Polymer- and Colloid-Functionalization Using a Combination Of ATRP and Click Chemistry
2009
A straightforward click reaction (i.e. copper catalyzed 1,3 dipolar Huisgen cycloaddition of azides and terminal alkynes) was used as a complementary tool for functionalizing well-defined polymers prepared by atom transfer radical polymerization (ATRP). The bromine chain-ends of polystyrene or poly(acrylate) backbones were first transformed into azide end-groups via nucleophilic substitution and subsequently involved in “click” cycloaddition reactions with various functional alkynes. This efficient ATRP/“click” dual synthetic strategy was employed for preparing a wide variety of tailor-made functional materials such as telechelics, polymer-bioconjugates or shell-functionalized polymeric micelles.
Keywords:
- Ring-opening polymerization
- End-group
- Living free-radical polymerization
- Reversible addition−fragmentation chain-transfer polymerization
- Atom-transfer radical-polymerization
- Click chemistry
- Azide
- Photochemistry
- Polymerization
- Organic chemistry
- Chemistry
- Polymer chemistry
- Cobalt-mediated radical polymerization
- Living polymerization
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