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Synthesis of fluorescent methoxy poly(ethylene glycol)‐ b ‐Poly(ethyl cyanoacrylate)–2‐( N ‐carbazolyl) ethyl methacrylate copolymer via living oxyanion‐initiated polymerization
Author(s) -
Lin Xiaona,
Deng Liandong,
Dong Anjie
Publication year - 2011
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/app.34879
Subject(s) - copolymer , ethylene glycol , polymer chemistry , polymerization , methacrylate , gel permeation chromatography , materials science , methyl methacrylate , molar mass distribution , carbazole , fluorescence , polymer , chemistry , organic chemistry , physics , quantum mechanics
The fluorescent amphiphilic block copolymer methoxy poly(ethylene glycol) (mPEG)‐ b ‐poly(ethyl cyanoacrylate) (PECA)–2‐( N ‐carbazolyl) ethyl methacrylate (CzEMA) was synthesized via living oxyanion‐initiated polymerization. mPEG‐ b ‐PECA–CzEMA was characterized by gel permeation chromatography, 1 H‐NMR, and Fourier transform infrared spectroscopy. The results indicate that the polymerization was well controlled with a narrow molecular weight distribution. The mPEG‐ b ‐PECA–CzEMA nanoparticles prepared by nanoprecipitation techniques showed a narrow size distribution with an average diameter of less than 100 nm. The mPEG‐ b ‐PECA–CzEMA exhibited a strong carbazole fluorescence. Furthermore, it was found that the fluorescence intensity of mPEG‐ b ‐PECA–CzEMA was sensitive to a change in solvent. The results indicate that a subtle change in the state of the polymer micellar association may have altered the state of carbazole groups, which was responsible for the fluorescence emission. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012