Fabiano Lever*, David Picconi, Dennis Mayer, Skirmantas Ališauskas, Francesca Calegari, Stefan Düsterer, Raimund Feifel, Marion Kuhlmann, Tommaso Mazza, Jan Metje, Matthew S. Robinson, Richard J. Squibb, Andrea Trabattoni, Matthew Ware, Peter Saalfrank, Thomas J. A. Wolf and Markus Gühr*,
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Near Edge X-ray Absorption Fine Structure spectroscopy (NEXAFS) can be used to observe electronic transitions in ultrafast molecular relaxation. We performed time-resolved UV-pump/X-ray probe absorption measurements at the sulfur 2<i>s</i> (L1) and 2<i>p</i> (L2/3) edges. We are able to identify absorption features corresponding to the S2 (<i>ππ*</i>) and S1 (<i>nπ*</i>) electronic states. We observe a delay of 102 ± 11 fs in the population of the <i>nπ*</i> state with respect to the initial optical excitation and interpret the delay as the time scale for the S2 → S1 internal conversion. We furthermore identify oscillations in the absorption signal that match a similar observation in our previous X-ray photoelectron spectroscopy study on the same molecule.</p>","PeriodicalId":62,"journal":{"name":"The Journal of Physical Chemistry Letters","volume":"16 16","pages":"4038–4046 4038–4046"},"PeriodicalIF":4.6000,"publicationDate":"2025-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.acs.org/doi/epdf/10.1021/acs.jpclett.5c00544","citationCount":"0","resultStr":"{\"title\":\"Direct Observation of the ππ* to nπ* Transition in 2-Thiouracil via Time-Resolved NEXAFS Spectroscopy\",\"authors\":\"Fabiano Lever*, David Picconi, Dennis Mayer, Skirmantas Ališauskas, Francesca Calegari, Stefan Düsterer, Raimund Feifel, Marion Kuhlmann, Tommaso Mazza, Jan Metje, Matthew S. Robinson, Richard J. Squibb, Andrea Trabattoni, Matthew Ware, Peter Saalfrank, Thomas J. A. Wolf and Markus Gühr*, \",\"doi\":\"10.1021/acs.jpclett.5c0054410.1021/acs.jpclett.5c00544\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >The photophysics of nucleobases has been the subject of both theoretical and experimental studies over the past decades due to the challenges posed by resolving the steps of their radiationless relaxation dynamics, which cannot be described in the framework of the Born–Oppenheimer approximation (BOA). In this context, the ultrafast dynamics of 2-thiouracil has been investigated with a time-resolved NEXAFS study at the Free Electron Laser FLASH. Near Edge X-ray Absorption Fine Structure spectroscopy (NEXAFS) can be used to observe electronic transitions in ultrafast molecular relaxation. We performed time-resolved UV-pump/X-ray probe absorption measurements at the sulfur 2<i>s</i> (L1) and 2<i>p</i> (L2/3) edges. We are able to identify absorption features corresponding to the S2 (<i>ππ*</i>) and S1 (<i>nπ*</i>) electronic states. We observe a delay of 102 ± 11 fs in the population of the <i>nπ*</i> state with respect to the initial optical excitation and interpret the delay as the time scale for the S2 → S1 internal conversion. 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Direct Observation of the ππ* to nπ* Transition in 2-Thiouracil via Time-Resolved NEXAFS Spectroscopy
The photophysics of nucleobases has been the subject of both theoretical and experimental studies over the past decades due to the challenges posed by resolving the steps of their radiationless relaxation dynamics, which cannot be described in the framework of the Born–Oppenheimer approximation (BOA). In this context, the ultrafast dynamics of 2-thiouracil has been investigated with a time-resolved NEXAFS study at the Free Electron Laser FLASH. Near Edge X-ray Absorption Fine Structure spectroscopy (NEXAFS) can be used to observe electronic transitions in ultrafast molecular relaxation. We performed time-resolved UV-pump/X-ray probe absorption measurements at the sulfur 2s (L1) and 2p (L2/3) edges. We are able to identify absorption features corresponding to the S2 (ππ*) and S1 (nπ*) electronic states. We observe a delay of 102 ± 11 fs in the population of the nπ* state with respect to the initial optical excitation and interpret the delay as the time scale for the S2 → S1 internal conversion. We furthermore identify oscillations in the absorption signal that match a similar observation in our previous X-ray photoelectron spectroscopy study on the same molecule.
期刊介绍:
The Journal of Physical Chemistry (JPC) Letters is devoted to reporting new and original experimental and theoretical basic research of interest to physical chemists, biophysical chemists, chemical physicists, physicists, material scientists, and engineers. An important criterion for acceptance is that the paper reports a significant scientific advance and/or physical insight such that rapid publication is essential. Two issues of JPC Letters are published each month.