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• W2043289049 endingPage "230" @default.
• W2043289049 startingPage "217" @default.
• W2043289049 abstract "Abstract Several variants of coupled electron pair type approximations are compared with respect to their accuracy in the prediction of bond distances, harmonic vibrational frequencies and anharmonic corrections for a range of closed-shell diatomic molecules. In the first part of the paper the coupled-electron pair (CEPA) methods (CEPA/1,2,3) are discussed. Extensions of these methods allow the derivation of the correlation energy from the stationarization of a correlation energy functional (CPF/1,2,3 methods). All methods are formulated as diagonally dressed configuration–interaction with single- and double-excitations (CISD) eigenvalue problems. Averaging the diagonal shifts of the CPF methods in various ways lead to the ACPF and AQCC methods. Several small modifications of the shifts for the single excitations are proposed that enhance the stability of the methods (NCPF/1,2,3, NCEPA/1,2,3, NACPF). The reduced shifts are justified by linear response arguments. The implementation of the methods for a closed-shell ground state is described. In the application part, we first tested the size-consistency, exactness for two-electron systems and unitary invariance of the methods. Extensive numerical studies with polarized quadruple-ζ basis sets are employed to test the accuracy of the coupled pair approaches relative to the more elaborate quadratic CI (QCISD) and coupled-cluster (CCSD and CCSD(T)) approaches. Not surprisingly, the CCSD(T) method is the most accurate approach on average. However, the proposed NCPF/1 variant led to even smaller average errors for bond distances (∼0.2 pm relative to ∼0.3 pm for CCSD(T)) while predicting still accurate harmonic frequencies (av. Error ∼25 cm−1 for NCPF/1, ∼8 cm−1 for CCSD(T) and ∼45 cm−1 for CCSD). All coupled pair methods are more accurate than present day DFT approaches (BP86, B3LYP). The exception is the recently proposed double-hybrid B2PLYP functional that approaches the coupled pair performance. Some more difficult copper containing diatomics are treated as well (CuH, CuF, CuCl and Cu2). We discuss why we believe that the coupled-pair approaches (and in particular the proposed NCPF/1 variant) are attractive for large-scale chemical applications." @default.
• W2043289049 created "2016-06-24" @default.
• W2043289049 creator A5003872223 @default.
• W2043289049 creator A5046820685 @default.
• W2043289049 date "2008-01-01" @default.
• W2043289049 modified "2023-09-27" @default.
• W2043289049 title "A comparative study of single reference correlation methods of the coupled-pair type" @default.
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