Energy-Degeneracy-Driven Covalency in Actinide Bonding.
Jing SuEnrique R BatistaKevin S BolandSharon E BoneJoseph A BradleySamantha K CaryDavid L ClarkSteven D ConradsonAlex S DitterNikolas KaltsoyannisJason M KeithAndrew KerridgeStosh Anthony KozimorMatthias W LöbleRichard L MartinStefan G MinasianVeronika MockoHenry S La PierreGerald T SeidlerDavid K ShuhMarianne P WilkersonLaura E WolfsbergPing YangPublished in: Journal of the American Chemical Society (2018)
Evaluating the nature of chemical bonding for actinide elements represents one of the most important and long-standing problems in actinide science. We directly address this challenge and contribute a Cl K-edge X-ray absorption spectroscopy and relativistic density functional theory study that quantitatively evaluates An-Cl covalency in AnCl62- (AnIV = Th, U, Np, Pu). The results showed significant mixing between Cl 3p- and AnIV 5f- and 6d-orbitals (t1u*/t2u* and t2 g*/eg *), with the 6d-orbitals showing more pronounced covalent bonding than the 5f-orbitals. Moving from Th to U, Np, and Pu markedly changed the amount of M-Cl orbital mixing, such that AnIV 6d - and Cl 3p-mixing decreased and metal 5f - and Cl 3p-orbital mixing increased across this series.