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  • Chemistry  (12)
  • 1 H-NMR spectroscopy  (1)
  • Desulfobulbus propionicus  (1)
  • 2015-2019
  • 1980-1984  (14)
  • 1984  (14)
Collection
Keywords
Publisher
Years
  • 2015-2019
  • 1980-1984  (14)
Year
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 139 (1984), S. 167-173 
    ISSN: 1432-072X
    Keywords: Propionate formation ; 13C NMR ; Desulfobulbus propionicus ; Sulfate reducing bacteria
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Whole cells of Desulfobulbus propionicus fermented [1-13C]ethanol to [2-13C] and [3-13C]propionate and [1-13C]-acetate, which indicates the involvement of a randomizing pathway in the formation of propionate. Cell-free extracts prepared from cells grown on lactate (without sulfate) contained high activities of methylmalonyl-CoA: pyruvate transacetylase, acetase kinase and reasonably high activities of NAD(P)-independent L(+)-lactate dehydrogenase NAD(P)-independent pyruvate dehydrogenase, phosphotransacetylase, acetate kinase and reasonably high activity of NAD(P)-independent L(+)-lactate dehydrogenase, fumarate reductase and succinate dehydrogenase. Cell-free extracts catalyzed the conversion of succinate to propionate in the presence of pyruvate, CoA and ATP and the oxaloacetate-dependent conversion of propionate to succinate. After growth on lactate or propionate in the presence of sulfate similar enzyme levels were found except for fumarate reductase which was considerably lower. Fermentative growth on lactate led to higher cytochrome b contents than growth with sulfate as electron acceptor. The labeling studies and the enzyme measurements demonstrate that in Desulfobulbus propionate is formed via a succinate pathway involving a transcarboxylase like in Propionibacterium. The same pathway may be used for the degradation of propionate to acetate in the presence of sulfate.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Reactions of insertion of components serving as bridges between a pharmacologically active constituent and a water-soluble telomeric chain, were carried out. Model compounds containing hydroxyl, amine or carboxylic functions were studied. In each case a bifunctional compound could be found, which is capable of reacting with the model. The resulting products could be fixed on a telomer. The results with the model compounds were applied to the fixation of the carboxylic drug indometacin.
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  • 3
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The telomerization of vinylidene chloride with CHCl3, CCl3Br, Cl3C—CO2CH3, Cl3C—CF3, Cl3C—CF2—CFClX (X = Cl, Br), and CCl3CF2CCl3 was carried out by redox catalysis. The first adducts of each reaction were isolated and identified. The hydrolysis of these telomers containing a CCl3 group at the chain-end by means of oleum led to a series of halogenated acids, some of them being olefinic ones.
    Additional Material: 3 Tab.
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  • 4
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The photodecomposition of several sulfonic esters of α-hydroxymethylbenzion (1a) was studied by means of ESR and 1H NMR-CIDNP techniques. An exclusive α-cleavage into benzoyl and α-hydroxy-α-sulfonyloxymethylbenzyl radicals (6 and 7) through a triplet excited state was observed. Radicals (7) were found to undergo elimination of sulfonic acid to give benzoylmethyl radicals (9) in an extremely fast process. Chemical confirmation was provided by naphthalene quenching and radical-trapping experiments using 1-dodecanethiol and 2,2,6,6-tetramethylpiperidin-1-oxyl, respectively. Photodecomposition of the sulfonic esters in the presence of 1,1-diphenylethylene as a model substrate for vinyl monomers indicated that both benzoyl and benzoylmethyl radicals are highly reactive towards the carbon-carbon double bond.
    Additional Material: 5 Tab.
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  • 5
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Ternary phase diagrams of linear tri-block and multi-block copolymers consisting of poly(dimethylsiloxane) with a constant segment mass of M̄n = 103 and varying poly(oxyethylene) segment masses in the range 100 ≤ M̄n ≤ 2000 with water and oil (cyclohexane) are reported. Also binary mixtures of the same copolymers with water and oil are investigated by differential scanning calorimetry (DSC). Microphase separation of the copolymers and different states of water are detected as a function of composition and structure of the copolymers as well as oil and water content, respectively. The results are discussed in terms of a model having an interphasial zone where intermixing of the dissimilar segments occurs.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Chain extension reactions involving α,β-bifunctional precursor polymers and bifunctional coupling agents of low molecular weight were investigated both theoretically and experimentally. The number and weight molecular weight distributions were calculated, and computer simulations were performed, neglecting the weight of the coupling agent with respect to that of the precursor polymer. Examples of such chain extension reactions include the polycondensation of “living” α,β-dicarbanionic polystyrene with 1,4-bis(bromomethyl)benzene, and the reaction of poly(oxyethylene)glycol with a low-molecular-weight diisocyanate. The characterization of the resulting polymers yields results that are in satisfactory agreement with the theoretical expectation.
    Additional Material: 5 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 185 (1984), S. 1583-1595 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The redox telomerization of vinylidene chloride with carbon tetrachloride catalyzed by iron or copper salts was thoroughly studied. The DP of the telomers obtained vary from 1 to 100, roughly. The concentration of the reactants and the nature of the solvents exert some effect on the molecular weight distribution. The first adducts 1a - 1d (n = 1 to 4) were isolated and identified by NMR spectroscopy and viscosimetry.
    Additional Material: 3 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 185 (1984), S. 453-458 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Isotopically substituted styrene, (phenyl-2H5) styrene (3), and selectively labled styrene, [alpha;, beta;-2H2] styrene (6), were prepared by the classical two step synthesis, starting with the correspondingly labeled compounds. By anionic polymerization in an inert atmosphere labeled high molecular weight polystyrences 10 and 11 were prepared.
    Additional Material: 4 Ill.
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  • 9
    ISSN: 1573-4986
    Keywords: 1 H-NMR spectroscopy ; glycopeptide ; rat hemopexin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Rat hemopexin is a plasma glycoprotein that contains 18.3% carbohydrate consisting of onlyN-glycosidically-linked oligosaccharide chains. Glycopeptides obtained from hemopexin by Pronase® digestion could be separated on Concanavalin A-Sepharose into three fractions. The lectin-binding fraction has been characterized as a mixture of monosialyl and disialyl di-antennary compounds ending inN-acetylneuraminic acid residues α(2-6)-linked to galactose in the respective branches [Bernard N, Lombart C, Strecker G, Montreuil J, Van Halbeek H, Vliegenthart JFG (1983) Biochimie 65:185–92]. The structures of the glycans in the Concanavalin A non-binding fractions were determined by a combination of methylation analysis and 500-MHz1H-NMR spectroscopy. Some of them appeared to be tri-antennary glycans. However, the major component of these fractions possesses the following structure: This type of structure has been encountered before in some bovine blood coagulation factors as well as in rat α-acid glycoprotein, but the1H-NMR parameters for it are first reported here. Furthermore, by methylation analysis, the occurrence of the NeuAcα2-8NeuAc disaccharide element was demonstrated in a minor part of the carbohydrate moiety of rat hemopexin. This element has also been reported previously for rat brain glycopeptides.
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  • 10
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The Lower Critical Solution Temperature (LCST) of polyethylene (PE), polypropylene (PP), and ethylene-propylene block and random copolymers have been measured in heptanes. A thermogram related to the variation of the turbidity of the solution is obtained between 100 and 210°C. The temperature of the onset of the turbidity peak is defined as the LCST of the system. The width and the area of the turbidity peaks are tentatively associated with the polymer polydispersity and the amount of polymer involved in the phase separation. The thermograms of solutions containing both homopolymers show two distinct turbidity peaks situated at a 70°C interval. Correlations of molecular orientations in the concentrated phase, possible in PE systems but not in PP solutions, are at the origin of the lower LCST values for PE solutions. The LCST of copolymers are situated between those of the homopolymers but the dependence of the LCST on the copolymer ethylene content is different for block and random copolymers. Examples of thermograms are also given for mixtures of copolymers with PE and PP. By analysis of their thermograms, some commercial block EP copolymers were also found to contain PK and PP. This method seems well suited for characterizing polymer mixtures.
    Additional Material: 10 Ill.
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