Iron Tris(bipyridine) PEG Hydrogels with Covalent and Metal Coordinate Cross-Links

Spontaneous gel formation of iron(II) tris(bipyridine)-centered poly(ethylene glycol) methacrylate ([Fe{bpy(PEG-MA)2}3]2+) was observed without the addition of a cross-linking agent. BpyPEG2 macroligands were first modified with methacrylate groups using methacrylic anhydride and then combined with...

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Veröffentlicht in:Biomacromolecules 2009-01, Vol.10 (1), p.128-133
Hauptverfasser: Fiore, Gina L, Klinkenberg, Jessica L, Pfister, Anne, Fraser, Cassandra L
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Sprache:eng
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Zusammenfassung:Spontaneous gel formation of iron(II) tris(bipyridine)-centered poly(ethylene glycol) methacrylate ([Fe{bpy(PEG-MA)2}3]2+) was observed without the addition of a cross-linking agent. BpyPEG2 macroligands were first modified with methacrylate groups using methacrylic anhydride and then combined with FeSO4 to produce [Fe{bpy(PEG-MA)2}3]SO4. End group analysis by 1H NMR spectroscopy verified quantitative methacrylation of the PEG hydroxyl chain ends. A series of experiments and control reactions were performed to investigate the conditions required for gel formation. Hydrogels of [Fe{bpy(PEG-MA)2}3]SO4 were produced both in the presence and in the absence of a photoinitiator. Controls using MA-PEG-MA also formed hydrogels in the presence of [Fe(bpy)3]2+; however, the addition of a radical scavenger, TEMPO, prevented formation of a polymer network, suggesting radical involvement. Treatment of preformed hydrogels of bpy(PEG-MA)2 with aqueous solutions of FeSO4, CuBr2, and CoCl2 also produced materials with color changes indicative of complexation.
ISSN:1525-7797
1526-4602
DOI:10.1021/bm800998g