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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 32 (1994), S. 1991-1995 
    ISSN: 0887-624X
    Keywords: allenyl ethers ; oligo(oxyethylene)s ; crosslinking ; nonionic hydrogel ; cationic catalyst ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Cationic crosslinking reactions of poly(allenyl ether)s having oligo(oxyethylene) moieties prepared by the radical polymerization of the corresponding allenyl ethers were carried out under some varied reaction conditions. For instance, a crosslinked polymer was obtained in 82% yield by the treatment of poly(ethylene glycol methyl allenyl ether) (1a) with 1.2 mol% of BF3·OEt2 (2) under high concentration in dichloromethane (46 wt %). The gels obtained showed good swelling properties in water, alcohols, and polar organic solvents such as dichloromethane. In particular, the degrees of swelling of these gels in aqueous sodium chloride (1M) were quite similar to those in ion-free water, indicating that these gels served as nonionic hydrogels. © 1994 John Wiley & Sons, Inc.
    Additional Material: 3 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 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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  • 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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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 1515-1519 
    ISSN: 0887-624X
    Keywords: sulfonyl isocyanate ; acrylamide ; sulfonylurea ; radical polymerization ; hydrolysis ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The radical polymerization of N-acryloyl-N′-(p-tolylsulfonyl)urea (2), prepared easily by the reaction of p-toluenesulfonyl isocyanate with acrylamide, was carried out in DMF, DMSO, or NMP at 60°C by use of AIBN as an initiator to give a polymer 3 in a good yield. Copolymerization parameters of 2 were evaluated by the copolymerization with MMA. Polymer 3 was readily hydrolyzed in an aqueous NaOH solution (1M) at room temperature to give poly(acrylic acid). The reason for the higher activity for hydrolysis of 3 compared to an ordinary amide is discussed. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 1515-1519, 1998
    Additional Material: 3 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 35 (1997), S. 787-793 
    ISSN: 0887-624X
    Keywords: β-alkoxyenoate moieties ; hydrolysis ; aminolysis ; displacement of the main chain ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The hydrolysis and the substitution reaction of the main chain of the polymer having β-alkoxyenoate moieties in the main chain are described. The hydrolysis of the polymer prepared from 2,2-dimetylpropylene-1,3-bis(propiolate) and p-xylene glycol under acidic conditions proceeded smoothly to obtain diols in quantitative yield by the cleavage of both ester and vinyl ether moieties. On the other hand, carboxylic acids were obtained by the hydrolysis of the polymer under alkaline conditions. The aminolysis with pyrrolidine gave the β-aminoenoate by the selective fission of vinyl ether moieties in quantitative yield. Furthermore, a polymer having β-aminoenoate moieties in the main chain was obtained by the reaction with piperazine via the displacement of the main chain. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 787-793, 1997
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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