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MO: Fachverband Molekülphysik

MO 16: Ultrafast Dynamics I

MO 16.3: Talk

Wednesday, March 13, 2024, 15:00–15:15, HS 3044

Investigating the Ultrafast Molecular Relaxation of 4-Thiouracil Using Time-Resolved X-Ray Photoelectron Spectroscopy — •Dennis Mayer1, David Picconi2, Matteo Bonanomi3,4, Miltcho Danailov5, Alexander Demidovich5, Michele Devetta4, Michele di Fraia5, Davide Facciala4, Raimund Feifel6, Cesare Grazioli7, Fabiano Lever1, Nitsh Pal8, Vasilis Petropoulos3, Kevin Prince5, Oksana Plekan5, Richard Squibb6, Caterina Vozzi4, Giulio Cerullo3,4, and Markus Gühr1,91DESY, Hamburg, Germany — 2University of Groningen, The Netherlands — 3Politecnico di Milano, Italy — 4CNR-IFN, Milan, Italy — 5Elettra-Sincrotrone Trieste, Italy — 6University of Gothenburg, Sweden — 7CNR-IOM, Trieste, Italy — 8Heriot-Watt University, Edinburgh, UK — 9University of Hamburg, Germany

Recent experiments on 4-thiouracil observed different time constants for the UV-induced relaxation into its triplet state that go beyond the difference between experiments in the gas and solution phase [1,2]. Utilizing the element- and site-selectivity of x-rays, we studied the relaxation process 4-thiouracil using gas-phase time-resolved x-ray photoelectron spectroscopy (XPS) at the free-electron laser FERMI. Lifetimes of the chemical shifts at the S 2p edge support previous gas-phase experiments [1]. In comparison to its isomer 2-thiouracil [3], the molecule shows an additional excited-state spectral feature.

[1] Chem. Phys. 515, 572 (2018); [2] J. Am. Chem. Soc. 140, 16087-16093 (2018); [3] Nat. Comm. 13, 198 (2022)

Keywords: free-electron laser; ultrafast molecular dynamics; photoelectron spectroscopy; x-rays; thiouracil

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