Abstract
The synthesis of a new series of tetrathiafulvalene (TTF) and π-extended TTF (exTTF) disulfides and the electrochemical properties of self-assembled monolayers derived from these compounds are described. When the intermediate bromides 3 and 7 were reacted with thiourea, followed by basic hydrolysis, the expected thiol formation was not observed and only disulfides were obtained. A mechanism is proposed to explain the self-oxidation process of these compounds. For the first time SAMs of exTTF derivatives were prepared. Electrochemical data for SAMs of 6 and 8 reveal a single two-electron chemically reversible oxidation process to form a dicationic state, typical of the exTTF system. The SAMs are stable over extended periods of time and show electrochemical stability upon repeated potential scans.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 8379-8385 |
| Number of pages | 7 |
| Journal | Journal of Organic Chemistry |
| Volume | 68 |
| Issue number | 22 |
| DOIs | |
| State | Published - Oct 31 2003 |
| Externally published | Yes |
All Science Journal Classification (ASJC) codes
- Organic Chemistry