Heteroarm core cross-linked star polymers via RAFT copolymerization of styrene and bismaleimide
We explored reversible addition-fragmentation chain transfer (RAFT) copolymerization of 1,2-bis(maleimidoethane) (BMI) with styrene (S) in the presence of polylactide macro-chain transfer agent (PLA-CTA) as a means to synthesize heteroarm core cross-linked star (CCS) polymers consisting of PLA and P...
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Veröffentlicht in: | RSC advances 2016, Vol.6 (53), p.47715-47722 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | We explored reversible addition-fragmentation chain transfer (RAFT) copolymerization of 1,2-bis(maleimidoethane) (BMI) with styrene (S) in the presence of polylactide macro-chain transfer agent (PLA-CTA) as a means to synthesize heteroarm core cross-linked star (CCS) polymers consisting of PLA and PS arms (PLA
n
PS
n
). Because of the strong alternating tendency of maleimide and styrenic double bonds, copolymerization of BMI with an excess of S depleted BMI in the early stage of polymerization forming a cross-linked core. The remaining S was successively polymerized to grow PS arms from the core, completing PLA
n
PS
n
via
“in–out” mechanism. Use of a stoichiometric amount of S produced PLA
n
, which could be used as a macro-CTA for the synthesis of more well-defined PLA
n
PS
n
. Compared with divinylbenzene, copolymerization of BMI with S was much more effective for core formation suggesting the importance of the alternating character of the copolymerization. While PLA
n
PS
n
existed as stable nanoparticles in a neutral solvent in contrast to linear PLA-
b
-PS, it also self-assembled to form microphase-separated structures in a selective solvent and in bulk indicating that PLA and PS arms can be intramolecularly segregated. |
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ISSN: | 2046-2069 2046-2069 |
DOI: | 10.1039/C6RA07527D |