Effect of dynamic correlation on the ultrafast relaxation of uracil in the gas phase. (10th February 2021)

• Record Type: Journal Article
• Authors: Chakraborty, Pratip; Liu, Yusong; Weinacht, Thomas; Matsika, Spiridoula
• Is Part Of: Faraday discussions. Volume 228(2021)
• Page Start: 266
• Page End: 285
• Publication Date: 2021-02-10
• Subjects: Chemistry -- Periodicals; Metallurgy -- Periodicals; Electrochemistry -- Periodicals; 540
• DOI: 10.1039/d0fd00110d
• Languages: English
• ISSNs: 1359-6640

Abstract

Abstract : High level multi-reference non-adiabatic dynamics simulations reveal that uracil's photoexcited S2 state decays very quickly without any significant trapping. Abstract : The photophysics and photochemistry of DNA/RNA nucleobases have been extensively investigated during the past two decades, both experimentally and theoretically. The ultrafast relaxation of the canonical nucleobases following photoexcitation is of significant interest when it comes to understanding how nature has ensured their photostability. Here we study the excited state dynamics of uracil which is a nucleobase found in RNA. Although theory and experiment have shed significant light on understanding the photoexcited dynamics of uracil, there are still disagreements in the literature about specific details. In order to examine how the dynamics is influenced by the underlying electronic structure theory, we have performed non-adiabatic excited state dynamics simulations of uracil using on-the-fly trajectory surface hopping methodology on potential energy surfaces calculated at different electronic structure theory levels (CASSCF, MRCIS, XMS-CASPT2, TD-DFT). These simulations reveal that the dynamics are very sensitive to the underlying electronic structure theory, with the multi-reference theory levels that include dynamic correlation, predicting that there is no trapping on the absorbing S2 state, in contrast to predictions from lower level electronic structure results. The dynamics are instead governed by ultrafast decay to the ground state, or trapping on the dark S1 state.