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dc.creatorStwalley, W. C.en_US
dc.date.accessioned2006-06-15T17:08:30Z
dc.date.available2006-06-15T17:08:30Z
dc.date.issued1973en_US
dc.identifier1973-X-06en_US
dc.identifier.urihttp://hdl.handle.net/1811/16185
dc.descriptionAcknowledgment is made to the Donors of the Petroleum Research Fund, administered by the American Chemical Society, for support of this research. William C. Stwalley has been an Alfred P. Sloan Foundation Fellow.en_US
dc.descriptionAuthor Institution: Department of Chemistry, University of Iowaen_US
dc.description.abstractA semiclassical procedure for obtaining the internuclear distance dependence of diatomic properties (e.g. dipole moment, dipole strength function, spin-orbit coupling constant) from measured expectation values of the property in specific vibrational-rotational states is outlined. It represents a generalization of the Rydberg-Klein-Rees method for obtaining the internuclear potential energy and thus (unlike known Dunham results valid only near $R_{e}$) is valid throughout the potential well.en_US
dc.format.extent164056 bytes
dc.format.mimetypeimage/jpeg
dc.language.isoEnglishen_US
dc.publisherOhio State Universityen_US
dc.titleA SEMICLASSICAL INVERSION PROCEDURE FOR THE INTERNUCLEAR DISTANCE DEPENDENCE OF DIATOMIC PROPERTIESen_US
dc.typearticleen_US


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