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  • Polymer and Materials Science  (2)
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  • 1
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Monomers containing several octadecyl groups, e.g., 2-isopropenyl-4,6-bis(octadecylamino)-1,3,5-triazine (2), 2-dioctadecylamino-4-isopropenyl-6-octadecylamino-1,3,5-triazine (3) and 2,4-bis(dioctadecylamino)-6-isopropenly-1,3,5-triazine (4) were prepared by the alkylation reaction of 2,4-diamino-6-isopropenyl-1,3,5-triazine (1) with 1-bromooctadecane in the presence of sodium hydride. In the free-radical homopolymerization of these monomers, the polymer yield of 3 was lower than that of 2 due to a decrease in the ceiling temperature, and the polymerization of 4 did not proceed. Copolymerizations of these monomers with styrene or methyl methacrylate were carried out and the monomer reactivity ratios (r1 and r2) were determined. The monomer reactivity decreased with increasing the number of octadecyl groups in the monomers. Crystallinity of the octadecyl side chains in the resulting comb-like polymers was evaluated by differential scanning calorimetry.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: New isopropenyltriazines, e.g., 2-diethylamino-4-dimethylamino-6-isopropenyl-1,3,5-triazine (2a) and 2-dimethylamino-4-dioctadecylamino-6-isopropenyl-1,3,5-triazine (2b) were prepared by the alkylation reaction of 2-amino-4-dimethylamino-6-isopropyl-1,3,5-triazine (1) with corresponding alkyl halides in the presence of sodium hydride. In the free-radical homopolymerization of these monomers, the polymerization yield of 2b was lower than that of 2a due to a lower ceiling temperature. Copolymerizations of these monomers with styrene and methyl methacrylate were carried out, and monomer reactivity ratios (r1 and r2) were determined. The monomer reactivity decreases by the introduction of two octadecyl groups into the monomer. Exothermic crystallization and endothermic melting peaks based on the octadecyl side chains were observed in differential scanning calorimetry of the resulting comb-like polymers. The thermal stability of the polymers is not affected by the long alkyl groups.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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