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  • 1
    Electronic Resource
    Electronic Resource
    Polyamides from 2,6,(7)-diamino-9,10-dihydro-9,10-ethanoanthracene and 2,6,(7)-diaminoanthraceneContribution No. 3529. (1985)
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 23 (1985), S. 2779-2790 
    Details
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: High-molecular-weight, film-forming, amorphous polyamides have been prepared from 2,6(7)-diamino-9,10-dihydro-9,10-ethanoantracene with adipic, sebacic, dodecanoic, isophthalic, 4,4′-oxybibenzoic, 2,6-naphthoic, 4,4′-bibenzoic, and terephthalic acid. Thermal elimination of ethylene from these polymers has yielded the corresponding polyamides from 2,6(7)-diaminoanthracene which were of high molecular weight, film forming, and crystalline.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1985.170231106
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  • 2
    Electronic Resource
    Electronic Resource
    Polyesters from 2,6-dihydroxy-9,10-dihydro-9,10-ethanoanthracene and 2,6-dihydroxyanthraceneContribution No. 3528. (1985)
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 23 (1985), S. 2791-2802 
    Details
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: High molecular weight, film-forming, amorphous polyesters have been prepared from 2,6-dilydroxy-9,10-dihydro-9,10-ethanoanthracene with adipic, sebacic, dodecanoic, isophthalic, 4,4′-oxybibenzoic, 2,6-naphthoic, 4,4′-bibenzoic, and terephthalic acid. Thermal elimination of ethylene from these polymers has yielded the corresponding polyesters from 2,6-dihydroxyanthracene which were of high molecular weight, film forming, and crystalline.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1985.170231107
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  • 3
    Electronic Resource
    Electronic Resource
    New linear polymers. Henry Lee, Donald Staffey and Rris Neville McGraw-Hill, New York, 1967. x + 374 pp, illus. (1969)
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 7 (1969), S. 2464-2464 
    Details
    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
    URL: http://dx.doi.org/10.1002/pol.1969.150070851
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  • 4
    Electronic Resource
    Electronic Resource
    Thermal behavior of polyhydrazides and poly-1,3,4-oxadiazoles (1966)
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 4 (1966), S. 1649-1664 
    Details
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The thermal properties of a series of polyhydrazides and corresponding poly-1,3,4-oxadiazoles have been investigated using differential thermometric and thermogravimetric techniques. In addition, the conversion rates of the polyhydrazides to the corresponding oxadiazole structures have also been measured. In general, weight loss in polyhydrazides occurs in three distinct stages corresponding, respectively, to loss of adsorbed water, cyclodehydration, and decomposition of the poly-1,3,4-oxadiazole formed in situ. The polyoxadiazoles generally exhibit only a single weight loss step (below 700°C.) corresponding to decomposition and volatilization of the substrate itself. These data clearly indicate that the presence of aliphatic carbon-carbon linkages in the polymer backbone reduces the temperature at which decomposition of the polyoxadiazoles is noted. Corresponding differential thermometry patterns give additional data on phase transitions in the polymers and indicate, in general, that the poly-1,3,4-oxadiazoles formed in situ decompose before reaching their intrinsic melting points (under the specific conditions of these experiments). Comparison of the poly-1,3,4-oxadiazoles prepared under the (rapid) dynamic conditions of the differential thermometry and thermogravimetry techniques employed (30°C./min.) with isothermal rate data clearly suggests subtle structural differences in the polyoxadiazoles prepared by the two different modes. In general, ΔE
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1966.150040701
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