Self-Assembled Monolayers of Aromatic ω-Aminothiols on Gold: Surface Chemistry and Reactivity

被引:18
作者
Dietrich, Paul M. [2 ]
Graf, Nora [2 ]
Gross, Thomas [2 ]
Lippitz, Andreas [2 ]
Schuepbach, Bjoern [1 ]
Bashir, Asif [4 ]
Woell, Christof [3 ]
Terfort, Andreas [1 ]
Unger, Wolfgang E. S. [2 ]
机构
[1] Goethe Univ Frankfurt, Inst Anorgan & Analyt Chem, D-60438 Frankfurt, Germany
[2] BAM Bundesanstalt Mat Forsch & Prufung, D-12203 Berlin, Germany
[3] Ruhr Univ Bochum, Lehrstuhl Phys Chem 1, D-44780 Bochum, Germany
[4] Max Planck Inst Eisenforsch GmbH, D-40237 Dusseldorf, Germany
关键词
RAY PHOTOELECTRON-SPECTROSCOPY; BIPHENYL-BASED THIOLS; X-RAY; ELECTRONIC-STRUCTURE; SULFUR; 2P; IMMOBILIZATION; MOLECULES; AU(111); SPECTRA; PHOTOEMISSION;
D O I
10.1021/la903293b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Amino-terminated self-assembled monolayers on gold substrates were studied by X-ray photoelectron spectroscopy (XPS), near-edge X-ray absorption Fine structure (NEXAFS) measurements,and atomic force microscopy (AFM). Two different omega-amino-4,4'-terphenyl substituted alkanethiols of the general structure H2N-(C6H4)(3)-(CH2)(n)-SH (ATPn) were used: 2-(4 ''-amino-1,1':4',1 ''-terphenyl-4-yl)ethane-1-thiol (n = 2, ATP2) and 3-(4 ''-amino-1,1':4',1 ''-terphenyl-4yl)propane-1-thiol (n = 3, ATP3). Moreover, the addressability of amino groups within the films was investigated by chemical derivatization of ATPn SAMs with 3,5-bis(trifluoromethyl) phenyl isothiocyanate (ITC) forming fluorinated thiourea ATPn-F Films. Evaluation of high-resolution C Is and N Is XPS data revealed successful derivatization of at least 50% of surface amino species. Furthermore, it could be demonstrated by angle-resolved NEXAFS spectroscopy that chemical derivatization with ITC has no noticeable influence on the preferential upright orientation of the molecules in the SAMs.
引用
收藏
页码:3949 / 3954
页数:6
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