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  • 1980-1984  (2)
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Year
  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 22 (1984), S. 1969-1977 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The cyclohexane ring-containing polyamide 1,3-CBMA-6 was synthesized from 1,3-cyclohexane-bismethylamine (1,3-CBMA) and adipic acid (6), and effects of cis/trans isomers of the ring on crystallinity and thermal properties were studied. Polymers with high cis and high trans contents, respectively, were made by polymerizing the 1,3-CBMA-6 salts of 98% cis and 93% trans derived from the salt of 75/25 (cis/trans) by fractional crystallization. A polymer with 97% cis content was highly crystalline, with a melting temperature of 253°C, while one with 93% trans contents was amorphous. In contrast to this, little difference was found in the glass transition temperature of 97 and 84°C. These results indicate that the isomers affect the conformation of the molecular chains, which determines the crystallinity and melting temperature, but they do not much affect the mobility of the chains as manifested by the glass transition.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 18 (1980), S. 697-706 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The effect of 1,3-cyclohexane rings in the chain backbone on the crystal structure of polyamides has been studied using polyamides (denoted 1,3-CBMA-n) obtained from 1,3-cyclohexane-bis(methylamine) (1,3-CBMA) and n-carbon dicarboxylic acids. The crystallinity of the 1,3-CBMA-n polymers changes greatly with variation in the value of n. This is attributed to hydrogen-bond changes associated with the relative length of the diacid moiety to the diamine moiety in the monomeric unit of each polymer. In 1,3-CBMA-6, the cis-1,3-cyclohexane rings are readily accommodated in the molecular chains to form crystals in a manner similar to the m-benzene rings in poly(m-xylylene adipamide) (MXD-6). The crystal lattice, however, is more expanded than in MXD-6 since the 1,3-cyclohexane rings is bulkier than the m-benzene ring. The crystal structure of the 1,3-CBMA-n polymers is essentially the same as that of MXD-6.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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