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  • 1995-1999  (2)
  • Polymer and Materials Science  (2)
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Rapid Communications 17 (1996), S. 493-501 
    ISSN: 1022-1336
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The structure of poly(L-lysine) containing 44% azobenzene units in the side chain was studied by X-ray diffraction between room temperature and 150°C. The polymer exhibits a mesomorphic structure of the smectic A1 type. In this structure, stable at least until 150°C, each smectic layer of thickness d results from the superposition of two layers: one of thickness dA contains the free lysine side chains, the other of thickness dB contains the azobenzene modified lysine side chains and the polypeptide main chains, that in their planes are arranged as in the “antiparallel” β-structure classical for polypeptides.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Polymers for Advanced Technologies 6 (1995), S. 32-41 
    ISSN: 1042-7147
    Keywords: Photochromism ; Polypeptides ; Acrylate polymers ; Photoresponsive macromolecules ; 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
    Notes: In this review paper the photoresponsiveness of photochromic macromolecules under different structural and environmental conditions is discussed with reference to results from the authors' laboratories. Polypeptides, in particular poly(L-glutamic acid) and poly(L-lysine), with spirobenzopyrane side chains show photoinduced conformational variations which are amplified by addition of organic acids or bases to hexafluoro-2-propanol (HFP) solutions. Thus combination of light and environment effects allows modulation of order-disorder conformational transitions.Such photoindiced conformational changes are not observed in the case of macromolecules with a hydrocarbon main chain and azobenzene or stilbene side chains, obtained by polymerization of acrylic monomers. However, even in these systems structural variations affect the dependence of optical properties on irradiation. Moreover, the combination of organic solvents and water shows that polymer solubility can be modulated by light.
    Additional Material: 19 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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