Chlorination of 2-substituted 1-hydroxyindoles

Russian Chemical Bulletin - Chlorination of 1-hydroxyindole-5,6-dicarbonitriles and 1-hydroxypyrrolo[3,4-f]indole-5,7(1H,6H)-diones with N-chlorosuccinimide afforded previously unknown...     

Synthesis of (polycyanoisopropyl)[60]fullerene

The reaction of fullerene with excess 2,2′-azobis(isobutyronitrile) in o-dichlorobenzene at 60°C was studied, and the chemical structure of the reaction product was determined.     

Decoration of Carbon Nanotubes with MnO2 Nanoparticles Under Potassium Permanganate Treatment

Russian Physics Journal -     

The role of the porous structure of the filler in the reinfo rcement of polymers

Composites consisting of polyethylene and porous fillers with various pore sizes (from 22 to 115 Å) and surface types have been investigated. It is shown that the polymer filling the pores takes part in the deformation processes. The modulus of elasticity of the filled polymers is directly proportional to the filler surface per gram polymer. It is proposed to characterize the activity of the fillers by reference to the slope of the straight lines E-S with the hydrodynamic effect excluded.Institute of Polymer Mechanics, Academy of Sciences of the Latvian SSR, Riga. Translated from Mekhanika Polimerov, No. 2, pp. 253–258, March–April, 1973.     

Interaction of nickel hydroxocarbonate,ammonium paramolybdate,and ammonium metatungstate under mechanical activation

The interaction of nickel hydroxocarbonate, ammonium paramolybdate, and ammonium metatungstate (Ni: Mo: W = 3: 1: 1) is reported. Under mechanical activation conditions, nickel hydroxocarbonate particles undergo comminution and ammonium paramolybdate and ammonium metatungstate particles soften and aggregate. It is demonstrated by DTA, X-ray diffraction, and IR spectroscopy that heat treatment of the mechanically activated mixture at 400–450°C yields the salts NiMoO₄ and NiWO₄.     

Formation of mixed J-aggregates of cyanine dyes stimulated by Eu<Superscript>+3</Superscript> cations

The block mechanism of the formation of J-aggregates from the dimers of various dyes in an aqueous solution under the action of the multiply charged Eu⁺³ cation was considered for the first time. It was shown that the structure and the position of the absorption maximum of the mixed J-aggregates are determined by the length of the dye chromophore moiety. It was concluded that the mixed J-aggregates are of interest as nanosized optical elements with varying optical and electronic properties depending on the structure of cyanines used.