Tailoring Triuranium Octoxide into Multidimensional Uranyl Fluoride Micromaterials.

Uranium microstructured materials with controlled size and shape are relevant to the nuclear industry and have found applications as targets for medical isotope production, fuels for nuclear reactors, standards for nuclear forensics, and energy sources for space exploration. Until now, most studies at the microscale have focused on uranium microspheres (oxides, nitrides, carbides, and fluorides), while micromaterials of uranium halides, carbides, and pnictides with other morphologies are largely unknown. A promising method to shape the morphology of uranium micromaterials is the replacement of O by F atoms in oxide materials using a solid-gas reaction. Here, with the aim to elaborate unexplored uranium fluoride micromaterials, the fluorination of uranium oxide (U3O8 and UO2) microspheres (ms), microrods (mr), and microplates (mp) in an autoclave at 250 °C with HF(g) (produced from the thermal decomposition of silver bifluoride (SBF)) and with ammonium bifluoride (ABF) was evaluated. We show that the reactions between U3O8 mr and U3O8 mp and SBF provided the most efficient way to elaborate mr and mp UO2F2 micromaterials in a high yield (∼90%). The resulting UO2F2 mr (length: 3-20 µm) and UO2F2 mp (width: 1-7.5 µm) exhibited a well-defined geometry that was identical to that of the U3O8 precursors. Agglomerated (NH4)3UO2F5 and UO2F2 ms (2-3.5 µm) were prepared from the reaction of U3O8 ms with ABF. It is noted that the reaction of UO2 ms with SBF and ABF did not provide any uranium fluoride micromaterials. The successful preparation of uranium fluoride microstructures (ms, mr, and mp) developed here opens the way to novel actinide fluoride micromaterials.

Speciation of Technetium Dibutylphosphate in the Third Phase Formed in the TBP/HNO3 Solvent Extraction System.

The speciation of technetium in the nitric acid/dibutylphosphoric acid (HDBP)-n-dodecane system was studied by extended X-ray absorption fine structure (EXAFS) spectroscopy and theoretical methods. Tetravalent technetium, produced by the hydrazine reduction of TcO4- in 3 M HNO3, was extracted by HDBP in n-dodecane (30% by volume). During extraction, the splitting of the organic phase into a heavy phase and a light phase was observed. EXAFS analysis is consistent with the presence of Tc(NO3)3(DBP)(HDBP)2 in the light phase and Tc(NO3)2(DBP)2(HDBP)2 in the heavy phase. Density functional theory calculations at the B3LYP/6-31G* level confirm the stability of the proposed species and indicate that stereoisomers -mer- and fac-Tc(NO3)3(DBP)(HDBP)2 for the light phase and cis- and trans-Tc(NO3)2(DBP)2(HDBP)2 for the heavy phase] could coexist in the system (in the n-dodecane solution). Mechanisms of formation of Tc(NO3)3(DBP)(HDBP)2 and Tc(NO3)2(DBP)2(HDBP)2 are proposed.

Structural Investigation of Technetium Dibutylphosphate Species Using X-ray Absorption Fine Structure Spectroscopy.

The speciation of Tc after the extraction of Tc(IV) from H2O and 1 M HNO3 by dibutylphosphoric acid (HDBP) in dodecane has been studied by X-ray absorption fine structure (XAFS) spectroscopy. Results show the formation of dimeric species with Tc2O2 and Tc2O units, and the formulas [Tc2O2(DBP·HDBP)4] (1) and [Tc2O(NO3)2(DBP)2(DBP·HDBP)2] (2) were, respectively, proposed for the species extracted from H2O and 1 M HNO3. The interatomic Tc-Tc distances found in the Tc2O2 and Tc2O units [2.55(3) and 3.57(4) Å, respectively] are similar to the ones found in Tc(IV) dinuclear species. It is likely that the speciation of Tc(IV) in dodecane is due to the extraction of a species with a Tc2O unit for (2) and to the redissolution of a Tc(IV)-DBP solid for (1). The XAFS results for (1) and (2) were compared to that obtained for the extraction of Tc(IV) with TBP/HDBP/dodecane from 0.5 M HNO3, (3) which highlight the formation of Tc mononuclear nitrate species {i.e., [Tc(NO3)3(DBP)] or [Tc(NO3)2(DBP·HDBP)]}. These results confirm the importance of the preparation and speciation of the Tc(IV) aqueous solutions prior to extraction and how much this influences and drives the final Tc speciation in organic extraction. These studies outline the complexity of Tc separation chemistry and provide insights into the behavior of Tc during the reprocessing of used nuclear fuel.

Synthesis and Morphological Control of UO2F2 Particulates.

Uranium-based microspheres are of interest due to their potential applications as targets for medical isotopes production, as fuel for nuclear reactors, and as standardized materials for nuclear forensics. Here, for the first time, UO2F2 microspheres (1-2 µm) have been prepared from the reaction between UO3 microspheres and AgHF2 in an autoclave. In this preparation, a new fluorination method has been applied, and HF(g)-produced in situ from the thermal decomposition of AgHF2 and NH4HF2-was used as the fluorinating agent. The microspheres were characterized by powder X-ray diffraction (PXRD) and scanning electron microscopy (SEM). Diffraction results indicated that the reaction performed with AgHF2 at 200 °C led to anhydrous UO2F2 microspheres, while at 150 °C, hydrated UO2F2 microspheres were obtained. Meanwhile, NH4HF2 led to the formation of contaminated products as driven by the formation of volatile species.

Pressure-induced metallization and 3d-like behavior in TcS2.

TcS2 undergoes a charge transfer insulator to metal transition above 28 GPa. Laser annealing reveals a kinetically hindered high pressure arsenopyrite phase that is recoverable to ambient. The new phase is similar to the Mn-dichalcogenides rather than the expected Re-dichalcogenides and involves the formation of S-S and Tc-Tc bonds.

Synthetic diversity in the preparation of metallic uranium.

Uranium metal is associated with several aspects of nuclear technology; it is used as fuel for research and power reactors, targets for medical isotope productions, explosive for nuclear weapons and precursors in synthetic chemistry. The study of uranium metal at the laboratory scale presents the opportunity to evaluate metallic nuclear fuels, develop new methods for metallic spent fuel reprocessing and advance the science relevant to nuclear forensics and medical isotope production. Since its first isolation in 1841, from the reaction of uranium chloride and potassium metal, uranium metal has been prepared by solid-state reactions and in solution by electrochemical, chemical and radiochemical methods. The present review summarizes the methods outlined above and describes the chemistry associated with each preparation.

Thermal Analysis of Benzotriazolium Perrhenate and Its Implication to Rhenium Metal.

The thermal analysis behavior of C6H6N3[ReO4] was studied by simultaneous thermal gravimetric analysis (TGA) and differential scanning calorimetry (DSC) up to 700 °C under argon. Such analysis afforded rhenium metal, which was characterized by powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), and energy-dispersive X-ray (EDX) spectroscopy. XRD peak broadening due to crystallite size and lattice strain was analyzed by both Williamson-Hall (W-H) and Debye-Scherrer (D-S) methods. Efforts to isolate Re metal from the thermal treatment of benzotriazole (BTA = C6H5N3) with NH4ReO4 and Re2O7 under various atmospheres and temperatures are also reported. The results provide a significant insight into the chemistry of group VII transition metals, investigate the potential use of benzotriazole as a reducing agent for metal productions, and demonstrate a successful convenient method for rhenium metal production, which could be applied to other refractory metals.

Synthesis and chemical stability of technetium nitrides.

We demonstrate the synthesis and phase stability of TcN, Tc2N, and a substoichiometric TcNx from 0 to 50 GPa and to 2500 K in a laser-heated diamond anvil cell. At least potential recoverability is demonstrated for each compound. TcN adopts a previously unpredicted structure identified via crystal structure prediction.

A 70-Year-Old Mystery in Technetium Chemistry Explained by the New Technetium Polyoxometalate [H7 O3 ]4 [Tc20 O68 ] ⋠4H2 O.

[H7 O3 ]4 [Tc20 O68 ] ⋅ 4H2 O [1] was prepared from an aqueous Tc2 O7 solution concentrated over anhydrous H2 SO4 . [Tc20 O68 ]4- is the first polyanionic species to be reported for Tc. The unit cell contains one centrosymmetric [Tc20 O68 ]4- polyanion as well as hydronium ions and water molecules. The core of the structure consists of four Tc(V)O6 octahedra that form a square Tc4 O4 ring. The four Tc(V)O6 octahedra are decorated by sixteen Tc(VII)O4 tetrahedra. Calculations show the bonding within the Tc4 O4 ring to consist of a 3-center bond formed between each neighboring pair of Tc atoms and their bridging oxygen. Calculations also indicate that a strong d→d electronic transition at 513 nm is the origin of the red color of [1]. The characterization of red HTcO4 solutions by X-ray absorption spectroscopy has complemented the description of this compound in aqueous solution. The formation mechanisms in solution, including the possible role of technetium's radioactivity in the formation of [1], are discussed.

Coexistence of metamagnetism and slow relaxation of magnetization in ammonium hexafluoridorhenate.

The (NH4)2[ReF6] (1) salt was studied by X-ray diffraction, Raman spectroscopy, theoretical calculations, and magnetic measurements. 1 crystallizes in the trigonal space group P3̄m1 (Re-F = 1.958(5) Å). In the Raman spectrum of 1, splitting of the observed peaks was observed and correlated to the valence frequencies of vibration of the [ReF6]2- anion. The study of the magnetic properties of 1, through DC and AC magnetic susceptibility measurements, reveals the coexistence of metamagnetism and slow relaxation of magnetization at low temperature, which is unusual in the molecular systems based on the paramagnetic 5d metal ions reported so far.

Bis(tetraphenylarsonium) hexafluoridotechnetate(IV) dihydrate: preparation, structure and spectroscopic analysis.

Reports of quadrivalent transition-metal fluoride salts containing bulky organic cations are limited. In this context, we prepared the bis(tetraphenylarsonium) hexafluoridotechnetate(IV) dihydrate salt, (C24H20As)2[TcF6]·2H2O, by a cation metathesis reaction of (NH4)2[TcF6] in water. This is the first report of an arsonium salt of the hexafluoridotechnetate(IV) dianion. (AsPh4)2[TcF6]·2H2O crystallizes in the triclinic space group P-1. The [TcF6]2- anion adopts a slightly distorted octahedral geometry with an average Tc-F bond length of 1.933 Å. The cyclic voltammogram of (AsPh4)2[TcF6]·2H2O in CH3CN shows a one-electron reversible oxidation wave at 1.496 V.

An Americium-Containing Metal-Organic Framework: A Platform for Studying Transplutonium Elements.

The synthesis, structure, and spectroscopic characterization of the first transplutonium metal-organic framework (MOF) is described. The preparation and structure of Am-GWMOF-6, [Am2 (C6 H8 O4 )3 (H2 O)2 ][(C10 H8 N2 )], is analogous to that of the isostructural trivalent lanthanide-only containing material GWMOF-6. The presented MOF architecture is used as a platform to probe Am3+ coordination chemistry and guest-enhanced luminescent emission, whereas the framework itself provides a means to monitor the effects of self-irradiation upon crystallinity over time. Presented here is a discussion of these properties and the opportunities that MOFs provide in the structural and spectroscopic study of actinides.

An unexpected rhenium(IV)-rhenium(VII) salt: [Co(NH3)6]3[ReVIIO4][ReIVF6]4·6H2O.

The title hydrated salt, tris-[hexa-amminecobalt(III)] tetraoxidorhenate(VII) tetra-kis-[hexa-fluorido-rhenate(IV)] hexa-hydrate, arose unexpectedly due to possible contamination of the K2ReF6 starting material with KReO4. It consists of octa-hedral [Co(NH3)6]3+ cation (Co1 site symmetry 1), tetra-hedral [ReVIIO4]- anions (Re site symmetry 1) and octa-hedral [ReIVF6]2- anions (Re site symmetries 1and ). The [ReF6]2- octa-hedral anions (mean Re-F = 1.834 Å), [Co(NH3)6]3+ octa-hedral cations (mean Co-N = 1.962 Å), and the [ReO4]- tetra-hedral anion (mean Re-O = 1.719 Å) are slightly distorted. A network of N-H⋯F hydrogen bonds consolidates the structure. The crystal studied was refined as a two-component twin.

Structures and Phase Transitions in Pertechnetates.

The temperature dependence of the structures of four pertechnetates (ATcO4 A = Ag, Tl, Rb, Cs) from 90 K to their melting points is described. Synchrotron X-ray diffraction measurements show that RbTcO4 undergoes a I41/a to I41/amd transition near 530 K that is associated with a change in the orientation of the TcO4- tetrahedra about the scheelite b axis. AgTcO4 also exhibits a tetragonal scheelite type structure, and this is retained between 90 and 750 K, above which it melted. CsTcO4 has an orthorhombic pseudo-scheelite structure at room temperature and this undergoes a first-order orthorhombic to tetragonal transformation (Pnma to I41/a) near 430 K. TlTcO4 is isostructural with CsTcO4 at 90 K, but the orthorhombic to tetragonal transformation proceeds via an intermediate orthorhombic phase. The different behavior found here and described previously for the analogous Re oxide TlReO4 highlights the differences in the chemistry of these two systems.

An Atomistic Understanding of the Unusual Thermal Behavior of the Molecular Oxide Tc2O7.

The thermal behavior of Tc2O7 has been investigated by single-crystal X-ray diffraction of the solid state over a range of 80-280 K and by ab initio molecular dynamics (MD) simulations. The thermal expansion coefficient of the solid was experimentally determined to be 189 × 10-6 Å3 K-1 at 280 K. The simulations accurately reproduce the experimentally determined crystal structures and thermal expansion within a few percent. The experimental melting point and vapor pressure for Tc2O7 are unusually high and low, respectively, in comparison to similar molecular solids. Through investigating the structure and the motion of the solid across a range of temperatures, we provide insights into the thermal behavior of Tc2O7.

Syntheses, Raman spectroscopy and crystal structures of alkali hexa-fluorido-rhenates(IV) revisited.

The A2[ReF6] (A = K, Rb and Cs) salts are isotypic and crystallize in the trigonal space group type P [Formula: see text] m1, adopting the K2[GeF6] structure type. Common to all A2[ReF6] structures are slightly distorted octa-hedral [ReF6]2- anions with an average Re-F bond length of 1.951 (8) Å. In those salts, symmetry lowering on the local [ReF6]2- anions from Oh (free anion) to D3d (solid-state structure) occur. The distortions of the [ReF6]2- anions, as observed in their Raman spectra, are correlated to the size of the counter-cations.

Zirconium tetrachloride revisited.

Zirconium tetrachloride, ZrCl4, is a strategic material with wide-ranging applications. Until now, only one crystallographic study on ZrCl4 has been reported [Krebs (1970). Z. Anorg. Allg. Chem. 378, 263-272] and that was more than 40 years ago. The compound used for the previous determination was prepared from ZrO2 and Cl2-CCl4, and single-crystal X-ray diffraction (SCXRD) studies on ZrCl4 obtained from Zr metal have not yet been reported. In this context, we prepared ZrCl4 from the reaction of Zr metal and Cl2 gas in a sealed tube and investigated its structure at 100, 150, 200, 250, and 300 K. At 300 K, the SCXRD analysis indicates that ZrCl4 crystallizes in the orthorhombic space group Pca21 [a = 6.262 (9), b = 7.402 (11), c = 12.039 (17) Å, and V = 558.0 (14) Å3] and consists of infinite zigzag chains of edge-sharing ZrCl6 octahedra. This chain motif is similar to that observed previously in ZrCl4, but the structural parameters and space group differ. In the temperature range 100-300 K, no phase transformation was identified, while elongation of intra-chain Zr...Zr [3.950 (1) Šat 100 K and 3.968 (5) Šat 300 K] and inter-chain Cl...Cl [3.630 (3) Šat 100 K and 3.687 (9) Šat 300 K] distances occurred.

Expanding the Chemistry of Rhenium Metal-Metal Bonded Fluoro Complexes: Facile Preparation and Characterization of Paddlewheel Complexes.

Quadruply bonded rhenium(III) dimers with the stoichiometry Re2L4F2 (1, L = hexahydro-2H-pyrimido[1,2a]pyrimidinate (hpp-); 2, L = diphenyl formamidinate (dpf-)) were prepared from the solid-state melt reactions (SSMRs) between (NH4)2[Re2F8]·2H2O and HL. Those compounds were characterized in the solid state by single-crystal X-ray diffraction and in solution by UV-visible spectroscopy and cyclic voltammetry. The compound [Re2(hpp)4F2]PF6 (3) was prepared from the one-electron oxidation of Re2(hpp)4F2 with [Cp2Fe]PF6. Compounds 1-3 are isostructural with the corresponding chloro derivatives. In solution, compound 1 undergoes two one-electron oxidations. Comparison with its higher halogen homologues reveals that Re2(hpp)4F2 (1) is more easily oxidized than its chloro and bromo analogues.

Thermal Expansion Behavior in TcO2. Toward Breaking the Tc-Tc Bond.

The structure of TcO2 between 25 and 1000 °C has been determined in situ using X-ray powder diffraction methods and is found to remain monoclinic in space group P21/c. Thermal expansion in TcO2 is highly anisotropic, with negative thermal expansion of the b axis observed above 700 °C. This is the result of an anomalous expansion along the a axis that is a consequence of weakening of the Tc-Tc bonds.

Molecular and Electronic Structures of M2O7 (M = Mn, Tc, Re).

The molecular and electronic structures of the group 7 heptoxides were investigated by computational methods as both isolated molecules and in the solid-state. The metal-oxygen-metal bending angle of the single molecule increased with increasing atomic number, with Re2O7 preferring a linear structure. Natural bond orbital and localized orbital bonding analyses indicate that there is a three-center covalent bond between the metal atoms and the bridging oxygen, and the increasing ionic character of the bonds favors larger bond angles. The calculations accurately reproduce the experimental crystal structures within a few percent. Analysis of the band structures and density of states shows similar bonding for all of the solid-state heptoxides, including the presence of the three-center covalent bond. DFT+U simulations show that PBE-D3 underpredicts the band gap by ∼0.2 eV due to an undercorrelation of the metal d conducting states. Homologue and compression studies show that Re2O7 adopts a polymeric structure because the Re-oxide tetrahedra are easily distorted by packing stresses to form additional three-center covalent bonds.