Graft copolymers via ROMP and Diels–Alder click reaction strategy

Abstract

Abstract Anthracene‐functionalized oxanorbornene monomer and oxanorbornenyl polystyrene (PS) with ω‐anthracene end‐functionalized macromonomer were first polymerized via ring‐opening metathesis polymerization using the first‐generation Grubbs' catalyst in dichloromethane at room temperature and then clicked with maleimide end‐functionalized polymers, poly(ethylene glycol) (PEG)‐MI, poly(methyl methacrylate) (PMMA)‐MI, and poly( tert ‐butyl acrylate) (P t BA)‐MI in a Diels–Alder reaction in toluene at 120 °C to create corresponding graft copolymers, poly(oxanorbornene)‐ g ‐PEG, poly(oxanorbornene)‐ g ‐PMMA, and graft block copolymers, poly(oxanorbornene)‐ g ‐(PS‐ b ‐PEG), poly(oxanorbornene)‐ g ‐(PS‐ b ‐PMMA), and poly(oxanorbornene)‐ g ‐(PS‐ b ‐P t BA), respectively. Diels–Alder click reaction efficiency for graft copolymerization was monitored by UV–vis spectroscopy. The d n /d c values of graft copolymers and graft block copolymers were experimentally obtained using a triple detection gel permeation chromatography and subsequently introduced to the software so as to give molecular weights, intrinsic viscosity ([η]) and hydrodynamic radius ( R h ) values. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2010