## Abstract From a series of antioxidants comprising 2,2′‐biphenyldiols, 2,2′‐thiobisphenols and 2,2′‐dithiobisphenol, free phenoxyls were prepared by oxidation with __tert__‐butylperoxyls co‐ordinated to Co(III) in non‐polar media at ambient temperature. Both the effect of extended conjugation as
Radical reactions in the co-ordinated sphere of transition metals. XIV—spin distribution of phenoxy radicals generated from biphenyldiols
✍ Scribed by P. Pelikán; A. Tkáč; L. Omelka; A. Staško
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- English
- Weight
- 447 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The phenoxy radicals obtained from 2,2′‐ and 4,4′‐biphenyldiols show, in nonpolar solvents, symmetrization of the unpaired electron spin density on the two phenyl rings in the temperature range 290–410 K. Below 270 K the paramagnetic systems became diamagnetic. This para‐diamagnetic conversion with temperature is reversible. According to INDO calculations the symmetrization of spin density is due to the formation of dimeric phenoxy radicals. The para‐diamagnetic conversion at various temperatures is explained by the reversible conversion of the radical dimer to the quinone‐hydroquinone pair.
📜 SIMILAR VOLUMES
## Abstract Using the analysis of the splitting constants of the ESR spectra, factor are described which affect the stability of free phenoxyls and of phenoxyls co‐ordinated on cobalt, generated by the reaction of __tert__‐butyleperoxyls and 4,4′‐biphenyldiols (1), 4,4′–thiobisphenols (2 and 5), 4,
## Abstract Radical species were generated from 4,4′;‐ and 2,2′;‐alkylidenebisphenols during oxidation with free and co‐ordinated [Co(III)]RO~2~^˙^Radicals. This simulates the participation of bisphenolic antioxidants in the process of stabilization of hydrocarbons. Phenoxyls are primarily formed,
## Abstract The formation of a ternary complex between phenols, Co (II)‐acetylacetonate and molecular oxygen has been established at ambient temperature and in non‐polar solvents. After intramolecular electron transfer the transient magnified image radical enhances the homolytic scission of the O