Multireference general-model-space state-universal and state-specific coupled-cluster approaches to excited states

被引:28
|
作者
Li, Xiangzhu [1 ]
Paldus, Josef [1 ,2 ,3 ]
机构
[1] Univ Waterloo, Dept Appl Math, Waterloo, ON N2L 3G1, Canada
[2] Univ Waterloo, Dept Chem, Waterloo, ON N2L 3G1, Canada
[3] Univ Waterloo, Guelph Waterloo Ctr Grad Work Chem GWC2, Waterloo, ON N2L 3G1, Canada
来源
JOURNAL OF CHEMICAL PHYSICS | 2010年 / 133卷 / 18期
基金
加拿大自然科学与工程研究理事会;
关键词
OPEN-SHELL SYSTEMS; SINGLE-REFERENCE FORMALISM; EXCITATION-ENERGIES; ELECTRONIC STATES; WAVE-FUNCTION; QUANTUM-CHEMISTRY; LINEAR-RESPONSE; EXTENSION; DIRADICALS; EQUATIONS;
D O I
10.1063/1.3494538
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
The concept of C-conditions, originally introduced in the framework of the multireference (MR), general-model-space (GMS), state-universal (SU), coupled-cluster (CC) approach with singles and doubles (GMS-SU-CCSD) to account for the internal amplitudes that vanish in the case of a complete model space, is applied to a state-selective or state-specific Mukherjee MR-CC method (MkCCSD). In contrast to the existing applications, the emphasis is on the description of excited states, particularly those belonging to the same symmetry species. The applicability of the C-conditions in all MR-SU-CC approaches is emphasized. Convergence problems encountered in the MkCCSD method when handling higher-lying states are pointed out. The performance of the GMS-SU-CCSD and MkCCSD methods is illustrated by considering low-lying vertical excitation energies of the ethylene molecule and para-benzyne diradical. A comparison with the equation-of-motion CCSD results, as well as with the available experimental data and recent multireference configuration interaction theoretical results, is also provided. c 2010 American Institute of Physics. [doi:10.1063/1.3494538]
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页数:15
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