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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 115 (1983), S. 103-114 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Copolymerisationsparameter einiger halogensubstituierter aromatischer Amine wurden nach der Methode von Kelen-Tüdős und Fineman-Ross graphisch bestimmt. Bei der Copolymerisation mit den Comonomeren p-Toluidin oder p-Nitrophenol erwies sich die Reaktivität der halogensubstituierten aromatischen Amine in der Reihenfolge der Basenstärke ansteigend. Jedoch kehrt sich diese Reihenfolge um, wenn diese halogensubstituierten Amine mit p-Nitroanilin copolymerisiert werden. Diese Umkehr der Reaktivität wurde mit der Polarisation und Resonanzstabilisierung der Monomeren erklärt.
    Notes: Reactivity ratios of some halogen substituted aromatic amines have been determined by using Kelen-Tüdős and Fineman-Ross linear graphical methods. On copolymerization with p-toluidine or p-nitrophenol as comonomer, the reactivity of halogen substituted aromatic amines was found to be in the order of their basic strength. However, this order of reactivity gets reversed when these halogen substituted amines are copolymerized with p-nitroaniline. This reversal of reactivity has been interpreted in terms of polarization and resonance stabilization of the monomeric species.
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 21 (1983), S. 1165-1171 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The Kelen-Tüdös linear graphical method was used to determine the copolymerization parameters of some halogen-substituted (e.g., Cl, Br, I) aniline monomers. It was found during copolymerization with p-aminobenzoic acid or p-aminophenol that the reactivity of these monomers followed the order of their basic strength. The order of their basic strength. The order of their reactivity, however, was reversed if they copolymerized with sulfanilic acid (SA). This reversal has been interpreted in terms of the resonance stabilization of monomers, the nature of the acidic functional groups present in the comonomer, and the influence of electron-accepting or electron-donating groups present in the comonomers.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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