Organocatalyzed Polymerization of PET-mb-poly(oxyhexane) Copolymers and Their Self-Assembly into Double Crystalline Superstructures

Double crystalline multi-block copolymers exhibit two well-defined melting temperatures associated with the two phases formed by their constituent blocks. The crystalline superstructure formed in these copolymers is complex and depends on the miscibility of both comonomers. In this work, an innovative series of double crystalline Poly(ethylene terephthalate)-mb-poly(oxyhexane) multiblock copolymers were prepared in one pot. Previously synthesized low molecular weight poly(oxyhexane) telechelic diol and poly(ethylene terephthalate) oligomers were reacted by transesterification using an organic catalyst (DBU:BA), in a solvent-free process. The copolymerization was demonstrated by 1H NMR and 13C NMR spectroscopies and the random distribution of poly(oxyhexane) chains was confirmed. We found that all compositions exhibited double crystallinity, but the crystallization of the copolymers was strongly affected by PET/poly(oxyhexane) composition. When PET content in the copolymer decreases, the crystallization and melting temperatures of the poly(oxyhexane) phase decrease as well as its crystallization rate. Poly(oxyhexane) content increases induce similar changes in the PET phase. PET and poly(oxyhexane) chain segments form a one-phase melt according to SAXS. When the material is cooled from the melt, the PET phase crystallizes first (at higher temperatures) forming superstructural (micron size spherulites) templates. Upon further cooling, the crystallization of poly(oxyhexane) lamellae occurs, within the interlamellar regions of PET spherulitic templates. Furthermore, during crystallization of the copolymer, the amorphous regions of both components undergo phase separation, as evidenced by the presence of two Tgs. PLOM/AFM studies were performed and demonstrated the presence of micro-spherulitic morphology in the whole composition range. Considering all results, including temperature-dependent synchrotron SAXS/WAXS, we demonstrate the ability of poly(oxyhexane) to crystal