Binuclear complexes of copper(II) with 1′-phthalazinylhydrazones of substituted salicylic aldehydes: Physico-chemical study and quantum-chemical simulation

Binuclear complexes of copper(II) with 1′-phthalazinylhydrazones of substituted salicylic aldehydes have been prepared and studied. Antiferromagnetic exchange interaction between copper(II) ions has been revealed in all the complexes. Taking advantage of quantum-chemical simulation, we have investigated the influence of the complexes structural isomerism on the character of the exchange interaction between the paramagnetic centers. X-ray absorbance spectroscopy afforded the structural parameters of coordination spheres of copper(II) ions; it has been demonstrated that dimerization occurred via the nitrogen atoms of phthalazine fragments.     

Copper(II) and nickel(II) complexes with bis(azomethine)—a condensation product of 1-phenyl-3-methyl-4-formyl-5-mercaptopyrazole with 1,3-diaminopropan-2-ol

The copper(II) and nickel(II) complexes based on bis(azomethine), which is the condensation product of 1-phenyl-3-methyl-4-formyl-5-mercaptopyrazole with 1,3-diaminopropan-2-ol, are synthesized. Bis-azomethines can form both binuclear and mononuclear complexes in which the hydroxy group is not involved in coordination. The binuclear copper(II) complexes with the acetate and pyrazolate bridges exhibit an antiferromagnetic exchange, which strength is determined by the nature of the bridge (2J = ?154 and ?424 cm^?1, respectively). The structure parameters of the coordination spheres of the complexes are determined by X-ray absorption spectroscopy. The structure of the CHCl₃ solvate of the binuclear copper(II) complex with the pyrazolate bridge is solved by X-ray diffraction analysis (CIF file CCDC 964655).     

Study of the chemical reactions' influence on semiconductor films structure formation by the Monte-Carlo method

The investigation by the Monte-Carlo method of the growth of the silicon epitaxial film at a chloride CVD system has allowed to find out the composition of adsorption layer, the micromechanism of the reactions of Si atoms building-in into the growing crystalline layer and the growth conditions influence on the growth rate and film surface roughness. The change of adsorptive layer composition in the system SiCl₄—HCl—H₂ (fraction of adaatoms, silicon atoms built-in a crystal and molecules SiCl₂) depending on temperature has been determined. The change of silicon film growth rate depending on temperature and concentration change of SiH₂Cl₂ has been established and the contribution of growth mechanism (with participation of adatom, silicon atoms and molecules SiCl₂) into the total rate of film growth has been shown.     

Physicochemical study of binuclear copper(II), oxovanadium(IV), and iron(III) complexes with bis-1′-phthalazinylhydrazone of 2,6-diformyl-4-tert-butylphenol

Binuclear copper(II), oxovanadium(IV), and iron(III) complexes with bis-1′-phthalazinylhydrazone of 2,6-diformyl-4-tert-butylphenol have been prepared. An antiferromegnetic exchange interaction between the paramagnetic centers was found. Redox properties of the complexes were studied by the methods of cyclic and differential pulse voltammetry; the reduction of Cu(II) complexes was shown to proceed in two consecutive one-electron steps.     

Why Does the Geometric Product Simplify the Equations of Physics?

In the last decades it was observed that Clifford algebras and geometric product provide a model for different physical phenomena. We propose an explanation of this observation based on the theory of bounded symmetric domains and the algebraic structure associated with them. The invariance of physical laws is a result of symmetry of the physical world that is often expressed by the symmetry of the state space for the system implying that this state space is a symmetric domain. For example, the ball of all possible velocities is a bounded symmetric domain. The symmetry on this ball follow from the symmetry of the space-time transformations between two inertial systems, which fixes the so-called symmetric velocity between them. The Lorenz transformations acts on the ball Sof symmetric velocities by conformal transformations. The ball Sis a spin ball (type IV in Cartan's classification). The Lie algebra of this ball is defined a triple product that is closely related to geometric product. The relativistic dynamic equations in mechanics and for the Lorenz force is described by this Lie algebra and the triple product.     

Polyoxometalates as Reduction Catalysts: Deoxygenation and Hydrogenation of Carbonyl Compounds

Excellent deoxygenation of ketones and aldehydes is achieved with Keggin-type polyoxometalates in the presence of hydrogen (see Equation (1) for an example). The mixed addenda phosphovanadomolybdate [PV(2)Mo(10)O(4)](5-) was found to be the best catalyst. X-ray diffraction and IR studies suggest that the polyoxometalates are structurally stable under the strongly reducing conditions.     

Effect of ultrasonic treatment on the molecular weight of carboxymethylated chitin-glucan complex from Aspergillus niger

Different factors affecting the efficiency of the ultrasonic depolymerization of the high-molecular-weight carboxymethylated chitin-glucan prepared from the fungal mycelium of Aspergillus niger have been investigated. The influence of the following parameters was examined: concentration of the chitin-glucan complex, duration of ultrasonic irradiation, reaction temperature and volume of the ultrasonicated solution. The optimized conditions for the efficient ultrasonic depolymerization include: polysaccharide concentration--0.2 mg ml-1; volume of the sonicated solution--25 ml; duration of the sonication--10 min; and constant cooling of the sonicated sample in an ice-water bath.     

3-Indolylphenylacetonitriles

The reaction of 2-carbethoxyindole with aromatic aldehydes in ether saturated with HCl gave 2-carbethoxy-3-(-chlorobenzyl)indoles. Reaction of the latter with sodium cyanide in dimethyl sulfoxide gave 3-indolylphenylacetonitriles in 47–85% yields. If the indole NH group is substituted, rearrangment to give 1-methyl-2-cyano-3-benzylindoles occurs simultaneously. The latter were reduced with LiAlH₄ to aminomethyl derivatives and were hydrolyzed with KOH in ethylene glycol to 1-methyl-3-benzylindole-2-carboxylic acids. The structures were proved by the UV, IR, and PMR spectra.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 11, pp. 1482–1486, November, 1978.