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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 2487-2492 
    ISSN: 0887-624X
    Keywords: alkoxyallenes ; living coordination polymerization ; block copolymerization ; allylnickel catalyst ; surfactants ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Block copolymers of alkoxyallenes were obtained in high yield by the two-stage living coordi-nation polymerization of two kinds of alkoxyallenes using an allylnickel catalyst. The resulting copolymers had narrow molecular weight distributions (∼ 1.1), regardless of the order of the monomer additions. When an alkoxyallene-bearing hydrophilic substituent was used as a co-monomer for the block copolymerization with that bearing a hydrophobic one, the resulting copolymer showed amphiphilic properties. For example, a block copolymer obtained by the copolymerization of n-hexyloxyallene with diethylene glycol allenyl methyl ether was soluble in water as well as n-hexane. © 1995 John Wiley & Sons, Inc.
    Additional Material: 2 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 35 (1997), S. 431-437 
    ISSN: 0887-624X
    Keywords: alkoxyallenes ; isocyanide ; block copolymerization ; allylnickel catalyst ; living coordination polymerization ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A living block copolymerization of allene derivatives with 1-phenylethyl isocyanide (3) using [(allyl)NiOCOCF3]2 (1) is described. After complete polymerization of allene monomers such as n-octyloxyallene (2A) with 1, further addition of 3 to the reaction system yielded the corresponding block copolymers in high yield. For instance, a block copolymer (4A, Mn = 39,600, Mw/Mn = 1.20) was obtained in 96% yield by the addition of 3 ([3]/[1] = 250) to the living solution of poly(n-octyloxyallene) (Mn = 14,400, Mw/Mn = 1.03) prepared by the polymerization of 2A in the ratio of [2A]/[1] = 90. The resulting copolymer was a brownish orange gum or a solid, depending on the length of each of the segments. The solubility of the block copolymers could be controlled by the allene components. The copolymer of 2A with 3 having appropriate length of segments was soluble in n-hexane, while that of methoxyethoxyethoxyallene (2D) with 3 was soluble in methanol. © 1997 John Wiley & Sons, Inc.
    Additional Material: 3 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 36 (1998), S. 1779-1784 
    ISSN: 0887-624X
    Keywords: poly(sulfonium salt) ; poly(2-vinyldibenzothiophene) ; 5-methyl-2-vinyldibenzothiophenium tetrafluoroborate ; sulfonium monomer ; radical polymerization ; polymer reaction ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A polymer having dibenzothiophenium salt moieties [poly(sulfonium salt), 2] was prepared by the reaction of poly(2-vinyldibenzothiophene) (1) with CH3I and AgBF4 in CH2ClCH2Cl at room temperature for 24 h. The obtained polymer 2 was found to contain 71% of the methyldibenzothiophenium tetrafluoroborate unit. A monomer carrying the sulfonium salt moiety, i.e., 5-methyl-2-vinyldibenzothiophenium tetrafluoroborate (4), was independently prepared and subjected to radical polymerization to give a polymer (5) in 88% yield (methyldibenzothiophenium tetrafluoroborate unit: 79%). The thermal decompositions of 2 and 5 took place in two steps; the first step involved the formation of polymer 1 by demethylation. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 1779-1784, 1998
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 2589-2592 
    ISSN: 0887-624X
    Keywords: polymer reaction ; oxidation ; push-pull olefin ; electron-deficient olefin ; vinyl sulfone ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Oxidation of a polymer (1) having β-alkylmercaptoenoate moieties in the main chain by m-chloroperbenzoic acid (MCPBA) is described. Oxidation of 1 proceeded selectively to give polymers having vinyl sulfoxide or vinyl sulfone moieties in the main chain by using an appropriate amount of MCPBA. In the case of 1.1 equiv of MCPBA (relative to the sulfur atom), a polymer (4) having vinyl sulfoxide moieties selectively in the main chain was obtained in quantitative yield without side reactions. Likewise, a polymer (5) having vinyl sulfone moieties was obtained in quantitative yield by using 2.6 equiv of MCPBA. © 1998 John Wiley & Sons, Inc. J. Polym. Sci. A Polym. Chem. 36: 2589-2592, 1998
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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