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Highly Stable Si-C Linked Functionalized Monolayers on the Silicon (100) Surface

Year: 1998

Journal: Langmuir 1998, 14, 1759-1768, 20111221

Authors: A. B. Sieval, A. L. Demirel, J. W. M. Nissink, M. R. Linford, J. H. van der Maas, W. H. de Jeu, H. Zuilhof, and E. J. R. Sudhölter

Organizations: Laboratory of Organic Chemistry, Department of Biomolecular Sciences, Wageningen Agricultural University, Dreijenplein 8, 6703 HB Wageningen, The Netherlands, FOM-Institute for Atomic and Molecular Physics, Kruislaan 407, 1098 SJ Amsterdam, The Netherlands, Department of Analytical Molecular Spectrometry, Faculty of Chemistry, Utrecht University, Sorbonnelaan 16, 3584 CA Utrecht, The Netherlands, and Rohm and Haas Company, Bristol, Pennsylvania 19007

Monolayers that are bonded via a covalent Si-C bond are prepared on a silicon(100) surface by reaction of a 1-alkene with the hydrogen-terminated silicon surface. The monolayers have been analyzed by infrared spectroscopy, X-ray reflectivity, and water contact angle measurements and display a remarkably high thermal stability. The reaction also works well for w-functionalized 1-alkenes, provided that the functional group is properly protected. After formation of the monolayer, the protecting group can be easily removed without noticeable disturbance of the monolayer integrity, and the now reactive sites at the monolayer can be used for further functionalization, as has been shown in the case of ester-protected alcohol and carboxylic acids. Functional groups that are too close to the alkene moiety interfere with monolayer formation and yield disordered monolayers.