Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/75478
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dc.titleA rapid method for determining excited state surface parameters and bond length in diatomic molecules and calculating wavefunctions for Franck-Condon factors using the quantum momentum method
dc.contributor.authorLee, S.C.
dc.contributor.authorLee, S.-Y.
dc.date.accessioned2014-06-23T05:30:51Z
dc.date.available2014-06-23T05:30:51Z
dc.date.issued1991
dc.identifier.citationLee, S.C.,Lee, S.-Y. (1991). A rapid method for determining excited state surface parameters and bond length in diatomic molecules and calculating wavefunctions for Franck-Condon factors using the quantum momentum method. Computers and Chemistry 15 (3) : 215-223. ScholarBank@NUS Repository.
dc.identifier.issn00978485
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/75478
dc.description.abstractA fast and simple method for determining molecular potential energy parameters for excited dectronic states is presented. This method uses the moments of the observed vibronic spectra. It is particularly accurate in determining equilibrium bond lengths and is a good substitute for an iterative, least-squares Franck-Condon analysis. The calculation of wavefunctions for Franck-Condon factors Using the quantum momentum method is also reported. This method is not limited to low vibrational numbers and does not have problems with overflow and insufficient precision that are associated with methods using analytic forms of the Morse potential wavefunction. A program incorporating both the spectral moment method and the quantum momentum method is described. It provides a package for evaluating excited state molecular potential parameters and for simulating electronic-vibrational spectra for one vibrational mode at a time. © 1991.
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.sourcetitleComputers and Chemistry
dc.description.volume15
dc.description.issue3
dc.description.page215-223
dc.identifier.isiutNOT_IN_WOS
Appears in Collections:Staff Publications

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