journal article·2010-10-27

Surface Modifications Using a Water-Stable Silanetriol in Neutral Aqueous Media

Stefan Spirk, Heike M. Ehmann, Rupert Kargl, Natascha Hurkes, Martin Reischl, Jiri Novak, Roland Resel, Ming Wu, Rudolf Pietschnig, Volker Ribitsch

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Abstract

Surface modifications of glass slides employing the sterically hindered tert-butyl substituted silanetriol are described. To the best of our knowledge, this is the first time that a stable silanetriol has been directly used for this purpose. So far unprecedented, this process runs under neutral aqueous conditions and in the absence of organic solvents, which makes coating protocols accessible to acid-sensitive substrates. The layer thickness and surface topography are investigated by the Sarfus technique, by X-ray reflectivity, and by atomic force microscopy (AFM). These techniques yield values of 0.8±0.1 (XRR) and 0.6±0.2 nm (Sarfus) for layer thickness and 0.33 nm for root mean square roughness (AFM). The modified surfaces have hydrophobic and oleophilic character and contact angles (CA) between 60° (formamide, CH2I2) and 90° (water) are obtained. The thin coatings allow a structuring by UV/ozone treatment in order to get hydrophilic and hydrophobic compartments on the surfaces. For all coatings, surface free energies are calculated using different models. To determine the isoelectric points (IEP) of the modified surfaces, we performed zeta-potential measurements. Correlations between zeta potentials and hydrophilicity of the surfaces are shown.
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Research context

OpenAlex topics: Surface Modification and Superhydrophobicity · Advanced Sensor and Energy Harvesting Materials · Gas Sensing Nanomaterials and Sensors

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Institut für Chemie, Karl-Franzens-Universität Graz, Heinrichstrasse 28/IV, 8010 Graz, Austria, Department of Chemical Technology of Materials, Graz University of Technology, Stremayrgasse 9, 8010 Graz, Austria, and Institute of Solid State Physics, Graz University of Technology, Petersgasse 16, 8010 Graz, Austria

References (48)

Show source-provided references
1. Takiguchi T. · J. Am. Chem. Soc. · 1959 · 81 · 235910.1021/ja01519a021 ↗
2. Buttrus N. H. · J. Chem. Soc., Chem. Commun. · 1985 · 138510.1039/c39850001385 ↗
3. Al-Juaid S. S. · J. Organomet. Chem. · 1989 · 371 · 28710.1016/0022-328X(89)85224-6 ↗
4. Winkhofer N. · Angew. Chem. · 1992 · 104 · 67010.1002/ange.19921040545 ↗
5. Murugavel R. · Organometallics · 1995 · 14 · 529810.1021/om00011a054 ↗
6. Jutzi P. · Organometallics · 1996 · 15 · 284210.1021/om9509756 ↗
7. Murugavel R. · Acc. Chem. Res. · 1996 · 29 · 18310.1021/ar950154x ↗
8. Jutzi P. · Organometallics · 1997 · 16 · 537710.1021/om970613t ↗
9. Kornev A. N. · Russ. Chem. Bull. · 1999 · 48 · 156310.1007/BF02496413 ↗
10. Schneider M. · Monatsh. Chem. · 1999 · 130 · 33
11. Cerveau G. · Angew. Chem. (Int. Ed.) · 2000 · 39 · 453310.1002/1521-3773(20001215)39:24<4533::AID-ANIE4533>3.0.CO;2-8 ↗
12. Pietschnig R. · Organometallics · 2004 · 23 · 489710.1021/om049410c ↗
13. Prabusankar G. · Organometallics · 2004 · 23 · 230510.1021/om0499299 ↗
14. Kim J. H. · J. Organomet. Chem. · 2005 · 690 · 137210.1016/j.jorganchem.2004.12.012 ↗
15. Spirk S. · Z. Anorg. Allg. Chem. · 2009 · 635 · 104810.1002/zaac.200801270 ↗
16. Unno M. · J. Organomet. Chem. · 2003 · 686 · 17510.1016/S0022-328X(03)00541-2 ↗
17. Pietschnig R. · Inorg. Chim. Acta · 2005 · 358 · 44410.1016/j.ica.2004.09.018 ↗
18. Lickiss P. D. · Adv. Inorg. Chem. · 1995 · 42 · 14710.1016/S0898-8838(08)60053-7 ↗
19. Lickiss P. D. · 2001
20. Unno M. · Organometallics · 1996 · 15 · 241310.1021/om950737a ↗
21. Spirk S. · Dalton. Trans. · 2009 · 16310.1039/B812974F ↗
22. Lickiss P. D. · J. Chem. Soc., Chem. Commun. · 1991 · 17310.1039/c39910000173 ↗
23. Suzuki J. · Chem.—Eur. J. · 2008 · 14 · 97310.1002/chem.200700914 ↗
24. Corriu R. J. P. · 2001
25. Avnir D. · 2001
26. Solomun T. · ACS Appl. Mater. Interfaces · 2010 · 2 · 217110.1021/am100263t ↗
27. Yang S. · ACS Appl. Mater. Interfaces · 2009 · 1 · 158510.1021/am900252v ↗
28. Koehler S. · J. Polym. Sci., Polym. Chem. · 2008 · 46 · 407010.1002/pola.22749 ↗
29. Kontturi E. · Langmuir · 2003 · 19 · 573510.1021/la0340394 ↗
30. van Oss C. J. · Chem. Rev. · 1988 · 88 · 92710.1021/cr00088a006 ↗
31. van Oss C. J. · 1994
32. Sauerbrey G. · Z. Phys. · 1959 · 155 · 20610.1007/BF01337937 ↗
33. Reischl M. · Rev. Sci. Instrum. · 2008 · 79 · 11390210.1063/1.3020699 ↗
34. Smoluchowski M. · 1921
35. Björck M. · J. Appl. Cryst. · 2007 · 40 · 117410.1107/S0021889807045086 ↗
36. Parratt L. G. · Phys. Rev. · 1954 · 95 · 35910.1103/PhysRev.95.359 ↗
37. Névot L. · Rev. Phys. Appl. · 1980 · 15 · 76110.1051/rphysap:01980001503076100 ↗
38. Ausserre D. · Nano Lett. · 2006 · 6 · 138410.1021/nl060353h ↗
39. Horcas I. · Rev. Sci. Instrum. · 2007 · 78 · 01370510.1063/1.2432410 ↗
40. Owens D. K. · J. Appl. Polym. Sci. · 1969 · 13 · 174110.1002/app.1969.070130815 ↗
41. Kaelble D. H. · J. Adhes. · 1970 · 2 · 5010.1080/0021846708544579 ↗
42. Rabel W. · Farbe Lack · 1971 · 77 · 997
43. Wu S. · 1982
44. Brook M. A. · 2000
45. Marx K. A. · Biomacromolecules · 2003 · 4 · 109910.1021/bm020116i ↗
46. The theoretical mass of a monolayer consisting of silanetriol1was calculated to be 251 ng/cm2on the basis of the structure obtained in single-crystal X-Ray diffraction.
47. Pietsch U. · 200410.1007/978-1-4757-4050-9 ↗
48. Schaub M. · Adv. Mater. · 1993 · 5 · 91910.1002/adma.19930051209 ↗