The "Simple" Photochemistry of Thiophene

TL;DR

This study combines advanced quantum simulations with vibronic coupling models to accurately reproduce and analyze the ultraviolet absorption spectrum of thiophene, revealing detailed excited-state dynamics and spectral features.

Contribution

It introduces a comprehensive vibronic coupling model with multi-state and vibrational interactions, providing new insights into thiophene's photo-excited dynamics.

Findings

Spectral features explained by vibronic coupling and vibrational interactions.

Population transfer between states occurs within 100 fs.

Ring-opening occurs at longer timescales.

Abstract

The simple ultraviolet absorption spectrum of thiophene is investigated using a combination of a vibronic coupling model Hamiltonian with multi-configuration time-dependent Hartree quantum dynamics simulations. The model includes five states and all twenty-one vibrations, with potential surfaces calculated at the complete active space with second-order perturbation (CASPT2) level of theory. The model includes terms up to seventh-order to describe the diabatic potentials. The resulting spectrum is in excellent agreement to the experimentally measured spectrum of Holland et al [PCCP (2014) 16: 21629]. The, until now not understood, spectral features are assigned, with a combination of strongly coupled vibrations and vibronic coupling between the states giving rise to a progression of triplets on the rising edge of the broad spectrum. The analysis of the underlying dynamics indicates that population transfer between all states takes place on a sub-100 fs timescale, with ring-opening occurring at longer times. The model thus provides a starting point for further investigations into the complicated photo-excited dynamics of this key hetero-aromatic molecule.