Influence of the organic cation on the formation of hexahalotechnetates: X-ray, thermal and comparative analyses of non-covalent interactions.

In this work, we have reviewed non-covalent interactions in technetium hexahalide compounds and obtained eight new compounds of the CatnTcHal6 type, where Cat = dimethylammonium, tetramethylammonium, caffeinium, benzothiazolium, nicotinamidium, and pyrazolium, and Hal = Cl, Br. SCXRD studies were carried out for new compounds. In some compounds, halide anions and/or crystallization water were present. In the compounds obtained, an essential influence on the formation of structures and crystal packing is exerted by the molecules of crystallization water and halide ions. Diethylammonium and nicotinamidium compounds, whose structures do not contain other ions and contain sufficiently strong non-covalent interactions, best bind hexahalotechnetates. π-Stacking interactions, anion-π interactions, and halogen bonds were found in the structures. The percentage contribution of the H⋯Hal/Hal⋯H interactions in the transition from fluorine to bromine in TcHal62- anions decreases, while the contribution of interactions of other types increases. The greatest variety of interactions in anions is observed for compounds of caffeinium and nicotinamidium with TcBr62-. The paper considers the processes of thermolysis of some new and previously known CatnTcHal6 compounds with various cations. It is shown that the thermal stability of the compounds is only due to the properties of the organic cation and does not depend on the nature of the halogen. The proposed stages of the process of thermolysis of the TcHal62- anion, accompanied by the reduction of technetium to metal, have been established.

Route to Stabilization of Nanotechnetium in an Amorphous Carbon Matrix: Preparative Methods, XAFS Evidence, and Electrochemical Studies.

Technetium-carbon nanophases are obtained by thermal decomposition of pertechnetates with large organic cations under an argon atmosphere. Parallel carbonization of organic cations (hexamethyleneiminium and triphenylguanidinium), which occurs during the thermal decomposition of their pertechnetates, leads to the formation of X-ray amorphous solid products. An X-ray absorption fine structure study revealed that they have a crystal structure containing technetium-carbon bonds with a length of 1.76 Å. After subsequent annealing treatment at 1073-1673 K, the synthesized technetium-carbon phase has a cubic lattice with an a of 4.01 ± 0.03 Å. The products of thermal decomposition of the same perrhenates are also X-ray amorphous; however, unlike that of pertechnetates, the distance between rhenium and carbon atoms in them is significantly greater (2.14 Å). After subsequent annealing, they have a hexagonal lattice. The electrochemical properties of technetium-carbon nanophases prepared by thermal decomposition of pertechnetates with large organic cations are different from the properties of those prepared with metallic technetium. The oxidation of technetium carbide to its oxides at the electrode surface observed in the first anodic scan of cyclic voltammograms can be used for the deposition of noble metal nanoclusters under open-circuit conditions to prepare composite catalysts for the hydrogen evolution reaction. Nanotechnetium in the amorphous carbon matrix can also be a prospective material for reactor transmutation of technetium to stable isotopically pure ruthenium-100.

Intramolecular Re···O Nonvalent Interactions as a Stabilizer of the Polyoxorhenate(VII).

The first polyoxorhenate(VII) compound, pyrazolium polyoxorhenate ((C4N2H5)2Re4O15), and two new rhenium(VII) and technetium(VII) salts have been synthesized and studied. The structure of Tc2O7 has been reinvestigated. The [Re4O15]2- polyoxoanion contains four Re(VII) atoms: one with an octahedral environment and three with a tetrahedral environment. Polyoxorhenate is formed in the presence of a buffering agent, pyrazole, the latter maintaining pH = 2.5 during the formation of crystals. The [Re4O15]2- polyoxoanion has novel stoichiometry and the cis-conformation, likely due to the stabilizing intramolecular nonvalence interactions. For the first time, intramolecular interactions of the Re···O, Re···µ-O, and O···O are described (previously known were only intermolecular ones). In all of the compounds, intermolecular Re···O interactions are observed, which, however, in other compounds, do not lead to the formation of polyoxometalates. The Hirshfeld surface analysis showed that the main contribution to intermolecular interactions is made by the O···H/H···O contacts, van der Waals interactions of the H···H for cations, and the O···O for anions. DFT calculations of the [Re4O15]2- geometry, compared with the crystallographic data, revealed a deviation in the angles. Mass spectroscopy of the red polyoxometalate [Tc20O68]4- was carried out for the first time. Comparison of the results of MALDI and LI for the first known polyoxometalates of the manganese subgroup made it possible to find general patterns of oligomerization for rhenium and technetium compounds. The ESI-MS and LI-MS methods applied to solution and crystals Re compounds made it possible to prove rhenium being able to form not only [Re4O15]2- but also heavier polyoxoanions.

Synthesis, crystal structure and Hirshfeld surface analysis of bis-(caffeinium) hexa-chlorido-platinum(IV) in comparison with some related compounds.

The mol-ecular and crystal structure of the title compound, (C8H11N4O2)2[PtCl6], synthesized from hexa-chloro-platinic acid and caffeine in methanol, was studied by single-crystal X-ray diffraction. The caffeinium cations form a double layer via hydrogen bonds and π-stacking inter-actions. The Hirshfeld surface analysis showed that the largest contribution to the crystal packing is made by H⋯H (31.2%), H⋯Cl/Cl⋯H (22.6%), O⋯H/H⋯O (21.9%) contacts for the cation and H⋯Cl/Cl⋯H (79.3%) contacts for the anion.

New Preparative Approach to Purer Technetium-99 Samples-Tetramethylammonium Pertechnetate: Deep Understanding and Application of Crystal Structure, Solubility, and Its Conversion to Technetium Zero Valent Matrix.

99Tc is one of the predominant fission products of 235U and an important component of nuclear industry wastes. The long half-life and specific activity of 99Tc (212,000 y, 0.63 GBq g-1) makes Tc a hazardous material. Two principal ways were proposed for its disposal, namely, long-term storage and transmutation. Conversion to metal-like technetium matrices is highly desirable for both cases and for the second one the reasonably high Tc purity was important too. Tetramethylammonium pertechnetate (TMAP) was proposed here as a prospective precursor for matrix manufacture. It provided with very high decontamination factors from actinides (that is imperative for transmutation) by means of recrystallisation and it was based on the precise data on TMAP solubility and thermodynamics accomplished in the temperature range of 3-68 °C. The structure of solid pertechnetates were re-estimated with precise X-ray structure solution and compared to its Re and Cl analogues and tetrabutylammonium analogue as well. Differential thermal and evolved gas analysis in a flow of Ar-5% H2 gas mixture showed that the major products of thermolysis were pure metallic technetium in solid matrix, trimethylammonium, carbon dioxide, and water in gas phase. High decontamination factors have been achieved when TMAP was used as an intermediate precursor for Tc.

Thiourea as a Stabilizer of Reduced Forms of Technetium─Tc(III) and Tc(IV): Experimental and Theoretical Studies of Complexes.

This paper presents synthetic methods for the preparation of Tc(III) and Tc(IV) coordination compounds with thiourea. We have shown that the main product of the synthesis is the complex [TcTu5X]X2, (Tu = (NH2)2CS, X = Cl, Br) and not [TcTu6]Cl3·4H2O, as previously thought. Tu2[TcX6]X2·3H2O is the main technetium-containing byproduct of the reaction. All reaction products, including byproducts, were characterized by X-ray diffraction analysis. We also measured the solubility for the obtained Tc(III) complexes. This research work considers the process of thermolysis of the obtained Tc(III) complexes and shows that the presence of sulfur atoms in the coordination sphere can inhibit the process of metal formation in an argon-hydrogen medium. The analysis of nonvalent interactions in Tc(III) complexes showed that the main contribution is made by van der Waals interactions of the H···H type (40.8-42.3%) and hydrogen bonds Hal···H/H···Hal and H···S/S···H, which are 41.6-44.5% in total. As the temperature decreases, the proportion of H···H contacts and H bonds decreases, and when the halogen (Cl by Br) is replaced, the proportion of H bonds increases and the proportion of van der Waals interactions decreases.

Synthesis, crystal structure and Hirshfeld surface analysis of 2-(perfluoro-phen-yl)acetamide in comparison with some related compounds.

The mol-ecular and crystal structures of the title compound, C8H4F5NO, were examined by single-crystal X-ray diffraction and Hirshfeld surface analysis. The title compound was synthesized by a new method at the interface of aqueous solutions of LiOH and penta-fluoro-phenyl-aceto-nitrile. In the crystal, hydrogen bonds and π-halogen inter-actions connect the mol-ecules into double layers. Analysis of the Hirshfeld surface showed that the most important contributions to the crystal packing are made by F⋯F (30.4%), C⋯F/F⋯C (22.9%), O⋯H/H⋯O (14.9%), H⋯F/F⋯H (14.0%) and H⋯H (10.2%) contacts. The Hirshfeld surfaces of analogues of the title compound were compared and the effect of perfluorination on the crystal packing was shown.

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.

5,5-Di-chloro-6-hy-droxy-dihydro-pyrimidine-2,4(1H,3H)-dione: mol-ecular and crystal structure, Hirshfeld surface analysis and the new route for synthesis with Mg(ReO4)2 as a new catalyst.

The mol-ecular and crystal structures of the title compound, C4H4Cl2N2O3, were investigated by single-crystal X-ray diffraction and a Hirshfeld surface analysis. The title compound was synthesized by a new type of reaction using Mg(ReO4)2 as a new catalyst and a possible mechanism for this reaction is proposed. The six-membered ring adopts a half-chair conformation. In the crystal, hydrogen bonds connect the mol-ecules into double layers, which are connected to each other by halogen bonds. The Hirshfeld surface analysis revealed that the most important contributions for the crystal packing are from O⋯H/H⋯O (35.8%), Cl⋯Cl (19.6%), Cl⋯H/H⋯Cl (17.0%), H⋯H (8.3%), C⋯O/O⋯C (4.3%), Cl⋯O/O⋯Cl (4.2%) and O⋯O (4.1%) contacts.

Finding a receptor design for selective recognition of perrhenate and pertechnetate: hydrogen vs. halogen bonding.

Receptors bearing hydrogen and halogen bond donors for recognition of perrhenate and pertechnetate were designed and studied. Acyclic hosts with N-H and C-H binding sites showed the best selectivity for TcO4- and ReO4- over spherical and more basic tetrahedral anions.

99 Tc NMR determination of the oxygen isotope content in 18 O-enriched water.

99 Tc NMR has been suggested as an original method of evaluating the content of oxygen isotopes in oxygen-18-enriched water, a precursor for the production of radioisotope fluorine-18 used in positron emission tomography. To this end, solutions of NH4 TcO4 or NaTcO4 (up to 0.28 mol/L) with natural abundance of oxygen isotopes in virgin or recycled 18 O-enriched water have been studied by 99 Tc NMR. The method is based on 16 O/17 O/18 O intrinsic isotope effects in the 99 Tc NMR chemical shifts, and the statistical distribution of oxygen isotopes in the coordination sphere of TcO4- and makes it possible to quantify the composition of enriched water by measuring the relative intensities of the 99 Tc NMR signals of the Tc16 O4-n18 On- isotopologues. Because the oxygen exchange between TcO4- and enriched water in neutral and alkaline solutions is characterized by slow kinetics, gaseous HCl was bubbled through a solution for a few seconds to achieve the equilibrium distribution of oxygen isotopes in the Tc coordination sphere without distortion of the oxygen composition of the water. Pertechnetate ion was selected as a probe due to its high stability in solutions and the significant 99 Tc NMR shift induced by a single 16 O→18 O substitution (-0.43 ± 0.01 ppm) in TcO4- and spin coupling constant 1 J(99 Tc-17 O) (131.46 Hz) favourable for the observation of individual signals of Tc16 O4-n18 On- isotopologues.

Redetermination of the crystal structure of NaTcO4 at 100 and 296†K based on single-crystal X-ray data.

The redetermination of the title compound, sodium pertechnate, from single-crystal CCD data recorded both at 296 and 100 K confirms previous studies based on X-ray powder diffraction film data [Schwochau (1962 ▸). Z. Naturforsch. Teil A, 17, 630; Keller & Kanellakopulos (1963 ▸). Radiochim. Acta, 1, 107-108] and neutron powder diffraction data using the Rietveld method [Weaver et al. (2017 ▸). Inorg. Chem.12, 677-681], but reveals a considerable improvement in precision. The standard uncertainties of the room-temperature structure determination are about seven times lower than those of the neutron diffraction structure determination and about 13 times lower at 100 K, due to the decrease in the amplitude of librations. The crystal expansion could be approximated linearly with a thermal volumic expansion coefficient of 1.19 (12) × 10-4 K-1. NaTcO4 adopts the scheelite (CaWO4) structure type in space group type I41/a with Na and Tc atoms (both with site symmetry -4) replacing Ca and W atoms, respectively.

Reactivity of HTcO(4) with methanol in sulfuric acid: Tc-sulfate complexes revealed by XAFS spectroscopy and first principles calculations.

The reaction between HTcO(4) and MeOH in 13 M H(2)SO(4) was investigated by (99)Tc NMR, UV-visible and X-ray absorption fine structure (XAFS) spectroscopy. Experimental results and first principles calculations show the formation of Tc(+5) sulfate complexes. The results expand the fundamental understanding of Tc in high acid solutions.

Macrocyclic receptor for pertechnetate and perrhenate anions.

The design and synthesis of a neutral macrocyclic host that is capable of perrhenate and pertechnetate recognition is described. The anion affinities and underlying coordination modes were estimated by several experimental and theoretical methods including a new technique--reverse (99)Tc NMR titration.

Morpholinium perchlorate.

In the title salt, C(4)H(10)NO(+)·ClO(4) (-), which has three independent formula units, the cations are linked into chains along [100] by N-H⋯O hydrogen bonds. Each cation acts both as a donor and as an acceptor, and every cation makes one N-H⋯O hydrogen bond with a ClO(4) (-) anion. The crystal studied was an inversion twin.

Characterization of technetium(vII) reduction by cell suspensions of thermophilic bacteria and archaea.

Washed cell suspensions of the anaerobic hyperthermophilic archaea Thermococcus pacificus and Thermoproteus uzoniensis and the anaerobic thermophilic gram-positive bacteria Thermoterrabacterium ferrireducens and Tepidibacter thalassicus reduced technetium [(99)Tc(VII)], supplied as soluble pertechnetate with molecular hydrogen as an electron donor, forming highly insoluble Tc(IV)-containing grayish-black precipitate. Apart from molecular hydrogen, T. ferrireducens reduced Tc(VII) with lactate, glycerol, and yeast extract as electron donors, and T. thalassicus reduced it with peptone. Scanning electron microscopy and X-ray microanalysis of cell suspensions of T. ferrireducens showed the presence of Tc-containing particles attached to the surfaces of non-lysed cells. This is the first report on the reduction in Tc(VII) by thermophilic microorganisms of the domain Bacteria and by archaea of the phylum Euryarchaeota.