Actinide Complexes Research Articles

Highly stable actinide(III) complexes supported by doubly aromatic ligands.

Owing to the electron-deficient nature of boron atoms, the structures and properties of boron clusters can be enriched by doping various metal atoms, including lanthanide metal atoms. Nevertheless, the viability of actinide analogues has not been fully elucidated up to now. Here we demonstrate a series of highly stable low-valent actinide(III) boron clusters AnB7 (An = Pa, U, Np, and Pu) using first-principles calculations. The predicted global minimum structures of all the AnB7 complexes possess half-sandwich geometries with C6v symmetry and belong to MIII[B7]3--type species. In each AnB7 species, the B73- ligand possesses double aromaticity features with six delocalized π electrons and six delocalized σ electrons. Bonding analysis shows that although there is a substantial contribution of electrostatic interaction in each cluster, covalent interaction is responsible for the stability of AnB7. All the AnB7 species show significantly high formation energies, especially for NpB7, which is in line with the stronger Np-B covalent bonds. In addition, the simulated photoelectron spectroscopy analysis confirms the high electronic stability of neutral AnB7. These results imply that these ultrastable actinide(III) complexes are accessible in the gas phase at room temperature. This work may provide a theoretical basis for the design of highly stable boron-based nanomaterials as well as preparation of low-valent actinide complexes.

Porphyrinoid actinide complexes.

The diverse coordination modes and electronic features of actinide complexes of porphyrins and related oligopyrrolic systems (referred to as "porpyrinoids") have been the subject of interest since the 1960s. Given their stability and accessibility, most work with actinides has focused on thorium and uranium. This trend is also seen in the case of porphyrinoid-based complexation studies. Nevertheless, the diversity of ligand environments provided by porphyrinoids has led to the stabilization of a number of unique complexes with the early actinides that are often without structural parallel within the broader coordination chemical lexicon. This review summarizes key examples of prophyrinoid actinide complexes reported to date, including the limited number of porphyrinoid systems involving transuranic elements. The emphasis will be on synthesis and structure; however, the electronic features and reactivity pattern of representative systems will be detailed as well. Coverage is through December of 2021.

New tetradentate N,O-hybrid phenanthroline-derived organophosphorus extractants for the separation and complexation of trivalent actinides and lanthanides

Comparison of the extraction and separation properties between two novel phenanthroline-derived organophosphorus ligands, Et-Ph-BPPhen and Et-Ph-PIPhen.

Aggregated germanium saponite: Removal and retention of polymeric thorium and uranium complexes

The present study concerns the removal of thorium and uranium from aqueous solution, and particularly the effect of clay particle size and morphology on the adsorption of polynuclear actinide complexes by synthetic saponite nanoscale powders. Saponites were synthesized from a reactant mixture containing aluminum nitrate, magnesium nitrate, and either sodium silicate or sodium germanate. The saponite powders were analyzed by TEM, XRD, SAXS, N2-adsorption-desorption isotherms and FT-IR. Ge-saponite contained randomly stacked platelets ≈ 100 nm long and 80 nm wide, while Si-saponite showed roughly spherical agglomerates ≈ 60–80 nm in size. Small-angle X-ray scattering measurements indicated a hierarchical pore network among the plates and their agglomerates. Thorium polymers composed of fractal aggregates of branched filaments were characterized by synchrotron radiation-SAXS. The distribution coefficient (Kd mL/g) values for thorium (20 μg/mL) at pH 4 were: Ge-saponite (105) ≈ Si-saponite (105) > raw saponite (104) ≈ raw saponite (washed) (104). The Kd values for uranium (20 μg/mL) at pH 5.5 were: Ge-saponite (103) ≈ raw saponite (washed) (103) ≈ Si-saponite (103) ≈ raw saponite (103). The difference in uranyl adsorption performance observed between the two nanoparticle forms of saponite was attributed to a larger pore width for Ge-saponite (3.5 nm) compared with Si-saponite (0.8 nm). The results have implications for mineral ore tailings containing thorium(IV) and, by analogy, Pu(IV) in a clay buffer environment within a geological repository for high-level nuclear waste.

How 5 f Electron Polarisability Drives Covalency and Selectivity in Actinide N-Donor Complexes.

We report a series of isostructural tetravalent actinide (Th, U−Pu) complexes with the N‐donor ligand N,N’‐ethylene‐bis((pyrrole‐2‐yl)methanimine) (H2 L, H2pyren). Structural data from SC‐XRD analysis reveal [An(pyren)2] complexes with different An−Nimine versus An−Npyrrolide bond lengths. Quantum chemical calculations elucidated the bonding situation, including differences in the covalent character of the coordinative bonds. A comparison to the intensely studied analogous N,N′‐ethylene‐bis(salicylideneimine) (H2salen)‐based complexes [An(salen)2] displays, on average, almost equal electron sharing of pyren or salen with the AnIV, pointing to a potential ligand‐cage‐driven complex stabilisation. This is shown in the fixed ligand arrangement of pyren and salen in the respective AnIV complexes. The overall bond strength of the pure N‐donor ligand pyren to AnIV (An=Th, U, Np, Pu) is slightly weaker than to salen, with the exception of the PaIV complex, which exhibits extraordinarily high electron sharing of pyren with PaIV. Such an altered ligand preference within the early AnIV series points to a specificity of the 5f 1 configuration, which can be explained by polarisation effects of the 5 f electrons, allowing the strongest f electron backbonding from PaIV (5f 1) to the N donors of pyren.

In vitro evidence of the influence of complexation of Pu and Am on uptake by human lung epithelial cells Calu-3

Understanding the mechanisms involved in retention and clearance of actinides from the lungs after accidental intake is essential for the evaluation of the associated radiological risks. Although the absorption of radioelements has been shown in vivo to depend on their nature and physico-chemical properties, their mechanisms of translocation remain unknown. In this study, we have evaluated in vitro the binding and uptake by bronchial epithelial cells Calu-3 of 2 transuranic actinides, plutonium (Pu) and americium (Am), as the first steps of translocation across the pulmonary barrier. For this purpose, Calu-3 cells grown to confluence in 24-well plates were exposed to the radioelements for 24 h under various culture conditions. Two compartments were identified for the association of actinides to cells, corresponding to the membrane bound and internalized fractions. Binding of Pu was slightly higher than of Am, and depended on its initial chemical form (nitrate, citrate, colloids). Uptake of Pu and Am nitrate was higher in serum-free conditions than in supplemented medium, with an active mechanism involved in Pu internalization. Overall, our results suggest that complexation of actinides to bioligands may have an influence on their uptake by pulmonary epithelial cells, and therefore possibly on their subsequent absorption into blood.

Radionuclide geochemistry evolution in the Long-term In-situ Test (LIT) at Grimsel Test Site (Switzerland)

The Long-term In-situ Test (LIT) of the Colloid Formation and Migration project (CFM) at the Grimsel Test Site, investigates the generation of bentonite colloids and, hence, radionuclide mobilization within a well-defined and controlled shear zone in a crystalline rock. In this context, the determination of radionuclide aqueous speciation is essential to understand whether radionuclides are easily transported or immobilized by precipitation or uptake processes in the bentonite barrier included in a repository concept for nuclear waste, and mimic in the LIT experiment. The objective of this work is to determine the aqueous speciation of seven radionuclides (i.e. 75Se(VI), 99Tc(VII),233U(VI), 237Np(V), 241Am(III), Th(IV) and 242Pu(IV)) by thermodynamic calculations in different water compositions representing the geochemical evolution through the LIT. A comparison of the results obtained from two different modelling groups allows the identification of the geochemical key parameters affecting radionuclide mobility in this context and the corresponding numerical and conceptual uncertainties. Particularly, silicate complexes of trivalent actinides and uranium(VI) carbonato complexes (i.e. CanUO2(CO3)3(4−2n) n = 1 or 2) seem to be crucial in these environments, even at reducing conditions. Conceptual uncertainties like inclusion/exclusion of tetravalent actinide-bearing colloids formation and polyselenides have clearly been identified.

Impact of increased temperatures on the geochemical behaviour of trivalent actinides in aquatic systems

Abstract. The Safety Case for a radioactive waste repository in deep geological formations requires detailed chemical and thermodynamic information on the stored radionuclides in their relevant oxidation states. Although a comprehensive summary of critically evaluated thermodynamic data is available via the blue book series of the NEA-TDB (“Nuclear Energy Agency – Thermochemical Database”), the majority of this data is limited to ambient conditions (Grenthe et al., 2020). In the case of the disposal of high-active, heat-producing waste, however, the near-field of the repository will experience increased temperatures at early operative phases for several hundred or a few thousand years. Radionuclides may come into contact with aquatic solutions or brines at elevated temperatures in the case of early canister failure. Besides other factors of the overall disposal concept (e.g. the geometry of the repository, type and amount of stored radionuclide inventories), host rock characteristics themselves limit the extent of the allowable temperature increase. For example, in clay formations the maximum temperature should stay at around or below ∼100∘C in order to avoid an irreversible change in the host rock retention capacity, whereas rock salt allows much higher temperatures of up to 200 ∘C. Increased temperatures will have a distinct impact on the geochemical behaviour of radionuclides, potentially affecting their mobility and retention in the near field. Besides reactions at the solid–liquid interface (e.g. dissolution/precipitation reactions of the waste matrix, sorption reactions of the radionuclides to surfaces), complexation reactions with inorganic and organic ligands present in the aqueous phase potentially affect migration behaviour of the radionuclides. A quantitative thermodynamic description of these processes requires standard stability constants (log⁡βn0(T)), as well as standard reaction enthalpies and entropies (ΔrHm,n0, ΔrSm,n0). The precise experimental determination of these data for all relevant radionuclide/ligand reactions requires a vast amount of time and effort. In this regard, reliable extrapolation methods in particular for standard stability constants valid for 25 ∘C to higher temperatures are considered to support a comprehensive description. Recently, the German Federal Ministry of Education and Research (BMBF)-funded collaborative research project “Therm AC” focused on the experimental determination of new thermodynamic data at higher temperatures, as well as the comparison with the analogous results yielded by extrapolation methods. The Thermochemical Database Project of the OECD-NEA (NEA-TDB) is currently in the process of preparing a comprehensive state-of-the-art report on the high temperature thermodynamics of radionuclides, further emphasizing the particular relevance of this interesting topic. Within this contribution, a critical overview on the recent advances in the field of high temperature studies of radionuclides in aqueous solutions will be given. Besides summarizing information on key technical aspects relevant for high temperature studies, the effect of increased temperatures on the complexation of trivalent actinides with chloride will be discussed in more detail in order to illustrate newly derived in-depth understanding of the impact of increased temperatures on the (geo)chemical behaviour of trivalent actinides on the molecular scale (Skerencak-Frech et al., 2014).

Covalency of Trivalent Actinide Ions with Different Donor Ligands: Do Density Functional and Multiconfigurational Wavefunction Calculations Corroborate the Observed "Breaks"?

A comprehensive ab initio study of periodic actinide-ligand bonding trends for trivalent actinides is performed. Relativistic density functional theory (DFT) and complete active-space (CAS) self-consistent field wavefunction calculations are used to dissect the chemical bonding in the [AnCl6]3-, [An(CN)6]3-, [An(NCS)6]3-, [An(S2PMe2)3], [An(DPA)3]3-, and [An(HOPO)]- series of actinide (An = U-Es) complexes. Except for some differences for the early actinide complexes with DPA, bond orders and excess 5f-shell populations from donation bonding show qualitatively similar trends in 5f n active-space CAS vs DFT calculations. The influence of spin-orbit coupling on donation bonding is small for the tested systems. Along the actinide series, chemically soft vs chemically harder ligands exhibit clear differences in bonding trends. There are pronounced changes in the 5f populations when moving from Pu to Am or Cm, which correlate with previously noted "breaks" in chemical trends. Bonding involving 5f becomes very weak beyond Cm/Bk. We propose that Cm(III) is a borderline case among the trivalent actinides that can be meaningfully considered to be involved in ground-state 5f covalent bonding.

Continuous Shape Measures Study of the Coordination Spheres of Actinide Complexes – Part 1: Low Coordination Numbers

AbstractStructural analyses of a large set of molecular structures of actinide compounds allow us to establish trends for stereochemical preferences, common distortion paths, geometrical constraints imposed by different ligand topologies, and the existence of incipient bonds or of Van der Waals intramolecular interactions on purportedly vacant coordination sites. In this study the relative abundance of coordination numbers in actinide chemistry appears to be on average higher than that among the lanthanides. The detailed continuous shape measures study of normalized coordination polyhedra with coordination numbers between 1 and 6 presented here is based on more than 1,800 solid state and gas phase structural data sets.

New Complexes of Actinides with Monobromoacetate Ions: Synthesis and Structures.

Synthesis, FTIR spectral study, and X-ray diffraction analysis of single crystals of (CH3)4N[UO2(mba)3] (I), (CH3)4N[NpO2(mba)2(NO3)] (II), (CH3)4N[PuO2(mba)2(NO3)] (III), and (CH3)4N[NpO2(mba)(NO3)2] (IV), where mba is a monobromoacetate ion (CH2BrCOO–), were conducted. The main structural units of crystals I–IV are mononuclear anionic complexes of the [AnO2(mba)3]−, [AnO2(mba)2(NO3)]−, or [AnO2(mba)(NO3)2]− composition. All these complex units are characterized with the same crystal-chemical formula AB013 (A = AnO22+ and B01 = CH2BrCOO– or NO3–). Using the method of molecular Voronoi–Dirichlet polyhedra, the contributions of various types of noncovalent interactions into the formation of supramolecular structures of the obtained complexes were characterized. The analysis of coordination modes of all monobromoacetate-containing compounds from the Cambridge Structural Database was accomplished. Actinide contraction in the studied compounds is discussed.

Structure of the {U13} polyoxo cluster U13O8Cl x (MeO)38-x (x = 2.3, MeO = methoxide).

The structure of a new type of polyoxo cluster complex that contains thirteen uranium atoms, {U13}, is reported. The complex crystallized from methanol containing tetra-valent uranium (UIV) with a basic organic ligand, and was characterized as di-chloridoocta-cosa-μ2-methano-lato-octa-kis-(methano-lato)octa-μ4-oxido-trideca-uranium, [U13(CH3O)35.7Cl2.3O8] or [U13(μ4-Ooxo)8Cl x (MeO)38-x ] (x = 2.3, MeO = methoxide) (I), by single-crystal X-ray diffraction. The characterized {U13} polyoxo cluster complex (I) possesses a single cubic uranium polyhedron at the centre of the cluster core. To the best of our knowledge, this is the very first example of a polyoxo actinide complex that bears a single cubic polyhedron in its structure. The cubic polyhedron in I is well comparable in shape with those in bulk UO2. The U-O bonds in the cubic polyhedron of I are, however, significantly shorter than those not only in bulk UO2 but also in another analogue in the {U38} cluster. This shortening of U-O bonds, together with BVS calculations and the overall negative charge (2-) of I, suggests that the central uranium atom in I, which forms the single cubic coordination polyhedron, is presumably oxidized to the penta-valent state (UV) from the original tetra-valent state (UIV). Complex I is, hence, the first example of a polyoxo cluster possessing a single cubic coordination polyhedron of UV.

Inside Cover Picture

This cover picture describes the synthesis of U(TrenTIPS)OCP and U(TrenTIPS)OCP via introduction of 2‐phosphaethynolate anion into the actinide complexes. The issue of covalency of actinide complexes is still controversial. In this work, computational analyses indicated that the U—O bond has more covalency than of the Th—O bond due to more 5f orbital contribution for U. More details are given in the article by Shi et al. on page 2125—2131.Five new terpenoid dimers were isolated from Resina Commiphora with one compound inhibiting extracellular matrix components dose dependently. More details are discussed in the article by Cheng et al. on page 2172—2180.image

Cover Picture

This cover picture describes the synthesis of U(TrenTIPS)OCP and U(TrenTIPS)OCP via introduction of 2‐phosphaethynolate anion into the actinide complexes. The issue of covalency of actinide complexes is still controversial. In this work, computational analyses indicated that the U—O bond has more covalency than of the Th—O bond due to more 5f orbital contribution for U. More details are given in the article by Shi et al. on page 2125—2131.image

Facile Access to Uranium and Thorium Phosphaethynolate Complexes Supported by Tren: Experimental and Theoretical Study

Main observation and conclusionThe issue of covalence of actinide complexes remains controversial to date. The introduction of 2‐phosphaethynolate anion into actinide complexes is expected to investigate the reaction mode and the bonding property. Herein, we describe the functionalization of An(TrenTIPS)Cl (1: An = U; 2: An = Th) precursors with NaOCP(dioxane)2.5through salt‐elimination method leading to the formation of the corresponding uranium and thorium phosphaethynolate species: [U(TrenTIPS)(OCP)] (3) and [Th(TrenTIPS)(OCP)] (4). These two complexes were fully characterized by nuclear magnetic resonance (NMR), FT‐IR spectrum, UV‐vis‐NIR spectroscopies as well as X‐ray crystal diffraction. Computational analyses of the two complexes reveal that the U—O bond has a more covalent bond property than the Th—O bond due to more 5f orbital contribution for U.

Anomalous magnetism of uranium(IV)-oxo and -imido complexes reveals unusual doubly degenerate electronic ground states

Anomalous magnetism of uranium(IV)-oxo and -imido complexes reveals unusual doubly degenerate electronic ground states

Remodeling of N-Heterocyclic Iminato Ligand Frameworks for the Facile Synthesis of Isoureas from Alcohols and Carbodiimides Promoted by Organoactinide (Th, U) Complexes.

A new class of actinide complexes [(L)An(N{SiMe3}2)3] (An = Th or U) (Th1–Th3 and U1–U3) supported by highly nucleophilic seven-membered N-heterocyclic iminato ligands were synthesized and fully characterized by single-crystal X-ray diffraction. These complexes were successfully exploited as powerful catalysts for the addition of alcohols to carbodiimides to yield the corresponding desirable isourea products at room temperature with short reaction times and excellent yields. Thorough stoichiometric, thermodynamic, and kinetic studies were carried out, allowing us to propose a plausible mechanism for the catalytic reaction.

Theoretical Insights into the Actinide–Silicon Bonding Nature and Stability of a Series of Actinide Complexes with Different Oxidation States

Theoretical Insights into the Actinide–Silicon Bonding Nature and Stability of a Series of Actinide Complexes with Different Oxidation States

Complexation of Lanthanides and Heavy Actinides with Aqueous Sulfur-Donating Ligands

The separation of trivalent lanthanides and actinides is challenging because of their similar sizes and charge densities. S-donating extractants have shown significant selectivity for trivalent actinides over lanthanides, with single-stage americium/lanthanide separation efficiencies for some thiol-based extractants reported at >99.999%. While such separations could transform the nuclear waste management landscape, these systems are often limited by the hydrolytic and radiolytic stability of the extractant. Progress away from thiol-based systems is limited by the poorly understood and complex interactions of these extractants in organic phases, where molecular aggregation and micelle formation obfuscates assessment of the metal-extractant coordination environment. Because S-donating thioethers are generally more resistant to hydrolysis and oxidation and the aqueous phase coordination chemistry is anticipated to lack complications brought on by micelle formation, we have considered three thioethers, 2,2'-thiodiacetic acid (TDA), (2R,5S)-tetrahydrothiophene-2,5-dicarboxylic acid, and 2,5-thiophenedicarboxylic acid (TPA), as possible trivalent actinide selective reagents. Formation constants, extended X-ray absorption fine structure spectroscopy, and computational studies were completed for thioether complexes with a variety of trivalent lanthanides and actinides including Nd, Eu, Tb, Am, Cm, Bk, and Cf. TPA was found to have moderately higher selectivity for the actinides because of its ability to bind actinides in a different manner than lanthanides, but the utility of TPA is limited by poor water solubility and high rigidity. While significant competition with water for the metal center limits the efficacy of aqueous-based thioethers for separations, the characterization of these solution-phase, S-containing lanthanide and actinide complexes is the most comprehensively available in the literature to date. This is due to the breadth of lanthanides and actinides considered as well as the techniques deployed and serves as a platform for the further development of S-containing reagents for actinide separations. Additionally, this paper reports on the first bond lengths for Cf and Bk with a neutral S donor.

Relativistic DFT Probe for Reaction Energies and Electronic/Bonding Properties of Polypyrrolic Hetero-Bimetallic Actinide Complexes: Effects of Uranyl endo-Oxo Functionalization.

A series of hetero-bimetallic actinide complexes of the Schiff-base polypyrrolic macrocycle (L), featuring cation-cation interactions (CCIs), were systematically investigated using relativistic density functional theory (DFT). The tetrahydrofuran (THF) solvated complex [(THF)(OUVIOUIV)(THF)(L)]2+ has high reaction free energy (ΔrG), and its replacement with electron-donating iodine promotes the reaction thermodynamics to obtain uranyl iodide [(I)(OUVIOUIV)(I)(L)]2+ (UVI-UIV). Retaining this coordination geometry, calculations have been extended to other An(IV) (An = Th, Pa, Np, Pu), i.e., for the substitution of U(IV) to obtain UVI-AnIV. As a consequence, the reaction free energy is appreciably lowered, suggesting the thermodynamic feasibility for the experimental synthesis of these bimetallic complexes. Among all UVI-AnIV, the electron-spin density and high-lying occupied orbitals of UVI-PaIV show a large extent of electron transfer from electron-rich Pa(IV) to electron-deficient U(VI), leading to a more stable UV-PaV oxidation state. Additionally, the shortest bond distance and the comparatively negative Eint of the Pa-Oendo bond suggest more positive and negative charges (Q) of Pa and endo-oxo atoms, respectively. As a result of the enhanced Pa-Oendo bond and strong CCI in UVI-PaIV along with the corresponding lowest reaction free energy among all of the optimized complexes, uranyl species is a better candidate for the experimental synthesis in the ultimate context of environmental remediation.