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Dibenzotetrathiafulvalene

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Dibenzotetrathiafulvalene Basic information

Product Name:
Dibenzotetrathiafulvalene
Synonyms:
  • Δ2,2'-Bi[4,5-[1,3]butadieno-1,3-dithiol]
  • Dibenzotetrathiafulvalene 97%
  • DBTTF
  • 1,3-Benzodithiole,2-(1,3-benzodithiol-2-ylidene)-
  • [2,2]Bi[benzo[1,3]dithiolylidene], DB-TTF
  • Dibenzotetrathiafulvalene
  • Δ2,2'-Bi(1,3-benzodithiol)
  • Δ2,2'-Bi[1,3-benzodithiole]
CAS:
24648-13-3
MF:
C14H8S4
MW:
304.47
Mol File:
24648-13-3.mol
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Dibenzotetrathiafulvalene Chemical Properties

Melting point:
239-243 °C
Boiling point:
367.1±42.0 °C(Predicted)
Density 
1.538±0.06 g/cm3(Predicted)
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Safety Information

Hazard Codes 
N
Risk Statements 
50/53
Safety Statements 
60-61
RIDADR 
UN 3077 9/PG 3
WGK Germany 
3
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Dibenzotetrathiafulvalene Usage And Synthesis

Uses

Dibenzotetrathiafulvalene(DBTTF, also known as 1,3-Benzodithiole,2-(1,3-benzodithiol-2-ylidene)-) is an organic electronic material that can be used to form semiconductor charge transfer salts with electron accepting (n-type) materials (TCNQ and F4TCNQ). It can also be used to form charge transfer complexes (TCNQ and DDQ) with a variety of semiconductor crystals for the manufacture of organic field effect transistors (OFETs) and organic light emitting diodes (OLEDs).

Synthesis

Dibenzotetrathiafulvalene was prepared from 2,2'-Bi-1,3-benzodithiol under reaction conditions with  2,3-dicyano-5,6-dichloro-p-benzoquinone and dichloromethane. The specific method of operation is described below:
General procedure: Dithioacetal (0.1 mmol) and DDQ (68 mg, 0.30 mol) were dissolved in CH2Cl2 (3 mL). The resultant dark blue mixture was stirred at room temperature for 16 h and was then washed with a saturated NaOH aqueous solution (2 mL) and CH2Cl2 (10 mL). The orange organic phase was dried over anhydrous Na2SO4, filtered, and then evaporated under reduced pressure. The crude solid was recrystallized from hexane to give the corresponding dibenzotetrathiafulvalene derivative. Dibenzotetrathiafulvalene. Yield: 30 mg (99%); orange solid; mp 239.8-243.0 °C. 1H NMR (500 MHz, CDCl3): δ = 7.27-7.24 (m, 4 H), 7.13-7.10 (m, 4 H). 13C NMR (125 MHz, CDCl3): δ = 136.6, 125.9, 121.9, 110.6. MS (FAB): m/z = 304 [M+]. HRMS (FAB): m/z calcd for [M]+ (C14H8S4): 303.9509; found: 303.9519.

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