The time-delayed forward scattering mechanism recently identified by Althorpe et al. [Nature (London) 416, 67 (2002)] for the reaction was analyzed by using quasiclassical trajectory (QCT) methodology. The QCT results were found to match the quantum wavepacket snapshots of Althorpe et al., albeit without the quantum scattering effects. Trajectories were analyzed on the fly to investigate the dynamics of the atoms during the reaction. The dominant reaction mechanism progresses from hard collinear impacts, leading to direct recoil, toward glancing impacts. The increased time required for forward scattered trajectories is due to the rotation of the transient HDD complex. Forward scattered trajectories display symmetric stretch vibrations of the transient HDD complex, a signature of the presence of a resonance, or a quantum bottleneck state.
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28 April 2008
Research Article|
April 23 2008
A quasiclassical trajectory study of the time-delayed forward scattering in the hydrogen exchange reaction
Stuart J. Greaves;
Stuart J. Greaves
a)
Department of Chemistry,
University of Durham
, South Road, Durham DHl 3LE, United Kingdom
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Daniel Murdock;
Daniel Murdock
b)
Department of Chemistry,
University of Durham
, South Road, Durham DHl 3LE, United Kingdom
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Eckart Wrede
Eckart Wrede
c)
Department of Chemistry,
University of Durham
, South Road, Durham DHl 3LE, United Kingdom
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a)
Present address: School of Chemistry, University of Bristol, Bristol, BS8 1TS, UK.
b)
Present address: Department of Chemistry, Yale University, P.O. Box 208107, New Haven, CT 06520-8107.
c)
Author to whom correspondence should be addressed. Electronic mail: [email protected].
J. Chem. Phys. 128, 164307 (2008)
Article history
Received:
May 10 2007
Accepted:
March 05 2008
Connected Content
A companion article has been published:
New, unexpected, and dominant mechanisms in the hydrogen exchange reaction
Citation
Stuart J. Greaves, Daniel Murdock, Eckart Wrede; A quasiclassical trajectory study of the time-delayed forward scattering in the hydrogen exchange reaction. J. Chem. Phys. 28 April 2008; 128 (16): 164307. https://doi.org/10.1063/1.2902973
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