Semiclassical wavepacket construction of quantum resonance states from classical resonant orbits for the F + H2 reaction
Abstract
The semiclassical interpretation of reactive resonances as dynamically confined orbits is extended for the F + H2 reaction by construction of resonant-state wavefunctions according to a time-dependent formalism for Gaussian wavepacket dynamics. The partitioning of nodal curves between entrance and exit channels for the collinear resonances agrees with adiabatic theory and nodal surfaces for the 3D probability density distribution qualitatively agree with quantal calculations.
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270776
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0x95644003c57E6F55A65596E3D9Eac6813e3566dA
Article ID:
270776
Unique Identifier:
10.1016/0009-2614(85)80564-9
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Scimatic Chain (ID: 481)
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