Determination of Uranium Central-Field Covalency with 3 d 4 f Resonant Inelastic X-ray Scattering.

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 3 d 4 f resonant inelastic X-ray scattering (RIXS). Through a systematic study of uranium(IV) halide complexes, [UX 6 ] 2- , 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 f interelectron repulsion and 4 f -5 f spin-exchange, caused by metal-ligand orbital mixing and the degree of 5 f radial expansion, known as central-field covalency. Thus, this study furthers electronic structure quantification that can be obtained from 3 d 4 f RIXS, demonstrating it as a technique for estimating actinide-ligand covalency.