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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 26 (1993), S. 5664-5670 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Fig. 1 Comparison of a segment of a nylon-3 derivative of the type described here (a) with a peptide unit in a protein (b). In a, R=COOCH2CH(CH3)2. The lateral group R is on the opposite side to that in proteins, as it would be in polypeptide chains prepared from D-amino acids. The polymer was ...
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 1271-1282 
    ISSN: 0887-624X
    Keywords: glycine ; synthesis ; biodegradation ; poly(ester amide)s ; thermal analysis ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of aliphatic poly(ester amide)s derived from 1,6-hexanediol, glycine, and diacids with a variable number of methylenes (from 2 to 8) have been synthesized and characterized. Infrared spectroscopy shows that the studied polymers present a unique kind of hydrogen bond that is established between their amide groups. Thermal properties as melting, glass transition, and decomposition temperatures are reported. The data indicate that all the polymers are highly crystalline. Thus, different kinds of spherulites (positive and/or negative) were obtained depending on the preparation conditions and on the polymer samples. Moreover, all the polymers crystallized from dilute diol solutions as ribbonlike crystals where a regular folding habit and a single hydrogen bond direction could be deduced. A test of enzymatic hydrolysis was employed to assess the potential biodegradability of these polymers. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 1271-1282, 1998
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 713-721 
    ISSN: 0887-624X
    Keywords: stereorgular polyamides ; stereoregular nylons ; chiral polyamides ; chiral nylons ; polytartaramides ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Stereoregular polyamides containing two chiral backbone carbons in the repeating unit were prepared by polycondensation of bis(pentachlorophenyl) 2,3-O-methylene-L-tartrate with 1,9 and 1,12-alcanediamines activated as N,N′-bis(trimethylsilyl) derivatives. The polymers were characterized by elemental analysis, IR, and 1H-NMR spectroscopy, and differential scanning calorimetry. Both viscosimetry and GPC were used to estimate the molecular weights which ranged between 6000 and 44000. These polytartaramides were readily soluble in chloroform, displayed moderate optical activity in solution, and formed highly crystalline films.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 58 (1995), S. 41-54 
    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: This article describes the hydrolytic degradation of a series of nylons based on methylated L-tartaric acid and diamines. These polytartaramides were prepared by a solution polycondensation process using bis(pentachlorophenyl)-2,3-O-dimethyl-L-tartrate and N,N′-bis(trimethylsilyl)alkanediamines with 6, 8, or 12 methylene groups. The stereoregular optically active polyamides obtained were soluble in chloroform and showed intrinsic viscosities between 1.0 and 2.7 dL g-1. The degradation of these polytartaramides in the form of discs has been investigated in buffered salt solutions of pH 2.3, 7.4, and 10.6, and at temperatures of 37, 55, and 70°C. The degradation was monitored by following the changes in molecular weight, mass loss, chemical constitution, and thermal properties. Our results show that these polytartaramides degrade slowly at 37°C, with a degradation rate highly depending upon the number of methylenes in the diamine unit of the polyamide. The pH of the medium has also a great influence on degradation, as well as the temperature, with an important hydrolysis rate enhancement at 70°C. © 1995 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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