Facile and efficient fabrication of photoresponsive microgels via thiol-Michael addition

Macromol Rapid Commun. 2012 Nov 23;33(22):1952-7. doi: 10.1002/marc.201200439. Epub 2012 Aug 21.

Abstract

A photoresponsive microgel is designed by the combination of a noncovalent assembly strategy with a covalent cross-linking method. End-functionalized poly(ethylene glycol) with azobenzene [(PEG-(Azo)(2))] was mixed with acrylate-modified β-CD (β-CD-MAA) to form photoresponsive inclusion complex through host-guest interaction. The above photoresponsive complex was cross-linked by thiol-functionalized PEG (PEG-dithiol) via Michael addition click reaction. The photoreversibility of resulted microgel was studied by TEM, UV-Vis spectroscopy, and (1)H NMR measurements. The characterization results indicated that the reversible size changes of the microgel could be achieved by alternative UV-Vis irradiations with good repeatability.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Azo Compounds / chemistry
  • Gels / chemistry*
  • Light
  • Polyethylene Glycols / chemistry
  • Sulfhydryl Compounds / chemistry*
  • Ultraviolet Rays
  • beta-Cyclodextrins / chemistry

Substances

  • Azo Compounds
  • Gels
  • Sulfhydryl Compounds
  • beta-Cyclodextrins
  • Polyethylene Glycols
  • azobenzene
  • betadex