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  • Wiley-Blackwell  (2)
  • 1970-1974  (2)
  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 12 (1974), S. 2327-2335 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetic and thermodynamic specific features of the process of heterogeneous alkaline saponification of the copolymer of acrylonitrile (92.2%), methyl acrylate (6.3%), and sodium monoithaconate (1.5%) were investigated. Chemical and infrared spectroscopic methods reveal that the saponification of the nitrile groups of copolymer of acrylonitrile proceeds faster to yield amide groups and then slower to yield carboxylate groups. The order of both stages of the process with respect to the accumulation of the respective groups was evaluated. The dependence of the rate of saponification on the packing density of the structural units was demonstrated. With increasing conversion, the fiber structure becomes looser, as demonstrated by density and sorption investigations. If acrylonitrile copolymer is treated with alkali, the carboxylate groups in the polymer substrate accumulate as a result of saponification of the ester groups of the copolymer, while the nitrile groups are predominantly transformed into the amide groups. If the degree of conversion (with respect to the CN groups) is higher than 62.7%, the copolymer abruptly suffers a marked change in its mechanical properties and gradually dissolves. The products of partial saponification of copolymer were investigated by thermomechanical methods and DTA. The polycyclization of the polymer substrate was found to proceed at a temperatures which decreases as the content of the amide groups increases.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 6 (1974), S. 240-244 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A relatively fast rotation around the α,β carbon-carbon double bond at the equilibrium of geometrical isomers and a comparatively slow rotation around the carbon-nitrogen single bond in compounds of the type \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm X}_1 ({\rm X}_2){\rm C}_{\rm \alpha}=\!={\rm C}_\beta {\rm H}-{\rm C}_\gamma {\rm H}=\!={\rm C}_\delta {\rm H}-{\rm N}({\rm R}_1){\rm R}_2 $$\end{document} (X1, X2 are electron-attracting substituents) were detected and investigated by the NMR technique. The relationships between the free energies of activation for these rotational processes and the character of the substituents, the number of double bonds, solvents and concentration were studied.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
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