Olefin polymerization and copolymerization with alkylaluminum-initiator systems. VII. Initiation by electrophilic halogens

Kennedy, Joseph P. ; Sivaram, S. (1973) Olefin polymerization and copolymerization with alkylaluminum-initiator systems. VII. Initiation by electrophilic halogens Journal of Macromolecular Science: Part A - Chemistry, 7 (4). pp. 969-989. ISSN 1060-1325

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Official URL: http://www.tandfonline.com/doi/abs/10.1080/0022233...

Related URL: http://dx.doi.org/10.1080/00222337308061183

Abstract

The discovery of initiation of cat ionic polymerization of isobutylene and styrene by electrophilic chlorine generated by the reaction of chlorine and trimethylaluminum in the temperature range -40 to -100° is reported. Bromine and trimethylaluminum is a very poor initiating system, and iodine and trimethylaluminum does not initiate the polymerization of either isobutylene or styrene. Polymerization of isobutylene initiated by chlorine and trimethylaluminum shows a linear plot of log Mv vs 1/T with an overall EDP of ~1.9 kcal, mole. The molecular weights (Mw) of polystyrene obtained with the Cl2/Me3Al system appear to be the highest ever reported for cationic polymerization of this monomer under comparable conditions. The mechanism of initiation has been investigated by model experiments: The reaction between Cl2/Me3Al and 2,2,4-trimethyl-l-pentene gave three chlorinated products (2-chloromechyl-4,4-dimethyl-l-pentene, 1-chloro-2,4,4-trimethyl-1-pentene, and 2-chioromethyl-2,4,4-trimethyl-pentane). The position of chlorine in these compounds indicate initiation by electrophilic chlorine, Cl. Some preliminary results obtained using diethylaluminum chloride-halogens as coinitiator-initiator systems are also described.

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