- Rubrene
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ImageFile = Rubrene.png
ImageSize =
IUPACName = 5,6,11,12-Tetraphenyltetracene
OtherNames = 5,6,11,12-Tetraphenylnaphthacene, rubrene
Section1 = Chembox Identifiers
CASNo = 517-51-1
EINECS = 208-242-0
PubChem = 68203
SMILES = c34c(c7ccccc7)c2c(c8ccccc8)c1ccccc1c(c6ccccc6)c2c(c5ccccc5)c3cccc4
Section2 = Chembox Properties
Formula = C42H28
MolarMass = 532.7 g/mol
Appearance =
Density =
MeltingPt = 315 °C
BoilingPt =
Solubility =
Section3 = Chembox Hazards
MainHazards =
FlashPt =
Autoignition =Rubrene (5,6,11,12-tetraphenylnaphthacene) is a red colored polycyclic
aromatic hydrocarbon . It has the appearance of a red crystalline powder. Rubrene is used as asensitiser inchemoluminescence . Inlightstick s it is used to produce yellow light.Rubrene is an
organic semiconductor , used in OLEDs and OLED-based displays. Single-crystaltransistors can be prepared using crystalline rubrene. Crystals of rubrene and other organic semiconductors are generally grown in a modified zone furnace on a temperature gradient, by a technique known as Physical Vapor Transport. This method was introduced in 1997 by R. A. Laudise, Christian Kloc "et al."Rubrene holds the distinction of being the highest mobility organic semiconductor, with Podzorov "et al." recording room-temperature field-effect mobilities of ~30 along the crystallographic b-axis using a novel air-gap dielectric architecture. It has also been employed to demonstrate the
Hall Effect in rubrene, cited (along with photoconductivity experiments) as evidence of diffusive, band-type transport in organic crystals.References
*cite journal | author = Darmanyan A. P. | date = August 1982 | title = Nature of lasting luminescence of rubrene in solution | journal = Russian Chemical Bulletin | volume = 31 | issue = 8 | pages = 1679–1682(4) | pmid = | doi = 10.1007/BF00956909 | url = http://www.springerlink.com/content/nwult88620538056/ | accessdate = 2007-07-05
*cite journal | author = Zhang Zhi-lin et al | date = 1998 | title = The effect of rubrene as a dopant on the efficiency and stability of organic thin film electroluminescent devices | journal = J. Phys. D: Appl. Phys. | volume = 31 | issue = 1 | pages = 32–35(4) | pmid = | doi = 10.1088/0022-3727/31/1/005 | url = http://www.iop.org/EJ/abstract/0022-3727/31/1/005 | accessdate = 2007-07-05 | format = abstract
*cite journal | author = Silva Filho D. A. da, Kim E.-G., Brédas J.-L. | date = 2005 | title = Transport Properties in the Rubrene Crystal: Electronic Coupling and Vibrational Reorganization Energy | journal = Advanced Materials | volume = 17 | issue = 8 | pages = 1072–1076(5) | pmid = | doi = 10.1002/adma.200401866 | url = http://www3.interscience.wiley.com/cgi-bin/abstract/110438510/ABSTRACT | accessdate = 2007-07-05 | format = abstract
*cite journal | url=http://www.nature.com/nature/journal/v451/n7177/full/451408a.html | title=Materials science: Lilliputian light sticks | accessdate=2008-04-15 | doi=10.1038/451408a | year=2008 | author=Fardy, Melissa | journal=Nature | volume=451 | pages=408External links
* [http://www.tnt2006.org/Abstracts/Posters/TNT2006_LuoYi.pdf AFM and SEM study of rubrene micro-crystal thin film and nanowires growth]
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