Shashank Pathak
Tracking the ultraviolet-induced photochemistry of thiophenone during and after ultrafast ring opening
Pathak, Shashank; Ibele, Lea M.; Boll, Rebecca; Callegari, Carlo; Demidovich, Alexander; Erk, Benjamin; Feifel, Raimund; Forbes, Ruaridh; Di Fraia, Michele; Giannessi, Luca; Hansen, Christopher S.; Holland, David M.P.; Ingle, Rebecca A.; Mason, Robert; Plekan, Oksana; Prince, Kevin C.; Rouzée, Arnaud; Squibb, Richard J.; Tross, Jan; Ashfold, Michael N.R.; Curchod, Basile F.E.; Rolles, Daniel
Authors
Lea M. Ibele
Rebecca Boll
Carlo Callegari
Alexander Demidovich
Benjamin Erk
Raimund Feifel
Ruaridh Forbes
Michele Di Fraia
Luca Giannessi
Christopher S. Hansen
David M.P. Holland
Rebecca A. Ingle
Robert Mason
Oksana Plekan
Kevin C. Prince
Arnaud Rouzée
Richard J. Squibb
Jan Tross
Michael N.R. Ashfold
Dr Basile Curchod basile.f.curchod@durham.ac.uk
Academic Visitor
Daniel Rolles
Abstract
Photoinduced isomerization reactions lie at the heart of many chemical processes in nature. The mechanisms of such reactions are determined by a delicate interplay of coupled electronic and nuclear dynamics occurring on the femtosecond scale, followed by the slower redistribution of energy into different vibrational degrees of freedom. Here we apply time-resolved photoelectron spectroscopy with a seeded extreme ultraviolet free-electron laser to trace the ultrafast ring opening of gas-phase thiophenone molecules following ultraviolet photoexcitation. When combined with ab initio electronic structure and molecular dynamics calculations of the excited- and ground-state molecules, the results provide insights into both the electronic and nuclear dynamics of this fundamental class of reactions. The initial ring opening and non-adiabatic coupling to the electronic ground state are shown to be driven by ballistic S–C bond extension and to be complete within 350 fs. Theory and experiment also enable visualization of the rich ground-state dynamics that involve the formation of, and interconversion between, ring-opened isomers and the cyclic structure, as well as fragmentation over much longer timescales.
Citation
Pathak, S., Ibele, L. M., Boll, R., Callegari, C., Demidovich, A., Erk, B., Feifel, R., Forbes, R., Di Fraia, M., Giannessi, L., Hansen, C. S., Holland, D. M., Ingle, R. A., Mason, R., Plekan, O., Prince, K. C., Rouzée, A., Squibb, R. J., Tross, J., Ashfold, M. N., …Rolles, D. (2020). Tracking the ultraviolet-induced photochemistry of thiophenone during and after ultrafast ring opening. Nature Chemistry, 12, 795-800. https://doi.org/10.1038/s41557-020-0507-3
Journal Article Type | Article |
---|---|
Acceptance Date | Jun 11, 2020 |
Online Publication Date | Jul 20, 2020 |
Publication Date | 2020 |
Deposit Date | Jul 21, 2020 |
Publicly Available Date | Jan 20, 2021 |
Journal | Nature Chemistry |
Print ISSN | 1755-4330 |
Electronic ISSN | 1755-4349 |
Publisher | Nature Research |
Peer Reviewed | Peer Reviewed |
Volume | 12 |
Pages | 795-800 |
DOI | https://doi.org/10.1038/s41557-020-0507-3 |
Public URL | https://durham-repository.worktribe.com/output/1266194 |
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