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- W2017282624 abstract "The recently introduced method of correlation energy extrapolation by intrinsic scaling is used to calculate the nonrelativistic electron correlations in the valence shell of the O2 molecule at 24 internuclear distances along the ground state Σ3g− potential energy curve from 0.9 to 6 Å, the equilibrium distance being 1.207 52 Å. Using Dunning’s correlation-consistent triple- and quadruple-zeta basis sets, the full configuration interaction energies are determined, with an accuracy of about 0.3 mhartree, by successively generating up to sextuple excitations with respect to multiconfigurational reference functions that strongly change along the reaction path. The energies of the reference functions and those of the correlation energies with respect to these reference functions are then extrapolated to their complete basis set limits." @default.
- W2017282624 created "2016-06-24" @default.
- W2017282624 creator A5060037115 @default.
- W2017282624 creator A5087969901 @default.
- W2017282624 date "2010-02-19" @default.
- W2017282624 modified "2023-10-17" @default.
- W2017282624 title "Accurate <i>ab initio</i> potential energy curve of O2. I. Nonrelativistic full configuration interaction valence correlation by the correlation energy extrapolation by intrinsic scaling method" @default.
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