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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 1987-1994 
    ISSN: 0887-624X
    Keywords: aromatic polyamides ; polyisophthalalamides ; pendent oligomeric benzamide groups ; 5-(4-benzoylamino-1-benzoylamino)isophthalic acid ; water uptake ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of polyisophthalamides having pendent oligomeric benzamide groups were prepared by the Yamazaki reaction from common aromatic diamines and 5-(4-benzoylamino-1-benzoylamino)isophthalic acid. The latter was synthesized from 5-aminoisophthalic acid in a three-step synthesis by successive incorporation of benzamido groups. The new polymers were characterized by NMR, DSC, TGA, and WAXD and the properties were compared to those of corresponding unsubstituted polyisophthalamides. All of the polymers were essentially amorphous and their Tgs were about 20°C higher than the reference polymers. Initial thermal decomposition temperatures ranged from 375 to 420°C. All of the polymers were soluble in aprotic polar solvents without added salts. Properties of particular note were: the water uptake, which was particularly high, ranging from 7.5 to 18.2%, and the temporary insolubilization in concentrated sulfuric acid of films of the polymers heated for a short time to ≥ 200°C. © 1995 John Wiley & Sons, Inc.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 31 (1993), S. 1383-1392 
    ISSN: 0887-624X
    Keywords: aromatic polyamides ; pendent groups ; 5-phenylsulfonylisophthalic acid ; polycondensation ; NMR, solubility ; water uptake ; mechanical strength ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of polyisophthalamides containing phenylsulfonyl groups was prepared from seven aromatic diamines and 5-phenylsulfonylisophthalic acid by the phosphorylation condensation method, and from 5-phenylsulfonylisophthaloyl chloride by the solution polycondensation method at low temperature. When compared to the analogous unmodified polyisophthalamides, the modified ones were found to be essentially amorphous, and they showed better solubility in organic solvents, and slightly higher glass transition temperatures. Thermogravimetric analysis showed that the polyisophthalamides containing pendent phenylsulfonyl groups have thermal stabilities similar to the unmodified ones. Mechanical strength of films and water sorption were also investigated. © 1993 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 919-927 
    ISSN: 0887-6266
    Keywords: dielectric relaxation ; aromatic polyamides ; rotational barrier ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dielectric relaxation spectroscopy (DRS) is presented for a family of four aromatic polyamides trying to relate the structure of the lateral groups to the molecular mobility. A prominent sub-Tg absorption is always seen followed in some cases by remanent dielectric activity at room temperature and a subsequent increase of the loss permittivity. The low temperature relaxation is analyzed in terms of a Fuoss-Kirkwood equation to obtain the broadness and the strength of these relaxations as well as the activation energy (ranging from 10 to 11 Kcal/mol). The low frequency conductive peak shows in each case a half-width higher (1.30) than those corresponding to a single relaxation time peak (1.144). These values of the half-width are an indication of the complex character of these phenomena. A final discussion of the rotational barriers of the lateral chains rules out that such motions are the only molecular origin for the gamma relaxation. Instead, some kind of motion involving the main chain and where the interchain interactions play a significant role should be considered as responsible for that relaxation. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 919-927, 1997
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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