Photochemistry of Acetanilide. I. Quantum Yields of the Rearrangement and Benzene Photosensitized Reaction

Abstract

Abstract The photochemical rearrangement of acetanilide under 2537 Å irradiation has been studied by spectrophotometry. The quantum yield of the rearrangement in cyclohexane solution was independent of the irradiation time, concentration of acetanilide, presence of oxygen and light intensity. It was found that electronic energy transfer from the electronically excited benzene to acetanilide occurred in the mixed solution, and the transfer mechanism was explained by singlet-singlet nonradiative energy transfer. It was observed that the energy transfer rate constant was about 22 times greater than that predicted by diffusion theory (the transfer rate constant, k3=1.45×1011 l·mol−1·sec−1). From these studies, it is proposed that the rearrangement of acetanilide is an introamolecular reaction and does not occur from the triplet state but from the lowest singlet excited state.