Polymers, methacrylates diene functionalized

More recently, the Diels Alder cycloaddition was used as a single-step strategy for attaching diene-capped polymers onto CNTs sidewalls through grafting to methods (see Section 3.3.1.6 for more details). Examples include attachment of furfuryl-functionalized polystyrene [35] and cyclopentadienyl-functionalized polymethyl methacrylate [36]. 

Thus, the synthesis of a styrene-methyl methacrylate block polymer requires that styrene be the first monomer. Further, it is useful to decrease the nucleophilicity of polystyryl carbanions by adding a small amount of 1,1-diphenylethene to minimize attack at the ester function of MMA [Quirk et al., 2000]. Block copolymers of styrene with isoprene or 1,3-butadiene require no specific sequencing since crossover occurs either way. Block copolymers of MMA with isoprene or 1,3-butadiene require that the diene be the first monomer. The length of each segment in a block copolymer is controlled by the ratio of each monomer to initiator. The properties of the block copolymer vary with the block lengths of the different monomers. 

The rapid progress and proliferation of metal-catalyzed living radical polymerization has allowed a variety of vinyl monomers to be polymerized into well-defined polymers of controlled molecular weights and narrow MWDs. Most of them are conjugated monomers such as methacrylates, acrylates, styrenes, acrylonitrile, acrylamides, etc., except dienes, which possess not only alkyl substituents but also aprotic and protic functional groups. This fact attests to the versatility and flexibility of metal catalysis for precision polymerization. 

Some functional oligomers were prepared by the degradation of a polymer for instance, Ebdon and Flint [68] obtained a,oxlialdehyde-[methyl oligo(metha-crylate)] by oxidative cleavage of statistical methyl methacrylate-buta-1,3-diene copolymers. 

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