Covalent biofunctionalization of silicon nitride surfaces

Covalently attached organic monolayers on etched silicon nitride (SixN4; x >/= 3) surfaces were prepared by reaction of SixN4-coated wafers with neat or solutions of 1-alkenes and 1-alkynes in refluxing mesitylene. The surface modification was monitored by measurement of the static water contact...

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Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1992. - 23(2007), 11 vom: 22. Mai, Seite 6233-44
1. Verfasser: Arafat, Ahmed (VerfasserIn)
Weitere Verfasser: Giesbers, Marcel, Rosso, Michel, Sudhölter, Ernst J R, Schroën, Karin, White, Richard G, Yang, Li, Linford, Matthew R, Zuilhof, Han
Format: Aufsatz
Sprache:English
Veröffentlicht: 2007
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Coated Materials, Biocompatible Oligopeptides Proteins Silicon Compounds silicon nitride QHB8T06IDK
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245 1 0 |a Covalent biofunctionalization of silicon nitride surfaces 
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520 |a Covalently attached organic monolayers on etched silicon nitride (SixN4; x >/= 3) surfaces were prepared by reaction of SixN4-coated wafers with neat or solutions of 1-alkenes and 1-alkynes in refluxing mesitylene. The surface modification was monitored by measurement of the static water contact angle, XPS, IRRAS, AFM, and ToF-SIMS, and evidence for the formation of Si-C bonds is presented. The etching can be achieved by dilute HF solutions and yields both Si-H and N-H moieties. The resulting etched SixN4 surfaces are functionalized by terminal carboxylic acid groups in either of two ways: (a) via attachment of a 10-undecenoic acid 2,2,2-trifluoroethyl ester (trifluoro ethanol ester) and subsequent thermal acid hydrolysis; (b) through attachment of a photocleavable ester, and subsequent photochemical cleavage, as this would allow photopatterned functionalized SixN4. The carboxylic acids are successfully used for the attachment of oligopeptides (aspartame) and complete proteins using EDC/NHS chemistry. Finally, an amino-terminated organic monolayer can be formed by reaction of HF-treated SixN4 surfaces with a N-(omega-undecylenyl)phthalimide, which yields an amino-terminated surface upon deprotection with hydrazine 
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650 4 |a Research Support, Non-U.S. Gov't 
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650 7 |a Silicon Compounds  |2 NLM 
650 7 |a silicon nitride  |2 NLM 
650 7 |a QHB8T06IDK  |2 NLM 
700 1 |a Giesbers, Marcel  |e verfasserin  |4 aut 
700 1 |a Rosso, Michel  |e verfasserin  |4 aut 
700 1 |a Sudhölter, Ernst J R  |e verfasserin  |4 aut 
700 1 |a Schroën, Karin  |e verfasserin  |4 aut 
700 1 |a White, Richard G  |e verfasserin  |4 aut 
700 1 |a Yang, Li  |e verfasserin  |4 aut 
700 1 |a Linford, Matthew R  |e verfasserin  |4 aut 
700 1 |a Zuilhof, Han  |e verfasserin  |4 aut 
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