Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/15895
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dc.contributor.authorWang, Y-L-
dc.contributor.authorSu, D-Z-
dc.contributor.authorWang, K-
dc.date.accessioned2013-02-05T09:27:48Z-
dc.date.available2013-02-05T09:27:48Z-
dc.date.issued2013-02-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/15895-
dc.description177-183en_US
dc.description.abstractBased on the adiabatic potential energy surface of the ground state 12A′ constructed by Lv et al. [J Chem Phys, 132 (2010) 014303], the influence of collision energy and reagent vibrational excitation on product polarization for the reaction Ne+HD+(v,0) → NeH++D are studied. The reaction probabilities of the title reaction have been revealed by time-dependent wave packet and quasi-classical trajectory approaches. The four generalized polarization dependent differential cross-sections have been calculated in the center of mass frame. The P(θ), P(φ) and P(θ,φ) distributions, k-kʹ-jʹ correlation and the angular distribution of product rotational vectors are presented in the form of polar plots. The results indicate that both the orientation and the alignment of the rotational angular moment are impacted by initial vibrational number, v, and collision energy. en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-A Vol.52A(02) [February 2013]en_US
dc.subjectTheoretical chemistryen_US
dc.subjectStereodynamicsen_US
dc.subjectQuasi-classical trajectoryen_US
dc.subjectTime-dependent wave packeten_US
dc.subjectNe+HD+ reactionen_US
dc.subjectVector correlationsen_US
dc.titleTheoretical study of the stereodynamics of the reaction Ne+HD+ → NeH++Den_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.52A(02) [February 2013]

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