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  • Physics  (558)
  • 2000-2004
  • 1980-1984  (558)
  • 1925-1929
  • 1980  (558)
  • 101
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of the polymerization of 1,3-butadiene initiated by bis(η3-allyl nickel trifluoroacetate) prepared in benzene was studied in methylene chloride at 40°C. The reaction is first order with respect to the monomer, second order with respect to the catalyst in contrast to the case in which solvent is benzene. We have shown that the presence of a polar molecule (fe, N-methyl phthalimide) decreases the overall rate of polymerization. The apparent reactivity ratios for the system 2-phthalimidomethyl 1,3-butadiene (1)-1,3-butadiene (2) are r1 = 0.65 ± 0.006 and r2 = 0.48 ± 0.015.
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  • 102
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ammonia used as both reactant and solvent has been shown to dehydrochlorinate 1,1,1-tri-chloro-2,2-bis(4-hydroxyphenyl)ethane smoothly to 1,1-dichloro-2,2-bis(4-hydroxyphenyl)ethylene. The reaction is complete in 1 hr at 100°C, and after two crystallizations from methanol/water affords polymerizable quality monomer for the synthesis of highly flame-resistant polycarbonates. The use of organic solvents in combination with ammonia does not offer any rate advantages over pure ammonia. Primary and secondary amines also can be used to effect the dehydrochlorination but, except for the methylamine, are significantly less reactive and lead to less pure product than amonia.
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  • 103
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2513-2521 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of p-benzoquinone with tin tetrachloride in the absence of solvents was investigated by isolation and identification of the reaction products. This reaction leads to the formation of polymeric quinone-tin derivatives free from combined chlorine, chlorinated quinones, quinhydrone, and minute amounts of CI2 and HCI gases. The tin content varies accroding to the molar ratios of the reactants and reaches its maximum (72%) at the smallest SnCI4 ratio. The existence of the Sn-Sn bond in the polymeric derivatives was confirmed chemically and spectroscopically. A mechanism based on the formation of radical intermediates which can account for the reaction products was developed. In view of their quinonoid nature, high thermal stability, and the presence of Sn-Sn bonds, the polytin derivatives are to be investigated as radical traps in the stabilization of polymeric arcticles against radical degradation process.
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  • 104
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2561-2565 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Glass transitions of four solid epoxide prepolymers are described. The rigidity of their molecular chains are measured. With them an equation is developed which relates the glass transition temperatures to the molecular parameters of these polymers.
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  • 105
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: N-phenyl and N-cyclopropylcitraconimides did not polymerize as free radicals with azobisisobutyronitrile (AIBN) as initiator. N-allylcitraconimide, however, depending on the temperature and concentrations of the reactions, readily polymerized to produce polymers of different molecular weights. These polymers contained as much as 85% cyclic repeating units when the polymer exhibited an average molecular weight of ca. 4000. The softening point of the polymer was higher than 350°C and the compound was highly soluble in many organic solvents. The allylic CH3group in N-substituted citraconimides and in their corresonding citraconamic acids could not be brominated with N-bromosuccinimide.
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  • 106
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2523-2533 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The polymeric p-benzoquinone-tin derivatives obtained from the reaction of p-benzoquinone with tin tetrachloride in the absence of solvent have been investigated as thermal stabilizers for rigid PVC at 200°C by measuring the rate of dehydrochlorination. The results reveal the greater stabilizing efficiency of the investigated products in relation to dibutyltin maleate and the basic lead stabilizers commonly used in industry. Evidence has been accumulated that the quinone and metallic elements (Sn—Sn bonds) of the stabilizer participate in the stabilization process by trapping the radical intermediates of degradation and blocking the odd electron sites formed on the polymer chains. Although stabilizers with high quinone content provide greater stabilization in the early stages of degradation, their efficiency sharply decreases in subsequent stages. On the other hand, stabilizers of high tin content effectively prohibit the dehydrochlorination reaction at all stages of degradation. On an equivalent basis of metal content, the results clearly demonstrate the greater stabilizing efficiency of tin atoms when found in direct contact in the stabilizer molecule. The mechanism of stabilization suggested to account for the results obtained may be considered as additional evidence in support of the radical nature of the dehydrochlorination reaction.
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  • 107
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2543-2560 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A study was made of the microstructural changes that occur in ultraviolet irradiation under vacuum of thin films of 1,2-poly(cis-1,4-hexadiene) (CHD), 1,2-poly(trans-1,4-hexadiene) (THD), 1,2-poly(trans-1,3-pentadiene) (TPD), equibinary (1,2,-1,4) polybutadiene (EB), and equibinary (3,4-1,4) polyisoprene (EI). These polymers - all containing pendant double bonds - undergo important photoinduced loss of unsaturation, presumably through cyclization of the double bonds, by analogy to the previously reported photocyclization of 1,2-polybutadiene (VB) and 3,4-polyisoprene (VI)films. For the equibinary polymers, which contain internal as well as external (or pendant) double bonds, the loss of unsaturation is considered to involve photocyclization of 1,2-1,4 and 1,2-1,2 dyads in EB and of 3,4-1,4 and 3,4-3,4 dyads in EI. Accompanying thecyclization process in CHD, THD, and TPD is a direct photochemical cis-trans isomerization of —CH=CH—double bonds analogous to that originally noted for 1,4-polybutadiene. The photorearrangements in the above polymers with pendant double bonds were compared to the corresponding thermally induced rearrangements reported previoulsy;for VB and VI, in particular, the thermal, photo-and radiation-induced cycli-zations were found to be very similar, possibly having a common nonradical, nonionic mechanism involving excited double bonds.
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  • 108
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2567-2575 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The following characterstics of four molten epoxide prepolymers are described: flow curvepeculiarities, shift factor and temperature-independent flow activation energy, shear stress and shear rate effects, and their graphical and analytical descriptions.
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  • 109
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2577-2583 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Availabilities of O(3)H relative to O(2)H (that is, [O(3)H]a/[O(2)H]a) on accessible surfaces of microstructural units of cotton fibers were measured by chemical microstructural analysis (CMA). CMA involves a mild chemical reaction with N,N-diethylaziridinium chloride, determination of substituent distribution for this product and a corresponding product from decrystallized cellulose, and simple computations. Measurements for fibers in commercial cotton fabric, for field-dried fibers, and for never-dried fibers are reported. The [O(3)H]a/[O(2)H]a, an inverse measure of intact O(3)H ·· O(5′) bonds, decreased in the stated order; thus, intact O(3)H ·· O(5′) hydrogen bonding increased in this same order. Results indicate a high degree of order in intramolecular bonding in the never-dried fiber and an increasing disruption of this bonding as the never-dried fiber is dried and processed.
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  • 110
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2585-2595 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ceric-thiol systems are good initiators for the acid aqueous polymerization of some water-soluble Vinyl monomers although not for styrene (in aqueous emulsion) and vinyl acetate. Thiols used are 2-mercaptoethanol, thioglycolic acid, 2-mercaptoethylamine hydrochloride, and L-cysteine hydrochloride. The polymerization proceeds through a radical mechanism. End-group analysis of poly(methyl methacrylate) obtained by initiation with various ceric-thiol systems has been carried out using Palit's dye testes. Hydroxyl, carboxyl, and amine end groups (to the extent of about one per polymer molecule) were incorporated in poly(methyl methacrylate)s obtained by initiation with 2-mercaptoethanol, thioglycolic acid, and 2-mercaptoethylamine hydrochloride, respectively, each in combination with Ce4+ ions; both amine and carboxyl end groups were obtained using C4+/L-cysteine hydrochloride initiator system. From the end-group results, the initiating species have been identified and the initiation mechanism prooposed. The probable termination mechanism also has been discussed.
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  • 111
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2609-2614 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A Mössbauer spectroscopic study of the γ-induced polymerization of iron methacrylate has been made. Iron-methacrylate is a solid monomer. This monomer, in a powdered form, was polymerized by irradiating with γ rays from a 60Co source. A number of Mössbauer spectra were taken after subjecting the sample to different cumulative doses of γ rays. The spectra were asymmetric doublets and the asymmetry changed as the polymerization proceeded. The changes in asymmetry have been correlated with the percentages of polymerization which were determined by two different methods, viz., chemical analysis and resistivity measurement.
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  • 112
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2597-2608 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Mixtures in various proportions of natural rubber (NR) and each of two tackifier resins, a poly-β-pinene and a modified pentaerythritol rosin ester, were used as the adhesive layer in joining a flexible polyester strip to a plane glass substrate. Measurements of the force required to peel the strip from the glass at a 90° angle were made over a range of pulling rates at several temperatures. Application of time-temperature superposition enabled a master curve of (reduced) peel force versus (log) pulling rate at a standard temperature (296 K) to be obtained for each adhesive composition. The master curves showed, in increasing order of pulling rate, some or all of four different modes of peeling: (i) peeling with viscous adhesive response, (ii) peeling with rubbery response, (iii) oscillatory or slip-stick peeling, and (iv) peeling with glassy adhesive response. In general, transitions between the different peeling modes were quite abrupt. Increase in concentration of tackifier resin caused displacement of the master curve toward lower pulling rates [an effect interpreted in terms of an increasing adhesive glass temperature (Tg)], and a superimposed displacement of the transition between peeling modes (i) and (ii) toward higher pulling rates-an effect attributed to reduction in adhesive average molecular weight. The influence of the tackifier resin in modifying the viscoelastic characteristics of the adhesive was further demonstrated in a comparison of the peel force master curves with corresponding master curves of dynamic storage modulus.
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  • 113
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2615-2627 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The method of spin labels based on stable iminoxyl radicals has been applied to the investigation of the topochemistry of polymer-supported polyethylene-grafting diallylamine (PE-gr-PDAA)and ofimmobilized catalytic systetms. The effective distances between fixed radicals are comparatively large (r̄ ∼ 25-35Å for the case of functional groups of PE-gr-PDAA and r̄ ≥ 35Å for the case of fixed components of the catalytic systems). The demonstration of step-by-step penetration of the label into the functional cover (100-300 Å) has been made. Correlation times were calculated in the temperature range 290-440K. The dependence of log τc on 1/T shows two linear parts to the curve.The activation energies in the α region for PE-gr-PDAA and for the product of its interaction with TiCl4. Ti(OC4H9)4, and Al(C2H5)2Cl are equal to 13, 14, 24, and 13 Kcal/mole, respectively. The method has been applied to the investigation of Ziegler-Natta immobilized catalytic systems. It has been noted that the labels are fixed not far from each other (r̄ ≤ 12Å) after the interaction of the catalytic components.
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  • 114
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2629-2640 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polymerization was made at 60°C in a lyotropic liquid crystal of sodium undecenoate and water. The liquid crystalline structure prior to polymerization was identified by optical microscopy and low-angle x-ray diffraction as an array of hexagonal closely packed cylinders with the hydrophobic part of the soap in the center of the cylinders. During polymerization the structure became isotropic at 60°C. Cooling to 20°C transformed the structure to a lamellar liquid crystal-a reversible transition. The structure of the lamellar phase was interpreted as a polyethylene backbone from which deformed decanoate chains reached toward the aqueous layer. Molecular models showed the model to accept head-tail, head-head, and tail-tail configurations in cis and trans conformations with the exception of the cis tail-tail configuration.
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  • 115
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2641-2648 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Phase diagrams for monomer (methyl acrylate containing microemulsions) are shown and described. Polymerizations of a series of microemulsified monomer reveals the expected linear dependence of 1/DS vs. [S]/[M] for pentanol acting as a chain transfer agent and giving a value of 5.1 × 10-4 for Cs. No break in molecular weight behavior was shown as a result of micellization at higher water contents. A comparison of molecular weights obtained by various classical methods (solution, emulsion, bulk) are also given.
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  • 116
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2649-2662 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 13Carbon chemical shifts are reported for polyimide and polyamic acid prepared from 3-aminophenylacetylene, 1,3-bis(3-aminophenoxy) benzene, and 3,3′,4,4′-benzophenoetetracarboxylic dicanhydride. The shielding parameters are correlated with the structure. A spectral analysis of model compounds, monomers, and other oligomers is also included. This analysis resulted in an analytical method by 13C-NMR spectroscopy of determining the amic acid-imide ratio in the partly cured polyamic acid. The development of the method is discussed.
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  • 117
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2715-2721 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The anhydrous formaldehyde polymerization is examined. The influence of initiator and monomer concentration on the molecular weight and molecular weight distribution are emphasized. A mechanism for the transfer to the monomer is introduced. This mechanism is confirmed by experimental results and leads to the formation of formyl end groups. The influence of various initiators on the transfer reaction also is evaluated.
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  • 118
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2663-2676 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Soluble tricarbonylchromium complexes were made by reacting Cr(CO)6 with a ladder polyphenylsilsesquioxane and a linear polydiphenylsiloxane. These new polymer Cr(CO)3 complexes were characterized by elemental Cr, infrared (IR), gel permeation chromatography (GPC), viscosity, and thermal analyses and were evaluated as stereoselective hydrogenation catalysts. Thermogravimetry studies demonstrated that the new complexes were more stable at 180-200°C in N2 than the corresponding complex from crosslinked polystyrene. These silicone polymer complexes catalyzed stereoselective hydrogenation of methyl sorbate to cis-3-hexenoate in cyclohexane and tetrahydrofuran (THF) and could be recovered from THF for recycling by precipitation-fiItration. Catalytic activity and recyclability, however, were highly influenced by the solvent. Loss of catalytic activity associated with loss of Cr(CO)3 was observed on recycling. These results support a mechanisim that involves dissociation of Cr(CO)3, a significant portion of which cannot become reassociated with the polymer phenyl groups.
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  • 119
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2677-2695 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Dilphenyl-4-thiophenoxyphenylsulfonium salts have been found to be more efficient cationic photoinitiators than the highly photoactive triphenylsulfonium salts. The former compounds were identified as by-products produced in the preparation of triphenylsulfonium chloride from benzene, chlorine, sulfur monochloride, and aluminum chloride. Confirmation of the structure was made by NMR and UV spectroscopy as well as by independent synthesis. The photoinitiated cationic polymerization of cyclohexene oxide and other epoxy monomers was carried out to demonstrate the higher efficiency of diphenyl-4-thiophenoxysulfonium hexafluoroarsenate as compared to the corresponding triphenylsulfonium salt.
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  • 120
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The title compounds were synthesized and their homopolymerizations and copolymerizations with styrene and a number of acrylic monomers were investigated. Methyl 3-vinylacetylsalicylate was prepared in a five-step synthesis from 2-ethylphenol in an overall yield of 40%. Methanolysis of this compound gave methyl 5-vinylsalicylate in 63% yield. Hydrolysis of methyl 3-vinylsalicylate gave a nearly quantitative yield of 3-vinylsalicylic acid which could be acetylated to 3-vinylacetylsalicyclic acid (3-vinyl aspirin). 3-Vinylsalicylic acid derivatives were readily homopolymerized and copolymerized with styrene, methyl methacrylate, and methacrylic acid, and 3-vinylsalicyclic acid was copolymerized with a number of vinyl and acrylic monomers. Copolymer compositions were determined by examination of 1H-NMR spectra.
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  • 121
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2803-2810 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: This article was written for the purpose of investigating the mechanisms of reactions between unsaturated polyester resins and base anhydridelike metal oxides (CaO, MgO, ZnO) which cause an increase in viscosity. As a model system ethyl-hydrogen-succinate (ESH) and ZnO were reacted in CCl4 and complexes that contained Zn-hydroxocarboxylate units took an essential part in this reaction. Solubility measurements of the model compounds and infrared (IR) spectra of the reaction products led to the conclusion that further molecular associates were formed from the mixed metal-hydroxocarboxylate complex by the carbonyl oxygens of ester groups, which resulted in end products of polymeric structure. It is suggested by IR spectroscopical analogies between the model compounds and reaction products of an adipic acid/butanediol-1,4 polyester with ZnO that similar reactions can account for the polyesters as well.
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  • 122
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2811-2821 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rate of soapless emulsion polymerization is studied experimentally and theoretically. The soapless emulsion polymerization of methyl methacrylate (MMA) in water is carried out with potassium persulfate as initiator. It is shown that the soapless emulsion polymerization of MMA gives different time-conversion and time-average molecular weight curves from those of bulk and emulsion polymerizations. Comparing the experimental results with those of the other types of polymerization, features of the rate of soapless emulsion polymerization are discussed and a kinetic model is proposed to apply the soapless emulsion polymerization of MMA in water. The experimental results can be well expressed by this model.
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  • 123
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2823-2855 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Linear relationships among molecular weight, polymerization time, and gelation for the condensation of any monomer, including those of unknown size and functionality, are developed and applied to data on soluble silicic acids generated from tetraethyl silicate and from sodium silicate. The results suggest the formation of monomers containing ca. 12-15 —OSi units with functionality of ca. 2.05 that condense with a rate constant of ca. 10-4 liter/mole sec and an activation energy of 40-70 kJ/mole. One model compatible with these characteristics and the stoichiometry involved is a ladder polymer ca. 3 —SiO units wide. Polymer isolation was achieved by replacing residual —OH with (CH3)3Sio—, as well as by freezing of of aqueous solutions, which yielded fibers under special conditions. Solutions of the uncapped and capped polymers and melts of the latter had low viscosity even for fractions with M̄n ∼100,000. This implies a coiled or globular nature for the polymers, which is supported by their limited propensity for film and fiber formation. Attemps to improve this situation by copolymerization, the use of other capping agents, and by the polymerization of precapped monomers were unsuccessful.
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  • 124
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2857-2866 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Thermally activated ethylene polymerization catalysts which contain chromium and titanium on silica differ from those catalysts which contain only chromium on silica. The characteristics of chromium-titanium catalysts vary with the method of incorporating the titanium and the thermal activation procedure. Titanated catalysts of the kind examined in this article have faster initiation and a higher polymerization rate per unit catalyst weight than corresponding catalysts without titanium. High-density polyethylene produced by this type of titanium-chromium catalyst tends to have a higher melt index and a broader molecular weight distribution than polyethylene made with chromium on silica catalysts. Iodometric titration showed that reduction from the initial hexavalent chromium to trivalent occurs when the dry, catalyst starting material is treated with titanium tetraisopropoxide. A study of the reaction between chromium trioxide and titanium tetraisopropoxide in carbon tetrachloride revealed that (1) it is not necessary to have a reaction between surface silanols and titanium tetraisopropoxide for the reduction to occur, and (2) the reaction product has an absorption near 660 nm in the visible range. Comparison of spectra showed that chromium trioxide on silica reduced by isopropyl alcohol has a shifted absorption, i.e., 600 nm. These findings are interpreted to mean that titanium atoms come sufficiently close to chromium atoms to change their electron density in the starting material and remain close neighbors in the activated catalysts. The interpretation is further supported by ESCA data and leads to the proposal that in this case the activated catalysts contain titanium chromate structures.
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  • 125
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2869-2873 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 126
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2867-2868 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 127
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2875-2877 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 128
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2883-2885 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2887-2899 
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    Keywords: Physics ; Polymer and Materials Science
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2879-2882 
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2901-2904 
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 3021-3028 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Indene, α-methylstyrene, and styrene were polymerized in liquid sulfur dioxide in the presence of hydroperoxides and peracids. With indene, depending on the molar ratio of the monomer to sulfur dioxide, homopolymerization and polysulfone formation could be observed. With α-methylstyrene spontaneous polymerization in liquid sulfur dioxide was observed; the addition of hydroperoxide increased the yield and molecular weight. Styrene was polymerized in this solvent with hydroperoxides and peracids, the latter being a more effective initiator. The initiation in these systems could be explained by the formation of a mixed anhydride between sulfuric acid and m-chlorobenzoic acid.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 3069-3080 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Nucleophilic displacement of activated aromatic nitro groups with aryloxy anion is a versatile and useful reaction for the synthesis of aromatic ethers. Preparation of various aromatic monomers and polymers containing ether linkages is described.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 3059-3067 
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
    Notes: The formation of two kinds of solvation complex of poly(ethylene oxide), polydimethoxyethylene, and polydioxene with some alkali derivatives of fluorene in dioxane was found, differing in the ionic species of the fluorenyl metal in the complex. Additional evidence was found for the existence of peripherally solvated ion pairs of fluorenyllithium, -sodium, and -potassium. It was shown that polydimethoxyethylene and polydioxane interact with different cations in a different manner. The complexing ability of poly(ethylene oxide) and polydioxane with respect to fluorenyllithium, -sodium, and -potassium, and of polydimethoxyethylene for fluorenyllithium, was proved to be stronger than that of their monomer analogs - dimethoxyethane and dioxane. This was explained by the effect of the polymer chain.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 3081-3088 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Copper(II), nickel(II), cobalt(II), and zinc(II) accelerated the carboxylate-catalyzed hydrolyses of 2,4-dinitrophenyl isonicotinate (DNPI) and 2,4-dinitrophenyl picolinate (DNPP). The rate enhancement effect of the metal ions in the partially neutralized poly(methacrylic acid)- or poly(acrylic acid)-catalyzed hydrolysis of DNPI was greater than that in the monomeric acetate ion-catalyzed hydrolysis of this ester. This feature of the reactions was explained by the formation of a ternary complex composed of the polymer, the metal ion, and the substrate, in which the metal ion serves as a template for the nucleophilic reaction between the carboxylate groups along the polymer chain and the coordinated substrate. In DNPP the metal ion effect on the polycarboxylate-catalyzed hydrolysis was smaller than that on the acetate ion-catalyzed hydrolysis. This was interpreted as the result of differences in the structure of the complex.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 3111-3118 
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    Topics: Chemistry and Pharmacology
    Notes: The contribution of different MgO supports to the coordination polymerization of ethylene was studied by x-ray diffractometry and infrared (IR) and electron spin resonance (ESR) spectroscopy of the supports and their products after treatment with TiCl4. It was concluded that TiCl4 was bonded on the surface OH groups of MgO mainly in inactive form, whereas the majority of the active sites was associated with the coordinatively unsaturated O2- ions.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 3089-3099 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Configuration rules were established for the polymerization of cyclic monomers with chiral initiators. The latter recognize in the monomer an asymmetric carbon of homochiral configuration. The chirality of the initiator is defined by the “local” asymmetry of the ligand and by the overall asymmetry of the particular arrangement of catalytic aggregates. Two types of process called “homosteric” and “antisteric,” which apply to the polymerization of resolvable monomers and achiral monomers of meso structure, are defined. These configurational rules have a general character and are verified in many examples of differently substituted three- or four-membered cyclic monomers (oxiranes, thiiranes, β-lactones). Stereoelective polymerization appears to be an original method for the determination of the absolute configuration of some monomers of unknown chirality.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 3101-3110 
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    Topics: Chemistry and Pharmacology
    Notes: The thermal decomposition of poly(vinyl chloride) (PVC) mixed with several metal oxides was investigated by direct pyrolysis in a mass spectrometer (MS) and flash pyrolysis-gas chromatography. Our results show that the thermal decomposition of PVC occurs in two stages. Unsubstituted aromatic hydrocarbons (benzene, naphthalene, and anthracene) are evolved mainly in the first stage, alkyl-aromatics (e.g., toluene) in the second. Although the addition of some metal oxides results in an overall suppression of aromatic hydrocarbons, the unsubstituted aromatics are much more suppressed with respect to alkyl-aromatics. Furthermore, the formation of ZnCl2 and SnCl4 was revealed by the mass spectra of PVC-metal oxide pyrolysates. This suggests that, at least in these two cases, metal chlorides are responsible for aromatic hydrocarbon suppression. With this information a detailed reaction mechanism could be formulated for the thermal degradation of PVC.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 3129-3131 
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 3119-3127 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Alternating copolymers containing 4,4-isopropylidene-bisphenol (BPA) and comonomers with various degrees of polarity have been evaluated to find comonomer structures which provide low melt viscosity and good thermal stability. The materials were prepared by pyridine-catalyzed nucleophilic displacement reactions similar to that for the preparation of BPA polycarbonate. The molecular weights of the polycarbonates depend on the concentration and nucleophilicity of the attacking diol and the concentration and stability of a colored pyridine-chloroformate adduct formed during polymerization. The greatest thermal stability occurs for BPA-DMS and BPA-DEG. Thermomechanical flow measurements and Tg measurements were used to evaluate melt viscosity. The shapes and magnitudes of the Tg vs. Tf curves are sensitive to the copolymer chemical structure.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 3133-3147 
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    Topics: Chemistry and Pharmacology
    Notes: Treatment of 2,7,8-trioxabicyclo [3.2.1] octane (I) with electrophilic initiators gave polyorthoester composed of five- (70-86%), six-, and seven- (the sum, 14-30%) membered rings. Treatment of 2,8,9-trioxabicyclo [3.3.1]nonane (VI) with electrophilic initiators gave mainly oligomers. Trifluoromethane sulfonic acid in dichloromethane was particularly effective for the formation of dimer, 2,8,10,16,17,18-hexaoxatricyclo[11.3.1.1]hexadecane. The analysis of the structures of poly-I and oligomer-VI suggests that I and VI are polymerized through an SN1 mechanism.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 3393-3401 
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    Topics: Chemistry and Pharmacology
    Notes: A charge-transfer-type complex formation between poly(4-vinyl-N-propylpyridinium bromide) (C3PVP), poly(4-vinyl-N-butylpyridinium bromide) (C4PVP) or poly(4-vinyl-N-benzylpyridinium chloride) (BzPVP), and indole derivatives or between polymer containing flavin mononucleotide residues and indole derivatives was studied in the presence of simple and polyelectrolytes. The association constant (K) of the complex formation with indole acetate increased in the order BzPVP 〉 C4PVP 〉 C3PVP, which indicated an important contribution by hydrophobic interaction. The addition of simple and polyelectrolytes decreased the association constants. This was explained by the “secondary salt effect” of the salts. The importance of the electrostatic interactions in the complexation systems was obvious. The influence of simple electrolytes on the K values was discussed theoretically according to Manning's theory.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 3469-3481 
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    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The dissolution of cellulose in solutions of liquid ammonia and ammonium thiocyanate is discussed. Viscosity measurements on dilute solutions of cellulose in this solvent over a range of shear rates and shear stresses are reported. A four-bulb Ubbelohde suspended level viscometer was used for the measurements. Plots of log [η] versus log M gave Mark-Houwink coefficients of a = 0.95 and K = 6.686 × 10-5 at 25°C for [η] as dl/g. The Bloomfield equation was used to calculate effective bond lengths (b) from limiting viscosity numbers of cellulose in solutions of ammonia/ammonium thiocyanate and Cuene, respectively. Results indicate that cellulose may have similar configurations in both solvents and also that the ammonia solutions are true cellulose solutions. Miscibility of the cell- ulose/ammonia/ammonium thiocyanate solutions with organic solvents, such as glycerol, is also reported. Further, a few interesting characteristics of the liquid ammonia/ammonium salt solutions, discussed briefly, are the convenient boiling point, the rheological behavior, and the relatively high concentration of cellulose obtainable.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 3463-3468 
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    Topics: Chemistry and Pharmacology
    Notes: In the present study radiation-induced polymerization of 3n-dodecyl-1-vinylimidazolium iodide (I) in micellar aggregates was investigated. For comparison, the corresponding isotropic polymerization of I was also studied. Micellization was obtained in concentrated aqueous solutions; that is, above the monomer's critical micelle concentration (CMC) polymers obtained by both modes of polymerization were treated similarly and subsequently subjected to physical characterization. The main purpose of this study was to investigate whether the degree of organization of the monomer in micelles would affect polymer properties. Attempts to determine tacticity by 13C-NMR spectrometry failed because of the particular structure of the polymer. Crystallization of these polymers from ethyl alcohol or acetone was not possible as indicated by x-ray powder diffraction patterns that were characteristic of amorphous polymers. On the other hand, viscosity data of polymers do not depend on the mode of polymerization. It is therefore concluded that micellar aggregates are not sufficiently organized to affect polymer properties.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 65-67 
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    Topics: Chemistry and Pharmacology
    Notes: The existence of inhomogeneities in the polymer structure of ion exchangers was demonstrated and their influence on catalytic properties was shown. The results are based on the differences in catalytic activity of two ion exchangers with low degrees of sulfonation differing in the distribution of active groups within the polymer particles.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 59-64 
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    Topics: Chemistry and Pharmacology
    Notes: Vinyl acetate and acrylonitrile were copolymerized with Co(acac)3-Al(C2H5)3 catalyst system in benzene at 40°C. The rate of copolymerization is linearly proportional to monomer concentration and catalyst concentrations up to a certain value. The overall activation energy was found to be 11.3 kcal/mole. The effect of hydroquinone on the rate of copolymerization indicates the presence of free radicals in this system. The possibility of simultaneous formation of coordinate anionic and free radical active sites has been proposed.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 75-90 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of poly(ester carbonate) copolymers based on bisphenol A, terephthalic acid, and phosgene is reviewed, and a new synthetic route is described leading to polymers which are different from those obtained by methods described in the literature. The most important features of the new method are quantitative incorporation of the dicarboxylic acid into the polymer and absence of undersirable side reactions. Synthesis of the random copolymer in which the dicarboxylic acid and carbonic acid groups are present in about equal molar amounts is discussed. Solution properties, effects of M̄n and copolymer composition on Tg, sequence length distribution, the effect of ester interchange reactions on molecular weight distribution, and effects of monofunctional chain termination on molecular weight of the final product are also discussed.
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  • 148
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    Notes: New thermally stable polyimidines have been synthesized from bis(3,3-diphenyl-6-phthalidyl) ketone and five diamines: o-phenylenediamine, m-phenylenediamine, 1,5-diaminonapthalene, 1,8-diaminonapthalene, and benzidine. Polymers of low molecular weight (inherent viscosity up to 0.24 dl/g) were obtained by solution and sealed-tube polymerizations. The structural differences of the amines provided information concerning the effects on the thermal stability properties of the resulting polyimidines. The yellow to black polymers exhibited a 10% loss ranging from 420-510°C in air and 460-555°C in nitrogen and were soluble in chloroform and dimethylformamide.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 101-107 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The Cu(II) complexes of copolymers having pendant sulfide and imidazolyl groups were prepared by a free radical copolymerization of ethylvinylsulfide with vinylimidazole, and their properties and function were studied spectrophotometrically in comparison with those of poly[4(5)-vinylimidazole]. The complexes were found to be effective as catalysts for the oxidation of hydroquinone. Visible and ESR spectra of the Cu(II)-copolymer complexes were similar to those of the Cu(II)-homopolymer complexes, while the catalytic activity for the oxidation was different between these complex systems. A rapid reaction followed by a slow reaction, particularly at high ethylvinylsulfide content in the copolymers, was observed in the Cu(II)-copolymer complex systems, but a continuous reaction proportional to the reaction time was observed in the Cu(II)-homopolymer complex systems. The reoxidation rate of Cu(I) to Cu(II) complex, which was little affected by the concentration of imidazolyl group, decreased with a rise of the ethylvinylsulfide content in the copolymer. It was suggested that the sulfur atom of the sulfide group was weakly coordinated to Cu(II) but strongly to Cu(I), and an electron transfer reaction from substrate to the Cu(II) complex was increased, while reoxidation reaction of the Cu(I) complex was decreased in the copolymer complex systems.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 91-100 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Photochemical reactions of N-vinylcarbazole (VCZ) in the binary solvent of benzonitrile (φCN) and nitrobenzene (φNO2) were investigated. Both solvent and oxygen effects on the final products were examined. Benzonitrile and nitrobenzene behaved differently in the photochemical reaction of VCZ. At higher concentrations of benzonitrile in the aerated system, cyclodimerization was favored and it was inhibited by a cation scavenger and retarded by a radical scavenger. Polymerization occurred in the deaerated system and was inhibited by a radical scavenger and not by a cation scavenger. Using picosecond laser photolysis it was concluded that cyclodimerization occurs through the diffusion-controlled encounter collision of the excited singlet state of VCZ with an oxygen molecule, producing the VCZ cation radical and oxygen anion radical, and that this oxygen anion radical plays a very important role in the cyclodimerization of VCZ. It was also suggested that radical polymerization in the deaerated system is initiated by the excited triplet state of VCZ. On the other hand, at higher concentrations of nitrobenzene, only cationic polymerization took place irrespective of the presence of oxygen, and it was suggested that a contact charge-transfer complex is produced by the mixing of VCZ with φNO2 producing VCZ cation radical and NO2 anion radical by an excited-state electron transfer.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 123-146 
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    Topics: Chemistry and Pharmacology
    Notes: The thermal degradation of poly(3-pentylidene carboxylate) has been studied kinetically over the temperature range 200-300°C using thermogravimetry, gas evolution analysis, and rheogoniometry together with isolation and analysis of the reaction products. The observed behavior is completely different from that previously reported for poly(isopropylidene carboxylate) and poly(methylene carboxylate). Whereas in the latter cases the decomposition occurs by a first-order intramolecular ester interchange process characterized by an activation energy in the region of 27 kcal mole-1, poly(3-pentylidene carboxylate) decomposition occurs by random chain scission superimposed on a first-order hydrogen abstraction process. The activation energy associated with this decomposition reaction is in the region of 47 kcal mole-1, and the major degradation products are cis- and trans-2-ethyl crotonic acid.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 203-222 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Triad cotacticities of alternating copolymers of methyl methacrylate with styrene prepared in the presence of zinc chloride, ethylaluminium sesquichloride, and ethylboron dichloride are investigated from the mechanistic point of view by means of 1H- and 13C-NMR. The cotacticities from 1H-NMR spectra are obtained accurately by using α-d-styrene in the place of styrene and by measuring the spectra on the copolymer in o-dichlorobenzene at 170°C. The relative intensities of three peaks of the splitting signal for the methoxy protons in the nonalternating copolymers obtained by the use of benzoyl peroxide in the absence of metal halides agree well with the cotacticity distribution calculated theoretically by the Lewis-Mayo mechanism with the stereoregulation following Bernoullian statistics. The splitting signals in the 1H- and 13C-NMR spectra of the alternating copolymers prepared in the presence of metal halides cannot be explained by the same mechanism. The relative intensities of three peaks of the splitting signals for the methoxy protons and for the carbonyl carbon in the methyl methacrylate unit (the contents of cotactic triads centered by the methyl methacrylate unit) are not equal to those for the aromatic C1 carbon in the styrene unit (the contents of cotactic triads centered by styrene unit). The value of f2Y - 4fxfz is not equal to zero, where fx, fy, and fz are the cosyndiotactic, coheterotactic, and coisotactic triad contents, respectively, in the alternating copolymer. Copolymers obtained in the presence of zinc chloride are not exactly equimolar alternating but always contain a methyl methacrylate unit in excess, and the relative intensities of the three peaks for the aromatic C1 carbon change with the copolymer composition. These results are explained by a proposed mechanism: the alternating copolymerization proceeds through the homopolymerization of a ternary molecular complex composed of a metal halide, methyl methacrylate, and styrene, accompanied with the stereoregulation following first-order Markovian statistics; the increase of methyl methacrylate content in the copolymer prepared in the presence of zinc chloride is caused by the participation of the binary molecular complex composed of a metal halide and methyl methacrylate in addition to the ternary molecular complex.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 235-240 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The polymerization of isobutyl vinyl ether was studied in a heterogeneous system using iron (II) sulfate calcined in air at various temperatures as a catalyst. The maximum activity was shown by the catalyst calcined at 700°C, which effected the polymerization at room temperature in a few seconds, while the sulfate treated at 750°C was totally inactive. Poly(vinyl ethyl ether) was also obtained by the FeSO4 (700°C) catalyst at room temperature. This catalyst formed the crystalline polymer (melting temperature 135-138°C) when the reaction was performed in toluene as solvent at room temperature. Poisoning experiments with Hammett indicators were carried out with the FeSO4 (700°C) catalyst. The treatment with n-butylamine rendered it inactive in the reaction of isobutyl vinyl ether, while its catalytic activity was little affected by dicinnamalacetone. On the basis of the observed results, the nature of active sites of catalyst is discussed.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 259-264 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Hexamethylenetetramine (HMT) has been examined for its effect on the binding of methyl orange homologs, methyl orange, ethyl orange, propyl orange, and butyl orange by polyvinylpyrrolidone (PVP). In the presence of HMT the entropy changes associated with the binding tend to become more positive and the absolute magnitude in the enthalpy changes becomes smaller compared with those in the absence of HMT. These tendencies are accounted for in terms of the water-structure-promoting effect of HMT, hence the enhancement of hydrophobic interactions in the binding. PVP undergoes changes in conformation on the addition of HMT and its conformation becomes more compact. This also increases the contribution of the hydrophobic interactions to the macromolecule-small molecule interaction. Some other effects exerted by the added HMT on the binding system are also described.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 283-293 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Solution polymerization of MMA, with pyridine as the solvent and BZ2O2 and AIBN as thermal initiators, was studied kinetically at 60°C. The monomer exponent varied from 0.45 to 0.91 as [BZ2O2] was increased from 1 × 10-2 to 30 × 10-2 mole/liter in a concentration range of 8.3-4.6 mole/liter for MMA. For AIBN-initiated polymerization the monomer exponent remained constant at 0.69 as [AIBN] varied from 0.4 × 10-2 to 1.0 × 10-2 mole/liter in the same concentration range for MMA. The k2p/kt Value increased in both cases with an increase in pyridine concentration in the system. This was explained in terms of an increase in the kp value, which was due presumably to the increased reactivity of the chain radicals by donor-acceptor interaction between the molecules of solvent pyridine and propagating PMMA radicals and in terms of lowering the kt value for the diffusion-controlled termination reaction due to an increase in the medium viscosity and pyridine content.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 295-309 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The block copolymers of the ABA type, poly(dimethyl siloxane-b-styrene-b-dimethyl siloxane), were synthesized by the anionic polymerization of styrene and cyclic siloxane monomer, hexamethyl cyclotrisiloxane (D3) or octamethylcyclotetrasiloxane (D4), with lithium or sodium biphenyl as initiator. The effect of initiator concentration, gegenion, and the polymerization temperature for styrene on molecular weight distribution (MWD) was investigated. Gel permeation chromatography (GPC) data show broader MWD of polystyrene prepared by sodium biphenyl in comparison to that produced by lithium biphenyl. The block copolymers have been characterized by infrared (IR) and nuclear magnetic resonance (NMR) spectra. The influence of dimethylsiloxy units on thermal stability of the copolymers has also been discussed.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 321-326 
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
    Notes: Cooling slowly from the melt and annealing at 250 K for a month isotactic polyhexylethylene becomes partially crystalline. The degree of crystallinity, calculated according to the method of Hermans and Weidinger, is 0.3. The wide-angle x-ray diffraction diagram shows seven reflections, not completely independent of one another. These x-ray data do not allow an exact determination of the structure. The main chins possibly form quaternary helices (e. g., 4/1 or 7/2 helices) and the side chains are arranged in triclinic structure. The unit cell may be monoclinic: a ∼ 0.56 nm, b ∼ 3.8 nm, c ∼ 0.76 nm (in case of a 4/1 helix), β ≃ 97° The melting temperature is 278 K and the heat of fusion amounts to 30 J/g.
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  • 158
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    Topics: Chemistry and Pharmacology
    Notes: The mechanism of the redox polymerization of methyl methacrylate in acid-aqueous medium was studied for ceric-thiourea initiator system by analysis of polymer end groups using the dye partition method. Polymerization at room temperature and at pH 2.30 with this initiator system incorporates mostly amino end groups in the polymers to the extent of 1.18-1.31 and a small amount of hydroxyl end group not exceeding 0.08 per polymer molecule. Under the same pH condition, a higher polymerization temperature increases the amine end group content to 2.17-2.30 and hydroxyl end group content to 0.14-0.18 per polymer molecule. A lower polymerization temperature (5°C), or a lower pH (ca. 1) of the reaction medium, produces polymers with exclusively amine end groups, hydroxyl end groups being totally absent. At pHs greater than 3, amine end group incorporation decreases significantly, with simultaneous increase in hydroxyl incorporation. On the basis of end group results the initiating radical has been identified and the mechanism of initiation has been suggested. The possible mode of termination has also been discussed.
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  • 159
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 327-333 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of the γ-ray-initiated polymerization of acrylonitrile in bulk are reexamined in broad ranges of temperatures and radiation dose rates. The discussion of the results coupled with an analysis of earlier data indicate that the polymerization of acrylonitrile proceeds by different mechanisms depending on the reaction temperature. Above 60°C the precipitated growing chains recombine readily; therefore, the autoaccelerated conversion curves cannot be accounted for by an “occlusion effect.” It is suggested that autoacceleration is caused by a fast propagation taking place in oriented monomer aggregates which result from dipole-dipole association of the monomer with the polymer chains formed in the early stages of the reaction (“matrix effect”). Below 10°C the precipitated growing chains are buried in the dead polymer and monomer diffusion toward the occluded chain ends is very limited (“occlusion effect”). Between 10 and 60°C the system gradually changes from one dominated by “occlusion” to one where the “matrix effect” determines the kinetic behavior. The conclusion based on kinetic data is in agreement with results obtained from studies of the postpolymerization in these various systems.
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  • 160
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 373-376 
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
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  • 161
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 377-377 
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  • 162
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 379-379 
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  • 163
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 380-380 
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  • 164
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    Topics: Chemistry and Pharmacology
    Notes: Liquid sulfur-olefinic reactions at 140°C forming crosslinked polysulfide polymers have been investigated. A systematic approach to the characterization and some structure-property studies on these new polymeric materials has been presented. The olefinic systems of interest are endo-and exo-dicyclopentadiene and an oligomeric alkenyl polysulfide. Equimolar S8-olefinic system copolymers are amorphous and they show no tendency for sulfur crystallization. A correlation has been drawn between chemical structure and glass transition temperature of the copolymers and terpolymers. Mechanical properties and, in particular, chemical stress relaxation of the crosslinked polysulfide polymers have been investigated.
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  • 165
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    Topics: Chemistry and Pharmacology
    Notes: The plasma polymers prepared from perfluorocyclohexa-1,3-diene, perfluorocyclohexa-1,4-diene, and perfluorocyclohexene have been investigated by ESCA. The carbon-to-fluorine stoichiometries of the diene-derived polymers are similar and close to that of the starting material. The polymer prepared from perfluorocyclohexene is depleted in fluorine compared to the fluorine content of the “monomer.” The polymers prepared in nonglow regions are also studied and shown to be high in CF2 derived species. The results are compared with those for perfluorobenzene and perfluorocyclohexane, and the polymerization rates are in the order C6F6 〉 C6F8 1,3 ∼ 1,4 〉 C6F10 ∼ C6F12. The variations in composition of the plasma polymer as revealed by ESCA as a function of the polymerization conditions are discussed.
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  • 166
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 533-539 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ESR studies of the formation of stable nitroxyl radicals in the photooxidation of polypropylene containing 2,2,6,6-tetramethyl-4-hydroxypiperidine (II) and the commercial light stabilizer bis(2,2,6,6-tetramethyl-4-piperidinyl)sebacate (III) are described. Spectra of the stable nitroxyl radicals in solid polymer and in solution after extraction from the polymer were obtained. The extract from photooxidized polypropylene containing the bifunctional stabilizer (III) showed only the mononitroxyl radical. The possible formation of polymer-bonded nitroxyl radicals from (III) is discussed.
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  • 167
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 559-563 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 13C-NMR gives sequence information in copolyesters synthesized from ethylene glycol (EG), 1,4-butane diol (BD), and methyl terephthalate (TP). The EG-TP-EG and BD-TP-BD blocks are distinguishable from the unsymmetrical diester sequence EG-TP-BD. The carbonyl and aromatic quaternary carbons of terephthalate have different chemical shifts but identical relaxation times and nuclear Overhauser enhancements in the three different triad sequences. Peak areas indicate random copolymerization of the three copolyesters studied.
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  • 168
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 541-557 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of a polyether-based polyurethane foam with dry atmospheric pressure steam was examined as one approach to waste polyurethane foam recovery. Complete reaction at temperatures between 190 and 230°C yielded high-quality polyol, isomeric toluenediamines, and carbon dioxide as primary products. Kinetic analysis of toluenediamine yields versus time suggested the occurrence of a parallel first-order reaction scheme wherein urethane linkages react up to 50 times faster than urea linkages. The results derived from kinetic experiments and ancillary thermochemical and spectroscopic studies indicated that urethane linkages are broken by direct hydrolysis, whereas urea linkages undergo thermal dissociation to parent isocyanate and amine. Subsequent rapid hydrolysis of the isocyanate produced was necessary to obtain high yields of toluenediamine products. The rate of the slower reaction, dissociation of urea linkages, can be enhanced by a factor of 20 by the addition of trace amounts of sodium hydroxide to the foam.
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  • 169
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 565-577 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The photocycloaddition of simple olefins to poly(4-vinylbenzophenone) (PVB) and poly(styreneco-4-vinylbenzophenone) (PS-VB) was studied in benzene solution and in the solid polymer. In solution oxetane yields of 61-82% were obtained with di-, tri-, and tetrasubstituted olefins, which are visualized as capable of giving a radical on a 3° carbon atom in the biradical preceding ring closure to form the oxetane. Photocycloaddition of isobutene to PVB and PS-VB occurs in solid polymer films to more than 90% conversion of the polymer ketone. Quantum yields of oxetane formation are 0.013 ± 0.003 on irradiation at 366 nm, independent of film thickness between 1.9 and 10.6 μm and of temperature between 23 and 65°C. The absence of a pronounced effect of the polymer glass transition on the efficiency of the cycloaddition in PVB suggests that large-scale molecular motion is not required by this solid-state photoreaction. Crosslinking by photochemical cycloaddition was demonstrated in mixed films of PVB and squalene, a polyfunctional olefin.
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  • 170
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 579-592 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Although the preparation of polycarbonates based on bisphenol A and 2,2-bis(4-hydroxyphenyl)-1,1-dichloroethylene was disclosed in 1964 by Porejko et al., little has been reported on their physical and flammability properties. To define the properties of this system these materials were prepared and evaluated. The results indicate that the copolymers and blends of the homopolycarbonates of the two different bisphenols result in transparent thermoplastics that have almost the same attractive physical properties as the homopolycarbonate from bisphenol A. In addition, many of these formulations possess flame-resistant properties that exceed those of other transparent thermoplastics; for example, highest OI and lowest smoke and lowest ratings in the ASTM E84 tunnel and E162 radiant panel tests. Preliminary bioassay results with rats of the products from 500°C air pyrolysis gave an ALC50 value greater than that of other common thermoplastics.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 681-689 
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    Topics: Chemistry and Pharmacology
    Notes: A transacetalization reaction occurs during the etherification of poly(oxymethylene)diol [α-hydro-ω-hydroxypoly(oxymethylene)] with orthoesters and an important modification of molecular structure takes place. The intermediates formed during the transacetalization reaction are emphasized. The connection between this reaction and the other reactions during the etherification of poly(oxymethylene)diols is discussed.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 691-699 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A search has been made for electroinitiators of postpolymerization. A number of hydroxycarboxylic acids and some of their sodium salts have been found to be quite efficient. Factors controlling the rate of polymerization and yield have been described. Surprisingly, citric acid, though not an electroinitiator of polymerization, is a good initiator of postpolymerization. Other active species that deserve mention are tartaric acid and its salts. A free radical mechanism involving formation of oligomeric initiator fragments, growth by attachment of imbibed monomer, and termination by chain transfer has been proposed to explain the observed facts.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 815-825 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The most effective mechanism of protective action of organic phosphites-linear termination of kinetic chains on the inhibitor - has been established and the relative contribution of the other phosphite reactions (with hydroperoxides, their chain “self-oxidation”) to the summary mechanism has been determined. The quantitative kinetic characteristics of efficiency and length of inhibitive action of different structure phosphites in the wide range of the phase state of the oxidized substrate (solid polymer, its melt, liquid phase) have been given. On this basis the regularities which allow the prediction of the structures of phosphites scavenging peroxy substrate radicals more effectively (effective inhibitors) have been formulated.
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  • 174
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 781-797 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: cis-1,4-Polybutadiene and polypentenamer having pendant functional groups such as formyl, aldoxime, hydroxymethyl, or cinnamoyloxymethyl groups have been prepared, and some of their properties were investigated in terms of structural effect on physical properties of these polymers. cis-1, 4-Polybutadiene and polypentenamer having a different content of formyl group were prepared by the hydroformylation reaction with rhodium catalyst under mild conditions. The pendant formyl group was reduced to a hydroxymethyl group by using various reducing agents such as sodium borohydride or sodium trimethoxyborohydride which were effective to avoid a crosslinking reaction among the formyl groups. Glass transition temperature of polypentenamer having hydroxymethyl groups increased with increasing the content of the hydroxymethyl groups in the polymer. Cinnamoyl group was introduced into the polypentenamer having hydroxymethyl groups by reacting with cinnamoyl chloride so as to prepare a photosensitive rubber. The relationships between the photosensitivity of the cinnamoylated polypentenamer and the mobility of polymer main chains have been elucidated. A linear relationship between the photodimerization rate constant and the difference between ultraviolet (UV) irradiation temperature and the glass transition temperature of the polymer was found. It has become apparent that the photosensitivity of cinnamoylated polypentenamer can be estimated by the glass transition temperature of the original polymer, UV irradiation temperature, activation energy of the dimerization, and γ, which is a coefficient of the relationship between the photosensitive group concentration and the glass transition temperature of the polymer.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 827-850 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The radical polymerization of several vinyl monomers has been studied in the presence of cupric chloride. A termination reaction with CuII species leads to the formation of CuI species which can also participate significantly in termination with some, but not all, of the monomers studied. A theoretical treatment of the kinetics of such systems is presented which takes full account of initiator depletion during extended inhibition during extended inhibition periods. Specific velocity constants for reactions of polymer radicals with both CuII and CuI moieties are derived from observations on the nonstationary phase at the end of the inhibition period and from the subsequent steady state of polymerization. On the basis of the results presented here, together with the work of other authors, the patterns-of-reactivity approach gives α = -5.4, β = 9.0 as the parameters for copper (II) chloride. The implications of the results in relation to the mechanisms of the reactions between polymer radicals and both copper(II) chloride and copper(I) chloride are discussed. The kinetic treatment also provides an improved method for the determination of the rate of initiator decomposition and the rate of initiation form studies of the inhibition period.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 851-856 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The polycondensation reaction of aromatic dicarboxylic acids and diamines by using triphenyl phosphite were carried out in N-methylpyrrolidone (NMP) in the presence of poly(4-vinylpyridine) (P4VP). The reaction, especially of terephthalic acid (TPA), was markedly facilitated to give the absence of P4VP. The reaction promoted by P4VP was further favored by the addition of various pyridine derivatives; of the pyridines examined, pyridine was most effective, giving the best results at a high level (pyridine/P4VP values up to 26). P4VP of the molecular weight in the range of 1.3 × 104-3.0 × 105 did not affect the viscosity of the resulting polymer. These favorable additive effects of P4VP on the reaction of TPA were not observed in the reactions of isophthalic acid, and m -and p-aminobenzoic acids.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 857-870 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Epoxy-amine curing reactions were theoretically studied using expectation theory taking into account the different reactivities of (1) the primary and secondary amine hydrogens and (2) the secondary hydroxyl group generated when an amine reacts with an epoxy group. The curing compositions and the fractional conversions at the gel point were computed. Generally the hydroxyl groups react slower than the amines and user these conditions, the reactivity of the OH group has a significant effect only when there is an intial excess of epoxide over the amine. The hydroxyl activity effectively increases the functionality of the epoxides and gelation can occur where it may not be expected.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 933-938 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The polycondensation reaction of diethyl mucate (DEM) with hexamethylenediamine (HMD) was carried out in dimethyl sulfoxide (DMSO) at 60°C in the presence of poly(vinyl pyridine) (P-VPy) as a matrix polymer, which was expected to interact with DEM or the resulting polyamide which had pendant hydroxyl groups due to a hydrogen bonding. It was found that the polycondensation of DEM with HMD in the presence of poly(4-vinyl pyridine) (P-4VPy) produced a polyamide with a higher molecular weight than those in the presence of poly(2-vinyl pyridine) (P-2VPy) or in the absence of P-4VPy. The rate of the polycondensation, however, was rarely enhanced by polymer matrixes such as P-4VPy and P-2VPy. During polycondensation in the presence of P-4VPy a gelation of the reaction mixture was observed when the solution was kept at 30°C for several days. This might be ascribed to the formation of the polymer complex between resulting polyamide and P-4VPy during the polycondensation.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 939-948 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The polycondensation reaction of dimethyl tartrate (DMT) with hexamethylenediamine (HMD) was carried out in dimethyl sulfoxide (DMSO) at 60°C in the presence of various polymer matrices, which were expected to interact with DMT or the resulting polyamide which had pendant hydroxyl groups due to hydrogen bonding. It was found that the rate of polycondensation was enhanced by polymer matrices such as poly(vinyl pyrrolidone) (PVP), Pullulan (polysaccharide) (PF), and poly(vinyl alcohol) (PVA). The rate enhancement became more pronounced with increasing molecular weight of the polymer matrix. When polycondensation in the presence of PVA was carried out in DMSO, a polymer complex was produced. The formation of the polymer complex between the resulting polyamide and PVA during polycondensation was dependent on the concentration of monomers and also on PVA; a gelation of the solution was observed at a concentration of PVA.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 1177-1187 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Studies of the initiation rate of the copolymerization reaction of acrylonitrile with p-bromophenyl acrylate initiated by azobisisobutyronitrile in dimethylformamide at 60°C are reported. The inhibition method involved use of stable Banfield's radical (N-[1,1-dimethyl 3-(N-oxidophenylimine)butyl]-N-phenylaminyl oxide). In the case of acrylonitrile, a side reaction effect of the initiation with the stable radical was observed along with a retarding effect resulting from inhibition reaction products (2kdf)60AN = 8.2 × 10-4 min-1. During the inhibited homopolymerization of p-bromophenyl acrylate a very strong side initiation reaction effect results from the Banfield radical; the inhibition reaction products do not influence the further course of the polymerization reaction. Side initiation effects of the Banfield radical (BR) increase with increasing concentration of p-bromophenyl acrylate. The overall contribution of the side initiation reaction changes for different comonomer mixtures; with their compositions the actual changes are nonadditive. The inhibition reaction products do not influence the further course of copolymerization. The initiation rate in monomer mixtures depends on their composition and may be described by the following relation: $$ 2k_d f = (2k_d f)_{{\rm AN}} \times X_{{\rm AN}}^{1.1} + (2k_d f)_{{\rm pBrPhA}} \times X_{{\rm pBrPhA}}^{1.7} $$
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 1213-1221 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Thermal-induced conversion of maleic and fumaric acid anion radicals produced by γ irradiation at 77 K in poly(methyl methacrylate) (PMMA) was studied by electron spin resonance (ESR) and optical absorption spectroscopic measurements. The ESR spectra of these acid anion radicals change into two-line spectra with a line separation of ca. 10 G by thermal annealing. This spectrum is assigned to a protonated radical of each acid anion radical. Anion radicals of the solutes are relatively stable below the γ transition point of PMMA and the conversion reaction takes place near this point. This means that the molecular motion of matrix molecule affects the radical conversion reaction.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 1203-1211 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The acid-catalyzed stepwise polymerization of 1,1-diphenylethylene derivatives, p-di(1-phenylvinyl) benzene, bis[p-(1-phenylvinyl)phenyl]methane, 1,2-bis[p-(1-phenylvinyl)phenyl]ethane, bis[p-(1-phenylvinyl)phenyl]ether, and bis[p-(1-phenylvinyl)phenyl]sulfide produced selectively indanic-unit-containing polymers in pertinent conditions. Their molecular weights (M̄n) were in the 1600-15, 700 region after the fractionation in hot ethnol. Melting points were in the 214-281°C region. They dissolved fairly well in conventional solvents like benzene, tetrahydrofuran, and carbon tetrachloride. According to TGA they started to decompose at 397-432°C and showed 10% weight loss at 478-502°C in air at a heating rate of 5°C/min. Focusing on the thermostability, we report on their physical properties.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 1233-1246 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The vacuum ultraviolet (UV) emission from inductively coupled radio-frequency (RF) plasmas excited in a series of inert gases has been studied as a function of the pressure and applied power of the system. The effects of discharge tube size and pulsing of the applied RF power are also considered and a comparison is made between RF and microwave excitation.
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  • 184
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 1223-1232 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A study was made on the AIBN-initiated polymerization of styrene in benzene and dimethyl formamide at 50°C. The overall rate and the rate of initiation of the polymerization were determined and the number-average and weight-average molecular weights of the polymers formed were measured. The decrease in the rate and degree of polymerization with the decrease in styrene concentration was caused by the corresponding decreases in the rate constants of chain propagation and initiation steps. In the systems studied no chain transfer process occurred with an experimentally measurable rate.
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  • 185
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 1279-1284 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: It has been observed that in a benzene medium the carbinol base of a cationic dye reacts with a polymer with —SO3 Na and similar end groups that give rise to a reversible color formation of the dye cation. This reaction can be pushed to completion and consequent intensification of color by adding a benzene-insoluble acid such as citric acid. This principle has been applied to develop an improved dye interaction method of determining such end groups. The end groups values thus obtained by this method for different poly(methyl methacrylate) and polystyrene samples were found to be in fairly good agreement with those obtained by the dye partition (extrapolation) method.
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  • 186
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2905-2907 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 187
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2908-2908 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 188
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new class of polyureas are reported which contain a crown ether analog in the backbone. Synthesis involves condensation of 1,10-diaza-4,7,13,16-tetraoxacyclooctadecane with either 2,4-toluene diisocyanate or hexamethylene diisocyanate in dichloromethane. The former gives tough, flexible polymers and the latter tacky, hygroscopic products. The infrared (IR) and proton nuclear magnetic resonance (NMR) spectra of these materials are given along with those of the polyurea from piperazine and hexamethylene diisocyanate. The carbon NMR chemical shifts and spin-lattice relaxation times are also reported. Comparison is made with monomer, other crown ethers, polyoxyethylene, and a model compound prepared from the diaza monomer and phenylisocyanate. The T1 values indicate a greater degree of backbone and macrocycle flexibility for the hexamethylene-containing polyurea than for the toluene analog.
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  • 189
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2921-2932 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The homopolymerization of trans-1,4-hexadiene, cis-1,4-hexadiene, and 5-methyl-1,4-hexadiene was investigated with a variety of catalysts. During polymerization, 1,4-hexadienes undergo concurrent isomerization reactions. The nature and extent of isomerization products are influenced by the monomer structure and polymerization conditions. Nuclear magnetic resonance (NMR) and infrared (IR) data show that poly(trans-1,4-hexadiene) and poly(cis-1,4-hexadiene) prepared with a Et3Al/α-TiCl3/hexamethylphosphoric triamide catalyst system consist mainly of 1,2-polymerization units arranged in a regular head-to-tail sequence. A 300-MHz proton NMR spectrum shows that the trans-hexadiene polymer is isotactic; it also may be the case for the cis-hexadiene polymer. These polymers are the first examples of uncrosslinked ozone-resistant rubbers containing pendant unsaturation on alternating carbon atoms of the saturated carbon-carbon backbone. Polymerization of the 1,4-hexadienes was also studied with VOCl3- and β-TiCl3-based catalysts. Microstructures of the resulting polymers are quite complicated due to significant loss of unsaturation, in contrast to those obtained with the α-TiCl3-based catalyst. In agreement with the literature, there was no discernible monomer isomerization with the VOCl3 catalyst system.
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  • 190
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2933-2940 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: For a series of menthol esters of increasing size and polarity, “mintyness” decreased rapidly as molecular weight increased. For molecular weights above about 700, the compounds were tasteless to a significant proportion of the taste panel. As polarity increased, the “sweet minty” taste of hydrophobic menthol esters became increasingly bitter, until water-soluble menthol esters were strongly bitter. Bitterness was still apparent in quite high-molecular-weight water-soluble esters; a different receptor may be involved for bitterness than for mint. An overall hypothesis relating flavor to molecular solubility parameters is proposed.
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  • 191
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2941-2948 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Kinetic studies were investigated with rigid copolymers composed of vinylimidazole (VIm) and 3,3′-substituted biphenyls. For neutral substrates, two different kinetic figures were observed by the influence of 3,3′-substituents. The second-order rate constants kinetically determined were largely enhanced by the reduction of ethanol content less than 30 vol % in contrast to the rapid decrease in viscosities of catalyst solutions. A parameter concerning the polymer conformation and the effect of hydrophobic interaction was obtained using a relationship between the kinetic constants with ethanol content. Maximum kinetic effect of electrostatic interaction appeared at about 50 mole % VIm content by attracting cationic substrates towards the COO- group of the polymer catalyst. This maximum rate profile was nearly coincident with a curve derived by calculating the sequence distribution of the (VIm—COOH) linkage unit.
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  • 192
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2949-2958 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Various wholly aromatic polyamides based on m-and p-phenylene diamines and isophthaloyl and terephthaloyl chloride have been synthesized and their thermal properties and oxygen index values have been studied. The effect of different substituents on the aromatic ring of the diamine have been explored by comparing their differential thermal analysis (DTA) and thermogravimetric analysis (TGA) behavior, their relative char yields at 700°C, and their oxygen indices. The —Cl, —NO2, and —OH substituted polyamides have been found to produce the highest char yields. The high char yields are probably associated with crosslinking occurring at high temperatures. Attempts at correlating char yield with oxygen index indicated enhancement for the chlorosubstituted aramids.
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  • 193
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2959-2969 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Cyclic derivatives of uracil and thymine were synthesized from their corresponding 1-(2′-chloroethyl) derivatives by dehydrochlorination. These compounds were found to undergo a variety of reactions, giving many valuable derivatives of uracil and thymine. The cyclic derivatives, as monomers, were polymerized with a cationic initiator by a unique ring-opening process. The polymerization proceeded by ring opening with isomerization of the pyrimidine ring to give a polymer in which pyrimidine rings were connected with ethylene between N-1 and N-3 or O-4 in the pyrimidine ring. The structure of these polymers was determined by nuclear magnetic resonance (NMR), ultraviolet (UV), infrared (IR), and mass spectra. The structure was affected by polymerization temperature.
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  • 194
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2983-2992 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The preparation of a new form of ionomer is described. This class of material is based on the polymerization of a neutral monomer with a small amount of a cationic-anionic monomer pair. The resulting ionomers are ampholytic in character and contain no inorganic ions. In this investigation, the polymerization of styrene with 3-methacrylamidopropyldimethylammonium and trimethylammonium 2-acrylamido-2-methylpropanesulfonate in a variety of solvents is described.
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  • 195
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 2,3-Dichloro-5,6-dicyano-p-benzoquinone (DDQ) was found to copolymerize alternatingly with styrene (St). DDQ-isobutyl vinyl ether and DDQ-2-chloroethyl vinyl ether systems gave homopolymers of vinyl ethers, while DDQ-phenyl vinyl ether and DDQ-vinyl acetate systems gave oligomers containing both monomer units. In the terpolymerization of DDQ, p-chloranil (pCA), and St, terpolymers obtained were found to have about 50 mole % of St units regardless of monomer feed ratio and DDQ was incorporated much more rapidly into the terpolymer than pCA. The difference in the reactivity of the acceptor monomers could be attributed to that in their electron-accepting character.
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  • 196
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 3009-3020 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Enantiomer-differentiating ester syntheses from acid salts, chlorides, and an anhydride were studied in the presence of optically active polyamines. Enantiomer selection occurred in reactions of a racemic salt with an achiral alkyl bromide and vice versa, which is good evidence of the importance of activation of the carboxylate group by complexation of the counterion and activation of alkyl bromide by the formation of a quaternary salt with polyamine under solid-liquid, phase-transfer reaction conditions. Only small optical activity was observed in the products of acid anhydride or chloride with alcohol.
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  • 197
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2993-3008 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The magnetic circular dichroism (MCD) spectra of syndiotactic and isotactic polymers which contain aromatic chromophores have been found to be sensitive to configurational and conformational differences. For isotactic polymers it was determined that as the aromatic ring moved farther from the main chain the ration of B terms of the polymers to those of their model compounds reached a minimum but increased significantly when the aromatic ring was separated from the main chain by four atoms. This enhancement of MCD is believed to be caused by the alignment of the more flexible side chains which would allow the interaction of the aromatic rings with neighboring groups and could result in a favorable mixing of the ester electronic transition with the aromatic 1A1g-1B2u transition. This effect was not felt to any great extent by the syndiotactic polymers because the necessary nearest-neighbor interaction was sterically unfavorable. The ratio of the B terms of isotactic poly(phenyl methacrylate) to its model compound decreased as the polymer coil expanded, whereas it increased for the syndiotactic polymer. This effect reflects the different changes that the side chain interaction and orientations undergo in these polymers during coil expansion. The MCD ratios for iso- and syndiotactic poly(phenylethyl methacrylate) were not so sensitive during coil expansion. The ratio of the dipole strengths of the polymers and model compounds paralleled the MCD results, but the ultraviolet (UV) technique was less sensitive than MCD to subtle conformational differences. Poly(benzyl methacrylate) and benzyl pivalate were unsuitable systems for studying the MCD effect because the B terms of these materials approached zero.
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  • 198
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 3029-3041 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polyenaminoesters are prepared by condensation of α,α′-bis(carbomethoxy)diacetylbenzenes with phenylene diamines in the presence of N,N-dimethylaniline hydrochloride. Thermogravimetric analysis allowed the determination of the optimum temperature at which to conduct cyclization of the polymers to form thermally stable polypyridoquinolones. The structures of the polymers were assigned by spectroscopic comparisons with appropriate model compounds.
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  • 199
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 3149-3161 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The radical grafting of methyl methacrylate (MMA) onto polybutadiene (PBD) in benzene solution at 60°C is more efficiently induced by benzoyl peroxide (BP) than by azoisobutyronitrile (AIBN). PBD exerts a pronounced retardation on the polymerization of MMA and the grafting efficiency is governed by the ratio of rubber to monomer in the system. With BP as initiator, a fairly simple kinetic expression, relating grafting efficiency with reactant concentrations, can be derived by making certain approximations, including the neglect of termination grafting. The experimental data are reasonably consistent with this equation and yield acceptable values of several kinetic parameters. With AIBN, termination grafting is more significant. In consequence the relevant kinetic equation can be only qualitatively validated.
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  • 200
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 3245-3251 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polypropylene (PP) and polyethylene (PE) peroxy radicals undergo photoreactions, but under commonly encountered photodegradation conditions these reaction rates are much lower than those of conventional radical reactions; for example, for PP peroxy radicals in noon summer sunlight at 25°C their rate of photolysis to alkyl radicals is less than one-tenth of their rate of hydrogen abstraction from the polymer. At lower temperatures( 〈 -10°C) or when more intense radiation is used, however, peroxy radical photolysis becomes a proportionately more important source of alkyl radicals. In addition, occurrence of photoinduced radical combination is confirmed but is shown to be important only when photolysis generates an alkyl radical sufficiently close to a peroxy radical that termination can occur before oxygen reconverts the alkyl radical to a peroxy radical. This termination mechanism therefore becomes more important for radicals generated at lower temperatures when the average separation of a radical pair is lower.
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