Abstract
It was found that the irradiation of aqueous solution of isocytosine with UVC light provokes an oxo-hydroxy phototautomerism of the compound with a rate constant of 5.29× 10-3 min-1. It was observed a backward reaction, after removing the UV light source, with a rate constant of 0.12×10-3 min-1. Two mechanisms of the phototautomerism were investigated at the B3LYP/aug-cc-pVDZ theoretical level in water surroundings (PCM). The first one showed a consecutive dissociation and association of a proton through conical intersections S0/S1 whose structures were located at the same theoretical level in the gas phase. It occurs along the 1πσ* excited-state reaction pathway. The more probable mechanism includes an excited-state H-transfer supported by a water molecule as a catalyst. It occurs along the 1ππ* excited-state reaction pathway which we found over the IRC ground-state energy curve. The water molecule drastically reduces the energy barrier in the ground state as well in the excited state.
Funder
Bulgarian National Science Fund
Publisher
The Turkish Chemical Society