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  • Chemistry  (12)
Collection
Publisher
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 100 (1967), S. 1602-1615 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die reversible 2:1-Cycloaddition von Benzyliden-alkylaminen oder 3.4-Dihydro-isochinolin and Senföle führt zu Hexahydro-s-triazin-thion-Derivaten, die Addition an Schwefelkohlenstoff zu Hydro-1.3.5-thiadiazin-thionen. Benzyliden-methylamin vereinigt sich mit Benzoylsenföl zu einem gelben Diels-Alder-Addukt. Der 1.4-Dipol aus Isopropyliden-isopropylamin and Schwefelkohlenstoff stabilisiert sich durch 1.5-Protonenverschiebung und Folgereaktionen zu einem Thiazolinthion.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 32 (1986), S. 4657-4661 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    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: An unusual one-component sealant based on a moisture cure has been developed. The chemistry involves the reaction of a 1,3-dipole (a difunctional nitrile oxide) with a dipolarophile (an unsaturated polymer); a difunctional hydroximoyl chloride, which forms a nitrile oxide on reaction with a latent base, reacts with the polymer on exposure to moisture by forming isoxazoline crosslinks. The hydroximoyl chloride was prepared from a bis(chloroketone) (e.g., 4,4′-bis(chloroacetyl)diphenyl ether), by reaction with nitrous acid; this avoided the use of expensive dialdehydes, as well as hydroxylamine. The preferred latent base was barium oxide, and almost any unsaturated polymer could be used. Such a system, stable indefinitely when dry, crosslinked rapidly when exposed to atmospheric moisture. Since water is generated when the initially formed barium hydroxide reacts with the hydroximoyl chloride, only catalytic amounts are required, and thick beads cure completely; skinning causes problems with other moisturecurable systems.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 11 (1967), S. 73-84 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    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: Complexes of aluminum alkyls with Lewis bases catalyze the polymerization of vinyl chloride. Triethylaluminum is most effective, but other compounds of type R3Al, R2AlCl, R2AlH, and LiAIR4 are operable. Dialkylmagnesiums are active, but Grignard reagents, as well as a number of other metal alkyls are inactive. Among Lewis bases, tetrahydrofuran (THF) and tetrahydropyran give the best yields of poly(vinyl chloride). Oxygen bases, such as ethers and esters, are more effective than nitrogen bases, e.g., tertiary amines. Cyclic compounds are better than acyclic ones. The polymerization occurs in a variety of hydrocarbon, chlorinated hydrocarbon, or ether solvents, but especially well in CCl4. Radical polymerization is probably initiated through the reaction R3Al:Base + CCl4 → R2AlCl: Base + R + Cl3C., to form trichloromethyl radical.
    Additional Material: 8 Tab.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The Effect of Water on the Catalytic Activity of Bis(π-cyclopentadienyl)titanium Dichloride-Dimethylaluminium Chloride for the Polymerization of Ethylene)The combination (C5H5)2TiCl2 -(CH3)2AlCl has little, if any, activity as a catalyst for the polymerization of ethylene. The addition of small amounts of water, ca. 0.2-0.5 mole per mole of aluminium, converts it into an extremely active catalyst. Other additives, e. g., alcohols or oxygen, do not show the same effect. The reaction is discussed.
    Notes: Die Kombination (C5H5)2TiCl2-(CH3)2AlCl hat, wenn überhaupt, nur geringe katalytische Aktivität für die Polymerisation von Äthylen. Die Zugabe geringer Mengen Wasser, ca. 0.2 -0.5 mol pro mol Aluminium, verwandelt diese Kombination in einen außerordentlich aktiven Katalysator. Andere Zusätze, z. B. Alkohole oder Sauerstoff, haben nicht die gleiche Wirkung. Der Reaktionsmechanismus wird diskutiert.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Sodium ethylenesulfonate polymerizes readily in aqueous solution under the influence of ultraviolet light or in the presence of peroxide catalysts. The most important variable in the polymerization has been found to be the concentration of monomer, increased concentration leading to more rapid polymerization and higher molecular weights. Poly(sodium ethylenesulfonate) has been isolated as a brittle, white solid with weight-average molecular weights as high as 150,000. Sodium ethylenesulfonate copolymerizes with a variety of water-soluble monomers: acrylamide, acrylic and methacrylic acids, and their sodium salts. Although copolymerization occurs, water-soluble copolymers of sodium ethylenesulfonate with acrylonitrile and with methyl acrylate could not be prepared. Water-soluble copolymers of sodium ethylenesulfonate with vinyl acetate and with vinyl chloride have been made, but they contain only small amounts of acetate and chloride. No copolymers could be prepared with butadiene, isobutylene, styrene, α-methylstyrene, n-butyl vinyl ether, allyl alcohol, N-allylacetamide, maleic acid, or fumaric acid. The copolymerization of sodium ethylenesulfonate with acrylamide and with sodium acrylate has been used to calculate reactivity ratios. From these, sodium ethylenesulfonate has been calculated to have a Q value of 0.19 and an e value of +1.51.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 31 (1958), S. 253-254 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 38 (1959), S. 274-275 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 41 (1959), S. 519-520 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Tab.
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  • 9
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 41 (1959), S. 520-521 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 41 (1959), S. 521-522 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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