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) |
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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