作者: G. Henrici-Olivé , S. Olivé , E. Schmidt
DOI: 10.1016/S0022-328X(00)88920-2
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摘要: Abstract The polymerization of butadiene catalyzed by π-allylnickel iodide proceeds predominantly a living polymer mechanism which may, however, be influenced to certain extent the solvent. rates propagation as well chain transfer reaction increase in series benzene stereospecific dimerization styrene trans-1,3-diphenyl-1-butene with same catalyst was found involve π-allylic mechanism, comparable that polymerization. Other monomers are unable form structure destroy catalyst. Styrene exerts strong action on drastically reducing molecular weight (styrene end groups); there is also some copolymerization (inner groups).