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    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 44 (1992), S. 1267-1274 
    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: The preparation of cyanate ester thermosetting resins by coreacting a fluorinated bisphenol A dicyanate (6F-BADCY) monomer with a monofunctional reactive cyanate, namely, the dinonyl phenol cyanate (DNPC), is described in this paper. Our objective in this study was to modify the 6F-BADCY system with reactive diluents of a nonpolar nature and produce matrix resins processable at FR-4 epoxylike conditions. By introducing the monofunctional cyanate as a reactive diluent, it is expected that the molar crosslink density of the resulting network will be reduced. Highly branched triazine polymers will result from this approach. Dinonyl phenol cyanate was quantitatively synthesized by reacting dinonyl phenol with cyanogen bromide in the presence of triethylamine.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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