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BielawskiChristopher W

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Synthesis of conjugated diblock copolymers: two mechanistically distinct, sequential living polymerizations using a single catalyst

Author(s)
Wu, Zong-QuanRadcliffe, Jonathan D.Ono, Robert J.Chen, ZhengLi, ZichengBielawski, Christopher W.
Issued Date
2012
DOI
10.1039/c2py00566b
URI
https://scholarworks.unist.ac.kr/handle/201301/33167
Fulltext
https://pubs.rsc.org/en/content/articlelanding/2012/PY/c2py00566b#!divAbstract
Citation
POLYMER CHEMISTRY, v.3, no.4, pp.874 - 881
Abstract
Block copolymers comprised of poly(3-hexylthiophene) and three different poly(isocyanide)s were synthesized in a single pot via the sequential addition of 2-bromo-3-hexyl-5-chloromagnesiothiophene followed by 2-(2-methoxyethoxy) ethyl 4-isocyanobenzoate, tert-butyl 4-isocyanobenzoate, or 1-isocyanohexadecane to a solution of 1,3-bis(diphenylphosphino) propane dichloronickel. Similarly, block copolymers of poly(1-dodecylpyrrole) along with poly(2,5-bis(hexyloxy) phenylene) and a poly(arylisocyanide) were also prepared using an analogous methodology. The respective mechanistically distinct polymerizations proceeded in a controlled fashion, were mediated by a common catalyst, and afforded well-defined block copolymers with tunable molecular weights and compositions. Selected block copolymers exhibited higher-order structures in solution and microphase separation characteristics in the solid state.
Publisher
ROYAL SOC CHEMISTRY
ISSN
1759-9954
Keyword
CHAIN-GROWTH POLYMERIZATIONSGRIGNARD METATHESIS METHODBLOCK-COPOLYMERSTRANSFER POLYCONDENSATIONLOW POLYDISPERSITYMOLECULAR-WEIGHTPHASE-SEPARATIONSOLAR-CELLSSIDE-CHAINPOLYTHIOPHENE

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