Synthesis, characterization, and interaction strengths of difluorocarbene-modified polystyrene-polyisoprene block copolymers

The effect of difluorocarbene (CF2) modification on the self-assembly of po lystyrene-b-polyisoprene (PS-b-PI) copolymers was investigated. We prepared a set of fully CF2-modified PS-b-PI copolymers (PS-b-FPI) with different m olecular weights (8-13 kg/mol) and located their order-disorder transition temperatures (T-ODT) by rheology and static birefringence. Using both mean- field and fluctuation theory, we determined the temperature dependence of t he interaction parameter between the styrene and CF2-modified isoprene segm ents (chi(SFI)) Two series of polystyrene-b-(partially CF2-modified polyiso prene) (PS-b-(FPI-s-PI)) materials with different levels of CF2 modificatio n were also prepared from the reaction between difluorocarbene and two near ly symmetric PS-b-PI precursors with molecular weights of 18 and 61 kg/mol, respectively. A lamellar morphology was established for all of the PS-b-(F PI-s-PI) copolymers below the T-ODT by small-angle X-ray scattering (SAXS) and rheology. The effective interaction parameter (chi(eff)) between the PS and FPI-s-PI blocks, calculated from the domain spacing determined by SAXS , passes through a minimum before increasing smoothly by a factor of 4 upon complete CF2 modification. Using the binary interaction model originally d eveloped for homopolymer/copolymer blends, we were able to understand the d ependence of the chi(eff) on the CF2-modification extent in a quantitative manner and extracted the three pairwise interaction parameters. Rheology an d static birefringence were also used to locate the T-ODT for the lower mol ecular weight PS-b-(FPI-s-PI) series. The T-ODT was found to behave in a ma nner similar to the chi(eff): a decrease was observed at initial CF2 modifi cation, and a sharp increase was observed upon further CF2 modification.