One-pot synthesis of ABC type triblock copolymers via in situ click [3+2] and Diels-Alder [4+2] reactions


Durmaz H. , DAĞ A., Altıntaş O., Erdoğan T., Hizal G. , TUNCA U.

MACROMOLECULES, vol.40, no.2, pp.191-198, 2007 (Journal Indexed in SCI) identifier identifier

  • Publication Type: Article / Article
  • Volume: 40 Issue: 2
  • Publication Date: 2007
  • Doi Number: 10.1021/ma0618191
  • Title of Journal : MACROMOLECULES
  • Page Numbers: pp.191-198

Abstract

We report a one-pot synthesis of ABC triblock copolymers of poly(ethylene glycol)- (PEG-) polystyrene- (PS-) poly(methyl methacrylate) (PMMA), and poly(epsilon-caprolactone)- (PCL-) PS-PMMA by combining in situ click [3 + 2] and Diels-Alder [4 + 2] reactions. For this purpose, furan-protected maleimide end-functionalized PMMA, PS with alpha-anthracene and omega-azide end-functionality, and PEG or PCL with an alkyne end-functional group were reacted in N,N-dimehtylformamide (DMF) for 36 h at 120 degrees C in order to give the corresponding triblock copolymers. All polymeric precursors with narrow molecular weight distribution and well-defined chain-end functionalities were achieved from living polymerization methods, except PEG. The obtained polymers were characterized by H-1 NMR (250 MHz), gel permeation chromatography (GPC), and differential scanning calorimetry (DSC) measurements.