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  • 1
    Electronic Resource
    Electronic Resource
    Esters of alternating copolymers of maleic or 2,3-dimethylmaleic anhydride with alkyl vinyl ethersThis paper is dedicated to Professor Junji Furukawa on the occasion of his seventieth birthday, with warmest personal wishes. (1983)
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 21 (1983), S. 891-911 
    Details
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Maleic anhydride or 2,3-dimethylmaleic anhydride was copolymerized with a number of alkyl vinyl ethers, with AIBN as the initiator. The comonomers were always alternating and were obtained in yields ranging from 15 to 99%. The acid anhydride group in both series of copolymers was converted to the corresponding methyl esters in a two-step reaction. The structure of these polymers was established by elemental analysis and by infrared, 1H-and 13C-NMR spectroscopy. Addtional characterization of these copolymers were carried out by viscosity measurements, differential scanning calorimetry for the determination of glass transition temperatures, and thermal degradation for the determination of the thermal stability of the copolymers.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1983.170210323
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  • 2
    Electronic Resource
    Electronic Resource
    Functional polymers. XIII.For Part XII see ref. 1. Synthesis and polymerization of 2(2-hydroxy-5-methylphenyl)-5-vinyl-2H-benzotriazoleDedicated to Prof. Vivian T. Stannett on the occasion of his 65th birthday, with warmest personal wishes. (1982)
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 20 (1982), S. 2215-2230 
    Details
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of 2(2-hydroxy-5-methylphenyl)-5-vinyl-2H-benzotriazole was accomplished in seven steps starting from 4-ethylaniline. Acetylation and nitration followed by hydrolysis gave 2-nitro-4-cthylaniline which was diazotized, condensed with p-cresol, and reduced to 2(2-hydroxy-5-methylphenyl)-5-ethyl-2H-benzotriazole. As in previous cases, the ethyl group was transformed to the vinyl compound by bromination with N-bromosuccinimide and dehydrobromination of the 1-bromoethyl compound. Monomer grade 2(2-hydroxy-5-methylphenyl)-5-vinyl-2H-benzotriazole was polymerized and copolymerized with styrene, methyl methacrylate, and n-butyl acrylate.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1982.170200824
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  • 3
    Electronic Resource
    Electronic Resource
    Functional polymers. XIXPart XVIII: M. Kitayama and O. Vogl, Polym. J. Jpn., in press.. Biuret oligomers and polymers of biologically active primary aliphatic amines (1982)
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 20 (1982), S. 2477-2499 
    Details
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Biuret oligomers and polymers from primary aliphatic amines and aromatic or aliphatic diisocyanates have been synthesized. To demonstrate the feasibility of the synthesis of polybiurets, aliphatic primary amines with n-propyl, n-hexyl, n-octyl, and n-dodecyl groups have been incorporated. For the synthesis of biuret oligomers of biologically active primary aliphatic amines [8-(4-amino-1-methylbutylamino)-6-methoxyquinoline] (primaquine) and adamantanamine were selected. Primaquine was also incorporated into polyepichlorohydrin by nucleophilic substitution of the chlorine of the chloromethyl group by the primary aliphatic amino group of primaquine. The structure of the biuret polymers was established by elemental analysis, and by infrared 1H- and 13C-NMR spectroscopic characterization. Several attempts to use primaquine as a diamine for the formation of condensation polymers, including reaction of primaquine with sebacoyl chloride (to form polyamides), or with diisocyanates (to form polyureas) were unsuccessful.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1982.170200910
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  • 4
    Electronic Resource
    Electronic Resource
    Functional polymers. XVI.For Part XIV see ref. 1. Synthesis and polymerization of 2(2-hydroxy-5-isopropenylphenyl)-2H-benzotriazole and a new synthesis of 2(2-hydroxy-5-vinylphenyl)2H-benzotriazole (1982)
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 20 (1982), S. 2735-2754 
    Details
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 2(2-Hydroxy-5-isopropenylphenyl)2H-benzotriazole was synthesized in 40% overall yield starting from o-nitroaniline. Diazotization in aqueous hydrochloric acid gave o-nitrophenyl diazonium chloride which was condensed with p-hydroxyacetophenone; the azo compound was reduced to 2(2-hydroxy-5-acetylphenyl) 2H-benzotriazole with zinc powder in sodium hydroxide solution and the 2-hydroxy group of the compound was acetylated. Treatment of the acetyl compound with methyl Grignard reagent resulted in the methylation of the 5-acetyl group to 2[2-acetoxy-5(2-hydroxy-2-propyl)phenyl]2H-benzotriazole which was then dehydrated with potassium hydrogen sulfate to the desired 2(2-hydroxy-5-isopropenylphenyl)2H-benzotriazole. This monomer did not homopolymerize, but was copolymerized readily with styrene, methyl methacrylate, and n-butyl acrylate with azobisisobutyronitrile as the initiator. 2(2-Acetoxy-5-acetylphenyl)2H-benzotriazole was also reduced with sodium borohydride to form 2[2-acetoxy-5-(1-hydroxyethyl)phenyl]2H-benzotriazole which was dehydrated and hydrolyzed to the known 2(2-hydroxy-5-vinylphenyl)-2H-benzotriazole. This route provides a novel and simpler synthesis of 2(2-hydroxy-5-vinylphenyl)2H-benzotriazole.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1982.170201001
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  • 5
    Electronic Resource
    Electronic Resource
    Poly(alkylene oxide) ionomers VIII.Part VII: D. Bansleben, M. Hersman, and O. Vogi, J. Polym. Sci. Polym. Chem. Ed., 22, 2489 (1984). Synthesis of methyl ω-alkenoates and methyl ω-epoxyalkanoates (1984)
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 2501-2521 
    Details
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ω-Alkenoic acids, either commercially available or synthesized, were esterified to their corresponding methyl esters. They were characterized by their infrared, 1H-, and 13C-NMR spectra. The ω-alkenoates prepared were: propenoate (acrylic acid), butenoate, pentenoate, hexenoate, heptenoate, octenoate, nonenoate, and decenoate. These compounds were epoxidized with m-chloroperoxybenzoic acid to the corresponding methyl ω-epoxyalkanoates. The rate of epoxidation of the double bond is found to increase as the double bond is separated from the carbomethoxy group by increasing numbers of methylene groups. When at least three methylene groups are inserted, the rate of epoxidation becomes constant and is similar to the epoxidation of ω-olefins. The methyl ω-epoxyalkanoates were characterized by their infrared, 1H-, and 13C-NMR spectra. Methyl ω-alkenoates and methyl ω-epoxyalkanoates were prepared and characterized, and their purification was studied in preparation for their investigation as monomers for olefin or epoxide polymerization using corrdination initiators.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1984.170221018
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  • 6
    Electronic Resource
    Electronic Resource
    Terpolymerization of acrylonitrile, styrene, and 2,3-dibromopropyl acrylate (1983)
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 21 (1983), S. 1913-1928 
    Details
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The terpolymerization of acrylonitrile with styrene and 2,3-dibromopropyl acrylate in emulsion and dimethyl formamide solution was investigated. Polymerizations, when stopped at low conversions, yielded terpolymers that showed good agreement between experimental and theoretical copolymerization composition data, calculated from the Alfrey-Goldfinger equation. The relationship between monomer feed and terpolymer compositions is displayed on triangular coordinate graphs proposed by Slocombe. By using a computer program the lines of unique composition and binary azeotropic composition for both systems were established. In the case of emulsion polymerization the azeotropic ternary point was determined at a molar ratio for acrylonitrile/styrene/2,3-dibromopropyl acrylate of 0.27/0.61/0.12. The experimental results of emulsion terpolymerization fit the calculated curves satisfactorily over a wide range of monomer compositions up to high conversions. The influence of 2,3-dibromopropyl acrylate on the thermal and flammability characteristics of the terpolymers is described.
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1983.170210704
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  • 7
    Electronic Resource
    Electronic Resource
    Poly(alkylene oxide) ionomers. XIII.Part XII: D. A. Bansleben and O. Vogl, J. Polymer Science, Polymer Chem. Ed., in press. Copolymers of trioxane with the epoxide and 1,3-dioxolane of methyl 10-undecenoate (1984)
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 3263-3288 
    Details
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Cationic copolymerization of 1,3,5-trioxane with methyl 10,11-epoxyundecanoate or methyl 7,8-epoxyoctanoate and terpolymerization with 1,3-dioxolane was successfully carried out. Co-and terpolymerization of 1,3,5-trioxane with 4-(1-carbomethoxynonyl)-1,3-dioxolane was also achieved. Feed compositions of the functional comonomers were varied from 5 to 40 mol %; in all cases the isolated copolymers contained less than 5% of the functional mer units. The composition of the copolymers showed that the methyl ω-epoxyalkanoates were much less reactive than 1,3,5-trioxane. A similar trend was observed with the functional dioxolane monomer, although significantly shorter induction periods were observed in comparison with the epoxy/trioxane copolymerizations. The oxymethylene copolymers and terpolymers were characterized primarily by their infrared spectra; however, the thermal and base stabilities of selected copolymers were also determined.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1984.170221143
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  • 8
    Electronic Resource
    Electronic Resource
    Poly(alkylene oxide) ionomers. X. Copolymerization of methyl ω-epoxyalkanoates and characterization of the polymersPart IX: J. Muggee and O. Vogl, J. Polym. Sci. Polym. Chem. Ed., to appear. (1985)
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 23 (1985), S. 649-671 
    Details
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Selected methyl ω-epoxyalkanoates ranging from methyl 3,4-epoxybutanoate to methyl 7,8-epoxyoctanoate were copolymerized with a number of oxiranes and with oxetane. Tetrahydrofuran did not take part in the attempted methyl ω-epoxyalkanote-tetrahydrofuran copolymerization, but acted only as the solvent. The oxirane copolymers had polymer compositions similar to the comonomer feed ratio. Oxirane comonomers used were propylene oxide (1,2-epoxypropane), butylene oxide (1,2-epoxybutane), 1,2-epoxyhexane, epichlorohydrin, and phenylglycidyl ether. The initiator system used was triethylaluminum/water/acetylacetone (1.0/0.5/1.0) in about 5 mol %. In the copolymerizations using methyl 3,4-epoxybutanoate as a comonomer, only small yields of polymer (in the range of 1 to 2%) were realized, while for methyl 4,5-epoxypentanoate the yields were generally in the range of 20 to 60%. Methyl 7,8-epoxyoctanoate copolymerized readily and gave yields of copolymers of 50 to 90%.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1985.170230306
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  • 9
    Electronic Resource
    Electronic Resource
    Poly(alkylene oxide) ionomers. XII. Hydrolysis of polymers and copolymers of methyl 10,11-epoxyundecanoatePart XI: D. A. Bansleben and O. Vogl, J. Polym. Sci. Polym. Chem. Ed., 23, 675 (1985). (1985)
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 23 (1985), S. 703-721 
    Details
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ester-substituted oxyethylene polymers and copolymers of methyl 10,11-epoxyundecanoate were prepared with an aluminumalkyl-water coordination initiator system modified with acetylacetone. Poly(ethylene oxide) ionomers, polyelectrolytes, and polycarboxylic acids were obtained by alkaline hydrolysis of the pendant carbomethoxy groups and by neutralizations with acetic acid. The high molecular weight substituted poly(ethylene oxide)s were characterized by spectral, thermal, and dilute solution measurements. The infrared spectra of carboxylate substituted poly(ethylene oxide)s, both homo- and copolymers, show the typical shifts in the carboxyl absorption when going from the ester to the carboxylate group to the free acid. Polymer transitions temperatures, as measured by DSC, changed accordingly. Wide-angle x-ray diffraction measurements strongly suggest the existence of ionic domains in the oxyethylene polymer matrix. Dilute solution properties of the ionomers show typical polyelectrolyte behavior, including a substantial change in viscosity when ionic solute is added.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1985.170230308
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  • 10
    Electronic Resource
    Electronic Resource
    Functional polymers. XIVPart XIII: S. Yoshida and O. Vogl, J. Polym. Sci. Polym. Chem. Ed., to appear.. Grafting of 2(2-hydroxy-5-vinylphenyl)2H-benzotriazole onto polymers with aliphatic groups (1981)
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 3307-3314 
    Details
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Successful grafting of 2(2-hydroxy-5-vinylphenyl)2H-benzotriazole onto saturated aliphatic C—H groups of polymers has been accomplished. When the grafting reaction was carried out in chlorobenzene at 150-160°C with di-tertiary butylperoxide as the grafting initiator, grafts as high as 20-30% at grafting efficiencies of 50 and 80% have readily been obtained. It was very important to carry out the grafting reaction in tubes sealed under high vacuum since trace amounts of oxygen cause complete inhibition of the grafting reaction by the phenolic monomer. Grafting reactions were carried out on a variety of different polymers including atactic polypropylene, ethylene/vinyl acetate copolymer, poly(methyl methacrylate), poly(butyl acrylate), and polycarbonate.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1981.170191223
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