Literature DB >> 18661929

Ultrafast dynamics and coherent oscillations in ethylene and ethylene-d4 excited at 162 nm.

K Kosma1, S A Trushin, W Fuss, W E Schmid.   

Abstract

The fifth harmonic (162 nm, 11 fs), generated in a short argon cell from 12 fs Ti-sapphire laser pulses, was used to excite C2H4 and C2D4 in the maximum of the first pi pi* transition. Around 10% of the molecules were excited to the pi3s Rydberg state instead. The subsequent motion of the wave packet, moving over the potentials from the Franck-Condon region down to the ground state, was monitored by nonresonant ionization at 810 nm with mass-selective detection of the ion yield. Five time constants (from approximately 20 fs in excited states to 0.6-11 ps in the hot ground state) and four coherent oscillations (CC stretch and torsion vibrations or hindered free rotation) were determined for each isotopomer. The initial relaxation follows a superposition of CC twist and stretch coordinates; this explains a surprisingly small deuterium isotope effect of the initial time constant (21 versus 24 fs). Also the vibrations in the Franck-Condon region have such a mixed character and a correspondingly small isotope shift. From the perpendicular minimum the wave packet reaches (within 17 or 21 fs for the two isotopomers) a conical intersection via a direction that also involves partial hydrogen migration. This is concluded from the detection of ethylidene (CH3CH), formed simultaneously with ground-state ethylene. This carbene isomerizes in the ground state within 0.6 ps (1.6 ps for CD3CD) to ethylene. Two time constants for dissociation (4.5 and 11 ps) in the hot ground state were also identified. The small yields of bimolecular reactions (photodimerization, addition reactions involving a "suddenly polarized" excited state, carbene reactions) are interpreted in terms of the short lifetimes. It is pointed out that the relaxation path starting from the Rydberg state merges into that from the pi pi* state; nevertheless, there is a wavelength dependence in the photochemistry of olefins, because due to a momentum effect the wave packet remembers from which state it came.

Entities:  

Year:  2008        PMID: 18661929     DOI: 10.1021/jp803548c

Source DB:  PubMed          Journal:  J Phys Chem A        ISSN: 1089-5639            Impact factor:   2.781


  3 in total

1.  Time-dependent view of an isotope effect in electron-nuclear nonequilibrium dynamics with applications to N2.

Authors:  Jayanth S Ajay; Ksenia G Komarova; Francoise Remacle; R D Levine
Journal:  Proc Natl Acad Sci U S A       Date:  2018-05-21       Impact factor: 11.205

2.  Time-resolved nuclear dynamics in bound and dissociating acetylene.

Authors:  C Burger; A Atia-Tul-Noor; T Schnappinger; H Xu; P Rosenberger; N Haram; S Beaulieu; F Légaré; A S Alnaser; R Moshammer; R T Sang; B Bergues; M S Schuurman; R de Vivie-Riedle; I V Litvinyuk; M F Kling
Journal:  Struct Dyn       Date:  2018-08-20       Impact factor: 2.920

3.  Photo-induced ligand substitution of Cr(CO)6 in 1-pentanol probed by time resolved X-ray absorption spectroscopy.

Authors:  Eric J Mascarenhas; Mattis Fondell; Robby Büchner; Sebastian Eckert; Vinícius Vaz da Cruz; Alexander Föhlisch
Journal:  Phys Chem Chem Phys       Date:  2022-08-03       Impact factor: 3.945

  3 in total

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