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Alkyllithium, anionic initiators copolymerization reactivity

Tapered Block Copolymers. The alkyllithium-initiated copolymerizations of styrene with dienes, especially isoprene and butadiene, have been extensively investigated and illustrate the important aspects of anionic copolymerization. As shown in Table 15, monomer reactivity ratios for dienes copolymerizing with styrene in hydrocarbon solution range from approximately 8 to 17, while the corresponding monomer reactivity ratios for styrene vary from 0.04 to 0.25. Thus, butadiene and isoprene are preferentially incorporated into the copolymer initially. This type of copolymer composition is described as either a tapered block copolymer or a graded block copolymer. The monomer sequence distribution can be described by the structures below ... [Pg.579]

Alkyllithium compounds are primarily used as initiators for polymerizations of styrenes and dienes (52). These initiators are too reactive for alkyl methacrylates and vinylpyridines. -Butyllithium [109-72-8] is used commercially to initiate anionic homopolymerization and copolymerization ofbutadiene, isoprene, and styrene with linear and branched structures. Because of the high degree of association (hexameric), w-butyllithium-initiated polymerizations are often effected at elevated temperatures (>50° C) to increase the rate of initiation relative to propagation and thus to obtain polymers with narrower molecular weight distributions (53). Hydrocarbon solutions of this initiator are quite stable at room temperature for extended periods of time the rate of decomposition per month is 0.06% at 20°C (39). [Pg.239]

Haddleton determined the reactivity ratios for copolymerization of MMA with BMA by classical anionic as 1.04 0.81 by alkyllithium/trialkylalu-minum initiation, 1.10 0.72 by GTP, 1.76 0.67 by ATRP, 0.98 1.26 by catalytic chain transfer, 0.75 0.98 by classical free radical, 0.93 1.22 [39]. The difference in reactivity ratios between GTP and classical anionic polymerization seems to indicate GTP is an associative process. However, Jenkins has also measured reactivity ratios for the same pair by GTP and reports different results rMMA=0.44 and rBMA=0.26 [40]. [Pg.19]

The alkyllithium-initiated anionic copolymerization of diene and styrene monomers continues to be of interest because one can tailor-make copolymers with a wide range of compositional heterogeneity. Recently, kinetic studies have provided rate constant data to further clarify the factors responsible for the predominant incorporation of the less reactive diene monomer in styrene/diene copol3naerizations carried out in hydrocarbon media.They confirm that the magnitude of the rate constants for butadiene-styrene copolymerizations fall in the order results of several... [Pg.335]




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Alkyllithium

Alkyllithium initiated

Alkyllithium initiator

Alkyllithiums

Alkyllithiums, reactivity

Anionic initiation

Anionic initiators

Anions initiating

Copolymerization, initiators

Initiators anions

Reactivity copolymerization

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