Abstract
Self-assembled monolayers (SAMs) of large π-conjugated aromatic thiols, 1-mercaptopyrene (MP), 6-mercaptobenzo[a]pyrene (MBP), and 1-(11- mercaptoundecyl)pyrene (MUP), prepared on Au(111) substrate at different temperatures were investigated by scanning tunneling microscopy. At room temperature, only MP and MBP molecules formed well-ordered SAMs with (3√3 × 3√3)R30° and (5 × √3) Rect symmetry, respectively. In contrast, MUP molecules were adsorbed randomly on the surface. At elevated temperatures, all three molecules produce well-ordered SAMs. At 343 K, the structure of MBP remains unchanged, while MP and MUP molecules undergo thermally induced rearrangement to form a (2 × √3) Rect symmetry due to improved ordering and denser packing. The results from the systematic study of controlled self-assembly of a series of pyrene-based thiols provide insights on the molecular structure-dependent and temperature-dependent organization of large π-conjugated aromatic thiols to obtain ordered SAMs. © IOP Publishing Ltd.
| Original language | English |
|---|---|
| Article number | 135605 |
| Journal | Nanotechnology |
| Volume | 19 |
| Issue number | 13 |
| Online published | 26 Feb 2008 |
| DOIs | |
| Publication status | Published - 2 Apr 2008 |
| Externally published | Yes |
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