Efficient electrochemical synthesis of pyrido[1,2-a]benzimidazoles

Electrochemical reduction of N-(2-nitroaryl)pyridinium chlorides in alcohol—dilute HCl mixtures gave pyrido[1,2-a]benzimidazoles in high yields in both divided and undivided cells. According to cyclic voltammetry measurements and DFT calculations (B3LYP/6-31+G(d)), the reaction involves intermediate formation of the corresponding hydroxylamine derivative followed by its heterocyclization.     

Cyclocondensation of methyl 2-(5-methylisoxazol-3-yl)imino-3,3,3-trifluoropropionate with 1,3-binucleophiles

Cyclocondensation of methyl 2-(5-methylisoxazol-3-yl)imino-3,3,3-trifluoropropionate with 1,3-binucleophiles such as benzamidines, aminothiazoline, and 2-aminocrotonic acid nitrile results in trifluoromethyl-containing 3,5-dihydro-4-ones, 2,3-dihydro-6H-imidazo[2,1-b]thiazol-5-one, and 4,5-dihydro-1H-pyrrole-3-carbonitrile.     

New Modulators of NMDA-Receptors Based on Alkyne-Azide Click-Reaction Between 2-Aminothiophene-3-carboxylic Acids Esters and N-Propargyl-Containing Pharmacophores

Russian Journal of General Chemistry - Copper-catalyzed alkyne-azide 1,3-dipolar cycloaddition of methyl esters of N-azidoacetyl-2-aminothiophene-3-carboxylic acids to N-propargyl-containing...     

Investigation of the mechanism of reaction of S-ethyl-N,N′-tetraethyldiamidothio-phosphite with [C5H 5Mn(CO)2NO]+BF by fourier transform infrared spectroscopy

FT-IR spectroscopy and a special mathematical program were used for the real-time monitoring of the mechanistic path of the reaction of S-ethyl-N,N-tetraethyldiamidothiophosphite with [CpMn(CO)-₂NO]⁺BFequation/tex2gif-stack-3.gif. The formation of a few intermediates is described.     

Magnetic,resonant, and thermal properties of Fe<Subscript>0.27</Subscript>Mn<Subscript>0.73</Subscript>S crystals

Fe_0.27Mn_0.73S single crystals were studied. A magnetic transition is detected near 197 K, which is accompanied by anomalies of the thermal, electrical, and resonant properties.     

Edge misfit dislocations in GexSi1 ? x/Si(001) (x ～ 1) heterostructures: role of buffer GeySi1 ? y (y < x) interlayer in their formation

The structure of dislocations in Ge _x Si_{1 − x} (x ∼ 0.4–0.8) films grown by molecular beam epitaxy on Si(001) substrates tilted by 6° toward the nearest (111) plane has been studied. The epitaxy of GeSi films on substrates deviating from the exact (001) orientation has allowed us to establish the main mechanism of formation of edge misfit dislocations (MDs), which most effectively (for heterostructures of the given composition) relieve stresses caused by the mismatch between lattice parameters of the film and substrate. Despite the edge MDs being defined as immobile (sessile) dislocations, their formation proceeds according to the gliding mechanism proposed by Kvam et al. [J. Mater. Res. 5, 1900 (1990)]. A comparative estimation of the propagation velocities of the primary and induced 60° dislocations, as well as the resulting 90° MDs, has been performed. It has been established that the condition providing for the most effective edge MD formation by the induced nucleation mechanism is the appearance of 60° MDs in a stressed film immediately after it reached a critical thickness. A source of these dislocations can be provided by a preliminarily grown buffer GeSi layer that occurs in a metastable state at the initial stage of plastic relaxation.     

Specific features of the combustion of hydrogen-oxygen mixtures near the lower concentration flammability limit

The combustion of hydrogen-air mixtures near the lower composition flammability limit in cylindrical reactors of various diameters is studied. The speed of flame propagation in the horizontal direction is lower than that in the upward direction. Chromatographic analysis showed that, during the combustion of these mixtures, hydrogen is consumed only partially. That the flame propagates despite a low adiabatic temperature can be explained by the formation of the well-known cellular structure.     

Magnetic and electrical properties of cation-substituted sulfides MexMn1 ? xS (Me = Co, Gd)

The temperature dependences of the specific magnetization σ and the electrical resistivity ρ of Me _x Mn_{1 − x} S single crystals (Me= Co, Gd; x= 0.05) have been studied in the temperature range 80 K < T < 1000 K. The samples under study have revealed the presence of a spontaneous magnetic moment below the Néel temperature (T _N) and ferromagnetic clusters in Gd_0.05Mn_0.95S in the temperature range 146 K < T < 680 K. Substitution of gadolinium for manganese initiates a transition from p-type to n-type conduction. The change in the conduction type is accompanied by an increase in the electrical resistivity at 300 K by approximately one order of magnitude and, accordingly, by a decrease in the activation energy. The magnetic and electrical properties of the crystals under study have been interpreted in terms of the cluster model with temperature-dependent ferromagnetic exchange and an electron localized in this cluster. Original Russian Text ? S.S. Aplesnin, L.I. Ryabinkina, O.B. Romanova, V.V. Sokolov, A.Yu. Pichugin, A.I. Galyas, O.F. Demidenko, G.I. Makovetskiĭ, K.I. Yanushkevich, 2009, published in Fizika Tverdogo Tela, 2009, Vol. 51, No. 4, pp. 661–664.     

Monodisperse spherical meso–macroporous silica particles: Synthesis and adsorption of biological macromolecules

Monodispersed spherical silica particles, including large mesopores (over 10 nm) and macropores (up to 100 nm) were obtained by chemical etching in an autoclave. A method for introducing globular protein myoglobin molecules into the pores is developed. The method of filling is based on a high adsorption capacity of the developed internal pore structure of the particles. The structure and adsorption properties of the materials are studied.