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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

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Authors

Shashank Pathak

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

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., …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

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