Effect of maltodextrins on the surface activity of small-molecule surfactants

We report on the effect of commercially important polysaccharides (maltodextrins with variable dextrose equivalent (Paselli SA-2, MD-6 and MD-10) on the surface activity at the air–water interface of small-molecule surfactants (sms), possessing different hydrophobic–lipophilic balance ((SSL (Na⁺), the main component is a sodium salt of stearol–lactoyl lactic acid, and PGE (080), polyglycerol ester of C18 fatty acid), and widely used in food products. A marked change of the surface activity of sms was found in the presence of maltodextrins by tensiometry. The combined data of laser multiangle light scattering and mixing calorimetry have suggested that this result is governed by specific complex formation between maltodextrins and sms in aqueous medium. Measurements have been made of the molar mass, the second virial coefficient and the enthalpy of intermolecular interactions in aqueous solutions. The implication of a degree of polymerization of maltodextrins in this phenomenon was shown. The interrelation between the molecular parameters of the formed complexes and their surface activity at the air–water interface has been revealed and discussed.     

Infrared reflection spectra in contactless nondestructive measurements of the electron density and mobility in indium phosphide

On the basis of numerical calculations and experimental studies we analyze the possibilities of measuring the electrophysical parameters of indium phosphide by means of infrared reflection spectra at wavelengths ranging from 5 to 200 m. We demonstrate that contactless nondestructive measurements of the electron density in the range 10¹⁶–10²⁰ cm^–3 can be made with a relative error not exceeding 15%, and of mobility with a relative error not exceeding 25%. A nomogram method is presented for rapid conversion of data from infrared reflection spectra into the parameters being measured.Translated from Izvestiya Vysshikh Uchebnykh Zavedenii, Fizika, No. 1, pp. 22–27, January, 1988.     

Crystal and molecular structure of 3β-acetoxy-22S,25-epoxyholosta-7,9(11)-dien-17α-ol

A complete x-ray structural investigation has been made of 3-acetoxy-22S,25-epoxyholosta-7,9(11)-dien-17-ol. Important conformational differences between this compound and its 17-deoxy derivative have been found which show the mobility of the conformation of rings B and C of the holostane series and the tetrahydrofuran ring of the side chain of the molecule. It has been shown that the conformation of the side chain of the molecule is stabilized by an 017-H...022 intramolecular hydrogen bond, without excluding the possibility of the participation of the hydroxy group in the formation of intermolecular hydrogen bonds (bifurcated).Pacific Ocean Institute of Bioorganic Chemistry, Far Eastern Branch, Russian Academy of Sciences, Vladivostok. Translated from Khimiya Prirodnykh Soedinenii, Nos. 3,4, pp. 341–344, May–August, 1992.     

Influence of alkali metal and ammonium cations on the structure of iron(II) and cobalt(III) hexacyanide complexes encapsulated in faujasite

Changing the cation composition (Na⁺ to K⁺, NH₄ ⁺ Cs⁺) of faujasite with hexacyanoferrate(II) encapsulated in the large pores causes distortion of the octahedral symmetry of the complex.Translated from Teoreticheskaya i Éksperimental'naya Khimiya, Vol. 30, No. 5, pp. 293–297, September–October, 1994.     

Interconnection between the Structures and Sorption Characteristics of Mesophase Materials of MCM-41 Type Containing Alkylpyridines

Under the conditions studied for the synthesis of mesophase materials with alkylpyridinium halides an increase in the density of packing of these molecules in the encapsulated micelles was observed with an increase in the length of the alkyl radicals. The difference in the density of packing of these surface active reagents (SAR) depended to a considerable extent on the perfection of the hexagonal structure and the characteristic absorption properties of the mesophase materials of MCM-41 type.     

Influence of the crystallinity of pentasil-type zeolites on their acidity

The acid properties of intermediate products in crystallization of pentasil-type zeolites have been investigated using programmed thermal desorption of ammonia and adsorption of pyridine. It was found that acidity increases with increasing crystallinity due to proton-donor centers. A correlation was established between this change in acidity and methanol TPSR data.Translated from Teoreticheskaya i Éksperimental'naya Khimiya, Vol. 31, No. 1, pp. 48–51, January–February, 1995.     

Mesoporous Titanium-containing Silicas. Synthesis and geometrical characteristics

Mesoporous titanium-containing silicas with TiO₂ contents from 1 up to 70 mol% were prepared. The obtained samples have been characterized by the powder X-ray diffraction data, the diffuse reflectance infrared Fourier transform method, and nitrogen adsorption at 77 K. Specific surface area, total pore volume, distribution pore volume on pore sizes were determined from nitrogen adsorption isotherm for synthesized titanosilicas. This revised version was published online in August 2006 with corrections to the Cover Date.     

Tetrabutylammonium Salts of Ruthenium(II) Nitroso Complexes

The paper describes synthesis of (nBu₄N)₂[RuNOCl₅](I), (nBu₄N)₂[RuNOCl₄OH](II), (nBu₄N)₂×[RuNOCl₄OH]·6H₂O (III), and (nBu₄N)₂[RuNOCl₅]· 2(nBu₄N)₂[RuNOCl₄(H₂O)]·2H₂O (IV). The complexes were studied by IR spectroscopy and powder Xray and crystal Xray analyses. The structures are built up of [RuNOCl₅]^2- (I, IV), [RuNOCl₄OH]^2- (II, III), and [RuNOCl₄(H₂O)]^- (IV) complex anions, (nBu₄N)⁺ cations, and crystal water molecules (III, IV). The substances are moderately soluble in water; highly soluble in polar organic solvents, such as acetone, ethanol, chloroform, methylene chloride; and almost insoluble in carbon tetrachloride and toluene. Under storage in light, the compounds decompose from the surface; in darkness I and II are stable, whereas III and IV can lose part of the crystal water.