For the initiating explosive, see tetrazene explosive.
Tetracene
Skeletal formula
Space-filling model of the tetracene molecule
Tetracene crystals
Names
Preferred IUPAC name
Tetracene[1]
Other names
Naphthacene
Benz[b]anthracene
2,3-Benzanthracene
Tetracyclo[8.8.0.03,8.012,17]octadeca-1,3,5,7,9,11,13,15,17-nonaene
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.001.945 Edit this at Wikidata
UNII
  • InChI=1S/C18H12/c1-2-6-14-10-18-12-16-8-4-3-7-15(16)11-17(18)9-13(14)5-1/h1-12H checkY
    Key: IFLREYGFSNHWGE-UHFFFAOYSA-N checkY
  • c1c2cc3cc4ccccc4cc3cc2ccc1
Properties
C18H12
Molar mass 228.29 g/mol
Appearance Yellow to orange solid
Melting point 357 °C (675 °F; 630 K)
Boiling point 436.7 °C (818.1 °F; 709.8 K)
Insoluble
-168.0·10−6 cm3/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Tetracene, also called naphthacene, is a polycyclic aromatic hydrocarbon. It has the appearance of a pale orange powder. Tetracene is the four-ringed member of the series of acenes.

Tetracene is a molecular organic semiconductor, used in organic field-effect transistors (OFETs) and organic light-emitting diodes (OLEDs). Tetracene can be used as a gain medium in dye lasers as a sensitiser in chemoluminescence. Napthacene is the main component of the tetracycline class of antibiotics.

History

German physicist Jan Hendrik Schön claimed to have developed an electrically pumped laser based on tetracene during his time at Bell Labs (1997–2002). However, his results could not be reproduced, and this is considered to be a scientific fraud.[2]

In May 2007, Japanese researchers from Tohoku University and Osaka University reported an ambipolar light-emitting transistor made of a single tetracene crystal.[3] Ambipolar means that the electric charge is transported by both positively charged holes and negatively charged electrons.

In 2024, it was used to produce lower-energy excitations in solar cells in a process known as singlet fission. An interface layer between tetracene and silicon transfers them into the silicon layer, where most of their energy can be converted into electricity.[4]

See also

Notes

References

  1. ^ International Union of Pure and Applied Chemistry (2014). Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013. The Royal Society of Chemistry. p. 208. doi:10.1039/9781849733069. ISBN 978-0-85404-182-4.
  2. ^ Agin, Dan (2007). Junk Science: An Overdue Indictment of Government, Industry, and Faith Groups That Twist Science for Their Own Gain. Macmillan. ISBN 978-0-312-37480-8.
  3. ^ T. Takahashi; T. Takenobu; J. Takeya; Y. Iwasa (2007). "Ambipolar Light-Emitting Transistors of a Tetracene Single Crystal". Advanced Functional Materials. 17 (10): 1623–1628. doi:10.1002/adfm.200700046. S2CID 135786504. Archived from the original on 2012-12-10.
  4. ^ Paderborn University (2024-03-09). "Hawk Supercomputer Improves Solar Cell Efficiency". CleanTechnica. Retrieved 2024-03-10.
source: http://en.wikipedia.org/wiki/Tetracene