Postformation Modification of SAMs : using click chemistry to functionalize organic surfaces

We have investigated a recently established strategy of modifying organic surfaces exposed by thiolate SAMs (self-assembled monolayers) deposited on Au substrates by employing so-called click chemistry. This term is used to denote a modified Huisgen 1,3-dipolar cycloaddition. We demonstrate the pote...

Ausführliche Beschreibung

Bibliographische Detailangaben
Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1992. - 25(2009), 19 vom: 06. Okt., Seite 11480-5
1. Verfasser: Chelmowski, Rolf (VerfasserIn)
Weitere Verfasser: Käfer, Daniel, Köster, Stephan David, Klasen, Tim, Winkler, Tobias, Terfort, Andreas, Metzler-Nolte, Nils, Wöll, Christof
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2009
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article
LEADER 01000naa a22002652 4500
001 NLM19167740X
003 DE-627
005 20231223191638.0
007 cr uuu---uuuuu
008 231223s2009 xx |||||o 00| ||eng c
024 7 |a 10.1021/la9012813  |2 doi 
028 5 2 |a pubmed24n0639.xml 
035 |a (DE-627)NLM19167740X 
035 |a (NLM)19788212 
040 |a DE-627  |b ger  |c DE-627  |e rakwb 
041 |a eng 
100 1 |a Chelmowski, Rolf  |e verfasserin  |4 aut 
245 1 0 |a Postformation Modification of SAMs  |b using click chemistry to functionalize organic surfaces 
264 1 |c 2009 
336 |a Text  |b txt  |2 rdacontent 
337 |a ƒaComputermedien  |b c  |2 rdamedia 
338 |a ƒa Online-Ressource  |b cr  |2 rdacarrier 
500 |a Date Completed 03.12.2009 
500 |a Date Revised 30.09.2009 
500 |a published: Print 
500 |a Citation Status PubMed-not-MEDLINE 
520 |a We have investigated a recently established strategy of modifying organic surfaces exposed by thiolate SAMs (self-assembled monolayers) deposited on Au substrates by employing so-called click chemistry. This term is used to denote a modified Huisgen 1,3-dipolar cycloaddition. We demonstrate the potential of this method by coupling ferrocene and azido acetic acid to alkyne/azide-terminated SAMs. After the surface reaction, the modified organic monolayers were analyzed using infrared spectroscopy (IR), X-ray photoelectron spectroscopy (XPS), and near-edge X-ray absorption fine structure (NEXAFS) spectroscopy. Under the conditions used in this study, only for the azide-terminated SAMs could successful grafting of the ferrocene be achieved whereas for the alkyne-terminated SAMs the spectroscopic studies reveal a rather low yield of the coupling reaction 
650 4 |a Journal Article 
700 1 |a Käfer, Daniel  |e verfasserin  |4 aut 
700 1 |a Köster, Stephan David  |e verfasserin  |4 aut 
700 1 |a Klasen, Tim  |e verfasserin  |4 aut 
700 1 |a Winkler, Tobias  |e verfasserin  |4 aut 
700 1 |a Terfort, Andreas  |e verfasserin  |4 aut 
700 1 |a Metzler-Nolte, Nils  |e verfasserin  |4 aut 
700 1 |a Wöll, Christof  |e verfasserin  |4 aut 
773 0 8 |i Enthalten in  |t Langmuir : the ACS journal of surfaces and colloids  |d 1992  |g 25(2009), 19 vom: 06. Okt., Seite 11480-5  |w (DE-627)NLM098181009  |x 1520-5827  |7 nnns 
773 1 8 |g volume:25  |g year:2009  |g number:19  |g day:06  |g month:10  |g pages:11480-5 
856 4 0 |u http://dx.doi.org/10.1021/la9012813  |3 Volltext 
912 |a GBV_USEFLAG_A 
912 |a SYSFLAG_A 
912 |a GBV_NLM 
912 |a GBV_ILN_22 
912 |a GBV_ILN_350 
912 |a GBV_ILN_721 
951 |a AR 
952 |d 25  |j 2009  |e 19  |b 06  |c 10  |h 11480-5