Synthesis and electrochemical studies of tetrathiafulvalene derivatives (TTFs) as redox active ligands
✍ Scribed by Abd El-Wareth A. O. Sarhan; Makoto Murakami; Taeko Izumi
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2002
- Tongue
- English
- Weight
- 56 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0022-152X
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✦ Synopsis
Abstract
A simple route for synthesis of new tetrathiafulvalene dimethyl ester (TTF‐DME) is reported. The tetrathifulvalene dimethylester (TTF‐DME) has been prepared by introducing an ester coordination function as a bifunctional new donor. The redox behavior of the TTF‐DME was investigated in comparison to the well‐known dibenzotetrathiafulvene (DB‐TTF) by cyclic voltammetry. A two‐electron redox behavior was observed as a two waves.
📜 SIMILAR VOLUMES
## Abstract The synthesis of the new ligand, BEDT‐TTF‐bipy [4,5‐ethylenedithio‐4′,5′‐(4′‐methyl‐2,2′‐dipyrid‐4‐ylethylenedithio)tetrathiafulvalene] is reported. The first Fe^II^ coordination complex, namely [Fe(NCS)~2~(BEDT‐TTF‐bipy)~2~]**·**CHCl~3~, with this redox‐active ligand is obtained. Magne
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