Unraveling the Relaxation Dynamics of Uracil: Insights from Time-Resolved X-ray Photoelectron Spectroscopy.

We report a study of the electronic and nuclear relaxation dynamics of the photoexcited RNA base uracil in the gas phase using time-resolved core-level photoelectron spectroscopy together with high-level calculations. The dynamics was investigated by trajectory surface hopping calculations, and the core ionization energies were calculated for geometries sampled from these. The molecule was excited by a UV laser and dynamics probed on the oxygen, nitrogen, and carbon sites by core electron spectroscopy. We find that the main de-excitation channel of the initially excited S(ππ*) state involves internal conversion to the S(nπ*) state with a time constant of 17 ± 4 fs, while a portion of S(ππ*) population returns directly to the ground state by internal conversion. We find no evidence that the S(nπ*) state decays to the ground state; instead, it decays to triplet states with a time constant of 1.6 ± 0.4 ps. Oscillations of the S(nπ*) state O 1s intensity as a function of time correlate with those of calculated C4═O8 and C5═C6 bond lengths, which undergo a sudden expansion following the initial π → π* excitation. Our calculations support our interpretation of the data and provide detailed insight into the relaxation processes of uracil.