Photochemistry of cerium(IV) ammonium nitrate (CAN) in acetonitrile

Abstract

Abstract Cerium ammonium nitrate (NH4)2CeIV(NO3)6 (CAN) is widely used as a photolytic source of NO3 radicals in acetonitrile. In spite of that, the mechanistic aspects of CAN photochemistry were poorly discussed in the literature. In this work CAN photochemistry in CH3CN was studied using the combination of stationary methods and laser flash photolysis. In accordance with the literature, the inner-sphere electron transfer was found to be the primary photochemical process. The (NH4)2CeIII(NO3)5(CH3CN) complex was found to be the only reaction product formed with the rather high quantum yield (0.6 and 0.4 upon 308 and 355\xa0nm excitation correspondingly). The NO3 radicals decay is mainly caused by the second-order reactions; their rate constants are determined. In addition to the direct release of the NO3 radicals, a part of the light-excited CAN molecules were found to form the radical complex [(NH4)2CeIII(NO3)5…NO3 ], which lifetime is ca. 2\xa0μs.