiquinones related to vitamins K and E
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2. Electron paramagnetic resonance, ENDOR and TRIPLE resonance studies on substitution reactions of 2-methyl-1,4-benzoquinone and 2,3-dimethoxy-5-methyl-1,4-benzoquinone in alkaline methanol;J. Chem. Soc., Faraday Trans.;1991
3. SPECTROSCOPIC STUDIES OF CUTANEOUS PHOTOSENSITIZING AGENTS-XIII.pH DEPENDENCE OF THE PHOTOCHEMISTRY OF PHOTO ALLERGENS BITHIONOL AND FENTICHLOR: AN ELECTRON spIN RESONANCE STUDY OF THE FREE RADICAL PHOTOPRODUCTS;Photochemistry and Photobiology;1989-01
4. Unrestricted Hartree—Fock calculations of methoxyl-substituted semiquinone radicals and the proton hyperfine coupling constants;Journal of Molecular Structure: THEOCHEM;1987-06
5. Anomalous electrochemical and electron spin resonance properties of some biologically relevant methoxyl-substituted quinones;International Journal of Quantum Chemistry;1984-03-12
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