A singlet and triplet excited-state dynamics study of the keto and enol tautomers of cytosine

Abstract

The photoinduced excited-state dynamics of the keto and enol forms of cytosine is investigated using ab initio surface hopping in order to understand the outcome of molecular beam femtosecond pump-probe photoionization spectroscopy experiments. Both singlet and triplet states are included in the dynamics. The results show that triplet states play a significant role in the relaxation of the keto tautomer, while they are less important in the enol tautomer. In both forms, the T${}_1$ state minimum is found too low in energy to be detected in standard photoionization spectroscopy experiments and therefore experimental decay times should arise from a simultaneous relaxation to the ground state and additional intersystem crossing followed by internal conversion to the T${}_1$ state. In agreement with available experimental lifetimes, we observe three decay constants of 7 fs, 270 fs and 1900 fs - the first two coming from the keto tautomer and the longer one from the enol tautomer. Deactivation of the enol form is due to internal conversion to the ground state via two S${}_1$/S${}_0$ conical intersections of ethylenic type.

References in corpus (1)

• Femtosecond Intersystem Crossing in the DNA Nucleobase Cytosine

Cited by in corpus (5)

• A general method to describe intersystem crossing dynamics in trajectory surface hopping
• Excitation of Nucleobases from a Computational Perspective II: Dynamics
• Perturbational treatment of spin-orbit coupling for generally applicable high-level multi-reference methods
• The DNA Nucleobase Thymine in Motion - Intersystem Crossing Simulated with Surface Hopping
• Simulating Nonadiabatic Dynamics in Benzophenone: Tracing Internal Conversion Through Photoelectron Spectra