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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 19 (1990), S. 425-436 
    ISSN: 1572-8927
    Keywords: Complexation ; lithium picrate ; competition method ; dioxane ; ion binding ligands
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The interaction of several cyclic ethers, poly(ethylene glycol dimethyl ether)s, nitriles, esters and ketones with lithium picrate in dioxane at 25°C was investigated by means of a competition method using cross-linked poly(ethylene oxide) (PEO) as the insoluble ligand. The Langmuir-Klotz isotherm of LiPi binding to the PEO gel gave an apparent binding constant, K′, as a function of the concentration of added ligand. Plots of 1/K′ vs. the ligand concentration then yielded the formation constant, K L , of the ligand complex with LiPi. The results demonstrate that in dioxane one ligand molecule binds to LiPi. While there is some dependence on the Gutmann donicity number of the respective ligands, steric factors often play a dominant role in determining the value of K L . The results were compared with complexation data obtained on similar systems but by different methods.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 61 (1962), S. 31-37 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Lack of termination in the “Living” polymer systems enables one to determine directly the absolute rate constant of propagation and of copolymerization. Anionic polymerizations in tetrahydrofuran are usually very fast, and a flow technique was developed to determine the rate of these reactions. The method is described and its use illustrated by studies on the following systems: styrene-p-methylstyrene, styrene-p-methoxystyrene, and styrene-2-vinylpyridine. The results indicate that the polarity of the reacting monomer is the dominant factor in determining the value of the copolymerization rate constant as long as the polarities of the monomers involved are similar. However, the results obtained on the system styrene-2-vinylpyridine clearly demonstrate that the terminal carbanion plays a major role when the polarities of the two monomers are very different. The technique can also be used to study the effect of the penultimate unit of a chain on the rate constant of propagation or copolymerization. Moreover, the chain length of the “living” polymer can be caried and its effect of the rate constant determined.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 108 (1967), S. 288-291 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 3 (1965), S. 3099-3106 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Anionic polymerization of vinylmesitylene was investigated in THF (counterion Na+) at temperatures ranging from +25° to -70°C. The homopropagation is slow (kp ∼ 11./mole-sec. at 25°C.), indicating the basically low reactivity of the monomer. Studies of conductivity and the retardation of the polymerization by the addition of Na+BPh4- demonstrate that free ions and ion pairs participate in the process. At 25°C. the kp of the free ion appears to be about 1000 times greater than that of ion pair. The outstanding feature of the polymerization is the proton transfer from the monomer to living end, producing an inert ion (or its isomer) which does not propagate. This reaction leads to retardation of the polymerization. Its contribution decreases on lowering the temperature, and the effect of Na+BPh4- indicates that the free ion, and not the ion-pair, acts as a base in the proton transfer.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 2 (1964), S. 735-737 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 3 (1965), S. 1037-1041 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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