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  • Wiley-Blackwell  (2)
  • American Institute of Physics (AIP)  (1)
  • 1
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Stable polymers with nonlinear optical side groups were synthesized from maleic anhydride copolymers and the azo dye Disperse Red 1 via esterification. After electrode poling under 135 V/μm at 185 °C, thermal stabilities were measured by pyroelectric and electro-optic thermal analysis and compared to a guest/host polymer of polymethylmethacrylate and the same dye. The pyroelectrically detected dipole orientation and the electro-optic activity of the side-chain polymers decreased only above 150 °C, and electro-optic r33 coefficients of up to 6 pm/V were achieved at 780 nm even without optimizing the dye content.
    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 36 (1998), S. 929-938 
    ISSN: 0887-624X
    Keywords: polyamidines ; chain conformation ; hydrogen bonds ; prototropic tautomerism ; thermal stability ; hydrolytic stability ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polymers with amidine groups —NH—CR=N— in the main chain were prepared by acid catalysed melt polycondensation of 4,4′-diaminodiphenyl methane (DAPM) with various orthoesters. The resulting polyamidines were characterized by 1H-, 13C- and 15N-NMR spectroscopy, differential scanning calorimetry (DSC), thermogravimetry (TGA) and wide angle x-ray scattering (WAXS) measurements. The properties of the polyamidines are strongly determined by the substituent R on the amidine group. Some peculiarities of the polyformamidine (R=H) could be attributed to the conformation of the amidine group. Glass transition temperatures varied from 106 to 161°C depending on the substituent R. All polyamidines possessed good thermal stability up to 370°C and, with exception of the polyformamidine, good solubility in common solvents. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 929-938, 1998
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 62 (1996), S. 1819-1833 
    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: Multiblock copolymers offer the possibility to combine the properties of different polymers. Thus, new materials with tailor-made unique properties are available by coupling of different suitable polymeric segments. The goal of the work discussed in this paper was to combine advantageous properties of liquid-crystalline polymers (LCP) with those of polysulfone (PSU). Therefore, liquid crystalline poly(ethylene terephthalate-co-1,4-oxybenzoates) were connected with PSU oligomers. Chemically homogeneous multiblock copolymers with high molecular weight were obtained by a melt transesterification procedure. It was demonstrated by wide angle x-ray scattering (WAXS), polarizing microscopy, transmission electron microscopy (TEM), and differential scanning calorimetry (DSC) that the properties of the multiblock copolymers (solid phase structure, phase behavior, morphology, glass transition, and melting behavior) can be balanced by the segment length of the incorporated blocks. The investigations clearly reveal the existence of a two-phase structure. However, a change of properties compared to the corresponding homopolymers refers to certain interactions between the phase due to the chemical connection of the LCP and PSU segments. © 1996 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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