TETRATHIAFULVALENE
TETRATHIAFULVALENE Basic information
- Product Name:
- TETRATHIAFULVALENE
- Synonyms:
-
- 1,3-Dithiole, 2-(1,3-dithiol-2-ylidene)-
- 1,4,5,8-Tetrathiafulvalen
- 1,4,5,8-Tetrathiafulvalene
- 2-(1,3-dithiol-2-ylidene)-1,3-dithiol
- Δ2,2μ-Bi-1,3-dithiole, TTF
- Delta2,2'-bi-1,3-dithiol
- [2,2']-Bi[1,3]-dithioylidene
- Tetrathiafulvalene, 99+% 1GR
- CAS:
- 31366-25-3
- MF:
- C6H4S4
- MW:
- 204.34
- EINECS:
- 250-593-7
- Product Categories:
-
- Functional Materials
- TTF Derivatives
- Building Blocks
- Chemical Synthesis
- Heterocyclic Building Blocks
- Materials Science
- Charge Transfer Complexes for Organic Metals
- Donors (Charge Transfer Complexes)
- Organic and Printed Electronics
- Organic Field Effect Transistor (OFET) Materials
- Others
- p-Type Organic Semiconductors
- p-Type Small Molecules
- S-Containing
- Mol File:
- 31366-25-3.mol
TETRATHIAFULVALENE Chemical Properties
- Melting point:
- 116-119 °C (lit.)
- Boiling point:
- 90℃ (1 Torr)
- Density
- 1.448 (estimate)
- refractive index
- 1.6000 (estimate)
- storage temp.
- 2-8°C
- form
- Crystals or Crystalline Powder
- color
- Orange to brownish
- Water Solubility
- It is insoluble in water. Soluble in organic solvents.
- Sensitive
- Air & Light Sensitive
- λmax
- 369nm(CHCl3)(lit.)
- Merck
- 14,9242
- BRN
- 1617956
- InChIKey
- FHCPAXDKURNIOZ-UHFFFAOYSA-N
- CAS DataBase Reference
- 31366-25-3(CAS DataBase Reference)
- EPA Substance Registry System
- 1,3-Dithiole, 2-(1,3-dithiol-2-ylidene)- (31366-25-3)
Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 43-52/53
- Safety Statements
- 36/37-61-24/25
- RIDADR
- 3335
- WGK Germany
- 3
- F
- 10-23
- TSCA
- Yes
- HS Code
- 29309090
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
TETRATHIAFULVALENE Usage And Synthesis
Chemical Properties
ORANGE TO BROWNISH CRYSTALS OR CRYSTALLINE POWDER
Uses
Electron donor for supramolecular synthesis,1 charge-transfer complex synthesis2 with 7,7,8,8-tetracyanoquinodimethane (cat. no. 157635), and for electron transfer to diazonium salts.3
Uses
Tetrathiafulvalene, holds wide application in HPLC, NMR. This heterocyclic compound contributed to the development of molecular electronics. They are used as a organic super conductors.
Uses
Molecular sensors; radical catalyst.
Definition
ChEBI: Tetrathiafulvalene is a member of the class of fulvalenes that is ethene substituted by 1,3-dithiol-2-ylidene groups at positions 1 and 2. It is an organosulfur heterocyclic compound and a member of fulvalenes.
General Description
Tetrathiafulvalene (TTF) is an electron-donor which consists of oligomers, dendrimers and polymers which can be used in the formation of redox macromolecules.
Purification Methods
Recrystallise it from cyclohexane/hexane under an argon atmosphere [Kauzlarich et al. J Am Chem Soc 109 4561 1987]. [Beilstein 19/11 V 380.]
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TETRATHIAFULVALENE(31366-25-3)Related Product Information
- TETRAKIS(OCTADECYLTHIO)TETRATHIAFULVALENE,Tetrakis(octadecylthio)tetrathiafulvalene [Organic Electronic Material]
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- BIS(CARBONYLDITHIO)TETRATHIAFULVALENE
- 4,4',5-TRIMETHYLTETRATHIAFULVALENE
- Bis(methylenedithio)tetrathiafulvalene [Organic Electronic Material],BIS(METHYLENEDITHIO)TETRATHIAFULVALENE
- TETRATHIAFULVALENE
- TRIS(TETRATHIAFULVALENE) BIS(TETRAFLUOROBORATE) COMPLEX,TETRATHIAFULVALENE FLUOROBORATE
- 4,4'-DIMETHYLTETRATHIAFULVALENE
- TPT-TTF
- TETRAKIS(METHYLTHIO)TETRATHIAFULVALENE,Tetrakis(methylthio)tetrathiafulvalene [Organic Electronic Material]
- Bis-cyclohexyl-tetrathiafulvalene,BIS-TETRAMETHYLENE-TETRATHIAFULVALENE
- 4,4'-DIMETHYL-5,5'-DIPHENYLTETRATHIAFULVALENE
- 4,4'-DI-PHENYL-TETRATHIAFULVALENE
- 2H4-Tetrathiafulvalene,TETRATHIAFULVALENE-D4
- 2,3,6,7-TETRAKIS(BENZOYLTHIO)TETRATHIAFULVALENE
- BIS(ETHYLENEDIOXY)TETRATHIAFULVALENE
- 2,3,6,7-TETRAKIS(ETHYLTHIO)TETRATHIAFULVALENE
- BIS(ETHYLENEDITHIO)TETRATHIAFULVALENE-D8