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- W2034852877 abstract "The electronic structures of oxides of selenium, SeO, SeO2, and SeO3, and their dimers, Se2O3 and Se2O5, were studied using the second-order Generalised van Vleck variant of multireference perturbation theory (GVVPT2), with comparison to the linked completely renormalised coupled cluster through perturbative triple excitations, i.e., CR-CC(2,3), theory. Geometry optimisations of SeO, SeO2, and SeO3 using GVVPT2 and the cc-pVTZ basis set show close agreement with CR-CC(2,3) results and, for SeO and SeO2, close agreement with experiment. In contrast, both GVVPT2 and CR-CC(2,3) predict that the r e bond length of SeO3 is significantly shorter (ca. 0.1 Å) than the r 0 experimental value. Calculations of energies of oxidation reactions predict the formation of SeO2 and SeO3 from SeO to be exothermic. The geometries and energetics of four isomers of both Se2O3 and Se2O5 have been characterised using a composite methodology; key transition states between the isomers were similarly calculated. Because of comparable energies, and relatively low transition barrier heights, several isomers of the dimeric species are predicted to be chemically relevant. Harmonic vibrational frequencies of monomeric and dimeric selenium oxides were obtained at the B3LYP/6-311G* level of theory and corroborate geometrical data that many of the characteristics of the monomeric selenium oxides are preserved in the dimeric species." @default.
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- W2034852877 date "2013-06-28" @default.
- W2034852877 modified "2023-09-26" @default.
- W2034852877 title "GVVPT2 multireference perturbation theory study of selenium oxides" @default.
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- W2034852877 doi "https://doi.org/10.1080/00268976.2013.809163" @default.
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