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Electronic Structure Tools for Transition Metal Complexes with Many Open Shells

机译:具有许多开壳的过渡金属配合物的电子结构工具

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摘要

In this thesis we present three different tools to model open shell transition metal electronic structure, commonly referred to as multi-reference (MR) or multi-configurational electronic structure. The first tool allows us to incorporate spin-orbit coupling into a method that also rigorously treats the multiple configurations arising from electrons in open shells. We call this method the state interaction spin-orbit (SISO) coupling method using density matrix renormalization group (DMRG) wavefunctions. We implement the DMRG-SISO scheme using a spin-adapted DMRG algorithm that computes transition density matrices between arbitrary wavefunctions of the interacting electronic states. To demonstrate the potential of this method, we present accurate benchmark calculations for the zero-field splitting (ZFS) of the copper and gold atoms and also calculate, for the first time, the ZFS of a [2Fe-2S] complex.;The second tool builds on the first to allow the calculation of electron paramagnetic resonance (EPR) g-values, one of the main spectroscopic methods used to characterize paramagnetic metals in transition metal complexes. We apply this to several benchmark systems such as TiF3 and CuCl 42-, as well as to determine the g-tensor for a [2Fe-2S] complex. This work opens up the possibility to model the g-tensor of the active site metals in bioinorganic systems.;Finally, we introduce the atomic valence active space (AVAS), which is a simple automated technique to identify the important orbitals to treat in a multi-configurational electronic structure method. We discuss the background, theory, and implementation of the idea, and several of its variations are tested. To demonstrate the performance and accuracy, we calculate the excitation energies for various transition metal complexes in typical application scenarios. The described technique makes MR calculations easier to execute, easier to reproduce by any user, and simplifies the determination of the appropriate size of the active space required for accurate results.
机译:在本文中,我们提出了三种不同的工具来模拟开壳过渡金属电子结构,通常称为多参考(MR)或多配置电子结构。第一个工具使我们能够将自旋轨道耦合纳入一种方法中,该方法还可以严格处理开放壳中电子引起的多种构型。我们将此方法称为使用密度矩阵重归一化组(DMRG)波函数的状态相互作用自旋轨道(SISO)耦合方法。我们使用自旋自适应DMRG算法实现DMRG-SISO方案,该算法计算相互作用电子状态的任意波函数之间的跃迁密度矩阵。为了证明该方法的潜力,我们提供了铜和金原子零场分裂(ZFS)的精确基准计算,并且首次计算了[2Fe-2S]配合物的ZFS。第二个工具基于第一个工具,可以计算电子顺磁共振(EPR)g值,这是表征过渡金属配合物中顺磁性金属的主要光谱方法之一。我们将此应用于几种基准系统,例如TiF3和CuCl 42-,以及确定[2Fe-2S]配合物的g张量。这项工作为在生物无机系统中对活性位点金属的g张量建模提供了可能性。最后,我们介绍了原子价活性空间(AVAS),这是一种简单的自动化技术,可确定要处理的重要轨道。多配置电子结构方法。我们讨论了该想法的背景,理论和实现,并对其中的几种变体进行了测试。为了证明性能和准确性,我们计算了典型应用场景中各种过渡金属配合物的激发能。所描述的技术使MR计算更容易执行,更容易被任何用户重现,并且简化了确定精确结果所需的活动空间的适当大小的确定。

著录项

  • 作者

    Sayfutyarova, Elvira R.;

  • 作者单位

    Princeton University.;

  • 授予单位 Princeton University.;
  • 学科 Chemistry.;Physical chemistry.
  • 学位 Ph.D.
  • 年度 2018
  • 页码 158 p.
  • 总页数 158
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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