Actinide Sulfate Structures from Caustic Solvents.

Four unique actinide sulfates were synthesized using solvothermal techniques with strong acids. The first plutonium(III) sulfate structure, Pu(HSO4)3, was synthesized and is isostructural with analogous lanthanide-based frameworks. A similar synthesis approach yielded crystals of NpNa0.5(HSO4)15(SO4)1.5, which has a comparable framework to the Pu(III) compound, but the neptunium metal is tetravalent and sodium is incorporated into the structure, as confirmed by chemical analysis. Anhydrous neptunium sulfate, Np(SO4)2, is reported and is isotypic with U(SO4)2. Finally, (H3O)2(UO2)(SO4)2, which contains a uranyl sulfate sheet structure, was synthesized and characterized. The corresponding sheet anion topology has previously been reported with various oxyanions, but this is the first report that contains sulfate. The sheets are charge balanced by hydronium cations in the interstitial space. This compound readily degrades and forms crystals of the synthetic analogue to the uranium mineral shumwayite, which is likely thermodynamically favorable. All four of these actinide sulfate compounds were synthesized in extremely acidic media, resulting in interesting and unique structures.

Plutonium and Cerium Perrhenate/Pertechnetate Coordination Polymers and Frameworks.

Spent nuclear fuel (SNF) contains transuranic and lanthanide species, which are sometimes recovered and repurposed. One particularly problematic fission product, 99TcO4-, hampers this recovery via coextraction with high valence metals, perhaps by complexation during aqueous reprocessing of SNF. There is limited molecular-level knowledge concerning the coordination chemistry between TcO4- or its well-known surrogate ReO4- and transuranic/lanthanide species. In the current study, we investigated the coordination of ReO4-/TcO4- with plutonium and cerium cations by structural and chemical characterization of a series of isolated extended solids. In this study, Ce represents both trivalent lanthanides and is considered a surrogate for Pu, respectively, in its common trivalent and tetravalent oxidation states. The structural elucidation of the seven isolated crystalline solids revealed that ReO4-/TcO4- directly connects to PuIV, PuVIO22+, CeIII, and CeIV in the terminal and bridging coordination modes, leading to 1-, 2-, and 3-dimensional frameworks. For example, ReO4- coordination to Pu(IV) formed a 1D chain or 2D framework, isostructural with previously isolated Th(IV) compounds. However, PuVIO22+ alternating with ReO4- led to a unique 1D chain, different from the prior-reported U(VI)/Np(VI)-ReO4-/TcO4- structures. Coordination of ReO4-/TcO4- with Ce(III) promotes the assembly of 3D frameworks. Finally, attempted synthesis of a Ce(IV)-ReO4- compound resulted in a 2D framework with a mixed-valence CeIII/IV. The highly acidic reaction conditions supported the reduction of both CeIV and TcVII, challenging isolation of compounds featuring these species. Only one TcO4-containing structure was obtained in this study (CeIII-TcO4 3D framework), vs the six total Ce/Pu-ReO4 compounds. Our three Pu-ReO4 crystal structures are the first reported and translated to atomic-level information about Pu-TcO4 coordination in nuclear fuel reprocessing scenarios, in addition to broadening our knowledge of bonding trends in the early, high-valence actinides.

Pu(VI) Oxalate Crystal Structure and Evidence of Photoreduction to Pu(IV) Oxalate.

We report the first crystal structure of a Pu(VI)-oxalate compound. This compound, [PuO2(C2O4)(H2O)]·2(H2O) (1), crystallizes in space group P21/c with a = 5.5993(3) Å, b = 16.8797(12) Å, c = 9.3886(6) Å, and ß = 98.713(6)°. It is isostructural with the previously reported U(VI) compound, [UO2(C2O4)(H2O)]·2(H2O). Each plutonyl ion (PuO22+) is coordinated in the equatorial plane by two side-on bidentate oxalates, creating an infinite chain along [001]. A coordinated water molecule and twisting of the oxalates lead to a distorted pentagonal bipyramidal geometry of the Pu. A photochemical degradation was observed for 1, which resulted in the formation of a secondary crystalline phase. The absorption spectrum of this secondary phase confirmed the presence of Pu(IV), but it did not match the spectrum of Pu(C2O4)2·6H2O, which is considered to be the primary product of Pu-oxalate precipitation. While compound 1 has previously been proposed to exist in solution, this is the first time it has been isolated via crystallization. Although redox interactions between Pu and oxalate have been documented in the literature, the present study is the first observation of a photochemical reduction of Pu(VI)-oxalate. As a result, this study has expanded on the limited understanding of the Pu(VI)-oxalate system, which is important for nuclear fuel cycle applications.

A spectrophotometric study of the impact of pH and metal-to-ligand ratio on the speciation of the Pu(VI)-oxalate system.

The oxalate ligand is prevalent throughout the nuclear fuel cycle. While the Pu(III)- and Pu(IV)-oxalate systems are well studied due to their use in plutonium metal and PuO2 production, the effect of oxalate on Pu(VI) remains understudied. Absorption spectroscopy was employed to probe the solution behavior of the Pu(VI)-oxalate system as a function of pH (1, 3, 7) and metal-to-ligand ratio (M/L; 10 : 1-1 : 10). Peak changes in the UV-vis-NIR spectra were associated with the formation of multiple Pu(VI)-oxalate species with increasing oxalate concentration. Some insight into identification of species present in solution was gained from the limited Pu(VI)-oxalate literature and comparisons with the assumed isostructural U(VI)-oxalate system. A peak in the UV-vis-NIR spectrum at 839 nm, which corresponds to the formation of a 1 : 1 PuO2(C2O4)(aq) complex, was observed and used to determine the formation constant (log ß° = 4.64 ± 0.06). A higher coordinated Pu(VI)-oxalate peak at 846 nm was tentatively assigned as the 1 : 2 complex PuO2(C2O4)22- and a preliminary formation constant was determined (log ß° = 9.30 ± 0.08). The predominance of both complexes was shown in speciation diagrams calculated from the formation constants, illustrating the importance of considering the Pu(VI)-oxalate system in the nuclear fuel cycle.

Insight into the Structural Ambiguity of Actinide(IV) Oxalate Sheet Structures: A Case for Alternate Coordination Geometries.

Invited for the cover of this issue is the group of Amy Hixon at the University of Notre Dame. The image depicts the newly identified structure of a PuIV oxalate sheet compared to the historically assumed structure. Read the full text of the article at 10.1002/chem.202301164.

Insight into the Structural Ambiguity of Actinide(IV) Oxalate Sheet Structures: A Case for Alternate Coordination Geometries.

Plutonium(IV) oxalate hexahydrate (Pu(C2 O4 )2 ⋅ 6 H2 O; PuOx) is an important intermediate in the recovery of plutonium from used nuclear fuel. Its formation by precipitation is well studied, yet its crystal structure remains unknown. Instead, the crystal structure of PuOx is assumed to be isostructural with neptunium(IV) oxalate hexahydrate (Np(C2 O4 )2 ⋅ 6 H2 O; NpOx) and uranium(IV) oxalate hexahydrate (U(C2 O4 )2 ⋅ 6 H2 O; UOx) despite the high degree of unresolved disorder that exists when determining water positions in the crystal structures of the latter two compounds. Such assumptions regarding the isostructural behavior of the actinide elements have been used to predict the structure of PuOx for use in a wide range of studies. Herein, we report the first crystal structures for PuOx and Th(C2 O4 )2 ⋅ 6 H2 O (ThOx). These data, along with new characterization of UOx and NpOx, have resulted in the full determination of the structures and resolution of the disorder around the water molecules. Specifically, we have identified the coordination of two water molecules with each metal center, which necessitates a change in oxalate coordination mode from axial to equatorial that has not been reported in the literature. The results of this work exemplify the need to revisit previous assumptions regarding fundamental actinide chemistry, which are heavily relied upon within the current nuclear field.

Snapshots of Ce70 Toroid Assembly from Solids and Solution.

Crystallization at the solid-liquid interface is difficult to spectroscopically observe and therefore challenging to understand and ultimately control at the molecular level. The Ce70-torroid formulated [CeIV70(OH)36(O)64(SO4)60(H2O)10]4-, part of a larger emerging family of MIV70-materials (M = Zr, U, Ce), presents such an opportunity. We elucidated assembly mechanisms by the X-ray scattering (small-angle scattering and total scattering) of solutions and solids as well as crystallizing and identifying fragments of Ce70 by single-crystal X-ray diffraction. Fragments show evidence for templated growth (Ce5, [Ce5(O)3(SO4)12]10-) and modular assembly from hexamer (Ce6) building units (Ce13, [Ce13(OH)6(O)12(SO4)14(H2O)14]6- and Ce62, [Ce62(OH)30(O)58(SO4)58]14-). Ce62, an almost complete ring, precipitates instantaneously in the presence of ammonium cations as two torqued arcs that interlock by hydrogen boding through NH4+, a structural motif not observed before in inorganic systems. The room temperature rapid assemblies of both Ce70 and Ce62, respectively, by the addition of Li+ and NH4+, along with ion-exchange and redox behavior, invite exploitation of this emerging material family in environmental and energy applications.

Beyond Biological Chelation: Coordination of f-Block Elements by Polyhydroxamate Ligands.

The promise of polyhydroxamic acid ligands for the selective chelation of the f-block elements is becoming increasingly more apparent. The initial studies of polyhydroxamic acid siderophores showed the formation of highly stable complexes with PuIV , but a higher preference for FeIII hindered effective applications. The development of synthetic routes toward highly pure and customizable ligands containing multiple hydroxamic acids allowed for the growth of new classes of compounds. Although the first round of these ligands focused on the incorporation of siderophore-like frameworks, the new synthetic strategies led to small molecules of various frameworks and even resins for applications in the field of f-block element separations and biological desorption. Unfortunately, a lack of consistent stability-constant data makes direct comparisons across this body of work difficult. More studies into the stability constants and separations of the f-block elements in a variety of pH ranges is necessary to truly realize the potential for polyhydroxamic acid ligands.