Reduction of Rare-Earth Metal Complexes Induced by γ Irradiation.
Article
Moore, William NG, White, Jessica RK, Wedal, Justin C et al. (2022). Reduction of Rare-Earth Metal Complexes Induced by γ Irradiation.
. INORGANIC CHEMISTRY, 61(44), 17713-17718. 10.1021/acs.inorgchem.2c02857
Moore, William NG, White, Jessica RK, Wedal, Justin C et al. (2022). Reduction of Rare-Earth Metal Complexes Induced by γ Irradiation.
. INORGANIC CHEMISTRY, 61(44), 17713-17718. 10.1021/acs.inorgchem.2c02857
The utility of γ irradiation for generating unstable, low oxidation state molecular species containing rare-earth metal ions in frozen solution has been examined. The method was evaluated by irradiating Ln(III) precursors (Ln = Sc, Y, and La) in a solid matrix of 2-methyltetrahydrofuran at 77 K with a 700 keV 137Cs source to generate free electrons capable of reducing the Ln(III) species. These experiments yielded EPR and UV-visible spectroscopic data that matched those of the known Ln(II) species [(C5H4SiMe3)3YII]1-, [(C5H4SiMe3)3LaII]1-, and {ScII[N(SiMe3)2]3}1-. Irradiation of the La(III) complex LaIII[N(SiMe3)2]3 by this method gave EPR and UV-visible absorption spectra consistent with {LaII[N(SiMe3)2]3}1-, a species that had previously eluded preparation by chemical reduction. Specifically, the irradiation product exhibited an axial EPR spectrum split into eight lines by the I = 7/2 139La nucleus (g⊥ = 1.98, g|| = 2.06, Aave = 519.1 G). The UV-visible absorption spectrum contains broad bands centered at 390 and 670 nm that are consistent with a La(II) ion in a trigonal ligand environment based on time-dependent density functional theory which qualitatively reproduces the observed spectrum. Additionally, the rate of formation of the [(C5H4SiMe3)3YII]1- species during the irradiation of (C5H4SiMe3)3YIII was monitored by measuring the concentration via UV-visible spectroscopy over time to provide data on the rate at which a molecular species is reduced in a glass via γ irradiation.
