• Source: Tetrathiafulvalene

Tetrathiafulvalene (TTF) is an organosulfur compound with the formula (C3H2S2)2. Studies on this heterocyclic compound contributed to the development of molecular electronics. TTF is related to the hydrocarbon fulvalene, (C5H4)2, by replacement of four CH groups with sulfur atoms. Over 10,000 scientific publications discuss TTF and its derivatives.




Preparation


The high level of interest in TTFs has spawned the development of many syntheses of TTF and its analogues. Most preparations entail the coupling of cyclic C3S2 building blocks such as 1,3-dithiole-2-thion or the related 1,3-dithiole-2-ones. For TTF itself, the synthesis begins with the cyclic trithiocarbonate H2C2S2C=S (1,3-dithiole-2-thione), which is S-methylated and then reduced to give H2C2S2CH(SCH3) (1,3-dithiole-2-yl methyl thioether), which is treated as follows:

H2C2S2CH(SCH3) + H[BF4] → [H2C2S2CH]+[BF4]− + CH3SH
2 [H2C2S2CH]+[BF4]− + 2 N(CH2CH3)3 → (H2C2S2C)2 + 2 [NH(CH2CH3)3]+[BF4]−




Redox properties


Bulk TTF itself has unremarkable electrical properties. Distinctive properties are, however, associated with salts of its oxidized derivatives, such as salts derived from TTF+.
The high electrical conductivity of TTF salts can be attributed to the following features of TTF:

its planarity, which allows π-π stacking of its oxidized derivatives,
its high symmetry, which promotes charge delocalization, thereby minimizing coulombic repulsions, and
its ability to undergo oxidation at mild potentials to give a stable radical cation. Electrochemical measurements show that TTF can be oxidized twice reversibly:
TTF → TTF+ + e− (E = 0.34 V)
TTF+ → TTF2+ + e− (E = 0.78 V, vs. Ag/AgCl in CH3CN solution)
Each dithiolylidene ring in TTF has 7π electrons: 2 for each sulfur atom, 1 for each sp2 carbon atom. Thus, oxidation converts each ring to an aromatic 6π-electron configuration, consequently leaving the central double bond essentially a single bond, as all π-electrons occupy ring orbitals.




History



The salt [TTF+]Cl− was reported to be a semiconductor in 1972. Subsequently, the charge-transfer salt [TTF]TCNQ was shown to be a narrow band gap semiconductor. X-ray diffraction studies of [TTF][TCNQ] revealed stacks of partially oxidized TTF molecules adjacent to anionic stacks of TCNQ molecules. This "segregated stack" motif was unexpected and is responsible for the distinctive electrical properties, i.e. high and anisotropic electrical conductivity. Since these early discoveries, numerous analogues of TTF have been prepared. Well studied analogues include tetramethyltetrathiafulvalene (Me4TTF), tetramethylselenafulvalenes (TMTSFs), and bis(ethylenedithio)tetrathiafulvalene (BEDT-TTF, CAS [66946-48-3]). Several tetramethyltetrathiafulvalene salts (called Fabre salts) are of some relevance as organic superconductors.




See also


Bechgaard salt




References






Further reading


Rovira, C. (2004). "Bis(ethylenethio)tetrathiafulvalene (BET-TTF) and Related Dissymmetrical Electron Donors: From the Molecule to Functional Molecular Materials and Devices (OFETs)". Chemical Reviews. 104 (11): 5289–5317. doi:10.1021/cr030663+. PMID 15535651.
Iyoda, M; Hasegawa, M; Miyake, Y (2004). "Bi-TTF, Bis-TTF, and Related TTF Oligomers". Chemical Reviews. 104 (11): 5085–5113. doi:10.1021/cr030651o. PMID 15535643.
Frere, P.; Skabara, P. J. (2005). "Salts of Extended Tetrathiafulvalene analogues: relationships Between Molecular Structure, Electrochemical Properties and Solid State Organization". Chemical Society Reviews. 34 (1): 69–98. doi:10.1039/b316392j. PMID 15643491.
Gorgues, Alain; Hudhomme, Pietrick; Salle, Marc. (2004). "Highly Functionalized Tetrathiafulvalenes: Riding along the Synthetic Trail from Electrophilic Alkynes". Chemical Reviews. 104 (11): 5151–5184. doi:10.1021/cr0306485. PMID 15535646.
Physical properties of Tetrathiafulvalene from the literature.
Segura, José L.; Martín, Nazario (2001). "New Concepts in Tetrathiafulvalene Chemistry". Angewandte Chemie International Edition. 40 (8): 1372–1409. doi:10.1002/1521-3773(20010417)40:8<1372::aid-anie1372>3.0.co;2-i. PMID 11317287.

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