## 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 c
Synthesis and Electrochemical Studies of Tetrathiafulvalene Derivatives (TTF′S) as Redox Active Ligands.
✍ Scribed by Abd El-Wareth A. O. Sarhan; Makoto Murakami; Taeko Izumi
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 29 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0931-7597
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1997 stereochemistry stereochemistry (general, optical resolution) O 0030 ## 12 -038 Chiral Oxazolines Linked to Tetrathiafulvalene (TTF): Redox-Active Ligands for Asymmetric Synthesis. -A number of novel homochiral oxazolines appended to TTF (cf. (IV)) are synthesized and applied as secondary li
## 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