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dc.creatorKotochigova, S.en_US
dc.creatorTupitsyn, I.en_US
dc.date.accessioned2006-06-15T19:02:25Z
dc.date.available2006-06-15T19:02:25Z
dc.date.issued1998en_US
dc.identifier1998-RB-07en_US
dc.identifier.urihttp://hdl.handle.net/1811/18869
dc.descriptionAuthor Institution: National Institute of Standards and Technology, Gaithersburg; Physics Department, St. Petersburg Universityen_US
dc.description.abstractAll electron ab initio configuration interaction valence-bond (CIVB) calculations have been performed for the ground and first excited states of the PdC molecule. Equilibrium geometries, dissociation energies, rotational and vibrational constants, and potential energy surfaces are computed. The properties of the metal-carbon bond as a function of internuclear separation are investigated with an electron population analysis. The hyperfine structure constant, the Fermi contact term, is derived using electron spin densities at the nuclear sites. Our version of the CIVB method is based on the Hartree-Fock and Sturm's type nonorthogonal basis functions of each atom. Molecular wave functions consist of a large number of determinants constructed from these atomic orbitals. Reexpansion of atomic orbitals from one nuclear center to another is used to simplify many-center integral calculations.en_US
dc.format.extent104478 bytes
dc.format.mimetypeimage/jpeg
dc.language.isoEnglishen_US
dc.publisherOhio State Universityen_US
dc.titleALL-ELECTRON CI VALENCE-BOND CALCULATION OF CARBIDE TRANSITION METAL MOLECULE: PdCen_US
dc.typearticleen_US


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