Facile and Efficient Fabrication of Photoresponsive Microgels via Thiol-Michael Addition
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 throug...
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Published in | Macromolecular rapid communications. Vol. 33; no. 22; pp. 1952 - 1957 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Weinheim
WILEY-VCH Verlag
23.11.2012
WILEY‐VCH Verlag Wiley Wiley Subscription Services, Inc |
Subjects | |
Online Access | Get full text |
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Summary: | 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 1H 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.
A light responsive microgel system based on host–guest interaction and Michael addition click reaction has been designed and synthesized under ambient conditions. The dissociation and association of β‐CD/azobene inclusion interaction could be tuned reversibly by alternative UV and visible light irradiations, which results in the reversible size control of the microgel particle. |
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Bibliography: | istex:3BD5733FDCBAECA9A4CDC7647DB411013167E739 ArticleID:MARC201200439 ark:/67375/WNG-BB6LSM38-9 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1022-1336 1521-3927 |
DOI: | 10.1002/marc.201200439 |