Single-Molecule AFM Study of Polystyrene Grafted at Gold Surfaces
Source abstract
Abstract
ABSTRACT Single-molecule studies under poor solvent conditions show that atomic force microscopy (AFM) measurements of contour lengths of polystyrene 12K and 17K relate well to gel permeation chromatography (GPC) data when grafting concentrations are low (not greater than 0.7 mM). Contact angles and ellipsometry have been used to characterize the surfaces and indicate low grafting densities at this grafting concentration. Persistence lengths (p) of different length polystyrene chains, when fitted to a WLC (worm-like chain) model, show values of p = 0.23 nm±0.10 nm and p = 0.25 nm±0.13 nm, for 12 K and 17 K polystyrene, respectively, when the persistence lengths are fitted to log-normal distributions. These values are close to the expected theoretical value of 0.23 nm and further confirm that mostly single molecules were studied on these polystyrene surfaces. Higher grafting concentrations (≥1 mM) resulted in pulling multiple molecules.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Molecular Junctions and Nanostructures · Force Microscopy Techniques and Applications · Polymer Surface Interaction Studies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (31)
Show source-provided references
1. Bemis J. E. · Langmuir · 1999 · 15 · 279910.1021/la980853t ↗
2. Desai N. P. · Biomaterials · 1991 · 12 · 14410.1016/0142-9612(91)90193-E ↗
3. Jones R. A. L. · 199910.1017/CBO9780511623196 ↗
4. Lin Y. · Nature · 2005 · 434 · 5510.1038/nature03310 ↗
5. Ulman A. · 1991
6. Al-Maawali S. · J. Phys. Chem. B · 2001 · 105 · 396510.1021/jp0037246 ↗
7. Nuzzo R. G. · J. Am. Chem. Soc. · 1987 · 109 · 235810.1021/ja00242a020 ↗
8. Bain C. D. · J. Am. Chem. Soc. · 1989 · 111 · 32110.1021/ja00183a049 ↗
9. Horton R. C. · J. Am. Chem. Soc. · 1997 · 119 · 1298010.1021/ja971329w ↗
10. Schwartz D. K. · Ann. Rev. Phys. Chem. · 2001 · 52 · 10710.1146/annurev.physchem.52.1.107 ↗
11. Ferry J. D. · 1970
12. Brandrup J. · 1989
13. Liu H. · Langmuir · 2003 · 19 · 237810.1021/la026378n ↗
14. Vercruyse K. · Eur. J. Org. Chem. · 2000 · 2 · 28110.1002/(SICI)1099-0690(200001)2000:2<281::AID-EJOC281>3.0.CO;2-2 ↗
15. Pandey P. C. · Biosen. Biotech. · 1995 · 10 · 669
16. Luo H. · Appl. Phys. Lett. · 1998 · 72 · 47710.1063/1.120791 ↗
17. Weisenhorn A. L. · Appl. Phys. Lett. · 1989 · 54 · 265110.1063/1.101024 ↗
18. Azzam R. M. A. · 1977
19. Wasserman S. R. · J. Am. Chem. Soc. · 1989 · 111 · 585210.1021/ja00197a054 ↗
20. Tompkins H. G. · 1993
21. Israelachvilli J. · 1992
22. Shastry M. · Bull. Mat. Science · 2000 · 23 · 15910.1007/BF02719902 ↗
23. Cuypers P. A. · Anal. Biochem. · 1978 · 84 · 5610.1016/0003-2697(78)90483-9 ↗
24. Udaya S. T. · European Poly. J. · 2001 · 37 · 113310.1016/S0014-3057(00)00231-7 ↗
25. Koutsos V. · Macromolecules · 1997 · 30 · 471910.1021/ma961625d ↗
26. Hadziioannou G. · Macromolecules · 1999 · 32 · 78010.1021/ma981245n ↗
27. Li H. · Adv. Mater. · 1998 · 3 · 31610.1002/(SICI)1521-4095(199803)10:4<316::AID-ADMA316>3.0.CO;2-A ↗
28. Flory P. J. · 1992
29. Grandbois M. · Science · 1999 · 283 · 172710.1126/science.283.5408.1727 ↗
30. Gardon J. L. · J. Phys. Chem. · 1963 · 67 · 193510.1021/j100803a515 ↗
31. Penn L. S. · Macromolecules · 2002 · 35 · 705410.1021/ma020618o ↗