Intramolecular friedel‐crafts cyclization and subsequent hydrogenation of styrene‐isoprene random copolymers prepared by anionic polymerization for thermally‐resistant and optical applications

To synthesize novel thermally and optically high‐performing thermoplastics from commodity monomers, random styrene (St)‐isoprene (Ip) rubbers ( r ‐SIRs) prepared by anionic copolymerization were subjected to intramolecular Friedel‐Crafts cyclization and subsequent hydrogenation via a sequence of simple postpolymerization modifications. The CF 3 SO 3 H‐catalyzed Friedel‐Crafts alkylation of r ‐SIR afforded cyclized r ‐SIR (C‐ r ‐SIR) via the predominant formation of bicyclic tetrahydronaphthyl units to give thermoplastics with a high glass transition temperature ( T g ∼130 °C), good mechanical properties, and good transparency. Subsequent hydrogenation of the small amount of remaining CC double bonds in the uncyclized Ip units and cyclized Ip‐Ip units yielded hydrogenated C‐ r ‐SIR (HC‐ r ‐SIR) and increased the degradation temperature by about 15 °C ( T d5 ≥ 380 °C). These HC‐ r ‐SIRs display good flexural moduli and strength, good transparency, and refractive indices similar to those of C‐ r ‐SIR. The birefringence of HC‐ r ‐SIR was successfully tuned by adjusting the comonomer content to obtain near‐zero birefringence high‐performance plastics.