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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 1901-1920 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Two closely related series of polyesters that contain mesogenic units interconnected by flexible spacers along the main chain were prepared and characterized for their liquid crystal properties. All of these polymers showed theotropic behavior, which was examined by DSC, hot-stage microscopy on a polarizing microscope, small-angle light and wide-angle x-ray scattering methods, and visual observation of stir-opalescence of the polymer melts. The effect of the length of the flexible spacer and the nature of the substituent, which is on the central aromatic ring of the mesogenic unit, on the stability and molecular order of the mesophase for each of the polymers was investigated and the results are discussed on the basis of the thermodynamic data obtained.
    Additional Material: 19 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 29 (1984), S. 547-554 
    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: A series of bis(benzylterephthaloyl-p-oxybenzoyl)esters (mesogen I) and bis(p-carboxybenzoyl-p-oxybenzoyl)esters (mesogen II) of several different polymeric glycols was prepared, and their thermotropic liquid crystalline behavior was studied by differential scanning calorimetry and by visual observation on the hot stage of a polarizing microscope. The polymeric glycols used were poly(ethylene oxide) (A), poly(tetramethylene oxide) (B), polybutadiene (C), and the hydrogenated polybutadiene (D) glycols, with molecular weights between 650 and 6000. With one exception, the benzyl ester derivations were not thermotropic, but the corresponding carboxylic acid derivatives were, and the related model compound, the bis(p-carboxybenzoyl-p-oxybenzoyl)ester of 1,12-dodecanediol, was also found to be liquid crystalline. The nature of the mesophases formed by the diacids derived from the macroglycol derivatives could not be clearly identified by their optical textures. Several of the diacid derivatives formed elastomeric films, even though they were still of low molecular weight, presumably because of chain extension by dimerization and association of the terminal mesogenic groups.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 6 (1968), S. 1065-1066 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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