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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 59 (1937), S. 111-112 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of organic chemistry 24 (1959), S. 643-644 
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of organic chemistry 25 (1960), S. 202-205 
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 59 (1937), S. 109-111 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 45 (1960), S. 83-89 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Data are presented for the preparation of high molecular weight and crystalline polymers of allylbenzene. With specific cationic catalysts, low molecular oligomers of β-methylstyrene are produced. With anionic catalysts, such as sodium and cesium, nonpolymerizable metallates are obtained from which the monomer may be regenerated. Stereospecific catalysts, prepared from triethylaluminum and titanium halides have been investigated as catalysts for allylbenzene. Solid polymers of allylbenzene have been obtained only under very specific catalytic conditions.
    Additional Material: 5 Tab.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 37 (1960), S. 25-38 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Synthese von substituierten Hydrazino-s-Triazinen auf zwei verschiedene Weisen sowie der entsprechenden Benzyliden-Verbindungen wird beschrieben. Ein Reaktionsmechanismus für die Bildung dieser Hydrazino-s-Triazine wird vorgeschlagen. Ausgehend von diesen Zwischenverbindungen wurden zwei neue Monomere, nämlich 2,4-Dimethoxy-6-(β-itaconylhydrazino)-s-triazin und 2,6-Diphenoxy-6-(β-itaconylhydrazino)-s-triazin dargestellt. Diese Monomere wurden mit Acrylnitril copolymerisiert und die Reaktionsfähigkeit der Monomeren bestimmt. Die Copolymere ließen sich leicht mit Methylenblau färben.
    Notes: Substituted hydrazino-s-triazines have been synthesized as intermediates by two methods and their benzal derivatives prepared. A possible mechanism for the formation of hydrazino-s-triazines is proposed. Two new monomers, 2,4-dimethoxy-6-(β-itaconylhydrazino)-s-triazine and 2,6-diphenoxy-6-(β-itaconylhydrazino)-sytriazine, prepared from these intermediates were copolymerized with acrylonitrile and the monomer reactivity ratios were determined. The copolymers were found to be readily dyeable with methylene blue.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 38 (1960), S. 56-71 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Methoden, die geeignet sind, die Anfärbbarkeit von Polyacrylnitril zu verbessern, werden eingeteilt und besprochen. Die Copolymerisation des Acrylnitrils mit Monomeren, die basische Farbstoffgruppen in die Polymerenkette einführen, wird als die praktischste Methode der Verbesserung der Färbbarkeit angesehen. Comonomere, die den Pyridin-Ring enthalten, verbessern die Färbbarkeit besonders gut. Um die durch den Pyridin-Ring verursachten basischen Eigenschaften zu verringern, wurden Comonomere mit Diazin-und Triazin-Ringen dargestellt. Die Basizität der Triazin-Comonomeren kann innerhalb weiter Grenzen durch Substitution geändert werden. Es stellt sich heraus, daß stark basische Eigenschaften zur Bindung der Farbstoffe nicht notwendig sind. Die Fähigkeit der Comonomeren zur Komplexbildung spielt für die Anfärbbarkeit der Polymeren ebenfalls eine wichtige Rolle.
    Notes: The methods of improving the dyeability of polyacrylonitrile are reviewed and classified, and the copolymerization of acrylonitrile with comonomers which introduce basic dye sites in the polymer chain is considered the most practical method. Comonomers containing the pyridine ring are especially effective in improving dyeability. To lower the basicity effect of the pyridine ring, comonomers based on diazine and triazine rings were synthesized. The basicity of the triazinyl comonomers can be varied greatly by substitution, and it is concluded that high basicity is not required to bind dyes and the ability of the comonomers to form complexes is also important with respect to dyeability.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 9 (1971), S. 552-552 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 3 (1965), S. 3675-3676 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 5 (1967), S. 287-306 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis and structure determinations of (2,2-dimethyl-1,3-dioxolan-4-yl)-methyl acrylate, 4-(2,2-dimethyl-1,3-dioxolan-4-yl)methyl itaconate, and [(2,2-dimethyl-1,3-dioxolan-4-yl)methyl] methyl fumarate are described. Reactivity ratios in the copolymerization of these monomers with other comonomers are reported and the Alfrey-Price Q and e values calculated. The post-polymerization study of the effects of ultraviolet light and heat on these polymers and copolymers is presented. The 1,3-dioxolane group when appended to the polymer chain performs as an internal ultraviolet sensitizer. A mechanism is offered to explain the crosslinking behavior of these polymers when treated with ultraviolet light.
    Additional Material: 22 Tab.
    Type of Medium: Electronic Resource
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