Aluminum hydroxocarboxylates in solution deposition of planarization alumina films

Aluminum hydroxocarboxylates derived from butyric, pivalic, valeric, and isovaleric acids were synthesized and characterized. The synthesized hydroxocarboxylates were suspended in isopropanol and reacted with diethylenetriamine and monoethanolamine, which acted as hydrolyzing and complex-forming agents, to obtain precursor solutions for chemical deposition of smooth amorphous alumina films on metal substrates.     

Helium-3 as a Perspective Fuel for Power Generation through Aneutronic Thermonuclear Fusion

Physics of Atomic Nuclei - The aneutronic D3–He (deuterium–helium-3) fuel cycle is considered as a viable alternative to D–T (deuterium–tritium) fusion since it is...     

The nature of the chemical bond in UO2

The nature of the chemical bond in UO₂ was analyzed taking into account the X-ray photoelectron spectroscopy (XPS) structure parameters of the valence and core electrons, as well as the relativistic discrete variation electronic structure calculation results for this oxide. The ionic/covalent nature of the chemical bond was determined for the UO₈ (D_4h) cluster, reflecting uranium's close environment in UO₂, and the U₁₃O₅₆ and U₆₃O₂₁₆ clusters, reflecting the bulk of solid uranium dioxide. The bar graph of the theoretical valence band (from 0 to ~35 eV) of XPS spectrum was built such that it was in satisfactory agreement with the experimental spectrum of a UO₂ single crystalline thin film. It was shown that unlike the crystal field theory results, the covalence effects in UO₂ are significant due to the strong overlap of the U 6p and U 5f atomic orbitals with the ligand orbitals, in addition to the U 6d atomic orbital (AO). A quantitative molecular orbital (MO) scheme for UO₂ was built. The contribution of the MO electrons to the chemical bond covalence component was evaluated on the basis of the bond population values. It was found that the electrons of inner valence molecular orbitals (IVMO) weaken the chemical bond formed by the electrons of outer valence molecular orbitals (OVMO) by 32% in UO₈ and by 25% in U₆₃O₂₁₆.     

Laser plasmatron for diamond coating deposition

An experimental installation with a laser plasmatron based on a continuous wave CO₂ laser with a radiation power of up to 3.5 kW has been created. The plasmatron design makes it possible to bring out the plasma jet into atmospheric air both along and across the laser beam direction. The spatial temperature distributions on the metal substrate surface heated by the plasma jet are measured. The threshold power for optical discharge maintenance as a function of the gas flow rate and the focal length of the focusing lens are obtained for an Ar and Ar/CH₄/H₂ gas mixture under atmospheric pressure; the radiation spectrum of the discharge plasma is measured. A one-dimensional model of the discharge for estimation of its geometrical parameters in a convergent laser beam with consideration of radiation refraction on the discharge is given.     

Electronic structure and properties of the ground state of copper in semiconducting cuprates

The spin-polarized discrete variational X_a method is used to calculate clusters that model the electronic structures of CuO, La₂CuO₄, and Nd₂CuO₄. It, is shown that in each of the compounds the unoccupied portion of the valence band involves mainly the O2p states, the contributions from the Cu3d orbitals being significantly smaller. The effects of the nature of holes in the valence band and of the structure of the close environment of copper on the low-energy CuK spectra and the X-ray photoelectron spectra of the above systems are discussed. Institute of Solid State Chemistry, Ural Branch, Russian Academy of Sciences. Translated fromZhumal Struktumoi Khimii, Vol. 36, No. 4, pp. 636–643, July–August., 1995. Translated by I. Izvekova     

Synthesis ofN-substituted 2-(5,6,7,8-tetrafluoro-4-oxo-1,4-dihydroquinolin-3-yl)glyoxylic acids

Methods for the synthesis of the earlier unknownN-substituted 2-(5,6,7,8-tetrafluoro-4-oxo-1,4-dihydroquinolin-3-yl)glycoxylic acids their esters from copper chelate of ethyl pentafluorobenzoylpyruvate were developed. The structure of intermediate ethyl 4-(R-amino)-2-oxo-3-pentafluorobenzoylbut-3-enoates is discussed. Published inIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 7, pp. 1234–1239, July, 2000.     

Measurement of the compressibility of a deuterium plasma at a pressure of 1800 GPa

The thermodynamic properties of a highly compressed deuterium plasma have been measured using an explosive spherical experimental chamber. The experiment has been performed with an X-ray diffraction complex consisting of three betatrons and a multichannel optoelectronic system of the detection of X-ray images of the process of the explosive spherical compression of deuterium. The density of the shock-compressed deuterium plasma ρ = (4.3 ± 0.7) g/cm³ at the pressure P = 1830 GPa has been detected at the initial pressure of gaseous deuterium P ₀ = 267 atm and the temperature T ₀ = 10.5°C. Under such conditions, the plasma is strongly nonideal (Γ ～ 450) with the degenerate (nλ _e ³ ～ 280) electron component and with an electron density of about 2.8 × 10²³ cm^?3.     

Reactions of 1-aryl(alkyl)-3-ethoxalyl-5,6,7,8-tetrafluoro-1,4-dihydrocinnolin(quinolin)-4-ones with aromatic dinucleophiles

The title compounds react with o-phenylenediamine and o-aminophenol at the ethoxalyl fragment to form heteryl-substituted quinoxalones and benzooxazinones, respectively. o-Aminobenzenethiol acts as both an S-nucleophile replacing the F atom and an N-nucleophile replacing the carbonyl group in the ethoxalyl fragment. Under more drastic conditions, cyclization proceeds to form benzothiazinones.     

Electronic structure,chemical bonding and X-ray photoelectron spectra of light rare-earth oxides

The electronic structure of the light RE oxides CeO₂, Pr₂O₃ and Nd₂O₃ has been studied by the cluster discrete variational DV-X method and X-ray photoelectron spectroscopy. The interpretation of XPE spectra basing on the MO model is given. The various electronic states contributions to the chemical bonding in the oxides are investigated.