Journal
POLYMER CHEMISTRY
Volume 8, Issue 45, Pages 6997-7008Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c7py01666b
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Funding
- National Natural Science Foundation of China [21274023]
- International Science & Technology Cooperation Program of China [2014DFE40130]
- Chinese Academy of Sciences [XDB20000000]
- Shanghai Scientific and Technological Innovation Project [16JC1402500, 16520710300]
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A series of ABA triblock copolymers, comprising double-bond-containing poly(phenoxyallene) (PPOA) and poly(methoxymethyl methacrylate) (PMOMMA) segments, was synthesized by a combination of conventional free radical polymerization, atom transfer radical polymerization (ATRP) and the site transformation strategy. A new bifunctional initiator containing azo and Br-containing ATRP initiating groups was employed to initiate the conventional free radical homopolymerization of phenoxyallene with a cumulated double bond to give a PPOA-based macroinitiator (Br-PPOA-Br) bearing ATRP initiating groups at both ends. Next, ATRP of MOMMA was initiated by Br-PPOA-Br macroinitiator to produce PMOMMA-b-PPOA-b-PMOMMA triblock copolymers, which were subsequently hydrolyzed to afford PMAA-b-PPOA-b-PMAA amphiphilic triblock copolymers. The critical micelle concentration (cmc) of PMAA-b-PPOA-b-PMAA amphiphilic triblock copolymer in aqueous solution was determined by fluorescence probe technique and the dependence of cmc on pH was also investigated. These amphiphilic triblock copolymers self-assembled into wormlike and large compound micelles in aqueous media.
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