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Synthesis and characterization of fluorine‐containing PAA‐b‐PTPFCBPMA amphiphilic block copolymer
Authors:Yongjun Li  Sen Zhang  Hao Liu  Qingnuan Li  Wenxin Li  Xiaoyu Huang
Institution:1. Key Laboratory of Organofluorine Chemistry and Laboratory of Polymer Materials, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, People's Republic of China;2. Laboratory of Nano‐Biology and Medicine, Shanghai Institute of Applied Physics, Chinese Academy of Sciences, 2019 Jialuo Road, Shanghai 201800, People's Republic of China
Abstract:A series of perfluorocyclobutyl (PFCB) aryl ether‐based amphiphilic diblock copolymers containing hydrophilic poly(acrylic acid) (PAA) and fluorophilic poly(p‐(2‐(p‐tolyloxy)perfluorocyclobutoxy)phenyl methacrylate) segments were synthesized via successive atom transfer radical polymerization (ATRP). 2‐MBP‐initiated and CuBr/N,N,N,N,N″‐pentamethyldiethylenetriamine‐catalyzed ATRP homopolymerization of the PFCB‐containing methacrylate monomer, p‐(2‐(p‐tolyloxy)perfluorocyclobutoxy)phenyl methacrylate, can be performed in a controlled mode as confirmed by the fact that the number‐average molecular weights (Mn) increased linearly with the conversions of the monomer while the polydispersity indices kept below 1.38. The block copolymers with narrow molecular weight distributions (Mw/Mn ≤ 1.36) were synthesized by ATRP using Br‐end‐functionalized poly(tert‐butyl acrylate) (PtBA) as macroinitiator followed by the acidolysis of hydrophobic PtBA block into hydrophilic PAA segment. The critical micelle concentrations of the amphiphilic diblock copolymers in different surroundings were determined by fluorescence spectroscopy using N‐phenyl‐1‐naphthylamine as probe. The morphology and size of the micelles were investigated by transmission electron microscopy and dynamic laser light scattering, respectively. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2010
Keywords:atom transfer radical polymerization  block copolymers  perfluorocyclobutyl  self‐assembly  synthesis
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