Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9559388 | Polymer | 2005 | 16 Pages |
Abstract
In a former article the dissociation of organolithium salts due to Ï-complexing additives is described. Durene and tetraphenylethylene tend to break up at least partly the dimeric structure of polystyryllithium in non-polar solvents, as well as higher aggregates such as those formed by polybutadienyllithium. In this research these Ï-complexing additives are used to break up a similar association, i.e. the formation of tridimensional insoluble multifunctional initiator mixtures, when a bifunctional initiator is synthesized, using a precursor and a 2-fold excess of butyllithium. As the precursor mainly 1,3-diisopropenylbenzene (m-DIB) is used, but also 1,3-di(1-phenylethenyl)benzene (PEB) is examined. Subsequent addition of styrene in the presence of durene and tetraphenylethylene gives satisfying results in the synthesis of SBS-triblock copolymers.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Jurgen Hofmans, Marcel Van Beylen,