Keywords
defluorination
denitration
nitration
organofluorine compounds
phenols
radiolysis
Abstract
Radiolysis of deaerated 1-nitro-3-(trifluoromethyl)benzene leads to mononuclear (predominantly) and binuclear arenes in which the nitro groups are replaced by NO or OH ones. The conversion of the nitro group to NO is caused by the action of the radiation-induced reducing intermediates. In parallel, the formed oxygen radical anions, atomic oxygen and OH radicals participate in the hydroxylation of the original molecules and radiolysis semi-products.
Funders
Russian Academy of Sciences
122011300061-3
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