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Living anionic polymerization of 4‐diphenylphosphino styrene for ABC triblock copolymers
Author(s) -
Schultz Alison R,
Chen Mingtao,
Fahs Gregory B,
Moore Robert B,
Long Timothy E
Publication year - 2017
Publication title -
polymer international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.592
H-Index - 105
eISSN - 1097-0126
pISSN - 0959-8103
DOI - 10.1002/pi.5253
Subject(s) - copolymer , polymerization , polymer chemistry , materials science , styrene , thermoplastic elastomer , monomer , fourier transform infrared spectroscopy , anionic addition polymerization , chemical engineering , polymer , composite material , engineering
Living anionic polymerization of 4‐diphenylphosphino styrene ( DPPS ) achieved unprecedented poly(S‐ b ‐I‐ b ‐ DPPS ) ABC triblock copolymers with predictable molecular weights and narrow polydispersities. In situ Fourier transform infrared spectroscopy probed the anionic polymerization, monitoring vinyl disappearance during sequential monomer addition for kinetic analysis. Varying the concentration of reinforcing, polystyrenic external blocks enabled diverse compositions with tunable thermomechanical properties and tailored morphology. Dynamic mechanical analysis confirmed the presence of microphase separation in the triblock copolymers and revealed a broad temperature range ( ca 100 o C ) for a plateau region and onset of flow temperatures above 100 o C . Small‐angle X‐ray scattering and atomic force microscopy collectively revealed solid state morphologies of the triblock copolymers and probed phase separation at the nanoscale. Well‐defined poly(S‐ b ‐I‐ b ‐ DPPS ) ABC triblock copolymers with tunable structure − property relationships now permit phosphorus‐containing thermoplastic elastomers for emerging applications. © 2016 Society of Chemical Industry