Burrow Timothy G, Alcock Nathan M, Huzan Myron S, Dunstan Maja A, Seed John A, Detlefs Blanka, Glatzel Pieter, Hunault Myrtille O J Y, Bendix Jesper, Pedersen Kasper S, Baker Michael L
Department of Chemistry, The University of Manchester, Manchester, M13 9PL, U.K.
The University of Manchester at Harwell, Diamond Light Source, Harwell Campus, OX11 0DE, U.K.
J Am Chem Soc. 2024 Aug 14;146(32):22570-22582. doi: 10.1021/jacs.4c06869. Epub 2024 Jul 31.
Understanding the nature of metal-ligand bonding is a major challenge in actinide chemistry. We present a new experimental strategy for addressing this challenge using actinide 34 resonant inelastic X-ray scattering (RIXS). Through a systematic study of uranium(IV) halide complexes, [UX], where X = F, Cl, or Br, we identify RIXS spectral satellites with relative energies and intensities that relate to the extent of uranium-ligand bond covalency. By analyzing the spectra in combination with ligand field density functional theory we find that the sensitivity of the satellites to the nature of metal-ligand bonding is due to the reduction of 5 interelectron repulsion and 4-5 spin-exchange, caused by metal-ligand orbital mixing and the degree of 5 radial expansion, known as central-field covalency. Thus, this study furthers electronic structure quantification that can be obtained from 34 RIXS, demonstrating it as a technique for estimating actinide-ligand covalency.
理解金属-配体键合的本质是锕系元素化学中的一项重大挑战。我们提出了一种新的实验策略,利用锕系元素L₃共振非弹性X射线散射(RIXS)来应对这一挑战。通过对卤化铀(IV)配合物[UX](其中X = F、Cl或Br)进行系统研究,我们识别出了具有与铀-配体键共价程度相关的相对能量和强度的RIXS光谱卫星峰。通过结合配体场密度泛函理论对光谱进行分析,我们发现卫星峰对金属-配体键合本质的敏感性源于金属-配体轨道混合以及被称为中心场共价性的5f径向膨胀程度所导致的5f电子间排斥作用和4f-5f自旋交换作用的减弱。因此,本研究进一步推进了可从L₃RIXS获得的电子结构量化,证明了它是一种估算锕系元素-配体共价性的技术。