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  • 1
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 31 (1993), S. 2929-2933 
    ISSN: 0887-624X
    Schlagwort(e): thermotropic polyamides ; polyethyleneglycol bis(4-carboxyphenyl)ether ; p-phenylenediamines ; 4,4′-diaminobiphenyls ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: New thermotropic liquid crystalline polyamides were prepared from polyethyleneglycol bis(4-carboxyphenyl)ether (PEGn, n = 2, 3, 4) and aromatic diamines by using triphenyl phosphite in pyridine as the condensing agent. Substituted p-phenylenediamines and 4,4′-diaminobiphenyls were successfully used; melting points and isotropization temperatures of the polyamides were changed by the kind and number of the substituents. Copolymerization of long chain aliphatic dicarboxylic acids was carried out at the lower melting point of the copolymer. Kink monomers were also incorporated into the polymer backbone. © 1993 John Wiley & Sons, Inc.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 32 (1994), S. 89-95 
    ISSN: 0887-624X
    Schlagwort(e): thermotropic copolyamide ; polyethyleneglycol bis(4-carboxyphenyl)ethers ; diamine segment length ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Thermotropic copolyamides were prepared from triethyleneglycol bis(4-carboxy-phenyl)ether (PEG3) and two types of diamines, substituted p-phenylenediamines and 4,4'-diaminodiphenyls, and depression of melting point and isotropization temperature of the copolymers produced were measured as a function of diamine combination. The depression was not practically observed by the combinations of homologous diamines with several kinds and numbers of substituents, but significant by those of the diamines with different lengths of the mesogenic segments, and by the molar ratios of the diamines employed. The effect was discussed in terms of deviation of interchain hydrogen bonding between amide bonds in the main chain. © 1994 John Wiley & Sons, Inc.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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