Abstract
The double click reactions (Cu catalyzed Huisgen and Diels-Alder reactions) were used as a new strategy for the preparation of well-defined heterograft copolymers in one-pot technique. The synthetic strategy to the various stages of this work is outlined: (i) preparing random copolymers of styrene (St) and p-chloromethylstyrene (CMS) (which is a functionalizable monomer) via nitroxide mediated radical polymerization (NMP); (ii) attachment of anthracene functionality to the preformed copolymer by the o-etherification procedure and then conversion of the remaining - CH2C1 into azide functionality; (iii) by using double click reactions in one-pot technique, maleimide end-functionalized poly(methyl methacrylate) (PMMA-MI) via atom transfer radical polymerization (ATRP) of MMA and alkyne end-functionalized poly (ethylene glycol) (PEG-alkyne) were introduced onto the copolymer bearing pendant anthryl and azide moieties.
Original language | English |
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Pages (from-to) | 6969-6977 |
Number of pages | 9 |
Journal | Journal of Polymer Science, Part A: Polymer Chemistry |
Volume | 46 |
Issue number | 20 |
DOIs | |
Publication status | Published - 15 Oct 2008 |
Keywords
- Atom transfer radical polymerization
- Click reactions
- Cu catalyzed Huisgen reaction
- Diels-Alder reaction
- Gel permeation chromatography
- Heterograft copolymer