Towards tailoring hydrophobic interaction with uranyl(VI) oxygen for C-H activation.

Bovine serum albumin (BSA) has a uranyl(VI) binding hotspot where uranium is tightly bound by three carboxylates. Uranyl oxygen is "soaked" into the hydrophobic core of BSA. Isopropyl hydrogen of Val is trapped near UO22+ and upon photoexcitation, C-H bond cleavage is initiated. A unique hydrophobic contact with "yl"-oxygen, as observed here, can be used to induce C-H activation.

Fate of Oxidation States at Actinide Centers in Redox-Active Ligand Systems Governed by Energy Levels of 5 f Orbitals.

We report the formation of a NpIV complex from the complexation of NpVI O2 2+ with the redox-active ligand tBu-pdiop2- =2,6-bis[N-(3,5-di-tert-butyl-2-hydroxyphenyl)iminomethyl]pyridine. To the best of our knowledge, this is the first example of the direct complexation-induced chemical reduction of NpVI O2 2+ to NpIV . In contrast, the complexation of UVI O2 2+ with tBu-pdiop2- did not induce the reduction of UVI O2 2+ , not even after the two-electron electrochemical reduction of [UVI O2 (tBu-pdiop)]. This contrast between the Np and U systems may be ascribed to the decrease of the energy of the 5 f orbitals in Np compared to those in U. The present findings indicate that the redox chemistry between UVI O2 2+ and NpVI O2 2+ should be clearly differentiated in redox-active ligand systems.

Solid-State Schikorr Reaction from Ferrous Chloride to Magnetite with Hydrogen Evolution as the Kinetic Bottleneck.

The selective formation of meta-stable Fe3O4 from ferrous sources by suppressing its oxidative conversion to the most stable hematite (α-Fe2O3) is challenging under oxidative conditions for solid-state synthesis. In this work, we investigated the conversion of iron(II) chloride (FeCl2) to magnetite (Fe3O4) under inert atmosphere in the presence of steam, and the obtained oxides were analyzed by atomic-resolution TEM, 57Fe Mössbauer spectroscopy, and the Verwey transition temperature (Tv). The reaction proceeded in two steps, with H2O as the oxide source in the initial step and as an oxidant in the second step. The initial hydrolysis occurred at temperatures higher than 120 °C to release gaseous HCl, via substituting lattice chloride Cl- with oxide O2-, to give iron oxide intermediates. In the first step, the construction of the intermediate oxides was not topotactic. The second step as a kinetic bottleneck occurred at temperatures higher than 350 °C to generate gaseous H2 through the oxidation of FeII by H+. A substantially large kinetic isotope effect (KIE) was observed for the second step at 500 °C, and this indicates the rate-determining step is the hydrogen evolution. Quantitative analysis of evolved H2 revealed that full conversion of ferrous chloride to magnetite at 500 °C was followed by additional oxidation of the outer sphere of magnetite to give a Fe2O3 phase, as supported by X-ray photoelectron spectroscopy (XPS), and the outer phase confined the conductive magnetite phase within the insulating layers, enabling kinetic control of magnetite synthesis. As such, the reaction stopped at meta-stable magnetite with an excellent saturation magnetization (σs) of 86 emu g-1 and Tv > 120 K without affording the thermodynamically stable α-Fe2O3 as the major final product. The study also discusses the influence of parameters such as reaction temperature, initial grain size of FeCl2, the extent of hydration, and partial pressure of H2O.

How does chemistry contribute to circular economy in nuclear energy systems to make them more sustainable and ecological?

While one should be aware that its zero CO2 emission is actually achievable only when electric power is generated, nuclear power is one of the most viable and proven "carbon-free" energy sources to provide baseload electricity to the current energy-demanding society. Even after the power generation, the major part of spent nuclear fuels still consists of recyclable nuclear fuel materials such as U and Pu, promising circular economy of nuclear energy systems in principle. However, actual situations are not very simple due to the following issues: (1) resource security of nuclear fuel materials, (2) issues of depleted uranium, and (3) treatment and disposal of high-level radioactive wastes. In this Perspective, I discussed how chemistry can contribute to resolving these problems and what task academic research in fundamental chemistry should take on there.

Crystal Structures of Ce(IV) Nitrates with Bis(2-pyrrolidone) Linker Molecules Deposited from Aqueous Solutions with Different HNO3 Concentrations.

We investigated the molecular and crystal structures of Ce(IV) compounds deposited under different [HNO3] with bis(2-pyrrolidone) linker molecules having a trans-1,4-cyclohexyl bridging moiety (L). As a result, we found that, after loading L, Ce(IV) in HNO3(aq) exclusively provides one of different crystalline phases, (HL)2[Ce(NO3)6] or [Ce2(µ-O)-(NO3)6(L)2]n 2D MOF, depending on [HNO3]. The former has been obtained at [HNO3] = 4.70-9.00 M and is isomorphous with the analogous (HL)2[An(NO3)6] we reported previously. In contrast, the deposition of the latter phase at the lower [HNO3] conditions (1.00-4.30 M) demonstrates that hydrolysis and oxolation of Ce4+ proceed even below pH 0 to provide a [Ce-O-Ce]6+ unit included in this compound. These different Ce(IV) phases are exchangeable with each other under soaking in HNO3(aq), implying that chemical equilibria of dissolution/deposition of these crystalline phases and hydrolysis and oxolation of Ce4+ and its complexation with NO3- occur in parallel. Indeed, such coordination chemistry of Ce(IV) in HNO3(aq) was well corroborated by 17O NMR, Raman, and IR spectroscopy.

Non-aqueous bonding of leuprorelin to ochratoxin A for peptide-based solid-phase extraction.

The anticancer therapeutic leuprorelin was found to have excellent affinity to the carcinogen ochratoxin A (OTA), with an equilibrium constant of 2.2 × 108 M-1 at 273 K (dissociation constant Kd = 4.5 nM) when functionalized into a mesoporous polymer. Binding between the surface-bound leuprorelin and mycotoxin was corroborated with DFT calculations, and it was extended to the extraction of OTA from the heavily fatty matrices of coffee, achieving 95% recovery with improved cyclability as compared with immunoaffinity. This work presents the potential of peptide-mycotoxin interactions for durable non-aqueous extraction.

Effects of coordinating heteroatoms on molecular structure, thermodynamic stability and redox behavior of uranyl(vi) complexes with pentadentate Schiff-base ligands.

Uranyl(vi) complexes with pentadentate N3O2-, N2O3- and N2O2S1-donating Schiff base ligands, tBu,MeO-saldien-X2- (X = NH, O and S), were synthesized and thoroughly characterized by 1H NMR, IR, elemental analysis, and single crystal X-ray diffraction. The crystal structures of UO2(tBu,MeO-saldien-X) showed that the U-X bond strength follows U-O ≈ U-NH > U-S. Conditional stability constants (ß X) of UO2(tBu,MeO-saldien-X) in ethanol were investigated to understand the effect of X on thermodynamic stability. The log ß X decrease in the order of UO2(tBu,MeO-saldien-NH) (log ß NH = 10) > UO2(tBu,MeO-saldien-O) (log ß O = 7.24) > UO2(tBu,MeO-saldien-S) (log ß S = 5.2). This trend cannot be explained only by Pearson's Hard and Soft Acids and Bases (HSAB) principle, but rather follows the order of basicity of X. Theoretical calculations of UO2(tBu,MeO-saldien-X) suggested that the ionic character of U-X bonds decreases in the order of U-NH > U-O > U-S, while the covalency increases in the order U-O < U-NH < U-S. Redox potentials of all UO2(tBu,MeO-saldien-X) in DMSO were similar to each other regardless of the difference in X. Spectroelectrochemical measurements and DFT calculations revealed that the center U6+ of each UO2(tBu,MeO-saldien-X) undergoes one-electron reduction to afford the corresponding uranyl(v) complex. Consequently, the difference in X of UO2(tBu,MeO-saldien-X) affects the coordination of tBu,MeO-saldien-X2- with UO2 2+. However, the HSAB principle is not always prominent, but the Lewis basicity and balance between ionic and covalent characters of the U-X interactions are more relevant to determine the bond strengths.

Synthesis and characterization of a uranyl(VI) complex with 2,6-pyridine-bis(methylaminophenolato) and its ligand-centred aerobic oxidation mechanism to a diimino derivative.

A uranyl(VI) complex with 2,6-bis(3,5-di-tert-butyl-o-phenolateaminomethyl)pyridine (UO2(tBu-pdaop), 1) was synthesized and thoroughly characterized by 1H NMR, IR, elemental analysis, and single-crystal XRD. Right after the dissolution of complex 1 in pyridine or DMSO, the solution was pale red, whereas it gradually turned to dark purple under an ambient atmosphere. 1H NMR spectra at the initial and final states suggested that both of the two aminomethyl groups in 1 were converted to azomethine ones through aerobic oxidation. Indeed, a uranyl(VI) complex with 2,6-bis(3,5-di-tert-butyl-o-phenolateiminomethyl)pyridine (UO2(tBu-pdiop), 2) was obtained from the concentrated solution once the reaction was completed, and was characterized by IR, and single-crystal XRD. Kinetic analyses as well as mechanistic studies based on quantum chemical calculations suggested that hydrogen atom transfer from one of the amino groups in complex 1 to nearby O2 initiates the stepwise oxidation processes to finally afford 2. The present findings demonstrate the novel reactivity of a uranyl(VI) complex, and provide new insights to construct thermally-driven molecular conversion systems by a UO22+ complex catalyst.

Fully Chelating N3O2-Pentadentate Planar Ligands Designed for the Strongest and Selective Capture of Uranium from Seawater.

Based on the unique fivefold equatorial coordination of UO22+, water-compatible pentadentate planar ligands, H2saldian and its derivatives, were designed for the strong and selective capture of UO22+ in seawater. In the simulated seawater condition (0.5 M NaCl + 2.3 mM HCO3-/CO32-, pH 8), saldian2- shows the strongest complexation with UO22+ to form UO2(saldian) (log ß11 = 28.05 ± 0.07), which is more than 10 order of magnitude greater than amidoxime-based or -inspired ligand systems most commonly employed for U capture from seawater. Good selectivity for UO22+ from other metal ions coexisting in seawater was also demonstrated.

Hydrophobic core formation and secondary structure elements in uranyl(VI)-binding peptides.

Cyclic peptides as well as a modified EF-hand motif of calmodulin have been newly designed to achieve high affinity towards uranyl(VI). Cyclic peptides may be engineered to bind uranyl(VI) to its backbone under acidic conditions, which may enhance its selectivity. For the modified EF-hand motif of calmodulin, strong electrostatic interactions between uranyl(VI) and negatively charged side chains play an important role in achieving high affinity; however, it is also essential to have a secondary structure element and formation of hydrophobic cores in the metal-bound state of the peptide.

Complexation-Distribution Separated Solvent Extraction Process Designed for Rapid and Efficient Recovery of Inert Platinum Group Metals.

Previously, we have demonstrated that thermal-assisted techniques can accelerate the extraction of inert platinum group metals (PGMs), while they still have several concerns about difficulty of temperature control in actual extraction contactors and safety risks arising from heating organic solvents. In this study, we report a complexation-distribution separated extraction process for the accelerated extraction of inert PGMs. This extraction method includes two steps: (1) complexation of PGMs with extractants in aqueous solution and (2) distribution of the formed complex from the aqueous phase to organic one. We separately investigated the complexation and distribution processes for typical inert PGMs such as Ru(III) and Rh(III) in the presence of water-soluble N,N,N',N'-tetra-alkylpyridinediamide ligands (PDA) and bis(trifluoromethylsulfonyl)amide (Tf2N-) counteranions. As a result, the water-soluble complexes of Ru(III) and Rh(III) with PDA can be formed in 0.5 M HNO3(aq) within 3 h under heating at 356 K. The formed complexes were extracted to the 1-octanol layer containing Tf2N- within 5 min at room temperature, where this hydrophobic anion plays an important role to promote extraction of PGMs as an anionic phase-transfer catalyst (PTC). Consequently, we successfully established and demonstrated the complexation-distribution separated extraction process for the accelerated extraction of inert PGMs using a water-soluble ligand and anionic PTC.

Effects of Substituents on the Molecular Structure and Redox Behavior of Uranyl(V/VI) Complexes with N3O2-Donating Schiff Base Ligands.

Uranyl(VI) complexes with pentadentate N3O2-donating Schiff base ligands having various substituents at the ortho (R1) and/or para (R2) positions on phenolate moieties, R1,R2-Mesaldien2-, were synthesized and thoroughly characterized by 1H nuclear magnetic resonance, infrared, elemental analysis, and single-crystal X-ray diffraction. Molecular structures of UO2(R1,R2-Mesaldien) are more or less affected by the electron-donating or -withdrawing nature of the substituents. The redox behavior of all UO2(R1,R2-Mesaldien) complexes was investigated to understand how substituents introduced onto the ligand affect the redox behavior of these uranyl(VI) complexes. As a result, the redox potentials of UO2(R1,R2-Mesaldien) in dimethyl sulfoxide increased from -1.590 to -1.213 V with an increase in the electron-withdrawing nature of the substituents at the R1 and R2 positions. The spectroelectrochemical measurements and theoretical calculation [density functional theory (DFT) and time-dependent DFT calculations] revealed that the center U6+ of each UO2(R1,R2-Mesaldien) complex undergoes one-electron reduction to afford the corresponding uranyl(V) complex, [UO2(R1,R2-Mesaldien)]-, regardless of the difference in the substituents. Consequently, the redox active center of uranyl(VI) complexes seems not to be governed by the redox potentials but to be determined by whether the LUMO is centered on a U 5f orbital or on one π* orbital of a surrounding ligand.

Crystallization of colourless hexanitratoneptunate(iv) with anhydrous H+ countercations trapped in a hydrogen bonded polymer with diamide linkers.

Colourless crystalline compounds of centrosymmetric [Np(NO3)6]2- were yielded from 3 M HNO3 aq in the presence of double-headed 2-pyrrolidone derivatives (L). In the obtained crystal structures, H+ was also involved as a countercation to compensate for the negative charge of [Np(NO3)6]2-, where the initial hydration around H+ was fully removed during crystallization despite it having the strongest hydration enthalpy. Instead, this anhydrous H+ was captured by L to form a [H+⋯L] n hydrogen bonded polymer. In [Np(NO3)6]2-, the Np4+ centre is twelve-coordinated with 6 bidentate NO3 -, and therefore, present in an icosahedral geometry bearing inversion centre. In such a centrosymmetric system, any f-f transitions stemming from the 5f3 electronic configuration of Np4+ are electric-dipole forbidden. This is the reason why the compounds currently obtained were colourless unlike ordinary Np(iv) species, which are olive-green.

Wet chemical processing for nuclear waste glass to retrieve radionuclides.

Here, we show unexpected and significant elution behavior of various elements from simulated nuclear waste glass (NWG) in ∼10° mol dm-3 acidic solutions below 100 °C, where a borosilicate-based glass matrix has been believed to be chemically durable. Most elements like glass main components (Li, B, Na, Ca, Al, and Zn, but except for Si) and simulated radionuclides (Rb, Cs, Sr, Ba, Se, Te, Mn, Pd, Mo, rare earths, Cr, Fe, and Ni) were remarkably eluted from the simulated NWG in ∼10° M HNO3 aq with Cl- at 90 °C. Especially, the elution of Pd is governed by its coordination chemistry including a redox reaction, because Pd(0) present in the simulated NWG has to be oxidized to Pd2+ which forms [PdCl4]2- for its dissolution. While Zr in simulated NWG is sparingly eluted even in this treatment, its elution actually proceeds in 1-3 M H2SO4 aq at 90 °C thanks to strong coordination of Zr(IV) with SO42-. Through design and optimization of the leaching conditions, a protocol of the wet chemical process to retrieve the radionuclides from simulated NWG has been proposed and demonstrated.

Crystal Structure of Regularly Th -Symmetric [U(NO3 )6 ]2- Salts with Hydrogen Bond Polymers of Diamide Building Blocks.

Hexanitratouranate(IV), [U(NO3 )6 ]2- , has been crystallized with anhydrous H+ -involving hydrogen bond polymers connected by selected diamide building blocks. Thanks to the significant moderation of electrostatic interactions between the anions and cations, the molecular structure of [U(NO3 )6 ]2- in these compounds is regularly Th -symmetric. The f-f transitions stemming from 5f2 configuration of U4+ are strictly forbidden by the Laporte selection rule in such a centrosymmetric system, so that the obtained compounds are nearly colourless in contrast to other UIV species usually coloured in green.

Controlling the lability of uranyl(vi) through intramolecular π-π stacking.

A reaction of UO22+ with cyclohexyldiphenylphosphine oxide (OPCyPh2) in ethanol resulted in a perchlorate salt of the 4-fold homoleptic complex, [UO2(OPCyPh2)4](ClO4)2·EtOH. X-ray structure determination revealed that [UO2(OPCyPh2)4]2+ shows a highly symmetric molecular structure supported by the intramolecular π-π stacking interactions between the phenyl groups of the neighbouring OPCyPh2 in the equatorial plane of UO22+. To clarify whether the reactivity of UO22+ is affected by such a unique coordination structure, the ligand exchange kinetics of [UO2(OPCyPh2)4]2+ in non-coordinating solvents has been studied using an NMR line-broadening method. In CD2Cl2 and CD3NO2 solutions, both signals of coordinated and free OPCyPh2 appeared distinctively even at 298 K, while 2D EXSY experiment provided evidence that a chemical exchange between [UO2(OPCyPh2)4]2+ and free OPCyPh2 occurs in these systems. Thus, this ligand exchange reaction is quite slow on the NMR time-scale. The dependency of the apparent first-order rate constant (kobs) on temperature and the free OPCyPh2 concentration suggested that this ligand exchange reaction involves associative and dissociative mechanisms both governed by large negative ΔS‡ terms predominantly. Compared with the kinetic data of ligand exchange reactions of other UO22+ complexes reported so far, the lability of UO22+ in [UO2(OPCyPh2)4]2+ is found to be significantly suppressed due to the intramolecular π-π stacking interactions as observed in the crystal structure. The DFT calculations successfully reproduced the intramolecular π-π stacking in [UO2(OPCyPh2)4]2+ by considering the empirical dispersion corrections, and provided theoretical rationales to the A and D mechanisms of the ligand exchange reaction of [UO2(OPCyPh2)4]2+.

The oxidation of borohydrides by photoexcited [UO2(CO3)3]4- .

The carbonate ion is an effective quencher of uranyl(vi) luminescence and makes uranyl(vi) tricarbonate barely luminescent and photochemically inactive. We demonstrate here that photoexcited uranyl(vi) tricarbonate, *[UVIO2(CO3)3]4-, can however oxidize borohydrides (BH3X-, X = H, CN) to give boric acid and H2 gas, reducing itself to [UVO2(CO3)3]5-. This hypothesis was supported by UV-vis and NMR spectroscopy as well as quantum chemical calculations. The charge transfer states associated with photoreduction processes were modelled by density functional theory calculations. These results suggest that the mechanism of photoreduction of [UVIO2(CO3)3]4- is similar to that of [UVIO2(H2O)5]2+ and that it occurs through a one-photon reduction process.

Molecular and Crystal Structures of Uranyl Nitrate Coordination Polymers with Double-Headed 2-Pyrrolidone Derivatives.

Double-headed 2-pyrrolidone derivatives (DHNRPs) were designed and synthesized as bridging ligands for the efficient and selective separation of UO22+ from a HNO3 solution by precipitation. The building blocks, UO2(NO3)2 and DHNRPs, were successfully connected to form an infinite 1D coordination polymer. The solubility of [UO2(NO3)2(DHNRP)]n is no longer correlated to the hydrophobicity of the ligand but is exclusively governed by the ligand symmetry and packing efficiency. The newly designed DHNRP family can be used to establish a new spent nuclear fuel reprocessing scheme.

An aqueous electrolyte of the widest potential window and its superior capability for capacitors.

A saturated aqueous solution of sodium perchlorate (SSPAS) was found to be electrochemically superior, because the potential window is remarkably wide to be approximately 3.2 V in terms of a cyclic voltammetry. Such a wide potential window has never been reported in any aqueous solutions, and this finding would be of historical significance for aqueous electrolyte to overcome its weak point that the potential window is narrow. In proof of this fact, the capability of SSPAS was examined for the electrolyte of capacitors. Galvanostatic charge-discharge measurements showed that a graphite-based capacitor containing SSPAS as an electrolyte was stable within 5% deviation for the 10,000 times repetition at the operating voltage of 3.2 V without generating any gas. The SSPAS worked also as a functional electrolyte in the presence of an activated carbon and metal oxides in order to increase an energy density. Indeed, in an asymmetric capacitor containing MnO2 and Fe3O4 mixtures in the positive and negative electrodes, respectively, the energy density enlarged to be 36.3 Whkg-1, which belongs to the largest value in capacitors. Similar electrochemical behaviour was also confirmed in saturated aqueous solutions of other alkali and alkaline earth metal perchlorate salts.

Emission properties and Cu(i)-Cu(i) interaction in 2-coordinate dicopper(i)-bis(N-heterocyclic)carbene complexes.

The synthesis, characterization, and emission properties of 2-coordinate dicopper(i) complexes bearing two trimethylene-bridged bis-NHC ligands, [Cu2(L3Me)2](PF6)2 (1), [Cu2(L3Et)2](PF6)2 (2), [Cu2(L3Bu)2](PF6)2 (3), [Cu2(L3MeOPh)2](PF6)2 (4) and [Cu2(L3Mes)2](PF6)2 (5), where L3R denotes trimethylene-bridged bis(N-heterocyclic)carbene (NHC) ligand substituted by two R groups at the nitrogen atoms of NHC, have been investigated. The quantum yield, Φ, and the lifetime, τ, of the emission of 2, are 0.21 and 25 µs, respectively in methanol, which is a well-known solvent for quenching the luminescence of many copper(i) complexes. The 8-shaped geometry of the dicopper(i) complexes brings a considerable copper(i)-copper(i) interaction which affects the luminescent properties. Additionally, we find that methoxyphenyl and mesityl groups substituted at the nitrogen atom of the NHC moiety drastically stabilize the bis(NHC) copper(i) complexes even in air-saturated acetone-d6.