4.7 Article

One Pot Synthesis of a Polyisoprene Polyrotaxane and Conversion to a Slide-Ring Gel

Journal

MACROMOLECULAR RAPID COMMUNICATIONS
Volume 37, Issue 1, Pages 67-72

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/marc.201500548

Keywords

1,4-polyisoprene; cyclodextrin; free radical polymerization; polyrotaxanes; slide ring gels

Funding

  1. Deutsche Forschungsgemeinschaft [WE 1090/17-1]

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Synthesis of a cyclodextrin (CD) polyrotaxane is achieved for the first time by simultaneous free radical polymerization of isoprene, threading by CD, and stoppering by copolymerization of styrene. This reaction is performed in an eco-friendly manner in an aqueous medium similar to classical emulsion polymerization. Threaded CD rings of the polyrotaxane are cross-linked by hexamethylene diisocyanate, leading to highly elastic slide-ring gels.

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