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  • 1
    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.
    Type of Medium: Electronic Resource
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  • 2
    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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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 56 (1962), S. 539-554 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The anionic polymerization of acrylonitrile by cyclopentadienyl sodium in tetrahydrofuran was studied. The effects of the concentration of monomer, catalyst, temperature, and added cyclopentadiene on the polymerization were investigated. Contrary to previously studied anionic polymerizations, the molecular weight was found to increase with monomer concentration as a result of the cyclopentadiene radical acting as a polyfunctional catalyst due to the following equilibrium: The cyclopentadienyl polymer anions thus formed (which have 5 resonance structures) initiate polymerization especially at high monomer concentration leading to increase in molecular weight as a result of the formation of several polymeric chains attached to the same cyclopentadienyl radical. Proof for the existence of such polymers was obtained on treatment of the polymers with ozone which caused considerable lowering of the molecular weight due to scission of polymer side chains as a result of the opening of the cyclopentadiene rings. X-ray diffraction diagrams of the branched polymers showed no strong reflection band at 5.3 A. which is associated with hydrogen bonding between chains of polyacrylonitrile. The molecular weight was independent of catalyst concentration and increased with lowering in temperature. Polymerization in the presence of free cyclopentadiene led to lowering in molecular weight due to termination by the acidic hydrogen of cyclopentadiene; plot of molecular weight against the reciprocal of the cyclopentadiene concentration gave a straight line. The polyacrylonitriles, having cyclopentadiene end groups, were utilized to introduce different end groups by the Diels Alder Reaction with dienophiles. Thus the adduct of the polymer with maleic anhydride gave an amide on reaction with amine.
    Additional Material: 6 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 1 (1963), S. 687-703 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The homogeneous anionic polymerization of acrylonitrile in dimethylformamide with n-butyllithium was studied. Two different termination reactions were found to exist depending on catalyst concentration. At high catalyst concentrations termination was bimolecular by chain transfer to monomer, while at relatively low catalyst concentrations termination was monomolecular, by an inner cyclization reaction of the growing chain end. The existence of chain transfer only at high catalyst concentrations suggests the possibility of free catalyst molecules participating in the transfer reaction. At intermediate catalyst concentrations, both monomolecular and bimolecular terminations were found to occur side by side, and DP = Kp[M]/(Ktr[C][M] + Kt). Study of the dependence of molecular weight on per cent conversion at low catalyst concentrations showed that, up to about 30% conversion, there is a linear relationship between molecular weight and concentration of monomer consumed which is independent of temperature and monomer. After this degree of conversion, molecular weight stopped to increase and remained constant due to monomolecular termination. All over the wide range of catalyst concentrations investigated, the catalyst efficiency in initiating polymerization was found to be low. In the lowest range where there is a linear dependence of molecular weight on per cent conversion it was also found that the molecular weights are proportional to [M]/[C], which is a property of “living” systems.
    Additional Material: 3 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 1 (1963), S. 1813-1837 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The anionic polymerization of styrene by phenyllithium was studied in various solvents The order of the decreasing molecular weights obtained depending on the solvent, was: tetrahydrofuran » toluene 〉 benzene 〉 petroleum ether 〉 diethyl ether. The molecular weight, due to absence of termination, is governed by the ratio of the rate propagation to the rate of initiation (Rp/Ri). Both these rates are influenced by the dielectric constant and the solvating power of the solvent for the phenyllithium and for the growing end, solvation of the growing end being greater due to the resonance of the propagating styryl anions. This leads to the fact that on passing from petroleum ether (low dielectric constant) to tetrahydrofuran (relatively high dielectric constant and high solvating power), Rp increases much more than Ri, leading to higher molecular weight. The polymerization of styrene in mixtures of petroleum ether and tetrahydrofuran was studied by the addition of increasing amounts of tetrahydrofuran while keeping the catalyst and monomer concentrations constant. Initially (up to 2 vol.-% tetrahydrofuran) there was a sharp decrease in molecular weight due to a greater dissociation of the phenyllithium, with a corresponding increase in Ri. On further addition of tetrahydrofuran (up to about 25 vol.-%), the molecular weight increased and approached the order of that obtained in petroleum ether. This is due to a greater increase in Rp over Ri due to greater solvation of the propagating end. At this relatively high tetrahydrofuran concentration we have maximum solvation both of the catalyst and of the growing end. With further addition of tetrahydrofuran there is a linear dependence of the molecular weight both on the concentration of the tetrahydrofuran and on the dielectric constant of the system. Ether gave the lowest molecular weights, in spite of its relatively high dielectric constant, due to greater dissociation of the catalyst associates (C6H5Li)x leading to an increased efficiency of the catalyst (greater Ri). Toluene and benzene led to higher molecular weights than petroleum ether, although the dielectric constants are of approximately the same order, due to the homogeneous nature of the polymerization in these solvents as compared with the heterogeneous polymerization in petroleum ether. The molecular weight increased with decrease in temperature in various solvents due to the increase in the dielectric constant and the lowering in Ri
    Additional Material: 5 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 1 (1963), S. 3643-3654 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The polymerization of acrylonitrile was studied using cyclopentadienyllithium, cyclopentadienyl sodium, fluorenylithium, and phenyllithium, and was compared to polymerization with butyllithium. With phenyllithium and fluorenyllithium in tetrahydrofuran, termination was found to be by chain transfer to monomer. The homogeneous polymerization in dimethylformamide carried out at both high and low catalyst concentrations showed that at high catalyst concentrations the molecular weights of polymer increased sharply with monomer concentration using cyclopentadienyllithium and cyclopentadienyl sodium, unlike the case of polymer obtained with butyllithium and fluorenyllithium. The increase in molecular weight is due to what has been previously found that the cyclopentadienyl anion acts as a polyfunctional catalyst leading to initiation of polymerization at various places on the ring. The basic strength of the catalyst investigated, as determined from the ability to polymerize monomers of decreasing acidity, was as follows: butyl ⋍ phenyl 〉 fluorenyl 〉 cyclopentadienyl.
    Additional Material: 10 Tab.
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  • 7
    Publication Date: 1966-08-01
    Print ISSN: 0014-3057
    Electronic ISSN: 1873-1945
    Topics: Chemistry and Pharmacology , Physics
    Published by Elsevier
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