Crystal structure of oxotitanium(IV) 2,2,6,6-tetramethyl-3,5-heptanedionate

The structure of titanyl dipivalylmethanate TiO(dpm)₂ has been studied by X-ray diffraction analysis. The compound has a molecular structure formed by isolated centrosymmetrical dimers [TiO(dpm)₂]₂; the unit cell contains two structurally related, crystallographically unique binuclear molecules. The Ti...Ti distance in the dimer is 2.73 Å. Crystal data for Ti₂C₃₆H₇₆O₁₀: a = 32.477(6) Å, b = 14.409(3) Å, c = 25.630(5) Å; β = 107.82(3)°, space group C2/c, Z = 8, d _calc = 1.002 g/cm³.     

Copolymers of the C9 hydrocarbon fraction of liquid pyrolysis products with maleic anhydride and their esterification products as additives to paper pulp

The influence exerted by copolymers of the C₉ fraction of liquid pyrolysis products of petroleum raw materials with maleic anhydride and by their esterification products, added to paper pulp, on the main paper properties was examined.     

Tandem purification of mouse IgM monoclonal antibodies produced in vitro using anion-exchange and gel fast protein liquid chromatography

A tandem chromatographic procedure was used to isolate rapidly mouse IgM monoclonal antibodies produced by cultivation of hybridomas in vitro. Hybridoma culture supernatants containing mouse IgM monoclonal antibodies were first chromatographed on an anion-exchange Mono Q column connected to a fast protein liquid chromatography system. This anion-exchange step offers the advantage of obtaining IgM antibodies in a concentrated form. The IgM-rich fractions from the Mono Q column were then injected on a gel filtration Superose 6 column equilibrated with a low-ionic strength buffer and eluted with a high-ionic strength buffer. Assessment of the purity of isolated IgM monoclonal antibodies was performed by sodium dodecyl sulphate polyacrylamide gel electrophoresis together with a Coomassie Brillant Blue R 250 staining technique. Assessment of the immunoreactivity of isolated IgM monoclonal antibodies was performed by an enzyme linked immunosorbent assay using a solid phase adsorbed antigen against which IgM monoclonal antibodies were directed. The chromatographic procedures described allows the rapid isolation of mouse IgM monoclonal antibodies produced in vitro at a high degree of purity and in an immunoreactive state.     

Azines and azoles. 64. Mass spectra and tautomerism of 2-aryl-4,6-dioxo-1,3-thiazines

Mass spectra of 2-aryl-4,6-dioxo-1,3-thiazines were studied and the general fragmentation paths of these compounds determined. Based on mass spectra of compounds with fixed structures, 2-aryl-5,5-dialkyl-4,6-dioxo-1,3-thiazines, 4-alkoxy- and 4-acyloxy-2-aryl-6-oxo-1,3-thiazines, the decomposition paths of the dicarbonyl and hydroxycarbonyl forms were determined. It was concluded on the basis of the obtained data that 2-aryl-4,6-dioxo-1,3-thiazines exist in the gas phase predominantly in the hydroxycarbonyl form.For Communication 63, see [1].Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1409–1412, October, 1987.     

Reaction of styrene with sulfur and triiron dodecacarbonyl and the molecular structure of the complex Fe2(CO)6(SCH2S)

Reaction of excess styrene with Fe₃(CO)₁₂ and sulfur (60°C, 15 h, Ar, S/Fe₃(CO)₁₂ 0.6 g-atom/mole) gave Fe₂(CO)₆S₂, Fe₃(CO)₉S₂, Fe₂(CO)₆(S₂CO), Fe₂(CO)₆S₂(PhCHCH₂), PhCHCH₂S₄, and a novel binuclear complex Fe₂(CO)₆(S₂CH₂S), whose structure was analyzed by x-ray crystallography. The crystals are monoclinic, a=7.764(3), b=13.205(4), c=6.628(6) Å, =98.97(3)°. V=671.2(7) ų, Z=2, space group P2₁/m. The bond lengths are Fe-Fe 2.520(2), Fe-S 2.236(2), S-S 2.078(4), C-S 1.825(12), Fe-CO 1.784(8), and CO 1.148(9) Å.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 4, pp. 930–934, April, 1991.     

519—Reduction of hydrophobic porphyrin at the octane/water interface controlled by the specific adsorption of halogen anions

The redox reaction between the ferric complex of hydrophobic porphyrin and sodium dithionite in two different phases occurring at the interface between two immiscible liquids has been investigated by Volta potential measurements and spectroscopy. The reduction of the ferric complex of hydrophobic porphyrin adsorbed at the interface was found to be accompanied by a potential shift in the negative direction and to depend significantly on the nature of the anion and the ionic strength of the supporting electrolyte. Specifically adsorbed halogen anions inhibited the redox reaction in the sequence: Cl^?, Br^?, I^?. Depending on pH, the ferric complex of hydrophobic porphyrin exists in the uncharged (FeP-O-PFe) form or in the cation FeP⁺ form. The interaction between the ferric complex hydrophobic porphyrin and water has also been investigated.     

Determination of metal traces in tantalum by proton activation analysis

Procedures for determining traces of calcium, titanium, vanadium, chromium, iron, copper, niobium, molybdenum and tungsten in tantalum are described utilizing 11 MeV proton activation. The instrumental method of analysis with the use of a Ge(Li) detector and the radiochemical separation of the corresponding fractions are described. The formula for the calculation of the concentration of traces with the use of thick target yields is given. Experimental data on the thick target yields of radioisotopes⁴⁴Sc,⁵²Mn,⁵⁶Co,⁶⁵Zn,^93mMo,⁹⁶Tc are presented. Based on the experimental data, the detection limits are estimated at 1–10 ppb for the above mentioned metal traces in tantalum. The successful solution of the task of the simultaneous determination of nine elements in tantalum confirms the wide applicability of proton activation analysis.     

Investigation of short lived radicals in aromatic nucleophilic substitution by use of nitroso compounds as scavengers

Radical intermediates formed in reaction of substituted nitrobenzene compounds with nucleophilic reagents have been trapped by t-nitrosobutane to yield nitroxide radicals which have been characterized in situ by ESR. The formation of short-lived radicals originating from reagents and solvents has been shown.     

Transformations of substituted tetrahydro-8h-indeno[1,2-d]imidazoles in concentrated sulfuric acid

The five-membered ring of the indene system in 2,8-dioxo-3a-hydroxy-8a-R-1,2,3a,8a-tetrahydro-8H-indeno[1,2-d]imidazoles is hydrolytically cleaved in concentrated sulfuric acid solutions. Depending on the reaction conditions, compounds for which substituted 4-(o-carboxyphenyl)imidazol-2-one (II), 1,8-dioxo-1,2-dihydro-8H-imidazo[4,3-a]isoindole (III), and spiro[imidazolidine-4,3′-phthalide] structures were assumed were isolated.