Abstract
2,6-Di-tert-butylphenols containing the Pt—SnCl3 and Pt—GeCl3 groups in the para position exert a dual effect on the oxidation of methyl oleate by molecular oxygen. Initially, these compounds act as antioxidants producing the corresponding phenoxyl radicals whose decomposition is accompanied by elimination of SnCl2 and GeCl2, which are oxidation promoters.
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