Publication | Closed Access
Synthesis, Electrochemistry and Self-Assembled Monolayers of Novel Tetrathiafulvalene (TTF) and π-Extended TTF (<i>e</i><i>x</i>TTF) Disulfides
30
Citations
44
References
2003
Year
π-Extended TtfEngineeringSelf-assembled MonolayersExpected Thiol FormationOrganometallic ElectrochemistryOrganic ChemistryNew SeriesChemistryTheoretical ElectrochemistryExttf DerivativesOrganic ElectrochemistryMaterials ScienceNovel TetrathiafulvaleneMolecular ElectrochemistryLayered MaterialElectrochemistryFundamental ElectrochemistryMolecule-based MaterialFunctional Materials
The synthesis of a new series of tetrathiafulvalene (TTF) and pi-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.
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