An experimental and theoretical study of the photoelectron spectra of cis-dichloroethene: valence shell vertical ionization and vibronic coupling in the low-lying cationic states

Trofimov, A.B.; Powis, I.; Menzies, R.C.; Holland, D.M.P.; Antonsson, E.; Patanen, M.; Nicolas, C.; Miron, C.; Skitnevskaya, A.D.; Gromov, E.V.; K�ppel, H.

Abstract

The valence shell photoelectron spectrum of cis-dichloroethene has been studied both experimentally and theoretically. Photoelectron spectra have been recorded with horizontally and vertically plane polarized synchrotron radiation, thereby allowing the anisotropy parameters, characterizing the angular distributions, to be determined. The third-order algebraic-diagrammatic construction (ADC(3)) approximation scheme for the one-particle Green's function has been employed to compute the complete valence shell ionization spectrum. In addition, the vertical ionization energies have been calculated using the outer valence Green's function method (OVGF) and the equation-of-motion (EOM) coupled cluster (CC) theory at the level of the EOM-IP-CCSD model. The theoretical results have enabled assignments to be proposed for most of the structure observed in the experimental spectra, including the inner-valence regions dominated by satellite states. The linear vibronic coupling model has been employed to study the vibrational structure of the lowest photoelectron bands, using parameters obtained from ab initio calculations. The ground state optimized geometries and vibrational frequencies have been computed at the level of the second-order Møller-Plesset perturbation theory, and the dependence of the ionization energies on the nuclear configuration has been evaluated using the OVGF method. While the adiabatic approximation holds for the ~X2B1 state photoelectron band, the ~A2B2, ~B2A1, and ~C2A2 states interact vibronically and form a complex photoelectron band system with four distinct maxima. The ~D2B1 and ~E2B2 states also interact vibronically with each other. The potential energy surface of the ~D2B1 state is predicted to have a double-minimum shape with respect to the out-of-plane a2 deformations of the molecular structure. The single photoelectron band resulting from this interaction is characterized by a highly irregular structure, reflecting the nonadiabatic nuclear dynamics occurring on the two coupled potential energy surfaces forming a conical intersection close to the minimum of the ~E2B2 state.

Citation

Trofimov, A., Powis, I., Menzies, R., Holland, D., Antonsson, E., Patanen, M., …Köppel, H. (2018). An experimental and theoretical study of the photoelectron spectra of cis-dichloroethene: valence shell vertical ionization and vibronic coupling in the low-lying cationic states. Journal of Chemical Physics, 149(7), Article 074306. https://doi.org/10.1063/1.5033425

• Journal Article Type: Article
• Acceptance Date: Jul 11, 2018
• Online Publication Date: Aug 20, 2018
• Publication Date: Aug 20, 2018
• Deposit Date: Sep 3, 2018
• Publicly Available Date: Sep 4, 2018
• Journal: The Journal of Chemical Physics
• Print ISSN: 0021-9606
• Electronic ISSN: 1089-7690
• Publisher: AIP Publishing
• Peer Reviewed: Peer Reviewed
• Volume: 149
• Issue: 7
• Article Number: 074306
• DOI: https://doi.org/10.1063/1.5033425
• Public URL: https://nottingham-repository.worktribe.com/output/986420
• Publisher URL: https://aip.scitation.org/doi/10.1063/1.5033425