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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2011-1-18
pubmed:abstractText
The efficacy of several multiconfiguration self-consistent field (MCSCF) methods in the subsequent spin-orbit coupling calculations was studied. Three MCSCF schemes to generate molecular orbitals were analyzed: state-specific, state-averaged, and dynamically weighted MCSCF. With Sn(2)(+) as the representative case, we show that the state-specific MCSCF orbitals lead to discontinuities in potential energy curves when avoided crossings of electronic states occur; this problem can be solved using the state-averaged or dynamically weighted MCSCF orbitals. The latter two schemes are found to give similar results when dynamic electron correlation is considered, which we calculated at the level of multiconfigurational quasidegenerate perturbation theory (MCQDPT). We employed the recently developed Douglas-Kroll spin-orbit adapted model core potential, ZFK3-DK3, and the dynamically weighted MCSCF scheme to calculate the spectroscopic constants of the mono-hydrides and compared them to the results obtained using the older set of potentials, MCP-TZP. We also showed that the MCQDPT tends to underestimate the dissociation energies of the hydrides and discussed to what extent coupled-cluster theory can be used to improve results.
pubmed:language
eng
pubmed:journal
pubmed:status
PubMed-not-MEDLINE
pubmed:month
Jan
pubmed:issn
1089-7690
pubmed:author
pubmed:issnType
Electronic
pubmed:day
14
pubmed:volume
134
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
024108
pubmed:year
2011
pubmed:articleTitle
Performance of dynamically weighted multiconfiguration self-consistent field and spin-orbit coupling calculations of diatomic molecules of Group 14 elements.
pubmed:affiliation
Department of Chemistry, University of Alberta, Edmonton, Alberta T6G 2G2, Canada.
pubmed:publicationType
Journal Article