Vibronic coupling in the ground and excited states of the imidazole radical cation

摘要

Vibronic interactions in the ground and two excited states of the imidazole radical cation, X(2)A " (pi(-1)), A(2)A' (n sigma(-1)), and B(2)A " (pi(-1)), and the associated nuclear dynamics were studied theoretically. The results were used to interpret the recent photoelectron measurements [M. Patanen et al., J. Chem. Phys. 155, 054304 (2021)]. The present high-level electronic structure calculations employing, in particular, the single, double, and triple excitations and equation-of-motion coupled-cluster method accounting for single and double excitation approaches and complete basis set extrapolation technique for the evaluation of the vertical ionization energies of imidazole indicate that the A (2)A' and B (2)A " states are very close in energy and subject to non-adiabatic effects. Our modeling confirms the existence of pronounced vibronic coupling of the A (2)A' and B (2)A " states. Moreover, despite the large energy gap of nearly 1.3 eV, the ground state X (2)A " is efficiently coupled to the A (2)A' state. The modeling was performed within the framework of the three-state linear vibronic coupling problem employing Hamiltonians expressed in a basis of diabatic electronic states and parameters derived from ab initio calculations. The ionization spectrum was computed using the multi-configuration time-dependent Hartree method. The calculated spectrum is in good agreement with the experimental data, allowing for some interpretation of the observed features to be proposed. Published under an exclusive license by AIP Publishing.