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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 12 (1974), S. 565-573 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A useful synthesis of a series of new aromatic sulfone ether diamines, H2NC6H4O\documentclass{article}\pagestyle{empty}\begin{document}$\hbox{---}\hskip-5pt[\ {\rm C}_{\rm 2} {\rm H}_{\rm 4} {\rm SO}_{\rm 2} {\rm C}_{\rm 6} {\rm H}_{\rm 4} \hbox{--} {\rm ORO}\hbox{---}\hskip-5pt ]_n {\rm OC}_{\rm 6} {\rm H}_{\rm 4} {\rm SO}_{\rm 2} {\rm C}_{\rm 6} {\rm H}_{\rm 4} \hbox{---} {\rm OC}_{\rm 6} {\rm H}_{\rm 4} {\rm NH}_{\rm 2} $\end{document}, where n = 0, 1, 2…, which increases the tractability of polyimides, polyamide-imides, and polyamides, was developed. These diamines were prepared by condensing various proportions of sodium p-aminophenate, sodium bisphenates, and dichlorodiphenyl sulfone. The synthetic procedures are now refined to the point where simply coagulating these diamines into water yields high purity polymer-grade sulfone ether diamines. The latter have good tractability; and in some cases, it is possible to extrude and injection-mold these high temperature polymers.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
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