Peroxide Clusters Research Articles

Flame Front Model with the Clusters Condensation

The processes model in a flame during the n-alkanes air mixture combustion initiation is proposed, taking into account the supramolecular structures formation possibility in the peroxide clusters form. This approach is justified by the n-alkanes melting temperatures correlation with their autoignition temperatures and anti-knock indexes. The condensation possibility is provided for such high molecular structures. Boiling temperatures values at flame front pressures characteristic were evaluated. To predict the peroxide clusters melting temperatures, a formula developed earlier for the hydrocarbons condensed state was used, which takes into account the length and molecular weight of modeled clusters. Expected peroxide clusters melting temperatures were predicted for conditions of dimeric and tetrameric structures. A linear dependence was used to recalculation the obtained values in boiling temperatures. It is shown that the calculated clusters phase transitions characteristic temperatures can be realized in the flame front preparatory zone. Based on the condensation theory, the flame front thickness and the minimum non-extinguishing sphere radius during ignition were estimated: the obtained data closely coincide with these parameters known values.

Formation of Uranyl Peroxide Compounds via Dissolution of Studtite, [(UO2)(O2)(H2O)2](H2O)2, in Ionic Liquids.

Four uranyl peroxide compounds with novel structures were formed following the dissolution of studtite, [(UO2)(O2)(H2O)2](H2O)2, in imidazolium-based ionic liquids. The compounds were characterized using single crystal X-ray diffraction (SCXRD), powder X-ray diffraction (PXRD), Raman and infrared (IR) spectroscopy, and scanning electron microscopy (SEM) with energy-dispersive X-ray spectroscopy (EDS). The ionic liquids used in the experiments were 1-ethyl-3-methylimidazolium (EMIm) diethyl phosphate, EMIm ethyl sulfate, and EMIm acetate. Each of the four uranyl peroxide compounds contain components from the ionic liquids as terminal ligands on uranyl peroxide molecular units, bridging ligands in uranyl peroxide sheet structures, or charge balancing cations located in the interstitial space. The studtite dissolved in and reacted with the ionic liquids, producing unique crystal structures depending on the anionic component of the ionic liquid, the temperature at which the synthesis was performed, and the introduction of additional ionic species into the solution. This is the first report of studtite dissolving in and reacting with ionic liquids to form uranyl peroxide compounds, which has the potential to vastly increase the number of synthetic routes for the formation of uranyl peroxide clusters and uranyl peroxide cage clusters.

Theoretical studies the structure and properties of bicyclic and tricyclic hydrogen peroxide clusters (H2O2)n, n = 8–21: MP2 and DFT calculations

DFT calculations of bicyclic and tricyclic hydrogen peroxide (HP) clusters Pn up to n = 21 in the gas phase have been performed for the first time. Three main types of coupling of two or more ring clusters P4-P7 (tetramer, pentamer, hexamer, heptamer) into a cyclic structure have been studied. The first, type A, involves the reorientation of hydrogen bonds and a change in the chirality of several HP molecules. The second, type B, consists in the formation of bridges between two HP molecules without changing the chirality. The third way in which two clusters can be connected is by forming nested structures in which the smaller cluster is inside the larger one. Thermodynamic parameters of the coupling of P4-P7 clusters with the formation of cyclic structures have been calculated. In the gas phase, heterochiral structures of type A are lower in energy than homochiral structures of type B with the same number of HP molecules. In low energy clusters, the largest number of hydrogen bonds (2n) is more favourable.

Electrochemical/computational analysis and the derivation of Pourbaix diagrams of redox-active structural and adsorbed species in uranyl peroxide clusters (U60)

Electrochemical analysis of U60 nanoclusters (Li40K20[UO2(O2)(OH)]60(H2O)214) and their natural analog, the mineral studtite (UO2)O2(H2O)2·(H2O)2, was carried out using cyclic voltammetry with a powder microelectrode setup. Voltammetric analysis was supplemented by ab initio quantum mechanical modeling to understand the mechanism, thermodynamics, and structural changes during redox transition (with a semi-quantitative kinetics evaluation). This research aims to better understand the redox behavior and transport of dissolved and structural (incorporated) uranyl units in the environment. Further analysis is performed to determine if redox switching of actinyl ions in clusters can be performed while leaving the cluster intact or at what redox transition it disintegrates. Quantum-mechanical calculations were applied to approximate electrochemical peak potential shifts and add them to standard reduction potentials to more accurately assign peaks to specific redox transitions between different species. These peak potentials are calculated from oxidation state-dependent binding energies between different uranyl species either within or adsorbed to U60. This theoretical approach incorporates extensive error cancellation and serves to predict electrochemical redox potentials and identify the reaction taking place. Voltammograms of U60 in electrolyte solutions exhibit kinetically-inhibited coupled redox peaks assigned to the U(VI)/U(V) transition of cluster structural uranyl units at −0.34 V (vs. standard hydrogen electrode), indicative of U60 reduction from UO22+ to UO2+. The U(V)/U(IV) transition at −0.71 V is assigned to the subsequent U60 reduction of UO2+ to UO20. A method of observing these transitions in situ using synchrotron x-ray absorption spectroscopy was explored. Voltammetry, modeling, and peak analysis indicate a kinetically-inhibited two-step, one-e- (per step) reduction of U60 from U(VI) to U(V) to U(IV). Voltammetry and x-ray absorption spectroscopy measurements performed before and after exhaustive cycling and the highly stable nature of U60 provide evidence that clusters typically do not break apart upon reduction. Voltammograms of U60 collected in varied uranyl solutions are indicative of UO22+ adsorption to the cluster surface and its subsequent reduction at +0.24 V (U(VI)/U(V)) and −0.05 V (U(V)/U(IV)). For uranyl solutions in electrolyte, the two-step, one-e- (per step) reduction of U60 is superseded by uranyl adsorption from solution to the electrode surface with subsequent reduction via U(V) disproportionation. This study represents the sole electrochemical investigation of U60 in the literature and only the second of any uranyl peroxide nanocluster. It is also one of the first to use quantum–mechanical approaches in combination with existing solution-based standard reduction potentials to calculate Pourbaix (EH-pH) diagrams for adsorbed and structural species.

Novel peroxosolvates of quinolone antibiotics containing large hydrogen peroxide clusters

Novel class of multicomponent quinolone antibiotics,crystalline hydrogen peroxide adducts of nalidixic acid C12H12N2O3 · H2O2 and ciprofloxacin C17H18F1N3O3 · 5 H2O2, were prepared from highly concentrated hydrogen peroxide, and their structures were determined by X-ray crystallography. The second compound contains decameric H-bonded hydrogen peroxide clusters, which makes this substance one of the richest in hydrogen peroxide among organic peroxosolvates.

A Cationic Octanuclear Zirconium Peroxide Ring with Unusual Thermal Stability.

Studies about the reaction of ZrIV ions with peroxides and the properties of the resulting zirconium peroxide clusters are significant for understanding zirconium chemistry in the nuclear fuel cycle and the advancement of less explored Group IV metal oxo clusters. Herein, an octanuclear zirconium peroxide cluster, designated as Zr8, was synthesized and characterized by using multiple techniques. Crystallographic analysis revealed that Zr8 has a ringlike structure and unusual positive charges, while tetravalent metal oxo clusters are mostly neutral. In situ variable-temperature Raman spectra indicated that Zr8 has unexpected thermal stability, which may be related to the strong interaction between ZrIV ions and peroxide groups. Small-angle X-ray scattering data showed that Zr8 self-assembled in the reactant solution prior to crystallization. In short, Zr8 expands the limited family of zirconium peroxide clusters and enriches the properties of metal peroxides.

Enhanced Hydrogen Bonds of the (H2O)n (n = 4-8) Clusters Confined in Uranyl Peroxide Cluster Na20(UO2)20(O2)30.

Water is a basic resource and an essential component of living organisms. It often exhibits some novel properties under confinement. The water clusters (H2O)n (n = 4-8) confined in the cavity of uranyl peroxide cluster Na20(UO2)20(O2)30 (U20) have been computationally investigated by using ab initio molecular dynamics (AIMD) simulations and density functional theory (DFT) calculations in this study. The results show that the confined water clusters can form hydrogen bonds with the internal oxygen atoms (Ouranyl) of U20, and their conformations changed significantly. The average lengths (2.553-2.645 Å) of hydrogen bonds in confined (H2O)n are shorter than those (2.731-2.841 Å) in the corresponding free water clusters. Moreover, these confined hydrogen bonds show better hydrogen bond patterns according to the quantified indices. The natural bond orbital (NBO) calculations determine that there is electron transferring from the U20 to its interior (H2O)n. It is the main reason for enhancing hydrogen bond interactions among the confined water molecules because their oxygen atoms are more negatively charged and their hydrogen atoms are more positively charged. The quantum theory of atoms in molecules (QTAIM) and interacting quantum atoms (IQA) analyses indicate that the confined hydrogen bonds are more covalent, based on the significant electron density ρ(r) and local energy density H(r) at the bond critical points (BCPs), and the stronger energies of interatomic exchange interactions (Vxc). These findings may help to promote the communication of confined water clusters and enrich the understating of confined hydrogen bonds.

Capture and Stabilization of the Hydroxyl Radical in a Uranyl Peroxide Cluster.

Here we describe the synthesis and characterization of a new uranyl peroxide cluster (UPC), U60 Ox30 *, which captures and stabilizes oxygen-based free radicals for more than one week. These radical species were first detected with a nitroblue tetrazolium colorimetric assay and U60 Ox30 * was characterized by single crystal X-ray diffraction as well as infrared (IR), Raman, UV-Vis-NIR, and electron paramagnetic resonance (EPR) spectroscopies. Identification of the free radicals present in U60 Ox30 * was done via room temperature solid and solution state X-band EPR studies using spin trapping methods. The spin trapping agent 5,5-dimethyl-1-pyrroline N-oxide (DMPO) was definitive for identifying the free radicals in U60 Ox30 *, which are hydroxyl radicals (⋅OH) that are stable for up to ten days that also persist upon addition of the metalloenzymes catalase and superoxide dismutase. Addition of the spin trapping agent α-(4-pyridyl N-oxide)-N-tert-butylnitrone (POBN) further confirmed the radicals were oxygen based, and deuteration experiments showed that the origin of the free radicals was from the decomposition of H2 O2 in water. These results demonstrate that highly oxidizing species such as the ⋅OH radical can be stabilized in UPCs, which alters our understanding of the role of free radicals present in spent nuclear fuel.

Organic Functionalization of Uranyl Peroxide Clusters to Impact Solubility.

Benzene-1,2-diphosphonic acid (Ppb) was introduced into the uranyl peroxide cluster system, resulting in three Ppb-functionalized uranyl peroxide clusters, (UO2)20(O2)20(C6H4P2O6)1040- (U20Ppb10), (UO2)26(O2)33(C6H4P2O6)638- (U26Ppb6), and (UO2)20(O2)24(C6H4P2O6)632- (U20Ppb6). Dissolution experiments were performed for the potassium salts of U20Ppb10 and U26Ppb6, which revealed the capacity of U20Ppb10 to dissolve in the organic solvent dimethyl sulfoxide (DMSO). Unlike U20Ppb10, the K salt of U26Ppb6 did not dissolve in DMSO but was more soluble in water, perhaps due to the lower proportion of Ppb ligands in its structure. In this work, U20Ppb10 and U20Ppb6 formed as potassium salts and both adopt the fullerene topology of previously reported U20. U20 contains 20 uranyl peroxide units and encapsulates 12 Na cations. It is not possible for unfunctionalized U20 to incorporate 12 K cations owing to space constraints, as is the case in the new clusters reported here. Transformation of U20Ppb10 in water over time to produce U24 was observed, possibly owing to its ability to incorporate K cations, which have been associated with the formation of U24.

Generation of localized highly concentrated hydrogen peroxide clusters in water by X-rays

The formation of highly concentrated hydrogen peroxide (H2O2) clusters (localized circumstance) in an aqueous solution during X-ray irradiation was demonstrated. The relationship between H2O2 concentration and hydrogen donor-independent reduction of nitroxyl radicals was examined. The method to measure the distance between the clusters (localized circumstance) was assessed by comparing the simulation and the experimental results. Reaction mixtures containing a nitroxyl redox probe, 4-hydroxyl-2,2,6,6-tetramethylpiperidine-N-oxyl (TEMPOL) and 3-carbamoyl-2,2,5,5-tetramethylpyrrolidine-N-oxyl (CmP) at 0.1 mM were prepared containing several different concentrations (1.0 mM‒9.8 M) of H2O2. The reaction mixture was irradiated by 12000 μW/cm2 UVB for 2 min, and reduction of the electron paramagnetic resonance (EPR) signal of the nitroxyl radicals was measured. An aliquot (2 µL) of 200 mM K3[Fe(CN)6] or FeCl3 solution was added to 200 µL of the reaction mixture, and the time course of the EPR signal of the nitroxyl radicals was measured. To estimate the distance between the H2O2 clusters, a series of nitroxyl radical solutions with several different concentrations (0.06 μM‒2.28 mM) was irradiated with X-rays, and the degree of reduction of nitroxyl radicals in each sample was measured. UVB, K3[Fe(CN)6], or FeCl3-induced EPR signal loss of the nitroxyl radicals was observed with H2O2 concentrations greater than 10 mM or 100 mM, respectively. The EPR signal loss of nitroxyl radicals, TEMPOL or CmP, may occur in highly concentrated H2O2 circumstances after oxidative stimulation. Plotting the X-ray-induced reduction of nitroxyl radicals versus their density revealed the high-concentration H2O2 clusters to be separated by 40‒47 nm. Ionizing irradiation of an aqueous solution creates a localized highly concentrated H2O2 environment.

LiOH Formation from Lithium Peroxide Clusters and the Role of Iodide Additive

Understanding the chemical formation of LiOH at a fundamental level is important for the development of Li-O2 batteries that employ moist oxygen. Previous studies revealed improved features for lit...

Dynamics of Cation-Induced Conformational Changes in Nanometer-Sized Uranyl Peroxide Clusters.

Conformational changes of the pyrophosphate (Pp)-functionalized uranyl peroxide nanocluster [(UO2)24(O2)24(P2O7)12]48- ({U24Pp12}), dissolved as a Li/Na salt, can be induced by the titration of alkali cations into solution. The most symmetric conformer of the molecule has idealized octahedral (Oh) molecular symmetry. One-dimensional 31P NMR experiments provide direct evidence that both K+ and Rb+ ions trigger an Oh-to-D4h conformational change within {U24Pp12}. Variable-temperature 31P NMR experiments conducted on partially titrated {U24Pp12} systems show an effect on the rates; increased activation enthalpy and entropy for the D4h-to-Oh transition is observed in the presence of Rb+ compared to K+. Two-dimensional, exchange spectroscopy 31P NMR revealed that magnetization transfer links chemically unique Pp bridges that are present in the D4h conformation and that this magnetization transfer occurs via a conformational rearrangement mechanism as the bridges interconvert between two symmetries. The interconversion is triggered by the departure and reentry of K (or Rb) cations out of and into the cavity of the cluster. This rearrangement allows Pp bridges to interconvert without the need to break bonds. Cs ions exhibit unique interactions with {U24Pp12} clusters and cause only minor changes in the solution 31P NMR signatures, suggesting that Oh symmetry is conserved. Single-crystal X-ray diffraction measurements reveal that the mixed Li/Na/Cs salt adopts D2h molecular symmetry, implying that while solvated, this cluster is in equilibrium with a more symmetric form. These results highlight the unusually flexible nature of the actinide-based {U24Pp12} and its sensitivity to countercations in solution.

Presence of X-ray Induced High Concentrated Hydrogen Peroxide Clusters

Presence of X-ray Induced High Concentrated Hydrogen Peroxide Clusters

Effects of H2O2 Concentration on Formation of Uranyl Peroxide Species Probed by Dissolution of Uranium Nitride and Uranium Dioxide.

Dissolution of uranium materials in alkaline aqueous conditions containing H2O2 results in uranyl peroxide species in solution, including anionic uranyl peroxide cage clusters. Uranyl peroxide cage clusters are generally highly soluble in water, where they persist as aqueous macroanions. Previous studies indicate that uranyl cluster speciation and dissolution of uranium materials is impacted by the concentration of alkali metal in solution, but in these studies, high concentrations of H2O2 were used. Herein, the role of hydrogen peroxide concentration is examined relative to the dissolution of powdered UN and UO2. Lower initial H2O2 concentrations reduce dissolution of UO2 and UN and tend to produce simple (small) uranyl peroxide species rather the highly soluble uranyl peroxide clusters. H2O2 availability will have implications for uranyl speciation and solubility where spent nuclear fuel is in contact with water and where alkaline peroxide conditions are used in dissolution of nuclear material.

Oxidative decomposition mechanisms of lithium peroxide clusters: an Ab Initio study

Oxidative decomposition of solid lithium peroxide is an important part of the charging process in a Li-O2 battery. In this paper, we investigate oxidative decomposition mechanisms of lithium peroxide clusters as molecular models for solid lithium peroxide using density functional methods to understand charging processes in advanced energy storage systems. Most calculations are done using a (Li2O2)4 cluster with similar results obtained from a larger (Li2O2)16 cluster. Reaction pathways of the clusters involving different sequences of oxidation, oxygen evolution, lithium cation removal, and spin excitation are investigated. The computations suggest that certain oxidative decomposition routes may not have dependence on the oxygen evolution or Li-ion removal kinetics due to the exothermicity of oxygen removal and Li+ removal (by solvent) upon oxidation. The computed charge potentials evaluated using a tetramer model indicates that it is possible to have low overcharge potential provided there exists a good electronic conductivity to facilitate the oxidative decomposition. Finally, oxidation potentials of a series of LixOy clusters are investigated to assess their dependence on stoichiometry and how the local site from which the electrons are being removed affects the charge potentials.

Structural and electronic properties of small lithium peroxide clusters in view of the charge process in Li-O2 batteries.

The Li-O2 battery is an ideal energy storage device due to its highest theoretical energy density; however, its high charge overpotential limits its practical application. Herein, through ab initio calculations, we systematically investigated the structural and electronic properties of small (Li2O2)nm+ (n = 1, m = 0, 1 and n = 2, m = 0, 1, and 2) clusters and calculated the reaction energies of various decomposition reactions. Results show that the (Li2O2)1 monomer has a low spin, whereas the (Li2O2)2 dimer has a high spin. The analysis of bond length, molecular orbitals, and projected density of states reveals that the interaction of O-O is stronger in the cationic cluster than in the neutral one, whereas the interaction of O-Li is weaker in the cationic cluster than in the neutral one; this facilitates the decomposition of cationic lithium peroxide cluster. Furthermore, the calculated reaction energies indicate that the peroxide lithium decomposition preferentially favors two-step reaction over one-step reaction. Finally, the lowest-energy reaction pathway for the decomposition of (Li2O2)2 dimer was predicted to be (Li2O2)2 → Li2O2 → (Li2O2)+ → LiO2 → O2, and the rate-determining step was predicted to be the first step.

In situ Raman spectroscopy of uranyl peroxide nanoscale cage clusters under hydrothermal conditions.

Aqueous solutions containing the nanoscale uranyl peroxide cage clusters U60, [(UO2)(O2)(OH)]6060-, and U60Ox30, [{(UO2)(O2)}60(C2O4)30]60-, were monitored by in situ Raman spectroscopy during stepwise heating to 180 °C. In solutions containing U60, clusters persist to 120 °C, although conversion of U60 to U24, [(UO2)(O2)(OH)]2424-, occurs above 100 °C. U60Ox30 persisted in solutions heated to 150 °C, although partial conversion to smaller uranyl peroxide clusters species was observed beginning at 100 °C. Upon breakdown of the uranyl peroxide cage clusters, uranium precipitated as a compreignacite-like phase, K2[(UO2)3O2(OH)3]2(H2O)7, and metaschoepite, [(UO2)8O2(OH)12](H2O)10. The role of the countercations, oxalate bridge, and solution pH are examined in order to better understand the mobility of these species at elevated temperatures.

Energetic Trends in Monomer Building Blocks for Uranyl Peroxide Clusters.

The uranyl triperoxide anionic monomer is a fundamental building block for uranyl peroxide polyoxometalate capsules. The reaction pathway from the monomer to the capsule can be greatly altered by the counterion: both the reaction rate and the resulting capsule structure. We synthesized and characterized uranyl triperoxides Mg2UO2(O2)3·13H2O (MgUT), Ca2UO2(O2)3·9H2O (CaUT), Sr2UO2(O2)3·9H2O (SrUT), and K4UO2(O2)3·3H2O (KUT) and compared their thermodynamic stabilities. The enthalpies of formation from oxides and elements of these compounds were calculated by thermochemical cycles from measurements by high temperature oxide melt drop solution calorimetry. Their formation enthalpies from oxides become more negative linearly as a function of the increasing basicity of the respective oxides on the Smith scale. This relationship holds for previously Li and Na analogues. Further affirming the trend, Δ Hf,ox of MgUT departs from linearity, due to the distinct bonding environment of Mg2+, as compared to the other alkalis and alkaline earths in the series.

Pyrophosphate and Methylenediphosphonate Incorporated Uranyl Peroxide Cage Clusters

Six uranyl peroxide cage clusters containing 18–54 uranyl ions, as well as 6–27 pyrophosphate or methylenediphosphonate ligands, have been synthesized and characterized. These uranyl peroxide clusters self-assemble and crystallize from aqueous solutions containing uranyl nitrate, hydrogen peroxide, and pyrophosphate or methylenediphosphonate over a pH range from 5.3 to 8.1. In their structures, uranyl hexagonal bipyramids are linked by bridging peroxide, hydroxide, and pyrophosphate or methylenedisphosphonate ligands. The incorporation of pyrophosphate or methylenedisphosphonate results in several interesting features in the coordination of uranyl ions and the topology of the uranyl peroxide clusters.

Charge Density Influence on Enthalpy of Formation of Uranyl Peroxide Cage Cluster Salts.

More than 60 unique uranyl peroxide cage clusters have been reported that contain as many as 124 uranyl ions and that have overall diameters extending to 4 nm. They self-assemble in water under ambient conditions, are models for understanding structure-size-property relations as well as testing computational models for actinides, and have potential applications in nuclear fuel cycles. High-temperature drop solution calorimetry has been used to derive the enthalpies of formation of the salts of seven topologically diverse uranyl peroxide cage clusters containing from 22 to 28 uranyl ions that are bridged by various combinations of peroxide, pyrophosphate, and phosphite. The enthalpies of formation of these seven salts, as well as three salts of other uranyl peroxide clusters reported earlier, are dominated by the interactions of the alkali countercations with the clusters. There is an approximately linear relationship between the enthalpies of formation of the cluster salts and the charge density of the corresponding uranyl peroxide cluster, wherein salts containing clusters with higher charge densities have more negative enthalpies of formation.