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The release of uranium and other transuranics into the environment, and their subsequent mobility, are subjects of intense public concern. Uranium dominates the inventory of most medium- and low-level radioactive waste sites and under oxic conditions is highly mobile as U(VI), the soluble uranyl dioxocation (UO2)2+. Specialist anaerobic bacteria are,… (More)
A Th(IV) compound, [Th(TFSI)4(HTFSI)].2H2O [where TFSI = N(SO2CF3)2], has been synthesized and characterized using elemental analysis, thermogravimetric analysis, and vibrational spectroscopy. The analysis suggests that the TFSI anion coordinates to the metal center via the sulfonyl oxygens as well as provides evidence for the coordination of HTFSI. The… (More)
The plutonyl(VI) dinitrate complex [PuO(2)(NO(3))(2)(H(2)O)(2)]·H(2)O (1) has been structurally characterized by single-crystal X-ray diffraction and spectroscopically characterized by solid-state vis-NIR and Raman spectroscopies. Aqueous solution spectroscopic studies indicate only weak plutonyl(VI) nitrate complexation, with the mononitrate complex… (More)
We report the syntheses and crystal structures of (NH4)11[Ln(III)(PMo11O39)2.xH2O (where Ln = every trivalent lanthanide cation except promethium) in which two lacunary [PMo11O39]7- anions sandwich an 8-coordinate Ln(III) cation to yield the complex anion, [LnIII(PMo11O39)2]11-. The 14 salts crystallise in two different space groups, C2/c or P1, but the… (More)
The crystal structure of the title compound, nonaammonium (arsenic decatungstido)(arsenic heptatungstido)diaqua-mu-hydroxo-(hydroxyarsenido)dizirconium hexacosahydrate, which was obtained from the reaction of [NaAs(4)W(40)O(140)](27-) with Zr(IV), has been determined. The anionic complex consists of two hydroxyl-bridged seven-coordinate capped… (More)
The ability of [TcO(4)](-) to coordinate directly to tetra- and hexa-valent actinides in the presence of organic P[double bond, length as m-dash]O ligands is confirmed in the crystallographically characterised complexes [UO(2)(TcO(4))(2)(Ph(3)PO)(3)] and [Th(TcO(4))(4)((n)Bu(3)PO)(4)].
The reduction of selected lanthanide cations to the zerovalent state in the room-temperature ionic liquid [Me3N(n)Bu][TFSI] is reported (where TFSI = bistriflimide, [N(SO2CF3)2]-). The lanthanide cations were introduced to the melt as the TFSI hydrate complexes [Ln(TFSI)3(H2O)3] (where Ln = La(III), Sm(III) or Eu(III)). The lanthanum compound… (More)
In situ EXAFS spectroscopic studies of uranium compounds in high temperature alkali chloride melts indicate the presence of oligomeric species. An investigation into UCl(3) and UCl(4) dissolved in LiCl reveals long range ordering of uranium atoms in the molten state which is not maintained on quenching. Studies of uranium dioxide dissolved in LiCl-KCl… (More)
The title compound, AgTcO4, contains close Ag-O contacts, and Raman spectroscopy shows a reduction in the Tc-O stretching frequencies on changing the pertechnetate counter-cation from K+ to Ag+.