Absolute rate constants for hydrocarbon autoxidation. 30. On the self-reaction of the α-cumylperoxy radical in solution

Abstract

Although it is generally accepted that the self-reaction of cumylperoxy radicals is a second-order process, recent reports have cast doubt on the overall validity of this assumption. Therefore we have reinvestigated some aspects of the self-reaction to clarify the kinetic and mechanistic features.Our product studies are entirely consistent with the accepted mechanism for the self-reaction of cumylperoxy radicals and no evidence was obtained for competing reactions. Results obtained with 36O2 labelled materials confirm the previous conclusion that reversible scission of cumylperoxy radicals to give oxygen and cumyl radicals does not compete significantly with the self-reaction at ambient temperatures. Kinetic studies, under both steady-state and transient conditions, establish clearly that the self-reaction of cumylperoxy radicals is a second order process. A possible explanation is proposed to account for the previous observations which indicated that the self-reaction was a first order process. Further, we show that the changes observed in the esr spectrum of the cumylperoxy radicals, which were attributed to the formation of a complex with cumyl hydroperoxide, are caused by changes in the viscosity of the solution.