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| Description | Tetrathiafulvalene (TTF) is an electron-donor which consists of oligomers, dendrimers and polymers which can be used in the formation of redox macromolecules. |
|---|---|
| IUPAC Name | 2-(1,3-dithiol-2-ylidene)-1,3-dithiole |
| Molecular Weight | 204.36 |
| Molecular Formula | C6H4S4 |
| Canonical SMILES | S1C=CS\C1=C2/SC=CS2 |
| InChI | 1S/C6H4S4/c1-2-8-5(7-1)6-9-3-4-10-6/h1-4H,FHCPAXDKURNIOZ-UHFFFAOYSA-N |
| InChI Key | FHCPAXDKURNIOZ-UHFFFAOYSA-N |
| Melting Point | 116-119 °C (lit.) |
| Application | TTF may be linked with lithium chloride (LiCl) to form a precipitated layer on the lithium oxide (Li2O2) for the fabrication of high performance Li-O2 batteries. Bio-sourced carbon nanodots can be surface modified by TTF which can be potentially used for electrochemical applications. |
| Storage | room temp |
| Assay | 0.97 |
| BeilsteinREAXYS Number | 1617956 |
| EC Number | 250-593-7 |
| MDL Number | MFCD00005492 |
| Packaging | 1 g in glass bottle |
| Quality Level | 200 |
