Poly(styrene-b-isobutylene-b-styrene) (PSt−PIB−PSt) triblock copolymers have been prepared for the first time via coupling of living PSt-PIB diblock copolymers in a one-pot procedure. The PSt−PIB diblock copolymer was synthesized by living sequential cationic polymerization in methylcyclohexane (MeChx)/methyl chloride (MeCl) or hexane (Hex)/MeCl solvent mixtures at −80 °C using TiCl4 as co-initiator. It was found that, due to decomposition of the living PSt ends, the crossover efficiency (Ceff) from living PSt to IB decreases precipitously with time at close to 100% St conversion. To obtain high Ceff, IB must therefore be added at ≤95% St conversion. It was also found that in the presence of unreacted St the rate of IB block copolymerization decreases with time; this was attributed to the formation of relatively unreactive −St−IB−Cl ends. Due to the relatively high concentration of these ends, coupling of living PSt−PIB was slow and incomplete. The obtained PSt−PIB−PSt triblock copolymers exhibited reasonable but significantly lower tensile strength (16−20 MPa) than that (23−25 MPa) reported for model PSt−PIB−PSt triblock copolymers of similar composition.
Yossef A. ElabdEugene NapadenskyCharles W. WalkerKaren I. Winey
Naifu ShenJinyu BuMarianne E. PrévôtTorsten HegmannJoseph P. KennedyWeinan Xu
Joseph P. KennedyS. C. FeinbergShuyue Huang
Younghwan KwonRudolf FaustCinti X. ChenEdwin L. Thomas