Models for estimating the non-specific toxicity of organic compounds in short-term bioassays

The solvation parameter model is used to construct equations for the estimation of the non-specific toxicity of neutral organic compounds to five organisms used for short-term toxicity testing. For the bacteria Vibrio fischeri (Microtox test) and Pseudomonas putida, the protozoan Tetrahymena pyriformis (Tetratox test), the green alga Scendesmus quadricauda and the brine shrimp Artemia salina, the main factors resulting in increased non-specific toxicity are size (dominantly) and lone-pair electron interactions, with hydrogen-bond basicity the most important solute property reducing toxicity. Species differences in relative non-specific toxicity are largely related to differences in cohesion and hydrogen-bond acidity of the biomembranes. The models for non-specific toxicity are proposed as an alternative to the octanol-water distribution constant for the determination of baseline toxicity. Failure of the octanol-water distribution constant to model non-specific toxicity is quantitatively explained by its inability to adequately characterize the sorption properties of the biomembranes for compounds with varied properties.     

Experimental setup for the determination of analytes contained in ultrasonically levitated drops

An automated technique for the determination of analytes in an ultrasonically levitated sample of 2 to 5 microL volume has been developed. Contactless dosing of reagents or solvents into an ultrasonically levitated drop was realized via piezoelectric micropumps. Drop size was continually controlled with a programmed CCD camera. A diode array spectrometer designed for the use with optical fibers was used for absorption and fluorescence measurements. Determinations via direct absorption measurements following the method of standard addition and acid-base titrations with an absorption indicator and a fluorescent indicator were carried out. The mean consumption of sodium hydroxide added via a piezoelectric micropump in five successive titrations with 18 nmol of sulfuric acid inside a levitated drop (indicator bromothymol blue) had a relative standard deviation of 0.7% and differed only by 0.2% from the expected value.     

An efficient synthesis of cyclodextrin-based carbohydrate cluster compounds

[formula: see text] The photoaddition of the thiol 2,3,4,6-tetra-O-acetyl-beta-D-1-thioglucopyranose to the allyl ether functions of per-2-allyl-, per-6-allyl-, and per-2,6-diallyl-beta-cyclodextrin derivatives provides a remarkably simple and efficient way for attaching glucopyranose units onto (1) the secondary face, as well as (2) the primary face, of beta-cyclodextrin--not to mention (3) both the primary and secondary faces, simultaneously--in yields of up to 70%.     

Kinetic parameters obtained from TG and DTG curves of acrylamide-maleic anhydride copolymers

The thermal behaviour of acrylamide-maleic anhydride copolymers was studied by thermogravimetric (TG and DTG) analysis. The obtained data permitted the calculation of activation energies and reaction orders of the decomposition steps by the Coats-Redfern and Freeman-Carroll methods.Thermal analysis shows four distinct peaks in the case of polyacrylamide and AAMA (71) copolymer and only three for AAMA (11) copolymer.In AA:MA (11) copolymers intermolecular imidization occurs only and thermal degradation is influenced more by the anhydride groups which are equal in number with the amide ones.

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Zusammenfassung Das thermische Verhalten von Acrylamid-Maleinsäureanhydrid-Kopolymeren wurde durch thermogravimetrische Analyse (TG und DTG) untersucht. Aus den erhaltenen Daten wurden die Aktivierungsenergien und Reaktionsordnungen der Zersetzungsschritte nach den Methoden von Coats-Redfern und Freeman-Carroll berechnet. Durch thermische Analyse können im Falle von Polyacrylamid und AAMA (71 (-Kopolymeren 4 Peaks und bei AA:MA (11) -Kopolymeren nur 3 Peaks unterschieden werden. Bei AAMA (1 1)-Kopolymeren verläuft nur eine intermolekulare Imidisierung und der thermische Abbau wird mehr durch die in gleicher Zahl wie die Amidgruppen vorliegenden Anhydridgruppen beeinflußt.

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T () — (). , - -, . : ( 71) , : 11 — . : 11 , , .

     

Detection and separation of two forms of cotton-plant pyrophosphatase

Two pyrophosphatase isoenzymes with identical molecular weights but differing in the pH optima of their action and also in their senstivity to some bivalent metal ions have been isolated from extracts of the cotyledons of three-day cotton-plant shoots by gel filtration and ion-exchange chromatography.V. I. Lenin Tashkent State University. Translated from Khimiya Prirodnykh Soedinenii, No. 3, pp. 375–378, May–June, 1985.     

Analytical Application of Silica Gel Modified with Didecylaminoethyl-beta-Tridecylammonium Iodide

Sorption of a high molecular weight quaternary ammonium salt, didecylaminoethyl-β-tridecylammonium iodide (DDATD) on different types of sorbents was investigated. The nature of reagent adsorption on silica gel was examined by spectroscopic and computer methods. The sorption of anionic metal complexes of cobalt, copper, zinc and manganese on silica gel modified with DDATD was studied. The possibility of recovery of cobalt and copper thiocyanate complexes and their further atomic absorption determination is shown. Modified sorbent was applied to cobalt chemiluminescence and determined in natural water and a nickel preparation (detection limit, 2 μg/l.).     

Structure of phenolic stabilizers for polymers VIII. Crystal structure of 2,2′-methylenebis(4-methyl-6-ter-butylphenol) monoacrylate

L. Ya. Karpov Scientific-Research Physicochemical Institute. Scientific-Research Institute of Rubber and Latex Goods. Translated from Zhurnal Strukturnoi Khimii, Vol. 32, No. 5, pp. 162–164, September–October, 1991.     

Formation of quasistationary states in polyatomic systems

Conclusions The results from our analysis of quasistationary states in real molecules and solid clusters provide us with grounds for stating that the proposed method can be used successfully to predict the number of resonances of form in molecules and to obtain approximate estimates of their characteristics.In studies in this area at the qualitative level, it is easy to establish the genealogy of the resonances (i.e., from which atomic states they have proceeded) and the effective value of the quantum number characterizing one resonance or another. In qualitative analysis, the mutual positions of the resonances are indicated approximately; with increasing number of atoms, the inaccuracy increases. Moreover, without carrying out the calculation, it is impossible to estimate the resonance energy, as it is impossible to distinguish reliably between resonances from collective free states of the discrete spectrum and from the rudiments of resonances.Nonetheless, it is possible to use the proposed method to judge trends in the change of resonances from one compound to another. Particularly valuable, in our view, is the possibility that is offered here for the use of very nearly the entire arsenal of the qualitative LCAO-MO theory.In order to obtain semiquantitative estimates of the characteristics of resonances, a model with potential wells is applicable. In simple cases, calculations using this model can be performed on a microcalculator.Rostov Institute of Agricultural Machinery Construction. Translated from Zhurnal Strukturnoi Khimii, Vol. 32, No. 5, pp. 3–8, September–October, 1991.     

Micellar enhanced cyanide ion determination in samples from synthetic organic processes

A method was developed for the recovery and determination of cyanide ion in organic sample matrices. To facilitate the solubilization of cyanide ions, cetyltrimethylammonium bromide (CTAB) was added at concentrations above the critical micelle concentration. Sample cyanation reaction products consisted of solvent mixtures of a hydroxynitrile in DMF-toluene or DMF-isopropylacetate (IPAC). Spectrophotometric determination of cyanide ion at 578 nm by the pyridine-barbituric acid method was automated by flow injection analysis. Recovery of cyanide ion from spiked samples was 93.2% in DMF-IPAC solvent matrix and 93.9% in DMF-toluene. Low alkali concentration was observed to favor solubilization of cyanide ion in the micellar solution.