## Abstract An acryloyl end-capped four-arm star-shaped poly(ethylene glycol)-branched-oligo(l-lactide) (4A-PEG-PLA) macromer was firstly prepared. A novel kind of hydrogels was synthesized via the Michael-type addition reaction between (2S,3S)-1,4-bis-sulfanylbutane-2,3-diol (dithiothreitol) and t
✦ LIBER ✦
Preparation of a Rapidly Forming Poly(ferrocenylsilane)-Poly(ethylene glycol)-based Hydrogel by a Thiol-Michael Addition Click Reaction
✍ Scribed by Xiaofeng Sui; Lennard van Ingen; Mark A. Hempenius; G. Julius Vancso
- Book ID
- 102496694
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 271 KB
- Volume
- 31
- Category
- Article
- ISSN
- 1022-1336
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✦ Synopsis
Abstract
The synthesis of a rapidly forming redox responsive poly(ferrocenylsilane)‐poly(ethylene glycol) (PFS‐PEG)‐based hydrogel is described, achieved by a thiol‐Michael addition click reaction. PFS bearing acrylate side groups (PFS‐acryl) was synthesized by side group modification of poly(ferrocenyl(3‐iodopropyl)methylsilane) (PFS‐I) and characterized by ^1^H NMR, ^13^C NMR, and FT‐IR spectroscopy. The equilibrium swelling ratio, morphology, rheology, and redox responsive properties of the PFS‐PEG‐based hydrogel are reported. magnified image
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