| Title | The Formation and Stability of Alkylthiol Monolayers on Carbon Substrates. |
| Publication Type | Journal Article |
| Year of Publication | 2010 |
| Authors | Lockett, MR, Smith, LM |
| Journal | J Phys Chem C Nanomater Interfaces |
| Volume | 114 |
| Issue | 29 |
| Pagination | 12635-12641 |
| Date Published | 2010 Jul 7 |
| ISSN | 1932-7455 |
| Abstract | The formation and stability of alkylthiol monolayers on amorphous carbon thin films are investigated. Alkylthiol monolayers were prepared via a two-step, wet chemical process in which the carbon surface was first halogenated and then incubated with (4-(trifluoromethyl)phenyl)methanethiol (4tBM). The 4tBM covalently attaches to the surface in a substitution reaction in which the 4tBM thiol replaces the surface halogen. Studies of the substitution mechanism showed that monolayer formation is affected by the nature of the surface-bound halogen as well as the concentration and nucleophilicity of the 4tBM sulfur atom, consistent with a bimolecular (S(N)2) substitution reaction mechanism. The alkylthiol monolayers are stable over a wide range of solvent, pH, and temperature conditions. |
| DOI | 10.1021/jp102821x |
| Custom 1 | |
| Alternate Journal | J Phys Chem C Nanomater Interfaces |
| PubMed ID | 20706614 |