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Vibrational Bound States of the He2Ne+ Cation
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    Vibrational Bound States of the He2Ne+ Cation
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    Departamento de Química Física, Universidad de Murcia, 3010 Murcia, Spain, Laboratoire Collisions, Agrégats, Réactivité, IRSAMC, Université de Toulouse, UPS, and CNRS, UMR5589, F-31062 Toulouse, France, and Department of Chemistry and Institute of Surface and Interface Science, University of California at Irvine, Irvine, California 92697-2025
    †Part of the “Vincenzo Aquilanti Festschrift”.
    ‡Universidad de Murcia.
    §Université de Toulouse.
    ∥University of California at Irvine.
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    The Journal of Physical Chemistry A

    Cite this: J. Phys. Chem. A 2009, 113, 52, 14896–14903
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    https://doi.org/10.1021/jp905043t
    Published October 7, 2009
    Copyright © 2009 American Chemical Society

    Abstract

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    The vibrational bound states of the He2Ne+ complex have been determined using a potential energy surface previously published by Seong et al. [J. Chem. Phys. 2004, 120, 7456]. The calculation was performed by sequential diagonalization−truncation techniques in a discrete variable representation using Radau hyperspherical coordinates. There are 52 bound levels. The ground state has an energy of 605.3 cm−1 above the absolute minimum and lies about half way to dissociation. The evaporation energy of one He atom is equal to 866.1 cm−1. Only four levels have energies below the classical energy for dissociation, and all the other 48 states are bound by the zero-point energy of the HeNe+ fragment. The implications of the properties of the eigenvalue spectrum and of the corresponding wave functions on the vibrational relaxation dynamics and infrared spectra of HeNNe+ clusters is discussed.

    Copyright © 2009 American Chemical Society

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    Cited By

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    This article is cited by 1 publications.

    1. Peter Bartl, Stephan Denifl, Paul Scheier, Olof Echt. On the stability of cationic complexes of neon with helium – solving an experimental discrepancy. Physical Chemistry Chemical Physics 2013, 15 (39) , 16599. https://doi.org/10.1039/c3cp52550c

    The Journal of Physical Chemistry A

    Cite this: J. Phys. Chem. A 2009, 113, 52, 14896–14903
    Click to copy citationCitation copied!
    https://doi.org/10.1021/jp905043t
    Published October 7, 2009
    Copyright © 2009 American Chemical Society

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