Literature DB >> 26484618

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

Gergely Kali1, Harley Eisenbarth1, Gerhard Wenz1.   

Abstract

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.
© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

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

Year:  2015        PMID: 26484618     DOI: 10.1002/marc.201500548

Source DB:  PubMed          Journal:  Macromol Rapid Commun        ISSN: 1022-1336            Impact factor:   5.734


  2 in total

1.  One-pot synthesis of block-copolyrotaxanes through controlled rotaxa-polymerization.

Authors:  Jessica Hilschmann; Gerhard Wenz; Gergely Kali
Journal:  Beilstein J Org Chem       Date:  2017-07-03       Impact factor: 2.883

2.  Superstructures with cyclodextrins: chemistry and applications III.

Authors:  Gerhard Wenz; Eric Monflier
Journal:  Beilstein J Org Chem       Date:  2016-05-10       Impact factor: 2.883

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.