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Title: Radiolytic studies of reduction and oxidation of aromatic systems

Miscellaneous ·
OSTI ID:7006287

The radiolytic reduction and oxidation of aromatic systems have been investigated intensively. The formation of initial radicals and the kinetics of their reactions were characterized and followed by pulse radiolysis using time-resolved absorption spectrophotometry. The stable products created in the gamma radiolysis of aqueous solutions of aromatic halides were quantitatively determined with the use of high performance liquid chromatography (HPLC). In the reduction of bromine substituted benzene, phenol and benzoic acid, the bromide yield was determined in 1mM neutral and basic solutions at pH5 {approximately} 11 to be {approximately} 2.7. These results indicate that the reactions of e{sup {minus}}{sub aq} with bromine substituted aromatic compounds are essentially quantitative. Studies of the competitive reactions of e{sup {minus}}{sub aq} in benzene and phenoxide substituted with both bromine and chlorine show that halide elimination is controlled by the site of attack on the solute. Intramolecular electron transfer appears not to be important. The combination of time-resolved and steady-state studies provides complete and detailed information of radiolytic reduction and oxidation of halogenated aromatic and phenol systems.

Research Organization:
Notre Dame Univ., IN (USA)
OSTI ID:
7006287
Resource Relation:
Other Information: Thesis (Ph. D.)
Country of Publication:
United States
Language:
English

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