Direct UV-induced functionalization of surface hydroxy groups by thiol-ol chemistry

A novel UV-initiated surface modification method for the direct functionalization of surface hydroxy groups with thiol-containing molecules (termed “thiol-ol” modification) is described. This method is based on the oxidative conjugation of thiols to hydroxy groups. We demonstrate that different thio...

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Hauptverfasser: Li, Linxian (VerfasserIn) , Li, Junsheng (VerfasserIn) , Du, Xin (VerfasserIn) , Welle, Alexander (VerfasserIn) , Grunze, Michael (VerfasserIn) , Trapp, Oliver (VerfasserIn) , Levkin, Pavel (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: March 5, 2014
In: Angewandte Chemie. International edition
Year: 2014, Jahrgang: 53, Heft: 15, Pages: 3835-3839
ISSN:1521-3773
DOI:10.1002/anie.201310692
Online-Zugang:Resolving-System, lizenzpflichtig, Volltext: https://doi.org/10.1002/anie.201310692
Verlag, lizenzpflichtig, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/anie.201310692
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Verfasserangaben:Linxian Li, Junsheng Li, Xin Du, Alexander Welle, Michael Grunze, Oliver Trapp, and Pavel A. Levkin
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Zusammenfassung:A novel UV-initiated surface modification method for the direct functionalization of surface hydroxy groups with thiol-containing molecules (termed “thiol-ol” modification) is described. This method is based on the oxidative conjugation of thiols to hydroxy groups. We demonstrate that different thiol-containing molecules, such as fluorophores, thiol-terminated poly(ethylene glycol) (PEG-SH), and a cysteine-containing peptide, can be attached onto the surface of porous poly(2-hydroxyethyl methacrylate-co-ethylene dimethacrylate). Direct functionalization of other hydroxy-group-bearing surfaces, fabrication of micropatterns, and double patterning have been also demonstrated using the thiol-ol method.
Beschreibung:Gesehen am 29.07.2020
Beschreibung:Online Resource
ISSN:1521-3773
DOI:10.1002/anie.201310692