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dc.creatorJulienne, P. S.en_US
dc.creatorMies, F. H.en_US
dc.date.accessioned2006-06-15T14:41:16Z
dc.date.available2006-06-15T14:41:16Z
dc.date.issued1981en_US
dc.identifier1981-RF-5en_US
dc.identifier.urihttp://hdl.handle.net/1811/11631
dc.descriptionAuthor Institution:en_US
dc.description.abstractMultichannel quantum defect theory has had considerable success in applications to atomic spectroscopy, where the potentials are coulombic. It is possible to develop a similar theory for molecules, where the long range potentials are noncoulombic. The scattering wavefunction above a molecular dissociation threshold can be analytically continued below the threshold to describe the bound states. Once a reference Hamiltonian is chosen, a simple analytic theory can be developed which relates the elastic and inelastic scattering above threshold and the level shifts and predissociation widths below threshold. The analytic theory will be illustrated by comparison to close coupling calculations on several curve crossing models.en_US
dc.format.extent66850 bytes
dc.format.mimetypeimage/jpeg
dc.language.isoEnglishen_US
dc.publisherOhio State Universityen_US
dc.titleA MULTICHANNEL QUANTUM DEFECT APPROACH TO MOLECULAR DISSOCIATIONen_US
dc.typearticleen_US


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