Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/9793
Title: Probing Nuclear Dynamics in Momentum Space: A New Interpretation of (e, 2e) Electron Impact Ionization Experiments on Ethanol
Authors: HAJGATO, Balazs 
DELEUZE, Michael 
MORINI, Filippo 
Issue Date: 2009
Publisher: AMER CHEMICAL SOC
Source: JOURNAL OF PHYSICAL CHEMISTRY A, 113(25). p. 7138-7154 + COVER
Abstract: Calculations of electron momentum distributions for equilibrium geometries, employing advanced Dyson orbital theories and statistical thermodynamics beyond the RRHO approximation, fail to quantitatively reproduce the outermost momentum distribution profile inferred from (e, 2e) electron impact ionization experiments on ethanol employing high-resolution electron momentum spectroscopy. A very detailed study of the influence on this momentum distribution of nuclear dynamics in the initial ground state and in the final ionized state is presented according to a thermal averaging over exceedingly large sets of model structures as well as Born - Oppenheimer molecular dynamical simulations on the potential energy surface of the radical cation. Our results give very convincing albeit qualitative indications that the strong turn-up of the (e, 2e) ionization intensities characterizing; the highest occupied molecular orbital (HOMO) of ethanol at low electron momenta is the combined result of (1) the extraordinarily flat nature of the conformational energy map of ethanol, which enables significant departures from energy minima in the ground electronic state, (2) strong anomeric interactions between an oxygen lone pair and the central C-C bond for the minor but significant fraction of conformers exhibiting a hydroxyl torsion angle (alpha) at around 90 degrees, and, last but not least, (3) the possibility to observe with this minor conformer fraction ultrafast and highly significant extensions of the central C-C bond, resulting, in turn, in an enhanced delocalization of the HOMO from the oxygen lone pair region onto the methyl group, immediately after the sudden removal of an electron. This charge transfer appears to occur at the very first stages, that is, within an effective time scale on the order of similar to 10 fs, of an ultrafast dissociation of the ethanol radical cation into a methyl radical and a protonated form of formaldehyde.
Notes: [Hajgato, Balazs; Deleuze, Michael S.; Morini, Filippo] Hasselt Univ, Dept SBG, Res Grp Theoret Chem, B-3590 Diepenbeek, Belgium. [Hajgato, Balazs] Vrije Univ Brussels, Fac Wetenschappen, B-1050 Brussels, Belgium.
Document URI: http://hdl.handle.net/1942/9793
ISSN: 1089-5639
e-ISSN: 1520-5215
DOI: 10.1021/jp9027029
ISI #: 000267205500037
Category: A1
Type: Journal Contribution
Validations: ecoom 2010
Appears in Collections:Research publications

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