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Thermally induced free-radical reactions in. cap alpha. -D-glucopyranose single crystals. An electron spin resonance-electron nuclear double resonance study. [X-radiation]

Journal Article · · J. Phys. Chem.; (United States)
DOI:https://doi.org/10.1021/j100217a030· OSTI ID:6440238

The dominant radical in single crystals of anhydrous ..cap alpha..-D-glucopyranose X-irradiated at 77 K, a C6 primary hydroxyalkyl radical, reorients slightly upon warming to approx. 200 K and converts to a C2 primary hydroxyalkyl radical upon warming to approx. 300 K. Annealing the sample at room temperature overnight results in several free-radical products, one identified as a C2 secondary hydroxyalkyl radical. The mechanisms of the free-radical reactions are discussed and compared to those postulated by using data from end-product analysis of irradiated crystalline ..cap alpha..-D-glucose.

Research Organization:
Univ. of Rochester, NY
DOE Contract Number:
AC02-76EV03490
OSTI ID:
6440238
Journal Information:
J. Phys. Chem.; (United States), Journal Name: J. Phys. Chem.; (United States) Vol. 86:20; ISSN JPCHA
Country of Publication:
United States
Language:
English