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多参考态量子化学:密度矩阵重整化群与正则变换理论的联合。

Multireference quantum chemistry through a joint density matrix renormalization group and canonical transformation theory.

机构信息

Institute for Molecular Science, 38 Nishigo-Naka, Myodaiji, Okazaki 444-8585, Japan.

出版信息

J Chem Phys. 2010 Jan 14;132(2):024105. doi: 10.1063/1.3275806.

Abstract

We describe the joint application of the density matrix renormalization group and canonical transformation theory to multireference quantum chemistry. The density matrix renormalization group provides the ability to describe static correlation in large active spaces, while the canonical transformation theory provides a high-order description of the dynamic correlation effects. We demonstrate the joint theory in two benchmark systems designed to test the dynamic and static correlation capabilities of the methods, namely, (i) total correlation energies in long polyenes and (ii) the isomerization curve of the Cu(2)O(2) core. The largest complete active spaces and atomic orbital basis sets treated by the joint DMRG-CT theory in these systems correspond to a (24e,24o) active space and 268 atomic orbitals in the polyenes and a (28e,32o) active space and 278 atomic orbitals in Cu(2)O(2).

摘要

我们描述了密度矩阵重整化群和正则变换理论在多参考量子化学中的联合应用。密度矩阵重整化群提供了在大的活性空间中描述静态相关的能力,而正则变换理论提供了对动态相关效应的高阶描述。我们在两个基准系统中演示了联合理论,这两个系统旨在测试方法的动态和静态相关能力,即(i)长聚烯烃中的总相关能量和(ii)Cu(2)O(2)核的异构化曲线。在这些系统中,联合 DMRG-CT 理论处理的最大完整活性空间和原子轨道基组分别对应于聚烯烃中的(24e,24o)活性空间和 268 个原子轨道,以及Cu(2)O(2)中的(28e,32o)活性空间和 278 个原子轨道。

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