Direct UV- Induced Functionalization of Surface Hydroxy Groups by Thiol- Ol Chemistry

被引:28
|
作者
Li, Linxian [1 ,3 ]
Li, Junsheng [1 ,4 ]
Du, Xin [1 ,4 ]
Welle, Alexander [2 ]
Grunze, Michael [2 ,4 ]
Trapp, Oliver [3 ]
Levkin, Pavel A. [1 ,3 ]
机构
[1] Karlsruhe Inst Technol KIT, Inst Toxicol & Genet ITG, D-76344 Karlsruhe, Germany
[2] KIT, Inst Funct Interfaces IFG, Karlsruhe, Germany
[3] Heidelberg Univ, Dept Organ Chem, D-69115 Heidelberg, Germany
[4] Heidelberg Univ, Dept Appl Phys Chem, D-69115 Heidelberg, Germany
关键词
alcohols; photopatterning; photochemistry; surface chemistry; thiols; ENE; KINETICS; FACILE; HYDROSILYLATION; PHOTOOXIDATION; MECHANISM; POLYMERS; BINDING; OXYGEN; FILMS;
D O I
10.1002/anie.201310692
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
引用
收藏
页码:3835 / 3839
页数:5
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