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- W2077889265 abstract "The selection of which configurations to include in a configuration interaction (CI) wave function is a compromise between accuracy and computational difficulty. A compact and accurate configuration interaction wave function can be constructed by inclusion of all single and double excitations and certain triple and quadruple excitations chosen in an a priori manner according to how many electrons are placed in several subsets of orbitals. Such a wave function, denoted CISD[TQ], has previously been shown to recover a large fraction of the energy of a CI wave function including all single, double, triple, and quadruple excitations (CISDTQ). A comparison of the molecular geometry and harmonic vibrational frequencies of hydrogen sulfide (H2S) predicted by two CISD[TQ] wave functions and the complete CISDTQ wave function are presented. With the largest basis set used, a triple-ζ plus double polarization basis with an additional set of d-type functions added to hydrogen, and an additional set of f-type functions added to sulfur [TZ2P(f,d)], the CISD[TQ] predictions differ from the CISDTQ by 0.0003 Å in the bond length and by 0.02° in the bond angle. The CISD[TQ] harmonic vibrational frequencies differ by less than 2 cm−1 from the full CISDTQ predictions. These results suggest that the CISD[TQ] wave function is an efficient and accurate truncation of the complete CISDTQ and are particularly impressive considering that with a TZ2P(f,d) basis, the larger CISD[TQ] wave functions included roughly 300 000 configurations while the CISDTQ includes almost nine million." @default.
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- W2077889265 date "1997-12-22" @default.
- W2077889265 modified "2023-10-18" @default.
- W2077889265 title "Comparison between molecular geometry and harmonic vibrational frequency predictions from CISD[TQ] and CISDTQ wave functions for hydrogen sulfide" @default.
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- W2077889265 doi "https://doi.org/10.1063/1.474176" @default.
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