The generalized active space concept in multiconfigurational self-consistent field methods

被引:238
作者
Ma, Dongxia [1 ,2 ]
Li Manni, Giovanni [3 ]
Gagliardi, Laura [1 ,2 ]
机构
[1] Univ Minnesota, Dept Chem, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Inst Supercomp, Minneapolis, MN 55455 USA
[3] Univ Geneva, Dept Phys Chem, CH-1211 Geneva, Switzerland
关键词
configuration interactions; gadolinium; manganese compounds; organic compounds; SCF calculations; wave functions; DIRECT CONFIGURATION-INTERACTION; 2ND-ORDER PERTURBATION-THEORY; QUANTUM-CHEMICAL METHODS; AB-INITIO CALCULATIONS; ANO BASIS-SETS; ELECTRONIC-SPECTRUM; SPECTROSCOPIC PROPERTIES; VARIABLE OCCUPATIONS; WAVE-FUNCTIONS; CU-II;
D O I
10.1063/1.3611401
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
A multiconfigurational self-consistent field method based on the concept of generalized active space (GAS) is presented. GAS wave functions are obtained by defining an arbitrary number of active spaces with arbitrary occupation constraints. By a suitable choice of the GAS spaces, numerous ineffective configurations present in a large complete active space (CAS) can be removed, while keeping the important ones in the CI space. As a consequence, the GAS self-consistent field approach retains the accuracy of the CAS self-consistent field (CASSCF) ansatz and, at the same time, can deal with larger active spaces, which would be unaffordable at the CASSCF level. Test calculations on the Gd atom, Gd-2 molecule, and oxoMn(salen) complex are presented. They show that GAS wave functions achieve the same accuracy as CAS wave functions on systems that would be prohibitive at the CAS level. (C) 2011 American Institute of Physics. [doi: 10.1063/1.3611401]
引用
收藏
页数:11
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