Abstract

The kinetics of the oxidation of isopropylbenzene by molecular oxygen in the presence of catalytic systems consisting of substituted N-hydroxyphthalimides and cuprous halides was studied. The effects of the structure of the N-hydroxyphthalimides, solvent, and nature of the cuprous salt on the oxidation rate were investigated. The system consisting of N-hydroxy-3,4,5,6-tetraphenylphthalimide and CuBr in chlorobenzene was found to be the most efficient.

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