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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 40 (1990), S. 1445-1452 
    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: Since 4-vinylbenzyl N,N-diethyldithiocarbamate (VBDC) polymer easily cleaves at the C - S bond and generates benzyl radical, graft copolymerization of methyl methacrylate (MMA) or 4-vinylpyridine (VPy) onto VBDC polymer is easily performed by UV irradiation. The structural analyses of the graft copolymers are performed through glass transition temperature measurements. The graft copolymers of MMA have one Tg and VPy graft copolymers have two Tg's arising from the main and side chains. It becomes clear that the mode of side chains propagation is significantly different for each of the second monomers used.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 2247-2250 
    ISSN: 0887-624X
    Keywords: polymer catalyst ; formose reaction ; thiazolium salt ; hydrocarbons ; dihydroxy acetone ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Thiazolium salt polymers synthesized by quaternization of 4-(4′-vinylphenyl)thiazole (VPT) polymers with methyl iodide had a highly catalytic activity for “the formose reaction.” Their catalytic activities were comparable to that of a low molecular weight analog, 3-methyl-4-phenylthiazolium iodide (MPTI). In the reaction catalyzed by the polymer catalyst, a main product, dihydroxyacetone (DHA), was detected by gas-liquid chromatography. The polymer catalysts were easily recovered from the reaction mixture and reused with a sustained catalytic activity. © 1992 John Wiley & Sons, Inc.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 32 (1994), S. 1711-1717 
    ISSN: 0887-624X
    Keywords: durable catalyst ; thiazolium salt ; aqueous system ; acyloin condensation ; enzyme model ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: We characterized three low-molecular-weight thiazolium salt analogues: N-methyl-5-(2′-benzyloxyethyl)-4-methylthiazolium iodide (MBMTI), N-methyl-4-phenylthiazolium iodide (MPTI), and N-methylbenzothiazolium iodide (MBTI). MBMTI, having high-electron density on the thiezolium ring, was found to be a durable thiazolium salt in buffer solution. Then, the polymer-supported thiazolium salt catalyst having MBMTI structure as a catalytic site for acyloin condensation was prepared by the polymerization of the corresponding thiazole monomer and the following quaternization. The polymer catalyst had excellent catalytic activity even in buffer solution, while the corresponding low molecular weight catalyst did not show any activity in aqueous system. Furthermore, the durable polymer catalyst could be reused under the aqueous condition. © 1994 John Wiley & Sons, Inc.
    Additional Material: 1 Ill.
    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 62 (1996), S. 1877-1885 
    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: A new three component photoinitiator system consisting of a dye, an iron arene complex, and a phenylglycine derivative was investigated by fluorescence quenching experiments and laser flash photolysis. The efficiency of a three-component system in photopolymerization reactions is higher by a two-fold factor compared to that of the two-component system. The first step of the photoreaction occurs between the dye and the iron arene complex. The iron arene complex reacts either with the singlet excited dye or with the triplet excited dye according to the nature of the dye. An electron transfer occurs in these systems. The mechanism was discussed in terms of the absence of the formation of a terminating radical in the three-component system. © 1996 John Wiley & Sons, Inc.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 52 (1994), S. 577-581 
    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: A thermotropic liquid crystal polymer with photosensitive groups (liquid crystal photoresist), copoly(4-methoxyphenyl) 4′-(2″-acroloyloxy ethoxy) benzoate (MPAEB)-4-vinylbenzyl cinnamate (VBC) was prepared, and its thermal behavior was characterized by a differential scanning calorimetry. The copolymer exhibited a liquid crystal mesophase between approximately 70°C and 120°C. In the mesophase, poly(MPAEB-VBC) (85/15) had a higher photo-crosslinking ability than that at room temperature and at 140°C, where the copolymer exhibited the isotropic phase. It was found that the liquid crystal photoresist had a high crosslinking ability owing to alignment of its photosensitive groups. © 1994 John Wiley & Sons, Inc.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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