Methyl substitution effects on the non-adiabatic dynamics of benzene: lifting three-state quasi-degeneracy at conical intersections

• Published in: Physical chemistry chemical physics : PCCP 2020, Vol.22 (5), p.2814-2818
• Main Authors: Adachi, Shunsuke, Suzuki, Toshinori
• Format: Article
• Language: English
• Subjects: Adiabatic flow; Benzene; Hydrocarbons; Intersections; Photoelectrons; Spectra; Substitutes; Toluene; Ultraviolet lasers; Wave propagation; Xylene
• ISSN: 1463-9076; 1463-9084
• DOI: 10.1039/c9cp06164a

Previously, theoretical calculations on the non-adiabatic dynamics of benzene from the S 2 state have indicated that the S 2 /S 1 and S 1 /S 0 conical intersections (CIs) facilitate ballistic nuclear wavepacket motion from S 2 to S 0 (fast channel) and branching to S 1 (slow channel). In this paper, we present time-resolved photoelectron spectra of benzene and its methyl-derivatives (toluene and o -xylene) measured with a vacuum-UV laser, which clearly reveal both the fast and slow channels. The extremely short propagation time of the wavepacket between the two CIs of benzene indicates that the two are in close proximity to each other, while methyl substitution extends the propagation time and decreases the branching ratio into the fast channel. The results suggest that the quasi-degeneracy of the three states in benzene is lifted by the geometrical shifts of the CIs by methyl substitution. Time-resolved photoelectron spectra of benzene and its methyl-derivatives (toluene and o -xylene) measured with a vacuum-UV laser clearly reveal both fast (A → B → C → D) and slow (B → C′ → D) relaxation channels from the S 2 state.