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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 823-832 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rate of anionic polymerization of pivalolactone with polystyrene dicarboxylates decreased with conversion, suggesting deactivation of the propagating chain end by precipitation of the polymer during polymerization. The presence of unreacted initiator was explained by slow initiation for formation of a living polymer of pivalolactone. Various factors affecting block efficiency were discussed, and high efficiency was obtained for the preparation of block copolymers containing a long pivalolactone segment by using more nucleophilic polystyrene dicarboxylates. Block copolymer of acrylonitrile and pivalolactone was prepared from polyacrylonitrile dicarboxylates.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 14 (1976), S. 783-792 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polycondensation of diethyl 2,3,4,5-tetrahydroxyadipate with various diamines was carried out in solutions under mild conditions. The polycondensation reaction occurred rapidly even at room temperature in polar solvents such as alcohols, and in aqueous solution a cyclic product was obtained instead of linear polymers although the reaction with diamines was completed within several minutes. Polymers obtained from diethyl 2,3,4,5-tetrahydroxyadipate were a linear polyamide having pendant hydroxyl groups, which decomposed on heating at around 200°C. A solid-phase polycondensation of the precursor polyamide yielded a high molecular weight polyamide.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 14 (1976), S. 961-971 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Graft copolymerization of styrene on rubber containing chlorine, e.g., chloroprene rubber (CR) and chlorosulfonated polyethylene (Hypalon), with chromous acetate (Cr2+) was carried out in DMF-THF mixed solvent at 50°C. From the kinetic study, the normal kinetic orders with respect to the concentration of initiator and monomer were obtained at low concentrations of CR, but the deviation from conventional first-order to second-order kinetics with respect to the monomer concentration was observed at high CR concentrations: Rp ∝ [CR]1/2 [Cr2+]1/2[styrene]1 (at low CR concentration); Rp ∝ [CR]1/2 [Cr2+]1/2[styrene]1 (at high CR concentration). This result was explained in terms of the high viscosity of the reaction medium due to the rubber contained in solution. An initiation site along the polymer chain was assumed from the graft copolymerization with three kinds of CR having different microstructures. The results of fractionation of obtained polymer showed that the graft efficiency was high but a large amount of gel was formed.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 16 (1978), S. 3035-3038 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 147-154 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In order to assess the effect of the methylol group at the 4-position of 1,3-dioxolane on polymerization, the photopolymerization of 2-vinyl-4-hydroxymethyl-1,3-dioxolane (VHDO) was carried out in benzene at 40°C. The reaction scheme of VHDO was considered to be the same as that of 2-vinyl-1,3-dioxolane (VDO). The rate of polymerization and the molecular weight of polymer were small because of the degradative chain transfer by allylidene group. Moreover, the rate of polymerization of VHDO was greater than that of VDO, whereas the molecular weight of polymer of VHDO was less than that of VDO.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effect of epoxy groups at the surface layer of ethyl acrylate-glycidyl methacrylate copolymer (1) emulsion particles on its crosslinking reactivity has been investigated. For this purpose two series of I emulsions were prepared. In the Y series, of which emulsion particles have epoxy groups at the surface layer, the epoxy content in the polymerization recipe was varied. For preparing the X series, of which emulsion particles have few epoxy groups at the surface layer, the high epoxy content of a given emulsion was reduced by various degrees of cleavage reaction with HCl-CaCl2. In emulsion blend films with amine-group-containing copolymer (II) emulsion, where the crosslinking reaction was expected to proceed only at the interfacial layer of I and II emulsion particles, the Y series, compared to the X series at the equal overall epoxy content in particles, showed less swelling and higher gel fraction in dioxane, less swelling in water, and higher tensile strength and modulus. On the other hand, this difference was not observed in the next two crosslinked films in which crosslinking was expected to be homogeneous. First, blends of I and II, which were isolated from the corresponding emulsions discussed above, were cast from dioxane solutions. Second, I emulsions were cast with BF3 ether complex which was expected to penetrate into the particles. It is concluded that the response of I emulsion cleaving the epoxy groups at the surface layer of particles to subsequent interfacial crosslinking is obviously reduced. However, even such an emulsion can be crosslinked to an extent similar to that of an uncleaved emulsion with similar overall epoxy content, if the crosslinking reaction is conducted so as to give an homogeneous effect.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 20 (1982), S. 3337-3350 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: It was found that structurally isomeric polymers were formed by the ring-opening polymerization of β-(2-acetoxy ethyl)-β-propiolactone with (EtAlO)n and Et(ZnO)2ZnEt catalysts; that is, the Al catalyst catalyzed normal polymerization which led to poly-β-ester and the Zn catalyst formed isomerized poly-β-ester as the main product. The polymer structure was determined by nuclear magnetic resonance (NMR), T1-value, thermal decomposition product, and (Tg). The NMR studies for the monomer-catalyst systems indicated that the Al catalyst interacted predominately with the lactone group, whereas the Zn catalyst interacted with the side-chain ester group. These site-selective interactions could be related to the difference in the stereoregulation by the two catalysts during the poly(β-ester)-forming polymerization process.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 21 (1983), S. 637-649 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: New active bisamides, 4,4′ -diacylbis-2-aryl-1,3,4-oxadiazoline-5-thiones and -ones having various electron accepting groups in the oxadiazoline units were synthesized, and their reactivities toward diamines were investigated. The polycondensation reactions of the bisamides derived from 2-aryl-1,3,4-oxadiazoline-5-thiones with both aliphatic and aromatic diamines occurred rapidly even at room temperature to form high-molecular-weight polyamides in quantitative yields. The reactivities of the bisamides having electron accepting groups such as p-chloro and p-nitro groups, particularly p-nitro groups, toward diamines were much higher than that of the corresponding bisamide having no such group. It was also found that reaction conditions such as solvent, monomer concentration, and temperature had a strong influence on the molecular weight of the resulting polyamides. Aminolysis of several benzoyl derivatives of 2-aryl-1,3,4-oxadiazoline-5-thiones and -ones was also carried out as a model reaction, and the effect of electron accepting groups on the reactivity of these compounds was discussed.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 21 (1983), S. 1559-1565 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The polymerization of γ-benzyl-DL-glutamate NCA in the presence of poly(γ-benzyl-L-glutamate) was investigated. At the initial stage the D-enantiomer was preferentially polymerized (ca. 35% ee) by using triethylamine as an initiator. Enantioselectivity was independent of the molecular weight of preformed poly(γ-benzyl-DL-glutamate).
    Additional Material: 3 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 21 (1983), S. 1671-1679 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Based on our recent discovery of the isomerization polymerization of β-(2-acetoxyethyl)-β-propiolactone into poly-δ-ester,1,2 we examined the generality of this phenomenon by using two related monomers. The catalysts were (EtAlO)n and Et(ZnO)2ZnEt. The side-chains in the monomers selected were the (CH3)2CHCOO—CH2CH2—(2) and (CH3)CICHCOO—CH2CH2—(3) groups in which steric effects are almost identical but electronic effects are in opposition. The monomers yielded isomerized poly-δ-ester units, depending on the terminal substituent groups in the side-chain. These observations can be interpreted with the bicyclic intermediate proposed in the earlier work. Monomer (2) was reactive and produced a poly-δ-ester structure most readily, probably because of the higher electron density at the side-chain ester group which coordinated with the catalyst. In contrast, monomer (3) was less reactive, and the probability of isomerization was the lowest, i.e., the electron deficient side-chain ester group apparently interfered with the formation of the intermediate, especially in the Zn-catalysis. Equibinary random copolymers were prepared from (2) and (3) according to the catalyst and polymerization conditions chosen.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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