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  • Polymer and Materials Science  (10)
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 9 (1965), S. 3383-3388 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The interfacial polymerization technique was used in the preparation of organotion polyesters. Dialkyltin dihalides dissolved in an organic solvent immiscible with water were reacted with the dialkali metal or ammonium salt of a dicarboxylic acid. High yields of polyesters were obtained after short reaction times. The polyesters were generally insoluble and were high melting. Copolymers were also obtained.
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 40 (1959), S. 149-158 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The low pressure polymerization of propylene was investigated using catalysts prepared from alkali metal alkyls and titanium tetrachloride. In all cases the efficiency of the catalysts depended on the molecular ratio of the metal alkyl to the titanium tetrachloride. In general the polymerization conditions were similar to those for ethylene although the propylene polymerized much more slowly. With n-butyllithium-titanium tetrachloride, optimum molecular ratios were found between 1.8-2.5, with sharp drops on both sides. With amylsodium-titanium tetrachloride the optimum extended over a wide range (5.7-15), the activity decreasing sharply with lower molecular ratios. The catalysts prepared from sodium alkyls were more active than those prepared from lithium alkyls. Increasing yield was obtained on lowering the concentration of the catalyst. Up to a pressure of about 3 atmospheres, increase in the rate of polymerization was observed with increase in pressure; above this no influence of the pressure was observed. Isotactic polymers were isolated from the polymerization products by successive fractionation of the crude polymers in acetone, ether, and isooctane which dissolved the atactic polymers. With butyllithium-titanium tetrachloride catalysts, at and above optimum ratios, the isotactic fractions were about 60%. At lower ratios there was a great increase in atactic polymers. With amylsodium-titanium tetrachloride catalysts the isotactic fractions were about 70%. Phenylsodium-titanium tetrachloride catalysts were found to be very weak in the polymerization of propylene.
    Additional Material: 3 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 28 (1958), S. 387-394 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The low and atmospheric pressure polymerizations of ethylene using catalysts prepared from n-butyl lithium or isoamyl lithium and titanium tetrachloride were studied. The efficiency of the catalyst depended on the molecular ratio of the alkyl lithium to titanium tetrachloride. Optimum molecular ratio for the n-butyl lithium-titanium tetrachloride was found to be between 2.15-2.47 with a sharp drop between 2.15-1.49; for the isoamyl lithium the optimum was between 2.5-4.3. Within the examined interval (of atmospheric pressure to a pressure of 60-70 lb./sq. in.) higher pressure caused an increase in the yield of polyethylene. No pronounced effect in polymerization was found in the temperature interval of -10-55°. The catalyst is stable for a few days if kept refrigerated. Petroleum ether, b.p. 40-80°, was the best solvent both for the preparation of the catalyst and for the polymerization. Ligroin, toluene, and especially ether interfered with the polymerization. The polyethylenes obtained melted between 125-135°.
    Additional Material: 1 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 33 (1958), S. 141-152 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The low pressure polymerization of ethylene with the use of catalysts prepared from various sodium alkyls and titanium tetrachloride was studied. Catalysts prepared from amylsodium were very active over a wide range of molar ratios of amylsodium to titanium tetrachloride (2-50); the activity decreased sharply with lower molar ratios. Rate of polymerization was found to decrease sharply, probably as a result of fusing of polyethylene particles to the catalyst surface during polymerization. Up to a pressure of about three atmospheres, the polymerization gave better yields with increase in pressure, but no increase in rate was observed on using higher pressures. Yields increased also with lowering of temperature; 0°C. gave the best yields. Molecular weight determinations showed that the polyethylenes produced had high molecular weights which did not vary over a wide range. With butylsodium, catalysts similar to those with amylsodium were formed; they showed a smaller optimum range (5-9) of molar ratios of alkyl sodium to titanium tetrachloride. Catalysts prepared from phenylsodium were much weaker, and the optimum molar ratio of phenylsodium to titanium tetrachloride, contrary to the other sodium alkyls, was found to lie at much lower molar ratios of alkyl sodium to titanium tetrachloride. Polymerizations were, in the case of phenylsodium, accompanied by an induction effect. Preliminary studies on the preparation of catalysts for the low pressure polymerization of ethylene in the presence of cyclopentadienylsodium and titanium tetrachloride were as yet not successful.
    Additional Material: 4 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 39 (1959), S. 347-356 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The low pressure polymerization of ethylene by use of catalysts prepared from either butyl or amyl potassium, or the reaction product of potassium with chlorobenzene and titanium tetrachloride was studied. The efficiency of the catalysts depended on the molar ratio of the potassium alkyl to titanium tetrachloride but was in every case considerably lower than that of the corresponding lithium or sodium alkyl containing catalysts. Optimum molar ratios of the butyl potassium-titanium tetrachloride catalysts were between 2.8 to 6.1 with sharp drops on both sides of the optimum; for the amyl potassium between 1.1 to 3.7. The reaction product of potassium with chlorobenzene yielded much weaker catalysts with titanium tetrachloride, and the properties of the polymers obtained were different. The physical properties of the polyethylenes obtained, as determined from x-ray diffraction diagrams, infrared spectra, and from melting points, showed similarity to those obtained with the lower alkali metal catalysts. The lower activity of the potassium catalysts may be related to the large ionic radius of the potassium, which influences the properties of the catalyst complex formed with titanium tetrachloride. Propylene did not undergo polymerization with the potassium alkyl containing catalysts at low pressure.
    Additional Material: 4 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2663-2676 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Soluble tricarbonylchromium complexes were made by reacting Cr(CO)6 with a ladder polyphenylsilsesquioxane and a linear polydiphenylsiloxane. These new polymer Cr(CO)3 complexes were characterized by elemental Cr, infrared (IR), gel permeation chromatography (GPC), viscosity, and thermal analyses and were evaluated as stereoselective hydrogenation catalysts. Thermogravimetry studies demonstrated that the new complexes were more stable at 180-200°C in N2 than the corresponding complex from crosslinked polystyrene. These silicone polymer complexes catalyzed stereoselective hydrogenation of methyl sorbate to cis-3-hexenoate in cyclohexane and tetrahydrofuran (THF) and could be recovered from THF for recycling by precipitation-fiItration. Catalytic activity and recyclability, however, were highly influenced by the solvent. Loss of catalytic activity associated with loss of Cr(CO)3 was observed on recycling. These results support a mechanisim that involves dissociation of Cr(CO)3, a significant portion of which cannot become reassociated with the polymer phenyl groups.
    Additional Material: 4 Ill.
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  • 7
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The polymerizations of the N-carboxyanhydrides of 1-aminocyclopropanecarboxylic acid, 1-aminocyclobutanecarboxylic acid, 1-aminocyclopentanecarboxylic acid, and 1-aminocyclohexanecarboxylic acid were investigated. These N-carboxyanhydrides did not polymerize in bulk when heated to their melting points under reduced pressure. In solution, they polymerized extremely slowly on initiation with n-hexylamine and relatively slowly when initiated by sodium methoxide-methanol. The polymerization rates of the above NCAs in dimethyl sulfoxide solution, initiated by sodium methoxide-methanol were found to increase in the following order: NCA of 1-aminocyclohexanecarboxylic acid, NCA of 1-aminocyclopropanecarboxylic acid, NCA of 1-aminocyclopentanecarboxylic acid and NCA of 1-aminocyclobutanecarboxylic acid. The influence of the alicyclic side rings on the relative rates of polymerization of the respective NACs is considered.
    Additional Material: 1 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 14 (1975), S. 173-196 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The Miyazawa-Blout-Krimm (M-B-K) treatment of polypeptide absorption in the infrared is extended to the calculation of circular dichroism (CD), linear dichroism, and oriented CD for the amide I and amide II transitions. Matrix methods are applied to the α helix and β structures using measured values for the strengths and directions of the transition dipole moments and empirical values from M-B-K for the coupling constants.Relatively small aggregates, a 36-residue helix, and 8-chain × 4-residue β sheets, are large enough to show calculated absorption agreeing with M-B-K results, which are based on infinite lattices.In all cases the predicted CD is an approximately conservative couple. The strongest CD should appear in the α helix, Δε/ε ≃± 10-3 for both transitions. The amide II transition should show moderate CD couples in both β structures, Δε/ε ≃ (+2 to -1) × 10-4. The amide I transitions in β structures should show weak CD couples, Δε/ε = (+3 to -2) × 10-5, except that the negative branch in the antiparallel structure may be detectable (Δε/ε ≃ -2 × 10-4) because absorption is very low at its wavelength peak.CD on oriented samples should be enhanced over the unoriented cases, giving values as large as Δε/ε = 3 × 10-3 because particular directions of observation allow the light to avoid much of the absorption in the sample.If all three structures are considered as helices, then the larger distance of the transition dipoles from the axis in the α helix, and the orientations of the transitions in the different structures, are the factors that, in terms of our previous theoretical work [Snir and Schellman (1973) J. Phys. Chem. 77, 1653] satisfactorily explain the calculated results. Simple dipole-dipole interaction is calculated to make a substantial contribution to the coupling between groups.
    Additional Material: 6 Ill.
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  • 9
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Aqueous solutions of quaternary ammonium hydroxides were used, for the first time, as initiators for the anionic homogenous polymerization of acrylonitrile and methacrylonitrile in dimethylformamide. The molecular weight of polyacrylonitrile was independent of catalyst and monomer concentrations, while that of polymethacrylonitrile increased linearly with monomer concentration. Infrared spectra showed the presence of primary alcohol groups in both polyacrylonitrile and polymethacrylonitrile. Polyacrylonitrile contained terminal double bonds which were absent in the methacrylonitrile polymers. On the basis of these and additional evidence, initiation by hydroxyl anion and termination by chain transfer to monomer is suggested for acrylonitrile polymerization; while termination of methacrylonitrile polymerization is by water. Molecular weight decreased with increase in size and electropositivity of the quaternary ammonium positive counterion in the following order: (CH3)4NOH 〉 (C2H5)4NOH 〉 (CH3)3C6H5CH2NOH.
    Additional Material: 1 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Propellants, Explosives, Pyrotechnics 15 (1990), S. 26-29 
    ISSN: 0721-3115
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Azidodinitromethyl compounds represent a new highly energetic class of propellant ingredients. Preparation of these materials was accomplished by means of electroxidative coupling of azide ions to dinitromethyl carbanions. Thus, anodic coupling of sodium azide with ethyl 4,4-dinitrobutyrate produced ethyl 4-azido-4,4-dinitrobutyrate. Similarly, 4-azido-4,4-dinitrobutyl acetate was prepared from 4,4-dinitrobutyl acetate and converted by way of the corresponding alcohol to the nitrate ester, 4-azido-4,4-dinitrobutyl nitrate.
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