The "Simple" Photochemistry of Thiophene
Fuente:
arXiv
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| Natura: | Preprint |
| Pubblicazione: |
2024
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| _version_ | 1866913450708434944 |
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| author | Parkes, Michael A. Worth, Graham A. |
| author_facet | Parkes, Michael A. Worth, Graham A. |
| contents | 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. |
| format | Preprint |
| id |
arxiv_https___arxiv_org_abs_2407_20039 |
| institution | arXiv |
| publishDate | 2024 |
| record_format | arxiv |
| spellingShingle | The "Simple" Photochemistry of Thiophene Parkes, Michael A. Worth, Graham A. Chemical Physics 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. |
| title | The "Simple" Photochemistry of Thiophene |
| topic | Chemical Physics |
| url | https://arxiv.org/abs/2407.20039 |