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  • 1985-1989  (16)
Material
Years
Year
  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of organic chemistry 53 (1988), S. 5187-5189 
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 21 (1988), S. 565-571 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary The imidazole-containing copolymeric surfactant, poly(N-methacryloyl-L-histidine methyl ester(la)-co-N,N-dimethyl-N-hexadecyl-N-(11-methacryloyloxyundecanyl)ammonium bromide(I)) was prepared and subjected to catalyze the hydrolyses of N-carbobenzoxy-d- and L-phenylalanine p-nitrophenyl esters (D-NBP and L-NBP). The copolymers exhibited enantioselective catalysis, viz., kcat(L)/kcat(D)=10.3 for poly(la-co-I) containing 3.7 mole % of la. The solvolytic systems employed were confirmed to form large ordered aggregate structure by electron microscopic observation.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 30 (1985), S. 1903-1926 
    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: Poly(methyl methacrylate)-polystyrene composite particle latexes were prepared by poly(methyl methacrylate)-seeded emulsion polymerization of styrene employing batch, swelling-batch, and semibatch methods. The changes in particle morphology taking place during the polymerization reaction were followed by electron microscopy. Anchoring effect exerted by ionic terminal groups introduced by ionic initiator was found to be the main factor in controlling the particle morphology. The polymer particles obtained by oil-soluble hydrophobic initiators such as azobisisobutyronitrile and 4,4′-azobis-(4-cyanovaleric acid) gave the inverted core-shell morphology. Water-soluble hydrophilic initiator, K2S2O8, also gave the inverted core-shell morphology. However, in this case the occurrence of the halfmoonlike, the sandwichlike, and the core-shell morphologies were also observed depending upon the polymerization conditions. The distribution of terminal —SO4- groups on the surface area of polystyrene particles could be controlled by initiator concentration and polymerization temperature. Viscosity of polymerization loci dictated the movement of polymer molecules, thus causing the unevenness of particle shape and phase separation at high viscosity state. Viscosity was controlled by the styrene/poly(methyl methacrylate) ratio, the addition of a chain transfer agent or a solvent which is common to polystyrene and poly(methyl methacrylate).
    Additional Material: 18 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 27 (1989), S. 3151-3159 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1-(p-Substituted phenyl)-2-vinylcyclopropanes such as 1-phenyl-2-vinylcyclopropane (Ia), 1-(p-chlorophenyl)-2-vinylcyclopropane (Ib), 1-(p-anisyl)-2-vinylcyclopropane (Ic), and 1-(p-tolyl)-2-vinylcyclopropane (Id) were prepared and polymerized radically, cationically and with Ziegler-Natta catalysts. Ia and Ib polymerized exclusively in 1,5-fashion with radical initiators. However, Ic and Id polymerized in 1,5-fashion only with Ziegler-Natta catalysts. All polymers were soluble in ordinary organic solvent and solution-cast films were clear and flexible, showing Tg values in the range of 39-71°C. Spectral data indicated that the double bonds of the polymer chains were in trans form in all cases. The difference between the polymerizabilities of different monomers are interpreted in terms of electronic properties of substituents.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 25 (1987), S. 19-23 
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 3089-3103 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 2-Methoxy-6-ethoxy-5-cyano-3,4-dihydro-2H-pyran (1a), 2-isobutoxy-6ethoxy-5-cyano-3,4-dihydro-2H-pyran (1b), and 2,6-diethoxy-3-methyl-5-cyano-3,4-dihydro-2H-pyran (1c) were prepared by (4 + 2) cycloaddition reaction of ethyl α-cyanoacrylate with the corresponding vinyl ethers. Compounds 1a-c were ring-open polymerized by cationic catalyst to obtain alternating head-to-head (H—H) copolymers. For comparison, head-to-tail (H—T) copolymer 3a was also prepared by free radical copolymerization of the mixture of the corresponding monomers. The H-H copolymer exhibited minor differences in its 1H-NMR and IR spectra, but in the 13C-NMR spectrum significant differences were shown between the H—H and H—T copolymers. Glass transition temperature (Tg) of H—H copolymer was higher than that of the corresponding H—T copolymer, but thermal decomposition temperature of the H—H copolymer was lower than that of the H—T copolymer. Compounds 1a and 1b copolymerized well with styrene by cationic catalyst, but compound 1c failed to copolmerize with styrene. All of the H-H and H-T copolymers were soluble in common solvents and the inherent viscosities were in the range 0.2-0.5 g/dL.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 27 (1989), S. 3789-3797 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Enantioselective solvolyses of optically active activated esters in the aggregate system of optically active polymeric surfactants containing imidazole and benzene moieties were performed. The catalyst polymers [copoly(MHis-DEVAB)] employed were copolymers of N-methacryloyl-L-histidine methyl ester (MHis) with N,N-dimethyl-N-hexadecyl-N-[10-(p-vinylcarboxanilido) decyl]ammonium bromide(DEVAB). In the solvolyses of N-carbobenzoxy-D- and L-phenylalanine p-nitrophenyl esters (D-NBP and L-NBP) by polymeric catalysts, copoly(MHis-DEVAB) exhibited not only increased catalytic activity but also enhanced enantioselectivity as the mole percent of surfactant monomers in the copolymers increased. The polymeric catalysts showed noticeable enantioselective solvolyses toward D- and L-NBP of the substrates employed. As the reaction temperature was lowered for the solvolyses of D- and L-NBP with the catalyst polymer containing 4.8 mol% of MHis, an increased reaction rate and enhanced enantioselectivity were observed. The coaggregate systems of the polymer and monomeric surfactants were also investigated. The case of a coaggregate system consisting of 70 mol% of cetyldimethylethylammonium bromide with polymeric catalyst showed maximum enantioselective catalysis, viz., kcat (L)/kcat(D) = 6.68. The catalyst polymers in the sonicated solvolytic solutions were confirmed to form large ordered aggregate structure by electron microscopic observation. From these results, it is concluded that hydrophobic interaction in ordered aggregate structure plays an important role in enantioselective catalysis of optically active imidazole-containing polymers.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 24 (1986), S. 109-111 
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 27 (1989), S. 85-91 
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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