X-ray diffraction study of CsZn<Subscript>2</Subscript>Br<Subscript>5</Subscript>

CsZn₂Br₅ crystals are studied by X-ray diffraction. The compound crystallizes in the monoclinic system with the unit cell parameters a = 6.8880(12) Å, b = 10.4703(19) Å, c = 6.5197(9) Å, β = 108.25°, V = 446.55 ų, ρ_calcd = 4.960 g/cm³. Refractive indices are n _p = 1.640 and n _p = 1.754.     

Synthesis,structure, and reactivity of germanium-containing derivatives of substituted diethanolamines

The reaction of dialkanolamines RN(CH₂CH₂O)(CHR’CHR’OH) (R = Me, Ph, PhCH₂; R’ = H, Ph) with tetraethoxygermane gives either 2,2-diethoxy-1,3,6,2-dioxazagermocanes RN(CH₂CH₂O)(CHR’CHR’O)Ge(OEt)₂ or 1,7,9,15-tetraoxa-4,12-diaza-8-germaspiro[7.7]pentadecanes [RN(CH₂CH₂O) (CHR’CHR’O)]₂Ge depending on the reactant ratio. The chemical behavior of the obtained compounds in substitution reactions at germanium was studied. The product structure was confirmed by elemental analysis data and ¹H, ¹³C, and ¹⁹F NMR spectroscopy. The cyclotrigermanoxane [MeN(CH₂CH₂O)₂GeO]₃ was studied by X-ray diffraction.     

Alkynyl and poly-ynyl derivatives of carbon-tricobalt clusters

A series of alkynyl-tricobalt carbonyl clusters, Co₃(μ₃-C_nR)(μ-dppm)(CO)₇ [R = Bu^t, Ph, C₆H₄I, C₆H₄CCPh, SiMe₃, Fc, Au(PPh₃)] containing three, five or seven carbons in the chain, have been prepared by elimination of phosphine-gold(I) halides in reactions between Co₃(μ₃-CBr)(μ-dppm)(CO)₇ and Au(CCR)(PPh₃) or between Co₃{μ₃-CCCAu(PR₃)} (μ-dppm)(CO)₇ (R = Ph, tol) and ICCR′ (R′ = SiMe₃, Fc). The use of poly-substituted arenes or ferrocenes has enabled preparation of the complexes 1,4-{(OC)₇(μ-dppm)Co₃ (μ₃-CCC)}₂C₆H₃X-5 (X = H, Br), 1,3,5-{(OC)₇(μ-dppm)Co₃(μ₃-CCC)}₃C₆H₃ and 1,1′-{(OC)₇(μ-dppm)Co₃ (μ₃-CCC)}₂Fc′ [Fc′ = Fe(η-C₅H₄-)₂]. The X-ray determined molecular structures of 12 of the complexes are reported.     

Molecular structures of tris(dipivaloylmethanato) complexes of the lanthanide metals, Ln(dpm)3, studied by gas electron diffraction and density functional theory calculations: a comparison of the Ln-O Bond distances and enthalpies in Ln(dpm)3 complexes and the cubic sesquioxides, Ln2O3

The molecular structures of tris(dipivaloylmethanato)neodymium(III), Nd(dpm)3, and tris(dipivaloylmethanato)ytterbium(III), Yb(dpm)3, have been determined by gas electron diffraction (GED) and structure optimizations through density functional theory (DFT) calculations. Both molecules were found to have D3 molecular symmetry. The most important structure parameters (r(a) structure) are as follows (GED/DFT): Nd-O = 2.322(5)/2.383 A, Yb-O = 2.208(5)/2.243 A, O-Nb-O = 72.1(3)/71.3 degrees , and O-Yb-O = 75.3(2)/75.8 degrees . The twist angles of the LnO6 coordination polyhedron, defined as zero for prismatic and 30 degrees for antiprismatic coordination, were theta = 19.1(3)/14.2 degrees for Nd and 20.4(2)/19.2 degrees for Yb. Structure optimizations of La(dpm)3, Gd(dpm)3 Er(dpm)3, and Lu(dpm)3 by DFT also yielded equilibrium structures of D3 symmetry with bond distances of La-O = 2.438 A, Gd-O = 2.322 A, Er-O = 2.267 A, and Lu-O = 2.232 A. The Ln-O bond distances in 12 Ln(dpm)3 complexes studied by GED decrease in a nearly linear manner with the increasing atomic number (Z) of the metal atom, as do the Ln-O bond distances in the cubic modifications of 14 sesquioxides, Ln2O3. The bond distances in the dpm complexes are, however, about 2% shorter. The mean Ln-O bond rupture enthalpies of the cubic sesquioxides calculated from thermodynamic data in the literature vary in an irregular manner with the atomic number; the La-O, Gd-O, Tb-O, and Lu-O bonds are nearly equally strong, and the remaining bonds are significantly weaker. The Ln-O bond rupture enthalpies previously reported for 11 Ln(dpm)3 complexes are on the average 13 kJ mol(-1) or about 5% smaller than in the sesquioxides, but they vary in a similar manner along the series: it is suggested that the pattern reflects variations in the absolute enthalpies of the gaseous Ln atoms.     

Acoustic anomalies in SrTiO<Subscript>3</Subscript>−BiFeO<Subscript>3</Subscript> solid solutions

The results of acoustic investigations of solid solutions SrTiO₃?BiFeO₃ in the temperature range from 100 to 650 K have been presented. The measurements of the velocity and attenuation of the longitudinal ultrasonic mode at a frequency of 10 MHz were carried out by the pulse-echo method. The observed anomalies in velocity and attenuation correlate with the maxima of the dielectric constant in the temperature range of the relaxor state. In addition, the attenuation peaks in the temperature range 400–600 K, which define Burns and T* temperatures, which are characteristic of relaxors, have been identified. The obtained results have allowed the clarifying of the phase diagram of the solid solution system SrTiO₃?BiFeO₃.     

Copolymerization of Magnesium and Calcium 2-Acrylamido-2-methylpropanesulfonates with N-Vinylpyrrolidone in Aqueous Solutions

The kinetics of radical copolymerization of magnesium and calcium 2-acrylamido-2-methylpropanesulfonates with N-vinylpyrrolidone in aqueous solutions at pH 9 and 50°C in the presence of an initiator, potassium peroxodisulfate, were studied dilatometrically, and the molecular characteristics of the resulting copolymers were determined.     

Kinetics of Radical Copolymerization of Acrylamide with Magnesium 2-Acrylamido-2-Methylpropanesulfonate in Aqueous Solutions

Kinetic features of homogeneous radical copolymerization of acrylamide with magnesium 2-acrylamido-2-methylpropanesulfonate in concentrated aqueous solutions in the presence of the initiating system potassium peroxosulfate-sodium hydrosulfite at pH 9 and 50°C were studied by dilatometric technique.     

Application of solution techniques for rapid growth of organic crystals

Single crystals of a pure hydrocarbon, 1,3,5-triphenylbenzene, with properties suitable for high-energy neutron detection were grown from toluene solutions using slow evaporation and temperature reduction methods with growth rates up to 10 mm/day. Application of the rapid growth technique developed earlier for growth of large water-soluble crystals shows that crystals of aromatic compounds can be successfully grown from solutions in large volumes required for their use as scintillator materials for radiation detection.     

6-m spectrometer of the Institute of Theoretical and Experimental Physics (ITEP, Moscow)

The history of the development and construction of the ITEP-MIS 6-m magnetic spectrometer is reported. Research studies performed by the ITEP-MIS group over a period of more than 30 years of spectrometer existence is surveyed. The results obtained by studying the narrow resonances f _j(2220) and X(1070) are presented.