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Borane groups, living radical polymerization

The unexpected good control in the incorporation of borane groups to polyolefin by metallocene catalysis and the subsequent radical chain extension by the incorporated borane groups prompted us to examine this free radical polymerization mechanism in greater details. Several relatively stable borane-based radical initiators were discovered, which exhibited living radical polymerization characteristics, with a linear relationship between polymer molecular weight and monomer conversion [27] and producing block copolymers by sequential monomer addition [28]. This stable radical... [Pg.292]

A radical initiator based on the oxidation adduct of an alkyl-9-BBN (47) has been utilized to produce poly(methylmethacrylate) (48) (Fig. 31) from methylmethacrylate monomer by a living anionic polymerization route that does not require the mediation of a metal catalyst. The relatively broad molecular weight distribution (PDI = (MJM ) 2.5) compared with those in living anionic polymerization cases was attributed to the slow initiation of the polymerization.69 A similar radical polymerization route aided by 47 was utilized in the synthesis of functionalized syndiotactic polystyrene (PS) polymers by the copolymerization of styrene.70 The borane groups in the functionalized syndiotactic polystyrenes were transformed into free-radical initiators for the in situ free-radical graft polymerization to prepare s-PS-g-PMMA graft copolymers. [Pg.41]


See other pages where Borane groups, living radical polymerization is mentioned: [Pg.79]    [Pg.91]    [Pg.91]    [Pg.264]    [Pg.42]    [Pg.262]    [Pg.264]    [Pg.273]    [Pg.367]   
See also in sourсe #XX -- [ Pg.91 ]




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