4.6 Article

Quantum stereodynamics of Li+HF reactive collisions: the role of reactants polarization on the differential cross section

期刊

PHYSICAL CHEMISTRY CHEMICAL PHYSICS
卷 13, 期 30, 页码 13656-13669

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c0cp02452j

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资金

  1. Ministerio de Ciencia e Innovacion [CSD2009-00038, FIS2010-18132, CTQ2008-02578, CTQ2007-62898]
  2. Comunidad Autonoma de Madrid (CAM) [S-0505/MAT/0303]

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A complete quantum study for the state-to-state Li + HF(v, j, m) -> LiF(v', j', Omega') + H reactive collisions has been performed using a wave packet method, for different initial rotational states and helicity states of the reactants. The state-to-state differential cross section has been simulated, and the polarization of products extracted. It is found that the reactivity is enhanced for nearly collinear collisions, which produces a vibrational excitation of HF, needed to overcome the late barrier. It is also found that LiF(v' = 0) products are preferentially forward scattered, while vibrationally excited LiF(v' = 1 and 2) are backward scattered. These results are interpreted with a simple reaction mechanism, based on the late character and bent geometry of the transition state, originating from a covalent/ionic crossing, which consists of two steps: the arrival at the transition state and the dissociation. In the first step, in order to get to the saddle point some HF vibrational excitation is required, which favors head-on collisions and therefore low values of m. In the second step a fast dissociation of H atom takes place, which is explained by the ionic Li(+)F(-)H character of the bent transition state: the FH(-) is repulsive making that H depart rapidly leaving a highly rotating LiF molecule. For the higher energy analyzed, where resonances slightly contribute, the orientation and alignment of product rotational states, referred to as reactants frame (with the z-axis parallel to k), are approximately constant with the scattering angle. The alignment is close to -1, showing that j' is perpendicular to k, while starting from initial states with well defined rotational orientation, as states with pure m values, the final rotational are also oriented. It is also found that when using products frame (with the z'-axis parallel to k') the rotational alignment and orientation of products varies a lot with the scattering angle just because the z' axis changes from being parallel to anti-parallel to k when varying from theta = 0 to pi.

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