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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.


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Radical pairs during photolysis of an im
✍ Georgii G. Lazarev; Francisco Lara; Federico Garcia; Anton Rieker 📂 Article 📅 1992 🏛 Elsevier Science 🌐 English ⚖ 303 KB

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