Strongly contracted canonical transformation theory

被引:69
作者
Neuscamman, Eric [1 ]
Yanai, Takeshi [2 ]
Chan, Garnet Kin-Lic [1 ]
机构
[1] Cornell Univ, Dept Chem & Chem Biol, Ithaca, NY 14853 USA
[2] Natl Inst Nat Sci, Inst Mol Sci, Okazaki, Aichi 4448585, Japan
基金
美国国家科学基金会;
关键词
nickel compounds; nitrogen; perturbation theory; renormalisation; SCF calculations; water; 2ND-ORDER PERTURBATION-THEORY; COUPLED-CLUSTER METHOD; CONFIGURATION-INTERACTION CALCULATIONS; MATRIX RENORMALIZATION-GROUP; REDUCED DENSITY-MATRICES; MOLECULAR WAVE-FUNCTIONS; FIELD REFERENCE FUNCTION; ANO BASIS-SETS; QUANTUM-CHEMISTRY; AB-INITIO;
D O I
10.1063/1.3274822
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Canonical transformation (CT) theory describes dynamic correlation in multireference systems with large active spaces. Here we discuss CT theory's intruder state problem and why our previous approach of overlap matrix truncation becomes infeasible for sufficiently large active spaces. We propose the use of strongly and weakly contracted excitation operators as alternatives for dealing with intruder states in CT theory. The performance of these operators is evaluated for the H(2)O, N(2), and NiO molecules, with comparisons made to complete active space second order perturbation theory and Davidson-corrected multireference configuration interaction theory. Finally, using a combination of strongly contracted CT theory and orbital-optimized density matrix renormalization group theory, we evaluate the singlet-triplet gap of free base porphin using an active space containing all 24 out-of-plane 2p orbitals. Modeling dynamic correlation with an active space of this size is currently only possible using CT theory.
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页数:13
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