首页> 外文期刊>The Journal of Chemical Physics >Independent amplitude approximations in coupled cluster valence bond theory: Incorporation of 3-electron-pair correlation and application to spin frustration in the low-lying excited states of a ferredoxin-type tetrametallic iron-sulfur cluster
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Independent amplitude approximations in coupled cluster valence bond theory: Incorporation of 3-electron-pair correlation and application to spin frustration in the low-lying excited states of a ferredoxin-type tetrametallic iron-sulfur cluster

机译:耦合簇价键合理论中的独立幅度近似:掺入3型 - 电子 - 对相关性和应用来旋转沉默令人生畏的富铁素型四硫酸铁 - 硫簇的激发态

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摘要

Coupled cluster valence bond (CCVB) is a simple electronic structure method based on a perfect pairing (PP) reference with 2-pair recouplings for strong electron correlation problems. CCVB is spin-pure, size-consistent, and can exactly (in its active space) separate any molecule into atoms for which unrestricted Hartree-Fock (UHF) at dissociation is the sum of the ground state UHF energies of the atoms. However CCVB is far from a complete description of strong correlations. Its first failure to exactly describe spin-recouplings arises at the level of 3 electron pairs, such as the recoupling of 3 triplet oxygen atoms in the dissociation of singlet ozone. Such situations are often associated with spin frustration. To address this limitation, an extension of CCVB, termed CCVB+i3, is reported here that includes an independent (i) amplitude approximation to the 3-pair recouplings. CCVB+i3 thereby has the same basic computational requirements as those of CCVB, which has previously been shown to be an efficient method. CCVB+i3 correctly separates molecules that CCVB cannot. As a by-product, an independent 2-pair amplitude approximation to CCVB, called PP+i2, is also defined. Remarkably, PP+i2 can also correctly separate systems that CCVB cannot. CCVB+i3 is validated on the symmetric dissociation of D-3h ozone. CCVB+i3 is then used to explore the role of 3-pair recouplings in an [Fe4S4(SCH3)(4)](2) cluster that has been used to model the iron-sulfur core of [Fe4S4] ferredoxins. Using localized PP orbitals, such recouplings are demonstrated to be large in some low-lying singlet excited states of the cluster. Significant 3 pair recoupling amplitudes include the usual triangular motif associated with spin frustration and other geometric arrangements of the 3 entangled pairs across the 4 iron centers. Published by AIP Publishing.
机译:耦合簇价键(CCVB)是一种基于完美配对(PP)参考的简单电子结构方法,其具有2对旋转的用于强电子相关问题。 CCVB是旋转纯的,尺寸一致的,并且可以完全(在其有源空间中)将任何分子分离成原子的原子,其中离解的不受限制的Hartree-Fock(UHF)是原子的地面状态UHF能量的总和。然而,CCVB远非完全描述强相关的相关性。其首先进行精确描述旋转旋旋在3个电子对的水平下产生,例如3个三重氧原子的再旋转在单线臭氧的解离。这种情况通常与旋转挫折相关。为了解决本限制,在此报告CCVB称为CCVB + I3的扩展,其包括与三对旋光夹的独立(i)幅度近似。因此,CCVB + I3与CCVB的基本计算要求具有相同的基本计算要求,其先前已被证明是一种有效的方法。 CCVB + I3正确分离CCVB不能的分子。作为副产物,还定义了与CCVB的独立的2对幅度近似,称为PP + I2。值得注意的是,PP + I2也可以正确地分离CCVB不能的系统。 CCVB + I3验证了D-3H臭氧的对称解离。然后使用CCVB + I3来探讨[Fe4S4(SCH3)(4)](2)簇中的3对再旋转的作用,该组簇用于模拟[Fe4S4]富勒莫汀的铁 - 硫核心。使用局部的PP轨道,在群体的一些低位单次激发态中表明这种锁定是大的。显着的3对循环振幅包括通常的三角形图案,与旋转挫折和其他4个铁中心的3个缠绕对的其他几何布置相关联。通过AIP发布发布。

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