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  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Phytochemistry 17 (1978), S. 591-592 
    ISSN: 0031-9422
    Keywords: 3,4'- and 7,4'-dimethylkaempferol. ; 3,4'-,3,7- and 7,4'-dimethyl-quercetin ; Angelonia grandiflora ; Scrophulariaceae ; methylated flavonols
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 16 (1978), S. 137-153 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Two monomeric N-substituted bisitaconimides, N,N′-bisitaconimido-p,p′-diphenylmethane and N,N′-bis(itaconimido-p,p′-diphenyl ether), were synthesized from the corresponding diamines. The synthesis was accomplished by reaction of the diamine with itaconic anhydride and cyclocondensation of the resultant bisitaconamic acid. Attempts to use p,p′-diaminodiphenylsulfone as the diamine gave N,N′-biscitraconimido-p,p′-diphenylsulfone and N-citraconimido-N′-itaconimido-p,p′-diphenylsulfone instead of the bisitaconimide. The two bisitaconimides polymerize thermally at 180°C and 225°C, respectively, and yield tough polymers with very high thermal stability.
    Additional Material: 8 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. 493-504 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polymerization of the monomers, methyl acrylate (MA) and methyl methacrylate (MMA) was carried out in sulfuric acid medium at 15°C. With the redox initiator system, ceric ammonium sulfate-malonic acid. There was no induction period, and a steady state was attained in a short time. There was found to be no polymerization even after 1 hr. in the absence of the reducing agent R. The initiation was by the radical produced from the Ce4+-malonic acid reaction. The rate of monomer disappearance was proportional to [M]1.5, [R]0.5, and [Ce4+]0.3-0.5, and the rate of ceric disappearance was directly proportional to [R] and [Ce4+]. Chain lengths of the polymers were directly proportional to [M] and inversely to [R]1/2 and [Ce4+]1/2. The experimental results were explained by a kinetic scheme involving the following steps: (a) oxidation of the substrate to give the primary radical which reacts with Ce4+ to give the products, (b) initiation by the primary radical, (c) propagation, and (d) termination of the growing polymer radicals by the mutual type. For the polymerization of acrylonitrile (AN) by the redox system, ceric ammonium sulfate-cyclohexanone (CH), in sulfuric acid at 15°C., the scheme was modified to include linear type of termination by Ce4+, along with the mutual termination to explain the results especially under conditions with [Ce4+] ≥ [CH].
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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