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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1983-1987 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The crystalline elastic modulus of poly(cis 1,4-isoprene) has been measured by x rays and calculated by molecular mechanics. The experimental modulus is E = (2.3 ± 0.3) × 109N m-2. The calculated modulus is E = (8.8 ± 0.1) × 109N m-2 for chains in S+ cis S-T conformation and E = (6.1 ± 0.1) × 109N m-2 for chains in S+ cis S+T conformation. The modulus calculated for a statistical structure including both conformation is E = (6.7 ± 0.1) × 109N m-2. The experimental modulus is thought to be a lower limit because of partial crystallinity of the sample. The chief mechanism of deformation is rotation around single bonds adjacent to the double bond.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 13 (1975), S. 1107-1118 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polyamides from n-alkylmalonic acids and linear aliphatic diamines, with paraffinic side chains of 3-18 carbon atoms, were prepared by melt polycondensation or by low-temperature interfacial polycondensation and were characterized by infrared, differential scanning calorimetry (DSC), and x-ray diffraction techniques. First-order transitions were found in the range of 130-210°C, depending on the number of carbon atoms in the side chain. The x-ray diffraction indicated substantially amorphous systems for polyamides with 8-18 carbon atoms in the side chain. However, long-range order arises in these polymers from a solid-state structure in which polyamide and hydrocarbon layers having partially disordered chain conformations alternate.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 15 (1977), S. 2151-2162 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new family of block copolymers have been synthesized and characterized. These copolymers have a central block deriving from the polyaddition of N,N′-dimethylethylenediamine to 1,4-bis-acryloylpiperazine, and lateral blocks of polystyrene. Preliminary biocompatibility tests have demonstrated that these new products show promise as long-acting nonthrombogenic materials.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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