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Synthesis of SBC, SC and BC block copolymers based on polystyrene (S), polybutadiene (B) and a crystallizable poly(ε‐caprolactone) (C) block
Author(s) -
Balsamo Vittoria,
von Gyldenfeldt Friederike,
Stadler Reimund
Publication year - 1996
Publication title -
macromolecular chemistry and physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.57
H-Index - 112
eISSN - 1521-3935
pISSN - 1022-1352
DOI - 10.1002/macp.1996.021970332
Subject(s) - polybutadiene , copolymer , polymer chemistry , caprolactone , polystyrene , materials science , block (permutation group theory) , polymer science , composite material , polymer , geometry , mathematics
The sequential anionic polymerization of polystyrene‐ block ‐polybutadiene‐ block ‐poly(ε‐caprolactone) (SBC) triblock copolymers as well as polystyrene‐ block ‐poly(ε‐caprolactone) (SC) and polybutadiene‐ block ‐poly(ε‐caprolactone) (BC) diblock copolymers was achieved in benzene. To initiate the polymerization of the highly reactive ε‐caprolactone, the nucleophilicity of the carbanion has to be reduced. For this purpose 1,1‐diphenylethylene (DPE) was used. To avoid inter‐ and intramolecular transesterification reactions of the growing caprolactone block, the reaction time of this monomer in the block copolymers was strictly controlled. The reaction between polybutadienyl anions and DPE is too slow, and an incomplete reaction results in side reactions when ε‐caprolactone is added. An alternative method was developed, which consisted in the addition of a small quantity of styrene, after the polymerization of butadiene, to diminish the total reaction time and reduce the probability of chain transfer.