Synthesis of aromatic derivatives of 1,5-benzodiazepine in the reaction of 4-nitro-o-phenylenediamine with chalcone dibromides

The reaction of 4-nitro-o-phenylenediamine with 4-nitro-4-R-chalcone dibromides affords the corresponding -(2-amino-4-nitroanilino)chalcones; x-ray diffraction data indicate that these are the Z-isomers. Experiments have been perfortned to determine the conditions required for cyclization of these compounds into 2, 4-diaryl7(8)-nitro-1, 5-benzodiazepines. In the solid phase or in ethanol solutions, these latter compounds exist primarily in the 3H tautomeric form; but in DMSO solutions, the 1H form predominates.Khar'kov State University, Khar'kov 310077. Institute of Heteroorganic Chemistry, Russian Academy of Sciences, Moscow 117813. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 950–958, July, 1995. Original article submitted June 30, 1994; revision submitted April 3, 1995.Deceased     

Spectrophotometric determination of ziram (dithiocarbamate fungicide) by thiocyanate and rhodamine 6G method

A sensitive spectrophotometric method has been developed for the determination of ziram in water, vegetables and grains. The method is based on the dissociation of dithiocarbamate complex of zinc with thiocyanate and rhodamine 6G at pH 4 to form a pink coloured complex that is stabilized by gelatin. The method is simple and Beer's law is obeyed over the concentration range of 0.05-1 ppm of ziram. The method is free from interference of similar dithiocarbamate fungicides containing Mn(2+) and Fe(3+) ions.     

Europium isotope separation in the HCl/HDEHP extraction system

The^153/151Eu isotope separation factor (q) for the Eu(II)/Eu(III) chemical exchange in the liquid-liquid extraction system, containing Eu (III) in di (2-ethylhexyl) phosphoric acid (HDEHP) and Eu(II) in water acidified with hydrochloric acid, was found to be 0.9993±0.0002 (2) for the single stage. Some theoretical aspects of separation of the Eu isotopes are discussed. The decisive role of the electron exchange reaction and complexation by the counter-ion in the aqueous phase is emphasized.     

The development of a sampler-sensor using a vanadium-oxinate-polymer film for the selective and direct determination of atmospheric ethanol

The development of a sensor for the direct and selective determination of atmospheric ethanol is in the initial stages. The sensor takes advantage of the selective chemical reaction between ethanol and vanadium oxinate. This reaction occurs in an organic medium where a red colored complex is the product. This reaction is determined spectrophotometrically where the absorbance maxima is 475 nm. The focus of this paper is to discuss the parameters necessary to develop a solid sorbent sampling-sensor which can be used to determine atmospheric ethanol.     

Shed plane leaves as a source ofα-tocopherol

A natural source of -tocopherol — shed plane leaves — has been found. The dynamics of the accumulation of a-tocopherol over the vegetation period of the plant has been studied, and a method has been developed for its isolation and quantitative determination.Deceased.Institute of the Chemistry of Plant Substances, Academy of Sciences of the Republic of Uzbekistan, Tashkent, fax (3712) 89 14 75. Translated from Khimiya Prirodnykh Soedinenii, No. 3, pp. 372–374, May–June, 1995. Original article     

A new convenient method for the synthesis of mixed-ligand β-diketonato Tc(III) complexes

A new convenient method has been proposed to synthesize mixed-ligand -diketonato Tc(III) complexes, using the ligand exchange reaction [Tc(acac)₂(CH₃CN)₂]⁺+L^–[Tc(acac)₂L]+ +2CH₃CN where L is bza, dpm or dbm. The yield was about 30–40%. UV-visible and IR spectra of these complexes were measured. Characteristic features of the compounds were compared with those of the corresponding complexes of ruthenium.     

Determination of aromatic sulfonic acids in industrial waste water by ion-pair chromatography

A method for the identification and quantification of aromatic sulfonic acids in industrial waste water has been developed. The preparation of the samples comprises a clean-up step and an enrichment step, utilizing i) reversed-phase extraction and ii) ion-pair solid phase extraction. The aromatic sulfonic acids are separated by ion-pair chromatography with diode-array detection. An advantage of the developed ion-pair chromatographic method is the separation of linear alkylbenzenesulfonic acids (LAS), lignosulfonic acids and aromatic sulfonic acids in one chromatographic run. Also described is an optimized clean-up procedure for collected fractions of a preparative chromatographic run to identify monosulfonic acids with GC/MS after methylation. The detection limits for aromatic sulfonic acids in industrial waste waters are at the g/l level.     

Influence of samarium on the electrocatalytic activity of platinum electrodes for the hydrogenation of benzene

The hydrogenation of benzene on platinum electrodes in 0.5 M sulfuric acid as supporting electrolyte has been studied in the presence and the absence of samarium in solution. The hydrogenation overpotential of preadsorbed benzene was diminished to 90 mV with samarium in the solution and the hydrogenation current was significatively increased. These results are interpreted in terms of a synergic effect of samarium on hydrogen adsorption and, consequently, on the electrocatalytic activity of the platinum electrode for the hydrogenation of benzene.     

An impedance analyzer method to simulate the oscillating characteristic of a series piezoelectric sensor in oscillators with zero or non-zero phases

An impedance analyzer method is employed to simulate the oscillation frequency of a series piezoelectric quartz crystal (SPQC) in electrolyte or non-electrolyte solutions. The influence of the oscillator phase on the oscillation frequency and response sensitivity are theoretically derived and experimentally verified. In non-electrolyte liquids, the oscillator phase has little effect on both the oscillation frequency and the response to the permittivity. But in electrolyte solutions, the oscillator phase has a significant influence on the oscillation frequency and the response sensitivity to the conductivity. Depending on the oscillator phase, the oscillation frequency of the SPQC may increase, be maintained or decrease with increasing conductivity in low or high conductive solutions. The dependence of the oscillation frequency of the SPQC on the supply voltage is explained. As an example of the applications, the SPQC is applied to the determination of the critical micelle concentration of ionic surfactants in aqueous solutions.