The role of dopant geometry in the photoinduced formation of radical pairs in crystals of 2,6-di-tert-butyl-4-methylphenol and 2,6-di-tert-butylphenol
✍ Scribed by Georgii G. Lazarev; Vladimir L. Kuskov; Francisco Lara; Federico García; Anton Rieker; Paul Tordo
- Publisher
- Elsevier Science
- Year
- 1993
- Tongue
- English
- Weight
- 550 KB
- Volume
- 212
- Category
- Article
- ISSN
- 0009-2614
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✦ Synopsis
Radical pairs are formed by photolysis of single crystals of 2,6-di-tert-butyl-4-methylphenol (ionol) (1) or 2,6-di-tert-butylphenol (2 ), doped by several different molecules, and investigated by the EPR method. A possible two-hydrogen-atom transfer is discussed as the photochemical act.
📜 SIMILAR VOLUMES
The formation of radical pairs with a dipole-dipole splitting constant D= 12.2 t 0.2 mT upon photolysis of single crystals of 2,6-di-tert-butyl-4-methylphenol doped with IO-' M 2,6-di-tert-butyl-1-imino-pquinone was studied by EPR spectroscopy in the temperature range between 77 and 140 K. The mecha
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