Poly[poly(isobornyl methacrylate-co-methyl methacrylate) (poly(IBMA-co-MMA))-b-polybutadiene-b-poly(IBMA-co-MMA)] Copolymers: Synthesis, Morphology, and Properties

Anionic random and block copolymerization of isobornyl methacrylate (IBMA) and methyl methacrylate (MMA) has been studied in THF at −78 °C by using (1,1-diphenyl-3,3-dimethylbutyl)lithium (DDBLi) as initiator in the presence of LiCl. The random copolymerization of MMA and IBMA has also been carried out at 0 °C, all the other conditions being kept unchanged. Poly[poly(IBMA)- b -poly(BD)- b -poly(IBMA)] (IBI), poly[poly(IBMA- co -MMA)- b -poly(BD)- b -poly(MMA- co -IBMA)] (I/MBM/I), and poly[poly(IBMA)- b -poly(MMA)- b -poly(BD)- b -poly(MMA)- b -poly(IBMA)] (IMBMI) block copolymers have been synthesized by sequential anionic polymerization of butadiene, MMA, and IBMA initiated by the m -diisopropenylbenzene ( m -DIB)/ tert -butyllithium ( t -BuLi) diadduct. These block copolymers of a monomodal and narrow molecular weight distribution ( M̄ w / M̄ n = 1.1) have been analyzed by size exclusion chromatography (SEC), NMR, differential scanning calorimetry (DSC), dynamic mechanical analysis (DMA), and transmission electron microscopy (TEM). Stereocomplexation of IMBMA and I/MBM/I with iPMMA has also been studied by DSC. Although IBI triblock copolymers show a lamellar morphology even for relatively low hard block content (33 wt %), cylindrical and lamellar morphologies have been observed for the other block copolymers under consideration. These new block copolymers exhibit high ultimate tensile strength (30 MPa), elongation at break (1000%), and upper service temperature (140−200 °C).