10.1007/s10975-008-2008-z

Abstract

The kinetics of the photolysis of substituted 1,2-dihydroquinolines (DHQ) in micellar solutions was studied by steady-state and flash photolysis. The photolysis mechanism depends dramatically on the location of DHQ molecules in micelles, which is governed by the surfactant nature. In micellar solutions of the anionic surfactant sodium dodecyl sulfate (SDS), where the DHQ molecules are located in the Stern layer, the intermediate species decay kinetics follows a first-order law. When DHQ is in neutral form (pH 4-12), the rate constant of the intermediate carbocation decay increases from 25 to 198 s -1 with an increasing concentration of DHQ in micelles. The positive micellar catalysis is caused by the acceleration of the final product formation with the DHQ molecule via proton abstraction from the intermediate cation. The formation of several types of intermediate species-carbocations in the aqueous phase and aminyl radicals in micelles-is observed in micellar solutions of the cationic surfactant cetyltrimethylammonium bromide (CTAB) due to the preferential location of DHQ molecules in the micellar core. The carbocation decays via a pseudofirst-order reaction with a rate constant close to that in the aqueous solution. The lifetime of the DHQ aminyl radicals in the micellar solutions is longer by several orders of magnitude than the lifetime observed for homogeneous solutions of hydrocarbons and alcohols.