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  • block copolymerization  (2)
  • 5-methyl-2-vinyldibenzothiophenium tetrafluoroborate  (1)
  • 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 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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  • 3
    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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