## Abstract A series of polystyrene‐__block__‐poly(__n__‐butyl methacrylate) (PS‐__b__‐P__n__BMA) diblock copolymers (di‐BCPs) with an azobenzene moiety [__trans__‐4‐methacryloyloxyazobenzene (MOAB)] in the P__n__BMA segment was prepared by atom transfer radical polymerization (ATRP). P(__n__BMA‐__
Synthesis of Polyacrylonitrile-block-Polystyrene Copolymers by Atom Transfer Radical Polymerization
✍ Scribed by Massimo Lazzari; Oscar Chiantore; Raniero Mendichi; M. Arturo López-Quintela
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 133 KB
- Volume
- 206
- Category
- Article
- ISSN
- 1022-1352
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✦ Synopsis
Abstract
Summary: The synthesis of polyacrylonitrile‐block‐polystyrene (PAN‐b‐PS) copolymers by atom transfer radical polymerization (ATRP) is reported. Chain extension of bromine terminated PAN macroinitiators with styrene was performed using a CuBr/N,N,N′,N″,N″‐pentamethyldiethylenetriamine catalyst system and 2‐cyanopyridine as a solvent. The first‐order kinetic plots of styrene consumption showed a significant curvature, indicating a progressive decrease in the concentration of active species during copolymerization. The loss of the bromide end group was mainly ascribed to the elimination of HBr, as shown by ^1^H NMR spectroscopy. By varying the molar ratio of either the catalyst or the monomer to the initiator, a series of PAN‐b‐PS copolymers were prepared, with polydispersities as low as 1.3, and molar compositions ranging from 8.6/91.4 to 35.5/64.5.
^1^H NMR spectra of PAN‐b‐PS in DMF‐d~7~ at 80 °C.
magnified image^1^H NMR spectra of PAN‐b‐PS in DMF‐d~7~ at 80 °C.
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