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  • 101
    Electronic Resource
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    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 1635-1637 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 102
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 1639-1642 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 103
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 1643-1646 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 104
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 1647-1650 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 105
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    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 1651-1664 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The absolute and relative binding energies for the C1s, O1s, and F1s core levels have been determined using x-ray photoelectron spectroscopy (ESCA) for a series of aliphatic, aromatic, and fluorine-containing polycarbonates. Comparisons of these experimentally determined, core-level binding energies with theoretical calculations using the ground-state potential model in the CNDO/2 SCF MO formalism as well as model compounds have been made on the C1s and O1s core levels. The degree of polymerization for low-molecular-weight fluorine-containing polycarbonates, as determined from ESCA measurements, is compared to measurements by vapor-phase osmometry and 19F-NMR.
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  • 106
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    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 2405-2418 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Alternating head-to-head (h-h) copolymers of methyl or n-butyl acrylates with the corresponding methacrylates were synthesized by alternating copolymerization of ethylene with citraconic anhydride, followed by esterification and Characterization. The respective equimolar (1:) head-to-tail (h-t) copolymers were also prepared by conventional radical copolymerization as comparison. The alternating, relatively low molecular weight h-h copolymers obtained showed softening, glass transition, and degradation temperatures somewhat higher than those displayed by the 1:1 h-t copolymers. After pyrolysis the main decomposition products from both h-h and h-t copolymers were alcohols, acrylates, and methacrylates. Furthermore, the ratios of alcohols to acrylates were larger for the h-h than for the h-t copolymers and smaller for the methyl than for the n-butyl esters.
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  • 107
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    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 2391-2403 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The alternating copolymer of ethylene with maleic anhydride was esterified with a number of aliphatic alcohols to yield its monoesters, which correspond structurally to equimolar (1:1) head-to-head (h-h) copolymers of acrylic acid with alkyl acrylates. In addition, they were methylated with diazomethane to 1:1 h-h copolymers of methyl acrylate with alkyl acrylates. For comparison the 1:1 head-to-tail (h-t) copolymers of methyl acrylate with alkyl acrylates were prepared by radical copolymerizations. Some chemical, physical, and thermal properties of these 1:1 h-h and h-t copolymers were evaluated and compared. The softening and glass transition temperatures of the 1:1 h-h copolymers were somewhat higher than those of the corresponding 1:1 h-t copolymers, which indicated that the h-h replacements made the polymer chain stiffer and less flexible. The 1:1 h-h copolymers were also observed to degrade thermally at somewhat higher temperatures and with higher rates than the 1:1 h-t copolymers. The ratio of alcohol to monomer found in the pyrolysis products was higher for the 1:1 h-h than for its respective 1:1 h-t copolymer.
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  • 108
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    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 2451-2455 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Adsorption of iodide-125, a γ emitter, was used as a quantitative methodology for polymer adsorption surface coverage analysis. Adsorption of I-125 on clean platinum produced surface elemental ratios of I:Pt of 1:4. The technique was applied to the adsorption of polyethylene glycol terephthalate from trifluoroacetic acid on platinum flags with a 2-cm2 surface area. This polymer adsorption is approximated by a logarithmic relationship similar to the Temkin isotherm. Polymer coverage attained up to 99.6% of the surface.
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  • 109
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 2443-2449 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Apparent glass transition temperature (Tg) measurements were made on smaples of a neat epoxy resin that had been cured at four different temperature and for four different times at each temperature. The apparent Tg data increase with cure time toward an asymptote that was dependent on cure temperature. The asymptotic dependence of Tg on cure temperature may be explained by the effect of cure temperature on the reaction rates and available reaction sites. The asymptotic increase with cure time may be understood in terms of the resin's extent of cure. Moisture-conditioning studies were also made and the amount of moisture absorbed was correlated with the extent of cure. The absorbed moisture's interaction with the resin's molecular structure was deduced to by primarily at hydroxyl sites.
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  • 110
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Photopolymerization of MMA was carried out with quinaldine-bromine (QN-Br2) and lutidine-bromine (LU-Br2) charge-transfer complexes as initiators. The rate of polymerization Rp increased with rising monomer concentration and the monomer exponent was computed as unity. At first the rate of polymerization accelerated and then reduced as the initiator concentration was increased. The initiator exponent was 0.5. The reaction was carried out at three different temperatures and overall activation energy was calculated at 4.0 kcal/mol. The kinetic data and other evidence indicate that the overall polymerization takes place in a radical mechanism. A suitable mechanism is suggested.
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  • 111
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 2519-2530 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The photodimerization reaction of oligo- and polyethyleneimine derivatives which contain pendant thymine bases in various amounts was studied in aqueous solution in a wide pH range and in N, N-dimethylformamide solution. The photodimerization reaction of these derivatives in poly(methyl methacrylate) was also studied. It was found that its quantum efficiency tended to increase as thymine units were added to the oligomers and copolymers. This result is discussed in terms of the effect of the nearest neighboring thymine units and singlet energy migration, particularly in the polymers.
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  • 112
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 2551-2560 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of polymers based on 4-chloroformyl phthalic anhydride (TMAC) and 4,4′-diaminodi-phenylether (DAPE) was prepared and shown to be soluble in N, N-dimethylacetamide which contained 0.1N LiBr. These solutions were characterized by light scattering, membrane osmometry, and viscosity. A relationship between the viscosity and molecular weight was formulated and the nature of the polymer chain in solution was postulated.
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  • 113
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 2571-2579 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Vinyl monomers bearing phenoxazine units, were synthesized: 2-vinyl-phenoxazine starting with phenoxazine in a five-step synthesis; 3-acrylamido- or 3-methacrylamido-phenoxazines with or without 10-PhCH2 or 10-Me-substituent starting with o-benzylideneaminophenol or o-anisidine via 3-aminophenoxazines; and 3-(p-styrenesulfonamido)phenoxazines with or without 10-PhCH2- or 10-Me-substituent, also via 3-aminophenoxazines. Polymerizations of these noval monomers proceeded smoothly, except those having no 10-substituent. Changes of the visible absorption spectrum of iodine in THF with addition of the polymers and oligomers thus prepared were considerable, with the appearance of new absorption peaks for polymers with 10-Me-substituent.
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  • 114
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 2581-2594 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: By the use of various boron compounds methyl methacrylate and styrene were copolymerized under photoirradiations at -20°C. The alternately regulating activities of the boron compounds in the copolymerizations were in the following order: boron trichloride 〉 ethylboron dichloride 〉 boron trifluoride 〉 diethylboron chloride ≫ triethylboron (≃0). Boron trichloride and ethylboron dichloride exhibited such high regulating activities that their presence in 1 mol% in the charged methyl methacrylate was sufficient to complete equimolar alternating copolymerization. The alternating copolymerization proceeded in the steady state. The copolymerization rates decreased in the following order: boron trichloride ≫ ethylboron dichloride 〉 diethylboron chloride ≫ triethylboron (≃0). The cotacticities of methyl methacrylate-centered triads in the resulting copolymers were identical to those prepared with boron trichloride, ethylboron dichloride, and diethylboron chloride. The mechanism of the alternating copolymerization is discussed.
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  • 115
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 2619-2633 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The compositions and sequence distributions of vinyl acetate-butyl acrylate copolymers obtained with batch and semicontinuous emulsion polymerizations have been studied by 1H and 13C NMR. The batch process gives heterogeneous copolymers while with the semicontinuous one the sequence distribution is statistical. These differences in sequence distributions have been related to the physical properties of the copolymers.
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  • 116
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 2647-2650 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 117
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 2651-2654 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 118
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 2659-2670 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Improved fire resistance occurs for phenolphthalein-related polycarbonates and polyesters compared to bisphenol-A polymers and emphasizes the importance of polymer composition and polymer structure in affecting the flammability of a polymer. Phenolphthalein-related polymers are able to produce a higher degree of crosslinking during pyrolysis which subsequently leads to higher char yields. The correlations between oxygen index and char yield for various polymers are obtained and discussed. Polycarbonates and polyamides usually show higher oxygen indices than the corresponding polyesters of related structures. This indicates that the nature of the pyrolysis products has a measurable effect on the flammability of a specific polymer. Among many factors, polycarbonates should release more CO2 from the breakdown of the carbonate group, and polyamides should produce relatively nonflammable nitrogen-containing products during pyrolysis, thus accounting in part for these results.
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  • 119
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 2689-2703 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A systematic investigation has been made of the composition, gross structural features, and rates of deposition of plasma polymer films produced from the excitation of inductively coupled RF plasmas in the isomeric tetrafluorobenzenes. ESCA data reveal that the dominant reaction involves rearrangement such that under a wide variety of experimental conditions the composition of the crosslinked products remains essentially the same as that of the starting material. Small differences in rates of deposition are observed for the different isomers, and theoretical SCF MO studies at the MNDO level provides a basis for discussion of the experimental data.
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  • 120
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 1807-1813 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Alkaline hydrolyses of p-nitrophenyl-3-indoleacetate (p-NPIA) and N-(indole-3-acryloyl)imidazole (IAI) were studied in the presence of poly(4-vinyl-N-propylpyridinium bromide) (C3PVP), poly(4-vinyl-N-benzylpyridinium chloride) (BzPVP), and copolymers of 4-vinyl-N-benzylpyridinium chloride and 4-vinyl-N-cetylpyridinium bromide (C16BzPVP). The hydrolyses were enhanced by the addition of these cationic polyelectrolytes. The magnitudes of the enhancement were in the order C16BzPVP 〉 BzPVP 〉 C3PVP, which is explainable in terms of the hydrophobicity of the polymers. The result and activation parameters obtained indicated that the substrates bound to polymers were more reactive than free substrates. The association constants obtained from the kinetic measurements (K) increased in the order BzPVP 〈 C3PVP 〈 C16BzPVP, which may suggest an important contribution of charge transfer interaction, in addition to electrostatic and hydrophobic interactions, between the polymers and the substrates. The association constants between the polymers and IAI were also obtained independently from the spectrophotometric measurements (K*) with the charge transfer absorption bands. The lack of a satisfactory agreement between K and K* is discussed.
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  • 121
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 1815-1820 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The complex formation of flavin mononucleotide (FMN) with tryptamine, indoleacetate, and trytophan was investigated in the presence of polyelectrolytes; that is, sodium polyethylene sulfonate (NaPES), sodium polystyrene sulfonate (NaPSS), and a copolymer of diethyldiallylammonium chloride and sulfur dioxide (DECS). The complexation of FMN and tryptamine was strongly retarded by the macrocations and macroanions, whereas that of FMN and indoleacetate was enhanced by the macrocations. Furthermore, the equilibrium constants of FMN-tryptophan complex were insensitive to the addition of polyelectrolytes. These results suggest that the complexation of FMN was strongly influenced by the electrostatic interactions between the reactant ions and macroions, in addition to those between the reactant ions, in conformity with the secondary salt effect.
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  • 122
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 1821-1834 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: New Processable polyaromatic ether-keto-sulfones were prepared from the acid chloride of bis-m-carboxyphenyl acetylene (XII), isophthaloyl chloride (XX), diphenyl ether (XVIII), and 4,4′-diphenoxydiphenyl sulfone (XIX) in a Friedel-Crafts-type polymerization. These polymers were cured by Diels-Alder cycloaddition with 1,4-diphenyl-1,3-butadiene. The cured polymers showed an increase in Tg and in thermal and heat stabilities. The polymers form colorless, transparent, brittle films and can be cast into a glass fiber laminate. Both meta-and para-substituted acid chlorides of biscarboxyphenyl-1,3-butadiene yielded insoluble polymers under the same conditions but form processable polymers where combined with acetylene units in the polymer chain. Polymers that contained both acetylene and butadiene units were prepared but could not be cured by an intramolecular Diels-Alder cycloaddition reaction.
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  • 123
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 1835-1840 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: New processable polyaromatic amides were prepared from the acid chloride of bis-m-carboxyphenyl acetylene (V), the acid chloride of 1,4-bis-m-carboxyphenyl-1,3-butadiene (VI), and several aromatic diamines. The polyamides that contained acetylene units were cured by Diels-Alder cycloaddition reaction with 1,4-diphenyl-1,3-butadiene, whereas the polyamides with 1,3-butadiene units were cured with N-phenyl maleimide. Cured polyamides showed an increase in tg, thermal, and heat stabilities. The polyamides can be cast into films and produce good glass-fiber laminates.
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  • 124
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 1841-1846 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Poly(α-amino acid)s of high molecular weight were obtained by the direct polycondensation reaction of α-amino acids in the presence of polyvinylpyrrolidone (PVP) as a matrix of triphenyl phosphite and LiCl in N-methylpyrrolidone (NMP). Molecular weights of the polymer produced were improved by use of an increasing amount of matrix of higher molecular weight. Most favorable results were obtained by the reaction at 80°C for 16 hr at a monomer concentration of 0.33 mole/liter in a NMP solution that contained about 3 wt % LiCl in the presence of an equivalent unit mole of PVP with the molecular weight of 3.6 x 105. The polymer from β-alanine with high molecular weight, which is difficult to obtain by the NCA method, was easily prepared by this process.
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  • 125
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 1847-1856 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Copolymers of L-lysine and L-lysine derivatives which contained nucleic acid bases substituted on the Nε position were synthesized by grafting nucleic acid derivatives onto poly-L-lysine. The conformation and interaction of these copolymers in solution were studied by using spectroscopic measurements. They existed in helical conformation at neutral pH values, and the polymer complex formation among them was examined by ultraviolet (UV) measurements in organic solvents. A decrease in the nucleic acid base content of the copolymers resulted in a decrease in helical structures and also in interactions with the polymer-containing complementary bases.
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  • 126
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 2773-2797 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Phenolphthalein polycarbonate underwent complicated thermal degradation which included random scission, rearrangement, hydrolysis, Friedel-Crafts acylation, and cross-linking. The carbonate group and lactone ring were both susceptible to thermal deterioration. Kinetic parameters were determined from the dynamic TGA thermograms. During early stages of degradation the measured reaction order was nearly 1, which suggested a random chain scission mechanism. The measured activation energy was 42.6 kcal/mol, compared with 41.2 kcal/mol calculated from isothermal aging. The Arrhenius preexponential constant was 3.09 × 1011 min-1. Below 80% weight residue the plot of fractional weight against 1/T revealed that complicated reactions with different activation energies occurred simultaneously and resulted in a final overlap of TGA curves for different heating rates indicative of cross-linking and a lower preexponential constant. The reaction order changed and kept increasing in the last stages of degradation. Pyrolysis of this polymer was performed at 350°C under vacuum, followed by GC-mass spectroscopic identification of products. The volatile products (17.5%) contained CO2, CO, O2, H2O, phenol, fluorenone, diphenyl carbonate, xanthone, anthraquinone, 2-hydroxylanthraquinone, 2-benzoxyanthraquinone, phenolphthalein, and trace amounts of benzoxyphenol and hydroquinone; the other 82.5% of products was insoluble gel. Functional group changes were examined by Fourier transform infrared spectroscopy (FT-IR). Lactone, carbonate, and aromatic absorptions decreased during degradation. Increasing absorptions at 1739, 1728, 1280-1200, and 1138-1075 cm-1 were believed to result from aromatic ester (1728 cm-1) and phenyl aromatic ester (1739 cm-1) cross-linkages ortho to the aromatic ether group (increases at 1155 cm-1 and 1280-1200 cm-1). Existence of 2-hydroxyanthraquinone and xanthone contained in the crosslinked polymer matrix were also detected. Mechanisms for random scission, rearrangement, Friedel-Crafts acylation, hydrolysis, and cross-linking were suggested.
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  • 127
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 2817-2834 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Thermal degradation behavior of poly(1,3-phenylene isophthalamide) and poly(chloro-2,4-phenylene isophthalamide) was investigated with the aid of some appropriate model compounds. The pyrolysis products of these materials were identified by gas chromatography (GC), gas chromatography/Fourier transform infrared spectroscopy (GC/FT-IR), and gas chromatography/mass spectrometry (GC/MS). The residual chars were characterized by IR spectroscopy. Thermogravimetric analysis (TGA) was applied to study the effect of end-group concentration on the degradation characteristics of the two polyamides. Kinetic parameters that describe the thermal degradation of the polyamides were also evaluated by TGA. The results of this investigation suggest that the thermal decomposition of these aromatic polyamides involves homolytic as well as hydrolytic cleavages of the amide units.
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  • 128
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 2841-2845 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Two aminophthalide monomers, 6-amino-3-benzylidenephthalide (I) and 3-(p-aminobenzylidene)phthalide (II), underwent self-polycondensation in o-phenylphenol at 250°C to yield polyphthalimidines with inherent viscosities up to 0.5 dL/g. These polymers were readily soluble in a variety of solvents such as dimethylformamide, dimethyl sulfoxide, m-cresol, pyridine, and methylene chloride. The temperatures at which a 10% weight loss occurred by thermogravimetry in nitrogen were 460°C for the polymer derived from I and 490°C for the polymer from II. The glass transition temperature of the polymer from I was 332°C, determined by thermomechanical analysis.
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  • 129
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 2847-2860 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ESCA is used to characterize the surfaces of high and low density polyethylenes, nylon-6,6, polyphenylene oxide, and polysulfone after exposure to the environment. Reactions that lead to degradation of the polymer surfaces can be detected straightforwardly and are discussed in terms of the known reactions found in the bulk polymers under similar conditions. The degree of surface oxidation is a strong function of polymer structure. The relative roles of different regions of the solar spectrum and other ambient conditions are examined by comparing the weathering characteristics in three mounting configurations.
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  • 130
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 2861-2868 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Trans-1-(3-vinyl-9-carbazolyl)-2-(9-carbazolyl)cyclobutane(I) was synthesized. Homopolymerization of I and copolymerization with 9-ethyl-3-vinylcarbazole(II) were conducted cationically. It was found that I polymerized to high molecular weight polymers (〈 105) with good yields, although its polymerizability was lower than that of II. Copolymer composition was determined by gel permeation chromatology (GPC) analysis, based on the remaining monomer ratio. Fluorescence spectroscopy indicated that poly(I) did not form excimer. Excimer emission gradually appeared with increasing II content in poly(I-co-II) to the homopolymer of II. This difference between poly(I) and poly(II) was attributed to the crowded and sterically distorted chromophore assemblies in poly(I). 1H- and 13C-NMR spectroscopy of cyclobutane groups in poly(I) compared with that in the monomer model compound supported the conclusion derived from fluorescence study.
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  • 131
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 1889-1903 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of new fluorinated ketone-containing polymers, poly(p-vinyltrifluoroacetophenone) (PVTFA), poly(p-vinyldifluoroacetophenone) (PVDFA), poly(p-vinylphenylheptafluoropropyl ketone) (PVHFK), and poly(o-and p-vinylbenzyltrifluoromethyl ketone) (PVTFK), were prepared by the free radical polymerization of the corresponding monomers. The monomers, p-vinyltrifluoroacetophenone (VTFA), p-vinyldifluoroacetophenone (VDFA), p-vinylphenylheptafluoropropyl ketone (VHFK), and o-and p-vinylbenzyltrifluoromethyl ketone (VTFK), were prepared by the reaction of Grignard reagent with the corresponding perfluoroacid or its lithium salt. Polymerization was a competitive side reaction during monomer preparation. Reduced side reaction and higher yields of monomer (based on the Grignard reagent) were obtained from the lithium salt of the perfluoroacid, compared with the perfluoroacid itself. These new substituted polystyrenes which contain fluorinated ketone functionality were characterized by their ability to (1) react with active hydrogen compounds such as alcohols or water; (2) have high glass transition temperatures and decreased solubility in nonpolar solvents (e. g., benzene) compared with polystyrene; and (3) be converted into other functional groups such as alcohols or acids by treatment with the appropriate chemical reagents. Beads of a styrene (ST) terpolymer with 2% divinylbenzene (DVB), which contained the CF3COCH2 function, were prepared by suspension polymerization of ST, VTFK, and DVB. The terpolymer, which contains 15-17% mole (or 0.70-0.71 meg/g) of CF3COCH2 swollen with a solvent, were shown to chemisorb alcohols.
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  • 132
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 1911-1916 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In an attempt to determine the role of a variety of amines in ceric-ion-initiated grafting, poly-(methyl methacrylate) was graft copolymerized onto Himachali wool in the presence of a variety of amines that included ammonia, diethylamine (DEA), dipropylamine (DPA), triethylamine (TEA), triethanol amine, and pyridine. All amines (with the exception of DEA) reduced the percent grafting. The reactivity of various amines toward graft copolymerization followed the order: DEA 〉 DPA 〉 NH3 〉 TEA 〉 triethanol amine 〉 Py. An explanation based on the basicity, nucleophilicity, and steric requirement of amines is given to explain the observed reactivity order shown by the various amines toward graft copolymerization.
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  • 133
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 1917-1922 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Thermal decomposition of α,α′-azobisisobutyronitrile (AIBN) and dimethyl α,α′-azobisisobutyrate (MAIB) in the presence of a large amount of tin tetrachloride was investigated to determine the effect of complex formation on the decomposition rates and yields of the recombination products. The addition of tin tetrachloride significantly increased the decomposition rates; the observed first-order rate constant increased by factors of 4.5 and 17 at molar ratios of [SnCl4]/[AIBN] = 21.65 and [SnCl4]/[MAIB] = 19.53, respectively. It was found that the decomposition of these azo compounds was also accelerated by the addition of a comparable amount of donor solvent such as ethyl acetate or propionitrile to tin tetrachloride and that the enhancement in rate was accounted for by a larger frequency factor in the Arrhenius equation. Furthermore, the addition of tin tetrachloride seemed to suppress the formation of recombination products, tetramethyl succinonitrile and dimethyl tetramethylsuccinate, of the radicals produced by decomposition.
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  • 134
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 1923-1931 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Direct pyrolysis in the mass spectrometer (MS) yielded unequivocal evidence regarding the mechanism of thermal decomposition of N-monosubstituted and N-disubstituted polyurethanes. It was ascertained that direct pyrolysis in the MS detects the primary thermal fragments that originate from polyurethane pyrolysis. This is particularly useful when, as in the thermal decomposition illustrated in eq. (1), it is necessary to distinguish between primary and secondary thermal fragments in order to assess the thermal degradation mechanism. Our results indicate that N-monosubstituted polyurethane V undergoes a quantitative depolycondensation process. Instead, the thermal decomposition of the N-disubstituted polyurethane VI which occurs selectively in eq. (1) is demonstrated by the detection of thermal fragments that contain secondary amine and olefinic end groups. Finally, polyurethane VI shows a higher thermal stability with respect to polymer V because of the absence of the depolycondensation process, which accounts for the thermal degradation of the N-monosubstituted polyurethane V.
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  • 135
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 1933-1943 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Radical polymerization of N-vinylpyrrolidone along poly(methacrylic acid) templates of high syndiotatic content was followed dilatometrically in dimethylformamide, which was used as solvent. The effects of template concentration, template molar mass, and temperature on polymerization rate and average molar mass of the formed polyvinylpyrrolidone (PVP) were examined. Template concentrations were varied around the critical concentration for homogeneous segmental distribution, C*. Below this concentration, template coils can act as separate microreactors wherein growing PVP radicals exhibit maximum rate enhancement, i. e., relative rate νR = νR,max. In the free solution, blank polymerization occurs, i. e., νR = 1. Consequently, νR can be approximated by the equation νR = φνR,max + (1 - φ), where φ represents the volume fraction occupied by template coils. The slight increase in UR and PVP molar mass with the template chain length is supposed to be caused by the influence of translational diffusion on the termination step. Over the investigated temperature range of 50-70°C, the activation energy and entropy were almost identical for blank and template polymerization. An expected decrease of ΔE≠ and ΔS≠ in template systems is supposed to be compensated by the effects of desolvation of the template macromolecules during the propagation step.
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  • 136
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 1945-1956 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polystyryllithium was prepared by anionic polymerization. This “living polymer” and the polystyrylmagnesium bromide derived from it were treated with carbon dioxide (solid or gas). The highest yields of carboxylic acid were obtained when solid carbon dioxide was used with polystyryllithium or by treatment of polystyrylmagnesium bromide with gaseous carbon dioxide. The products from the reaction of polystyryllithium with oxygen were polymeric ketone X, the alcohols IXa and IXb, and coupling products (e. g., XI). The various functionalized and unfunctionalized polystyrene products were isolated by chromatography on silica gel and were characterized by gel permeation chromatography (GPC), thin layer chromatography (TLC), and high-performance liquid chromatography (HPLC) in combination with chemical transformations.
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  • 137
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 1957-1966 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A technique has been developed for initiating a graft copolymerization electrochemically. A copoly(styrene/vinylbenzophenone) linear copolymer was prepared to serve as the electroactive starting material. The benzophenone sites on this molecule are readily activated at the cathode. Macroradical ions result from the direct transfer of electrons to benzophenone groups of the electroactive backbone polymer. In solution in N,N-dimethylformamide with tetraethylammonium perchlorate (TEAP) as supporting electrolyte the passage of current produced a dark blue solution similar to that observed with radical anions obtained with benzophenone directly. When monomer such as acrylonitrile or methyl methacrylate was added, a graft copolymer was formed. Electrolysis of solutions of the backbone polymer in tetrahydrofurn (THF), with sodium tetraphenylboride as supporting electrolyte, produced relatively stable, persistent macroradical anions and, under appropriate conditions, the reddish-violet macrodianions. Both types initiated graft copolymerization of acrylonitrile and methyl methacrylate. Graft copolymers were characterized by gel permeation chromatography (GPC), infrared (IR), and solvent extraction. High grafting efficiency (i. e., free from homopolymer) can be obtained under appropriate conditions. Suitable mechanisms are proposed, compared, and discussed.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 1967-1977 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of amylose block co-and terpolymers is described. Fully acetylated amylose triacetate was hydrolyzed by hydronium ions to give a hydroxy-terminated amylose triacetate oligomer (HATA), which was reacted with diisocyanates to produce block copolymers. Prepolymers of HATA and MDI or TDI were reacted with both hydroxy-terminated polybutadiene and polypropylene glycol to form block terpolymers. Block co- and terpolymer formation was demonstrated by intrinsic viscosity increases, gel permeation chromatographic results, and NMR and IR spectroscopy. The products were easily deacetylated by NaOMe in methanol to yield amylose block co- and terpolymers. These polymers were readily degraded by α-amylase. The enzymatic hydrolysis was monitored by intrinsic viscosity measurements. The rate of biodegradation was influenced by the DS of the amylose block and the composition of the block terpolymers.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 1979-1993 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: As the first phase in the study of the emulsion polymerization of acenaphthylene (AcN), the oligomerization kinetics of the in-aqueous-phase soluble portion of the AcN monomer was investigated. The reactions were carried out in the absence and presence of anionic emulsifiers. The monomer disappearance rate was followed by ultraviolet (UV) spectroscopy and spectra were established for these species. It was found that aqueous phase AcN oligomerized with K2S2O8 initiator at 50°C to yield SO-4K+ -ended oligo -AcN species which showed a UV hypsochromic shift in polar solvents. The oligomerization had a second-order dependence on monomer concentration. The presence of sodium oleate (SO) and sodium dodecyl sulfate (SDS) emulsifiers at below and above their critical micelle concentrations decreased the rate constant of the aqueous phase oligomerization. These observations led to the suggestion of a mixed micellization concept in the particle nucleation mechanism.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 1995-2000 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Improved methods for the synthesis of 4-halogeno 1-vinylnaphthalenes are proposed. Reactivity ratios are determined for the following systems: 4-fluoro-1-vinyl naphthalene-styrene, 4-chloro-1-vinyl naphthalene-styrene, and 4-bromo-1-vinyl naphthalene-styrene. The determinations are performed at various specific temperatures and the relative activation parameters are obtained. It appears that the reactivity of 1-vinyl naphthalene is drastically decreased when substituted by a halogen. In the case of 1-vinyl naphthalene the selection is enthalpically controlled.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2001-2010 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Kinetics of the polymerization of acrylonitrile has been investigated in aqueous sulfuric acid in a temperature range of 25-45°C. The rate of polymerization (Rp) and the rate of managanic ion disappearance, etc., have been measured. The effect of the various additives, such as water-miscible organic solvents, neutral electrolytes, complexing agents, and surfactants, on the rate has been thoroughly studied. A mechanism that involves the initial complex formation between the thiol form of the thioamide and Mn3+, whose decomposition yields the initiating free radical with the polymer chain terminated by mutual combination of growing radicals, has been suggested.
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 3031-3034 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 3027-3029 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new method is proposed to calculate the reactivity ratios based on the polynomial approximation of unreacted monomers during the reaction period. From the published data of Meyer the reactivity ratios were recalculated in reasonable agreement with the original author.
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  • 144
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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 block copolymers in three-step reactions from linear polycondensates (e.g., nylon 6. nylon 6,6, nylon 6,10 and polyurethane) and olefinic monomers (e.g., styrene, acrylic acid and acrylonitrile, methyl methacrylate, vinyl acetate, vinyl chloride, and isoprene) is reported. Macromolecular radicals are formed by the thermal decomposition of partly nitrosated peptide group containing polycondensates at elevated temperatures (60-200°C). These polyradicals initiate the copolymerization of the olefinic monomers. The conversion and reaction rates were generally high (up to 100% within a few hours). Most of the block copolymers prepared were soluble in organic solvents. Some, however, were insoluble or rubberlike. The reaction mechanism involved are analyzed. Applications are discussed.
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  • 145
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2033-2043 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The action of hydrazine on desulfurized tetrasulfide polymer obtained from bis-2-chloroethyl formal leads to S—S bond splitting and depolymerization. Our studies show that successful depolymerization can be initiated only in a strong alkali medium at 95-98°C. During this process cleavage of the disulfide bonds and the formation of polymers of lower molecular weight with —SH end groups takes place. From the results of the experiments performed it can be seen that the degree of depolymerization increases with an increase in the amount of hydrazine, in the mole ratio of sodium hydroxide, and in the time of reaction. When 0.7-1.0 mole of hydrazine per segment of polymer and 4 mole of sodium hydroxide per mole of hydrazine are used, a polymer of low average molecular weight in the form of water-soluble sodium salt (fraction I) and a polymer in dispersion form (fraction II) are obtained. Similar results could be attained if the amount ot hydrazine were decreased and the mole ratio of sodium hydroxide were simultaneously increased to more than 4 mole per segment of hydrazine used. In a constant amount of sodium hydroxide with a smaller quantity of hydrazine or a shorter reaction time the amount of water-soluble polymer (as a sodium salt) decreases and the amount of polymer in dispersion form increases. If a portion of the polymer in dispersion is coagulated with a portion of the polymer in the mother liquid, the yield of the depolymerized product is higher, but the average molecular weight is also higher than those of fraction I. The influence of the average contents of sulfur on the efficiency of the depolymerization is tested in polymers that contain 2.5 (i.e., 3) atoms of sulfur per segment of polymer. The result is that the depolymerization of the polysulfide polymer could be carried out without previous desulfurization, but the molecular weights of the products obtained with an equivalent quantity of hydrazine are much higher than those obtained by depolymerization of the disulfide polymer.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2045-2050 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Kinetics for the polymerization of ethylene and the copolymerization of ethylene and propylene were studied by using highly effective heterogeneous metal organic catalysts produced by coating different organic and inorganic supports with the components of Ziegler systems. The activity of a supported Ziegler catalyst is characterized by the physical parameters of the support structure and its chemical nature. The active role of magnesium-containing supports was established for the formation and functioning of the propagating species on their surfaces. This role is expressed not only by an increase in the portion of transition metal included in the propagating species, compared with typical Ziegler catalysts, but also by an increase in the reactivity of the propagating species, change in the nature of the elementary processes for polymerization and copolymerization, including control of copolymerization constants, and modification of the molecular structure of the polymers and copolymers. It was shown that by choice of support it is possible to control the activity of the same catalytic system and characteristics of the structure and properties of the polymers it produces under identical polymerization conditions.
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 3063-3068 
    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 dibutyltin diacetate (DBTDA)-catalyzed reaction of phenyl isocyanate with methanol in DMF and cyclohexane have been studied by monitoring the rate of change of the absorbance of the reaction mixture at 281.6 and 280.9 nm, respectively. Our results indicate that the mechanism of the reaction is independent of the nature of the (inert) solvent. The subsequent reaction steps are (i) complexation of methanol to DBTDA, (ii) dissociation of the complex into a proton and an anion of composition [(n-C4H9)2Sn(OCOCH3)2(OCH3)]-, (iii) insertion of the isocyanate into the tin - alkoxy bond (the rate-determining step), and (iv) methanolysis of the thus-formed urethane precursor with simultaneous regeneration of the anion. The rate of the catalyzed reaction increases on goin from coordinating to noncoordinating solvents. The following sequence in order of increasing rate constant was observed: DMF 〈 dibutyl ether 〈 cyclohexane. This is because in coordinating solvents, DBTDA and methanol, apart from forming a complex with each other, also form complexes with the solvent.
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 3069-3079 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The interaction of silica and oligomeric methylsiloxanes, methylsilicone oil as well as silicone gum at elevated temperature was studied. It was found that a reaction takes place between surface silanols and octamethylcyclotrasiloxane (D4) above 180°C. Part of the methylsiloxane replaces the surface silanols forming loops with the surface, while the other part is redistributed to its neighboring homologoues. The methylsiloxy surface groups thus formed can undergo further reaction with the other methylsiloxanes above 250°C. Methylsilicone oil behaves similarly. The reaction with silicone gum was demonstrated by the formation of “chemically bound rubber.” The mechanism of the reaction is discussed.
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 3081-3092 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In the presence of ZnEt2 the CoCl2-quinoline complex polymerizes NVC with a rate increasing with ZnEt2 and CoCl2-Q concentrations up to a certain concentration of ZnEt2 or CoCl2-Q, thereafter becoming independent of either. At a fixed concentration of ZnEt2 and CoCl2-Q the rate is second order with respect to NVC. The poly(NVC) obtained is freely soluble in benzene but leaves some insoluble fraction in methyl ethyl ketone, which has been characterized by 13C-NMR to be a stereoblock polymer. X-ray diffraction, IR, and thermal characteristics of the polymer have also been reported. [η] is virtually independent of monomer, in the concentration range 0.1-0.25 mol/L ZnEt2 and CoCl2-Q concentrations. Oxygen as an additive inhibits the polymerization. A cationic coordination mechanism has been proposed and appropriate rate and degree of polymerization equations have been suggested.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2121-2128 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Alloxan or ninhydrin radical anions which are obtained from alloxantin or hydrindantin, respectively, by treatment with triethylamine could be trapped in stable condition by polymer cations that contains 1-benzyl-3-carbamoyl pyridinium or 1-benzylpyridinium salts structure.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2103-2119 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The air oxidation of poly-p-xylylene films was studied at temperatures between 125 and 200°C. The oxidation kinetics were obtained from neutron activation (NA) oxygen analyses and infrared (IR) Spectroscopy. A correlation between the NA oxygen analyses and mechanical properties indicated that the amount of oxygen incorporated into these polymers before a significant degradation mechanical properties is about 1000 ppm for poly(dichloro-p-xylylene) and 5000 ppm for poly(monochloro-p-xylylene) or poly-p-xylylene. The activation energy for the oxidation of these polymers was about 30 kcal/mole. Long-term-use (100,000 hr) temperatures were also estimated for each of the poly-p-xylylenes studied. The 100,000-hr maximum continuous-use temperature is 112°C for poly(dichloro-p-xylylene), 72°C for poly(monochloro-p-xylylene), and 57°C for poly-p-xylylene.
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 3137-3143 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ce(IV)-induced polymerization of allyl methacrylate (AMA) with cotton cellulose was investigated under a variety of conditions. Polymer add-on was directly related to AMA concentration. The same holds good for Ce(IV) ion concentration up to a certain concentration (30 mmol/L), after which it decreases. Polymer add-on was higher at 60 than at 50 and 70°C. A methanol/water mixture (20/80) offers the best medium for polymerization. Addition of nitric acid (up to 400 mol equivalent/L) or perchloric acid (up to 800 mol equivalent/L) to the polymerization system caused significant enhancement in polymer add-on. The reverse was the case with sulphuric acid irrespective of the concentration used. A comparison between polymer add-on values based on increase in weight and those based on estimated allyl double bonds indicated that the latter undergo partial homopolymerization.
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 3123-3136 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polyesterification of diacid and diol in the absence of foreign acid is carried out under constant reaction temperatures from 140 to 180°C (rather than under constant oil bath temperature as is usually done) and molar ratios r of diol to diacid from 1 to 3.55. The experimental data obtained cannot fit conventional rate equations as they appear in the literature. Based on ion pair formation and considering additional proton transfer from acid to alcohol, we propose a reaction mechanism and rate equations. The rate equation is found to fit our experimental data very well except for r = 1. At r = 1, the kinetic plot shows two straight lines rather than one as predicted. This is attributed to unremoved water due to the higher molecular weight (and therefore higher viscosity) at r = 1 which causes a reverse reaction and slower apparent reaction rate.
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 3145-3153 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The chemical structure of polymers produced by the γ irradiation of monovinylsilanes was studied. γ-ray addition polymerization of monovinylsilanes such as trialkylvinylsilane was very slow, and only the liquid oligomers were formed from them by large radiation dose. The presence of silethylene or silmethylene linkage was ascertained in these polymers by infrared absorption spectroscopy and 1H-NMR measurement, even when no Si—H bond existed in the monomers. The polymers were supposed to be produced by addition polymerization with intervening silalkylene linkage.
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  • 155
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2143-2153 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The radical-induced grafting of styrene onto polyisoprene (PIP) in benzene solution at, 60°C was studied in rubber concentration (up to 0.5 monomer mole liter-1) in which the polymerization of styrene shows ideal kinetics with no retardation by PIP. The proportion of polystyrene incorporated as graft is independent of the initiator (benzoyl peroxide) concentration and was found to be consistent with the kinetic expression derived by Cameron et al. The graft fraction of polystyrene which is higher than in the corresponding styrene-polybutadiene system reflects the higher reactivity of PIP toward radicals. Azobisisobutyronitrile produces no graft copolymer in this system.
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  • 156
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2163-2174 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of polyamides which contained thianthrene, phenoxatiin, and dibenzo-p-dioxin units was synthesized from tricyclic fused-ring diamines and aromatic diacid chlorides by solution polycondensations at a low temperature. The amorphous polyisophthalamides were highly soluble in polar organic solvents, whereas some of the polyterephthalamides with a fair degree of crystallinity were insoluble. The solubility of the series of polyamides increased in the order of the dibenzo-p-dioxin-containing polymers 〈 phenoxatiin-containing polymers 〈 thianthrene-containing polymers. The thermal stability increased in the reverse order and the dibenzo-p-dioxinpolyamides were more thermostable than the corresponding open-chain polymers with diphenyl ether linkages. The polyamides derived from 2,8-oriented tricyclic diamines showed somewhat lower glass transition temperatures than those from 2,7-oriented diamines.
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  • 157
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
    Notes: Polyphosphate and polyphosphonate esters of molecular weights 〉 10,000 were synthesized by base-promoted, liquid-vapor and liquid-liquid interfacial polycondensations of hydroquinone (HQ) with 4-methylthiophenyl phosphorodichloridate (MTPP) and phenylphosphonic dichloride (PPD). The barium hydroxide-initiated liquid-vapor polycondensation of PPD and HQ in the temperature range of 15-95°C shows that [η] increases with reaction temperature and unfractionated yields exhibit a maximum at about 45°C. The analogous liquid-vapor polycondensation of MTPP and HQ between 25 and 854C also shows a maximum yield at 45°C, whereas [η] decreases with increase in reaction temperature. The results are contrasted with temperature dependencies of base-catalyzed, liquid-liquid polycondensation of HQ with MTPP and PPD. A different insight is obtained by analyzing the temperature effects on fractionated products. The relative importance of degradative saponification reactions are ranked as attack on chain ester linkages 〉 phosphorus chloride reactant 〉 end groups of growing chains.
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  • 158
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2189-2196 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polycondensation of bis-N-hydroxyimides, N,N′ dihydroxypyromellitic diimide, and N,N′ -dihydroxybenzophenonetetracarboxylic diimide with dicarboxylic acid chlorides was carried out in dimethylacetamide in the presence of triethylamine to produce novel polyimide-esters. The resulting polymers had inherent viscosities up to 0.27 dl/g. These polyimide-esters and model compounds exhibited high reactivity toward nucleophiles such as aniline and n-butylamine, which brought about rapid reductions in the viscosity of the polymers. These polymers were fairly resistant to organic solvents but soluble in m-cresol. Thermal stability oft he polyimide-esters was evaluated by thermogravimetry and their good heat-resistant properties were confirmed.
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  • 159
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 3237-3246 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polyion complexes of sodium poly(methacrylate) and piperidinium cationic polymers [I], which are insoluble in water and have an equal number of positive and negative charges, bind organic anions (methyl orange, ethyl orange, propyl orange, butyl orange, and pentyl orange) in aqueous solution. The strength of the binding is enhanced by an increase in the hydrophobicity of the polyion complex and the small cosolute. Moreover, strong cooperative interactions appear with increased uptake of the small molecule. Urea and an inorganic electrolyte (KCl) were examined for their effect on the binding, the amount of which is strongly suppressed by these additives. The significance of hydrophobic and electrostatic interactions which accompany the binding is described.
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  • 160
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 3247-3255 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The thermal and/or catalytic degradation of chloride-containing polymers causes dehydrohalogenation which produces hydrochloric acid. A nonaqueous method has been developed for the termination of hydrochloric acid. The sample is dissolved in tetrahydrofuran and titrated potentiometrically with a standard tetrabutylammonium hydroxide solution in a 7.5% (V/V) aqueous tetrahydrofuran solution with a combination glass-calomel electrode. The method has a relative precision of ±3.7% at the 95% confidence limit and a sensitivity of 25 ppm HCI.
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  • 161
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2209-2219 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Vinyl copolymers with pendant porphyrin dimers were synthesized first by the dimerizations of chlorophyll-α and protoporphyrin IX via the ethylenebisamide linkage, then by copolymerization of the vinylbenzyl esters of the resulting dimers with N-vinylpyrrolidone or the esterification reaction of the dimers with chloromethylstyrene copolymers. Dimer-pendant copolymers with vinyl pyrrolidone catalyzed photoredox systems in aqueous solutions more efficiently than the corresponding monomer analogs, presumably because of the interactions exerted between the two combined porphyrin rings, which are manifested in the hypochromic effect in absorption spectra. The effect of the central Mg atom in the protoporphyrin IX ring was also considerable.
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  • 162
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2197-2207 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Radical polymerization and copolymerization of some o-alkylphenyl methacrylates were carried out and the effect of the ortho-substituents on the ability to homopolymerize, on the monomer reactivities, and on the ceiling temperatures of the monomers was studied. The effect of the substituent on tacticities and thermal stabilities of the polymers formed was also discussed. The ability to honiopolymerize and the monomer reactivity were considerably decreased by the introduction of the o-substituent. 2,6-Di-tert-butylphenyl methacrylate formed no methanol-insoluble polymer at 60°C. On the basis of the tacticity determined it was noted that the o-substituted phenyl methacrylates preferred syndiotactic addition in the propagation reaction less than did phenyl methacrylate or methyl methacrylate. The polymers formed from the o-substituted monomers were thermally less stable than poly(phenyl methacrylate), and, consistent with this finding, ceiling temperatures of the o-substituted phenyl methacrylates seemed to be lower than that of phenyl methacrylate. The effects observed were characteristic of the o-substituents conformationally close to the carbon-carbon double bond of the monomer or the carbon carrying the unpaired electron of the polymer radical.
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  • 163
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2221-2238 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Studies have been made of the photochemistry of ethylene copolymers with carbon monoxide (CO), methyl vinyl ketone (MVK), and methyl isopropenyl ketone (MIPK) in solid films. Infrared (IR) evidence is presented to show that a variety of unexpected ketone structures is present in these polymers as a result of 1,5-hydrogen transfer or “back-biting” during the high-pressure polymerization reaction. These additional structures complicate the analysis of the quantum yield data. The overall quantum yield for carbonyl disappearance (φ-co) which increases from 0.074 to 0.24 to 0.26 in the series PE-1% CO, PE-2% MVK, and PE-20% MIPK reflects the increasing stability of the alkyl radicals produced from the type I process in the respective ketone structures. It is also shown that ketone groups located in the backbone of the polymer, as in the 1% CO copolymer, have lower quantum yields for photochemical reactions, particularly those that produce free radical intermediates. Studies of the gaseous products from extensive photodegradation under nitrogen show that in all three cases carbon monoxide is the major product (46-65% of the total). Acetaldehyde and methane, expected from the type I reaction, are major products only for the MVK and MIPK copolymers. Reaction schemes are presented to explain the major products observed.
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  • 164
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2239-2246 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The copolymerization of acrylonitrile (r1) and p-acetoxystyrene (r2) in bulk yields reactivity ratios r1 = 0.08 and r2 = 0.42. Crosslinked resins are readily obtained by a new type of precipitation copolymerization of acrylonitrile, p-acetoxystyrene, and divinylbenzene. After deacetylation, the phenolic groups afford useful attachment sites for protected amino acids as a first stage in solid-phase peptide synthesis. Reactivity of typical 10% functionalized polyacrylonitrile-based resins is comparable to that of the more usual polystyrene-based equivalents, although swelling characteristics of the two types of resin are very different.
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  • 165
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2247-2255 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The graft copolymerization of methyl methacrylate (MMA) onto silk in aqueous media initiated by the potassium peroxydiphosphate-thiourea redox system was studied at 50°C. The rate of grafting was determined by changing [monomerl], [thiourea], [initiator], acidity of the medium, reaction medium, and temperature. A significant increase percent of grafting was noticed with increasing monomer concentration to 84.49 × 10-2 mole/liter and the further increase is associated with the decrease of graft yield. The graft yield increases with an increase of thiourea (Tu) concentration to 25 × 10-5 mole/liter; then it decreases. A measurable increase in graft yield was observed with an increase in acidity of the medium. Graft yield increases to a certain temperature, i.e., 50°C, and then it decreases. The graft yield increases with an increase of initiator concentration to 60 × 10-4 mole/liter; then it decreases. The graft yield is medium dependent. A suitable kinetic path has been proposed and the rate equation has been derived.
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  • 166
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2257-2265 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A detailed kinetic study of the γ-ray-induced surface grafting of methyl acrylate (MA) onto polyethylene (PE) has been investigated by using quartz helix microbalances. Under typical graft conditions, the grafting rate increases, levels off, and then accelerates with irradiation time; i.e., the typical growth process of the surface grafting consists of an initial stage having an increasing rate of grafting, an intermediate stage having a constant rate, and an advanced stage having an accelerated rate. A homopolymer layer (consisting only of an MA component) begins to be formed on the inner graft copolymer layer (consisting both of MA and PE components) at the transition zone in grafting rate after a duration of a constant rate of grafting. Therefore, the increasing rate in increasing rate in the intial stage of grafting reflects the graft copolymerization in the graft copolymer layer (inside the PE sheet), and the increasing rate in the advanced stage reflects the growth of the homopolymer layer. Under grafting reflects the graft tage reflects the growth of the homopolymer layer. Under grafting conditions by which the homolymer layer is not formed throughout the whole grafting process, the surface grafting remains remains in the initial stage. On the order hand, under grafting conditions by which the homopolymer layer begins to be formed from an early stage of grafting, the surface grafting proceeds rapidly from the initial stage to the advanced stage and thus skips the intermediate stage.
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  • 167
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2281-2291 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The Macosko-Miller approach is used to obtain an expression for the polydispersity index for AA, BB, CC linear step polymerization system in which B and C are the same type of functional group. The dependence of the polydispersity index, as a function of the extent of reaction, on the monomer masses and on the relative reactivities of B and C groups toward A, is examined in detail.
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  • 168
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2293-2306 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Treatment of cyclopentadiene-blocked acrolein with α,β-unsaturated ketones, esters, and nitriles in the presence of a thiazoliurn salt under basic conditions led to a simple method for the preparation of acetonylmethyl Vinyl ketone, 2-carboxymethylethyl vinyl ketone, and 2-cyanoethyl vinyl ketone. In addition, the cyclopentadiene-blocked acetonylmethyl vinyl Ketone was converted to heterocyclic furan and pyrrole monomers.
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  • 169
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2267-2280 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Graft polymerization was carried out on carbon fibers subjected to various types of oxidation treatment and on acrylate (methyl, ethyl, and n-butyl) with benzene solvent and mainly benzoyl peroxide as initiator according to the nitrogen-displacement sealed-tube polymerization method. In comparison with carbon fibers subjected to air oxidation treatment, carbon fibers subjected to nitric acid oxidation treatment showed easier graft polymerization, and grafting became easier with increasing degree of nitric acid oxidation. The following relationship is established between the graft reaction ratio (a) and the polymerization time (t): da/dt = K(100-a). For graft polymerization with lauroyl peroxide (LPO), benzoyl peroxide (BPO), and α,α′-azobisisobutyronitrile (AIBN) as initiator, LPO showed the largest transfer reaction constant, followed by BPO; AIBN showed the smallest value. Grafting showed a tendency to become easier for monomers with a larger displacement radical group. For the graft polymerization reported in this article, it was believed that the affinity between carbon fibers subjected to oxidation treatment and to monomer influenced the result. For graft polymerization using acrylic acid as the comonomer, percent grafting increased notably. It is believed that, in this, in this case, apparent grafting by dipole-dipole interaction of the —COOH group of the carbon fiber subjected to oxidation treatment and the —COOH group of the polymer occurs according to the theory of Riess et al. Tensile strength and breaking elongation of graft carbon fibers showed a tendency to increase with an increase in percent grafting, whereas Young's modulus showed a tendency to decrease. The contact angle with water showed a tendency to increase with increasing percent, whereas the contact angle with ethylene glycol and phenylglycidilethyl showed a tendency to decreasing percent grafting.
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  • 170
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 3325-3331 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 171
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 3293-3306 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Methyl acrylate and styrene have been copolymerized in the presence of zinc chloride either by photoinitiation or spontaneously. The copolymerization mechanism is investigated by analyses of copolymers composition and monomer sequence distribution. The resulting copolymers are not always alternating, their composition being dependent especially on the monomer feed ratio. Appreciable deviation to higher methyl acrylate unit content from an equimolar composition occurs at monomer feed fractions of methyl acrylate over 0.7. The larger deviation is induced by higher temperature, by photoirradiation, and by greater dilution of the reaction mixture with toluene. The 13C-NMR spectrum of the alternating copolymer shows a sharp singlet at the carbonyl region, whereas the spectra of random copolymers prepared by benzoyl peroxide initiation at 60°C show a triplet splitting at the carbonyl carbon region, irrespective of copolymer composition. The relative intensities of the triplet peaks for the random copolymers are in good correspondence to the contents of triad sequences calculated by means of conventional radical copolymerization theory. These results clearly indicate that the carbonyl splitting is caused predominantly by variation of the monomer sequence and not by variation of the stereosequence. The monomer sequence distribution in the copolymers is thus directly and quantitatively measured from the split carbonyl resonance. Although the same triplet splitting appears in the spectra of methyl acrylate-rich copolymers prepared in the presence of zinc chloride at high feed ratios (〉0.7) of methyl acrylate, the relative intensities of the split peaks do not fit the sequence distributions of random copolymers calculated by means of the Lewis-Mayo equation. The copolymerization yielding these peculiar sequences and the alternating sequence in the presence of zinc chloride is fully comprehended by a copolymerization mechanism proceeding between two active coordinated monomers, i.e., the ternary molecular complex composed of zinc chloride, methyl methacrylate, and styrene, and the binary molecular complex composed of zinc chloride and methyl methacrylate.
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  • 172
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    Topics: Chemistry and Pharmacology
    Notes: Photodimerization reactions of polyacrylate and polymethacrylate derivatives and the dimer model compound containing thymine bases were studied in the presence of adenine derivatives in dimethyl sulfoxide; N,N-dimethylformamide; and dimethyl sulfoxide-ethylene glycol solutions. The photodimerization of thymine bases both in the polymers and in the dimer model compound was found to be quenched by the addition of adenine derivatives. Base-base interaction in the ground state was also studied by ultraviolet (UV) spectroscopy in the three solvents. The quenching of the photodimerizationof thymine bases in the presence of adenine derivatives was discussed in terms of the specific interaction between adenine and thymine bases both in ground and excited states.
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  • 173
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2347-2355 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: It was found that the addition reaction between poly(4-vinylpyridinium chloride) and electrophilic vinyl compounds, such as acrylic acid, acrylamide, methylacrylate, and acrylonitrile. leads to ammonium quaternary polymers with a transformation degree that depends oil the reactivity of vinyl compounds. The structure of addition compounds was established by using 1H-NMR IR, and UV spectral methods. NMR-determined values of transformation degree indicate that the reactivity of vinyl compounds decreases as follows: \documentclass{article}\pagestyle{empty}\begin{document}${\rm CH}_{\rm 2} \hbox{=\hskip-1.5pt=} {\rm CH} \hbox{---} {\rm COOH} 〉 {\rm CH}_{\rm 2} \hbox{=\hskip-1.5pt=} {\rm CH} \hbox{---} {\rm CONH}_{\rm 2} 〉 {\rm CH}_{\rm 2} \hbox{=\hskip-1.5pt=} {\rm CH} \hbox{---} {\rm COOCH}_{\rm 3} 〉 {\rm CH}_{\rm 2} \hbox{=\hskip-1.5pt=} {\rm CH} \hbox{---} {\rm CN}$\end{document}
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2357-2369 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Homogeneous trimethylsilylation of silicic acid in nonaqueous media was studied. The silylation process consisted of three steps: acidification of sodium silicate, solvent extraction. and trimethylation of silicic acid. Sodium silicate was first acidified with dilute sulfuric acid to form silicic acid: extraction followed with hydrophilic organic solvents. The Silicic acid obtained was finally allowed to react with trimethylchlorosilane to give trimethylsilylates with molecular weights of 1000-12,000. Optimum conditions for each step have been intensively sought to achieve trimethylsilylates in high yield. The trimethylsilylates exhibited excellent thermal stability and surface properties, such as water repellency and antifoaming properties, comparable to those of conventional polydimethylsiloxanes.
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  • 175
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2371-2390 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Vinylpyridine-N-oxide units were introduced in polymeric chains in order to study their photocrosslinking. Copolymers of styrene and 4-vinylpyridine-N-oxide were especially synthesized and studied. The methods used for characterization of photocrosslinked films were a “photoresist test” or the measurement of the insolubility and of the swelling ratio. The Cleavage of the N-oxide bond was responsible for the photocrosslinking. The competitive formation of carbonyl compounds took place and decreased the rate of photocrosslinking. This last reaction is favored by triplet-state quenchers. The photosensitivity of the copolymers was determined as a function of the wavelength of the radiation used. When the photocrosslinking proceeded, a film of the copolymeric material became transparent in the 280-320-nm range. Thick films could therefore be completely photocrosslinked when irradiated in this range of wavelength.
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  • 176
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2391-2410 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 2-Methyl-5-vinylpyridine-N-oxide, 4-vinylquinoline-N-oxide. 9-vinylacridine-N-oxide, p-N,N-dimethylaminostyrene-N-oxide units were introduced in polymeric chains as homopolymers or/and as styrene copolymers to study their photocrosslinking. The method used for characterization of photocrosslinked films was a “photoresist test” described in Part I of this series. The photosensitivity of the different chromophores bound to the different polymer has also been studied by UV, IR, and fluorescence spectrophotometries. The use of aromatic amine N-oxide groups in polymers seems to be a general means to produce their photocrosslinking by radical reactions. Among the different polymeric materials prepared, 4-vinylpyridine-N-oxide and 4-vinylquinoline-N-oxide are the most photosensitive.
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  • 177
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2423-2436 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A reinvestigation of the oligomeric and polymeric products obtained from furan and trichloroacetic acid was carried out to establish their structures. Comparison of spectral data with those of authentic materials indicated that the major oligomeric products are IV and V. The ratio of the products IV:V was 1:52. Comparison of the polymeric material with IV and V suggests that V is the primary component of the larger chains. In addition, microanalytical and molecular weight data were obtained. These findings are in disagreement with the structural designation of Wassermann et al., who proposed the presence of units that possessed aliphatic unsaturation (I), and of Kresta and Livingston, who put forth structure III for the same product. Mechanistic aspects are discussed. A limited study was carried out on insoluble polyfuran which was isolated from the reaction of furan with hydrochloric acid.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2411-2422 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Four typical bioactive esters of acrylic monomers, N-p-acryloxybenzoyloxysuccinimides, 3-ac-ryloxy-4-oxo-3,4-dihydro-1,2,3-benzotriazines, N-acryloxy-5-norbornene-2,3-dicarboximides, and I-p-acryloxybenzoyloxybenzotriazoles, were Synthesized and polymerized as reactive polymers. Twelve new monomers were prepared by coupling acrylic acid, methacrylic acid, p-acryloxybenzoic acid, or p-methacryloxybenzoic acid with four N-hydroxy compounds such as N-hydroxysuccinimide (HOSu), 3-hydroxy-4-oxo-3,4-dihydro-1,2,3-benzotriazine (HOObt), N-hydroxy-5-norbornene-2,3-dicarboximide (HONB), and I -hydroxybenzotriazole (HOBT) in the presence of dicyclohexylcarbodimide. All monomers polymerized readily in solution with azobisisobutyronitrile (AIBN) as free radical initiator. The resulting reactive polymers with reactive —OSu, —OObt, —ONB, or —OBT group on the side chain are equally reactive toward n-butylamine at room temperature in the formation of corresponding polyacrylamides. Reactive polymers were used to immobilizetrypsin. It has been found that poly(N-p-methacryloxybenzoyloxy-5-norbornene-2,3-dicarboximide)-trypsin matrix had high activity around three times that of the poly(N-methacryloxy-5-norbornene-dicarboximide)-trypsin matrix. It is proposed that this activity may be due to the presence of a long spacer arm with a hydrophobic and rigid benzene ring between the ligand and matrix. The reactive poly(N-p-methacryloxybenzoyloxysuccinimide-p-methacryloxybenzoic acid) copolymer was used to immobilize the serum protein. This immobilized protein was a hopeful bioactive solid immunoadsorbent.
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  • 179
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2437-2449 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polymorphic behavior and γ-ray-initiated postpolymerization of the even-numbered long-chain Methacrylates (C18-C12) have been investigated. Phase transition behaviors of octadecyl, hexadecyl, tetradecyl, and dodecyl methacrylates are respectively, which become simpler with shortening of the chain length. The methacrylate monomers with sufficiently long hydrocarbon chains, such as octadecyl and hexadecyl, can be polymerized rapidly in the α-form crystal (hexagonal packing) by a fully two-dimensional mechanism, whereas in the β-form crystal (triclinic packing), polymerization can hardly occur. In the case of dodecyl methacrylate, however, an accelerated polymerization in the β form occurs after an induction period of several hours and the resultant polymer is gel-like. This can be interpreted by the propagation reaction across the polymer chain already formed. It has been found that the solid-state post-polymerization of n-alkyl methacrylates is affected by the chain length through the packing mode of the monomer molecules and also by the aggregation state of side chains in the resultant comblike polymer.
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  • 180
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2461-2470 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A general detailed model of polymer oxidative degradation in the presence of a stabilizer-oxygen acceptor was considered. The motion of the degradation zone boundary and the sample lifetime were obtained for various conditions of the process. In particular, it is shown that within the given concentration immobile oxygen acceptor has the best stabilizing properties. The theoretical results are compared with the experimental data obtained by using two independent methods: polymer sample cracking and a change in the ESR signal. Good agreement between theory and experiment was obtained.
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  • 181
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effect of epoxy groups at the surface layer of ethyl acrylate-glycidyl methacrylate copolymer (1) emulsion particles on its crosslinking reactivity has been investigated. For this purpose two series of I emulsions were prepared. In the Y series, of which emulsion particles have epoxy groups at the surface layer, the epoxy content in the polymerization recipe was varied. For preparing the X series, of which emulsion particles have few epoxy groups at the surface layer, the high epoxy content of a given emulsion was reduced by various degrees of cleavage reaction with HCl-CaCl2. In emulsion blend films with amine-group-containing copolymer (II) emulsion, where the crosslinking reaction was expected to proceed only at the interfacial layer of I and II emulsion particles, the Y series, compared to the X series at the equal overall epoxy content in particles, showed less swelling and higher gel fraction in dioxane, less swelling in water, and higher tensile strength and modulus. On the other hand, this difference was not observed in the next two crosslinked films in which crosslinking was expected to be homogeneous. First, blends of I and II, which were isolated from the corresponding emulsions discussed above, were cast from dioxane solutions. Second, I emulsions were cast with BF3 ether complex which was expected to penetrate into the particles. It is concluded that the response of I emulsion cleaving the epoxy groups at the surface layer of particles to subsequent interfacial crosslinking is obviously reduced. However, even such an emulsion can be crosslinked to an extent similar to that of an uncleaved emulsion with similar overall epoxy content, if the crosslinking reaction is conducted so as to give an homogeneous effect.
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  • 182
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2471-2479 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of redox -initiated polymerization of acrylic acid (AA) by the systerm Mn3+-isobutyric acid (IBA) in sulfuric acid was studied in the temperature range of 35-50°C. The overall rates of polymerization (Rp), disappearance of manganic ion (-Rm), and degree of polymerization (Xn), were measured with variation in [monomer], [Mn3+], [IBA], H+, μ, [Mn2+], and temperature. The polymerization is initiated by the organic free radical that develops from the Mn3+-isobutyric acid oxidation reaction. Two types of termination reactions, one by the metal ion (Mn3+) and the other by the MN3+-isobutyric acid complex are proposed to explain the kinetic results. The various rate parameters were evaluated an discussed.
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  • 183
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    Topics: Chemistry and Pharmacology
    Notes: 2-Phthalimidomethyl 1,3-butadiene was homopolymerized and copolymerized with butadiene by free radical initiators; r1 and r2 were close to 1. All the attempts to polymerize 2PMB anionically have been unsuccessful. Preliminary studies of various η3-allylic catalysts showed that η3-allyl M0(CO)3OOCCF3 initiates the polymerization of butadiene and is not sensitive to N-methyl phthalimide (NMP); neither does it initiate the copolymerization of butadiene and 2PMB. On the other hand, a catalyst that results from the reaction of allyl trifluoroacetate with nickel tetracarbonyl is efficient for the copolymerization of butadiene and 2PMB. η3-Allyl nickel trifluoroacetate was prepared in heptane or benzene and used in benzene or methylene chloride. In all cases it initiated the copolymerization of butadiene with 2PMB
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  • 184
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    Keywords: Physics ; Polymer and Materials Science
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    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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  • 185
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    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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  • 186
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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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  • 187
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2561-2565 
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    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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  • 188
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    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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  • 189
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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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  • 190
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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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  • 191
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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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  • 192
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2577-2583 
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    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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  • 193
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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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  • 194
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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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  • 195
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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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  • 196
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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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  • 197
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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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  • 198
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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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  • 199
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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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  • 200
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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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