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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 194 (1993), S. 1377-1386 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: 1,2-Diketones may serve as starting materials for various carbo- or heterocyclic organic compounds. Two different synthetic routes towards poly(arylene)s containing structural units derived from the 1,2-diketo building block are presented. The first route involves the generation of polymeric 1,2-diketones via aryl-aryl coupling, followed by polymer-analogous derivatisation. The second synthetic sequence includes formation of the 1,2-diketo derivatives on the stage of monomeric compounds and subsequent polycondensation of these monomers. In this manner, aromatic polymers possessing the quinoxaline, 1,2,4-triazine and tetraphenylcyclopentadienone subunits are available. The polymeric 1,2,4-triazines are particularly attractive because they offer the possibility of a thermal conversion into polymers containing the diphenylacetylene building block.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Basel : Wiley-Blackwell
    Die Makromolekulare Chemie, Rapid Communications 14 (1993), S. 217-222 
    ISSN: 0173-2803
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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