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Now showing 1 - 3 of 3
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    Correlated rotational alignment spectroscopy of isolated molecules and molecular mixtures
    (Les Ulis : EDP Sciences, 2013) Schröter, C.; Kosma, K.; Schultz, T.
    We present a novel multi-pulse spectroscopic method for the correlated analysis of molecular mass, rotational structure and electronic structure. First experiments investigate carbon disulfide and butadiene.
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    Probing nucleobase photoprotection with soft x-rays
    (Les Ulis : EDP Sciences, 2013) McFarland, B.K.; Farrell, J.P.; Berrah, N.; Bostedt, C.; Bozek, J.; Bucksbaum, P.H.; Coffee, R.; Cryan, J.; Fang, L.; Feifel, R.; Gaffney, K.; Glownia, J.; Martinez, T.; Mucke, M.; Murphy, B.; Miyabe, S.; Natan, A.; Osipov, T.; Petrovic, V.; Schorb, S.; Schultz, T.; Spector, L.; Tarantelli, F.; Tenney, I.; Wang, S.; White, W.; White, J.; Gühr, M.
    Nucleobases absorb strongly in the ultraviolet region, leading to molecular excitation into reactive states. The molecules avoid the photoreactions by funnelling the electronic energy into less reactive states on an ultrafast timescale via non-Born-Oppenheimer dynamics. Current theory on the nucleobase thymine discusses two conflicting pathways for the photoprotective dynamics. We present our first results of our free electron laser based UV-pump soft x-ray-probe study of the photoprotection mechanism of thymine. We use the high spatial sensitivity of the Auger electrons emitted after the soft x-ray pulse induced core ionization. Our transient spetra show two timescales on the order of 200 fs and 5 ps, in agreement with previous (all UV) ultrafast experiments. The timescales appear at different Auger kinetic energies which will help us to decipher the molecular dynamics.
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    Excited state dynamics of liquid water near the surface
    (Les Ulis : EDP Sciences, 2013) Buchner, F.; Ritze, H.-H.; Beutler, M.; Schultz, T.; Hertel, I.-V.; Lübcke, A.
    Time resolved photoelectron spectroscopy explores the excited state dynamics of liquid water in presence of cations close to the surface. A transient hydrated electroncation complex is observed.