dc.creator Stwalley, W. C. en_US dc.date.accessioned 2006-06-15T17:08:30Z dc.date.available 2006-06-15T17:08:30Z dc.date.issued 1973 en_US dc.identifier 1973-X-06 en_US dc.identifier.uri http://hdl.handle.net/1811/16185 dc.description Acknowledgment 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.description Author Institution: Department of Chemistry, University of Iowa en_US dc.description.abstract A 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.extent 164056 bytes dc.format.mimetype image/jpeg dc.language.iso English en_US dc.publisher Ohio State University en_US dc.title A SEMICLASSICAL INVERSION PROCEDURE FOR THE INTERNUCLEAR DISTANCE DEPENDENCE OF DIATOMIC PROPERTIES en_US dc.type article en_US
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