Browsing by Author "McCabe, J. F."

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    Kinetics of Reaction of Metal Alkyls with Alkenes: Part 7.—n-Butyl Lithium and N : N : N' : N'-Tetramethyl Ethylene Diamine with Butadiene
    (Journal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1972, 68 (1), 1972) Hay, J. N.; McCabe, J. F.; Robb, J. C.
    The polymerization of butadiene, initiated by the complexes of n-butyl lithium and tetramethyl ethylene diamine, has been studied in the range 230-280 K by dilatometry. Initial rates of polymerization were second order in monomer, and first in both amine and butyl lithium concentrations. Maximum rates were observed at molar ratios of lithium alkyl/amine below' I /2. Rates of polymerization decreased with conversion, consistent with first-order dependence on unconverted monomer. Molecular weights of the polymers increased with conversion, and at ratios below' 1 /2 in alkyl/amine compared exactly with moles of monomer consumer per mole of butyl lithium initially present. The micro-structure of the polymers varied with polymerization temperatures between 70-90 % of 1,2 addition product. All the polymers had narrow molecular weight distributions independent of the final degree of conversion. It was concluded that the polymerization of butadiene occurred by a “ living” anionic addition mechanism, initiated by the 1 /2 amine complex. The nature of the active polymerizing species was confirmed by a molecular weight study of the complexes present at various molar ratios, and their concentration dependence.