Perylene

Chembox new
ImageFile = Perylene.svg
ImageSize = 114px
IUPACName = perylene
OtherNames =
Section1 = Chembox Identifiers
CASNo = 198-55-0
PubChem = 9142
InChI=1/C20H12/c1-5-13- 6-2-11-17-18-12- 4-8-14-7-3-10-16 (20(14)18)15(9-1)19 (13)17/h1-12H
SMILES = c1ccc5cccc4c5c1c2cccc3cccc4c23

Perylene or perilene is a polycyclic aromatic hydrocarbon with the chemical formula carbon₂₀hydrogen₁₂, occurring as a brown solid. It or its derivatives may be carcinogenic, and it is considered to be a hazardous pollutant. In cell membrane cytochemistry, perylene is used as a fluorescent lipid probe.

Emission

Perylene displays blue fluorescence. It is used as a blue-emitting dopant material in OLEDs, either pure or substituted. Perylene can be also used as an organic photoconductor. It has an absorption maximum at 434nm, and as with all polycyclic aromatic compounds, low water solubility (1.2 x 10-5 mmol/l). Perylene has a molar extinction coefficient of 38,500 M-1cm-1 at 435.75 nm.

tructure

The perylene molecule consists of two naphthalene molecules connected by a carbon-carbon bond at the 1 and 8 positions on both molecules. All of the carbon atoms in perylene are sp² hybridized. When drawing the structure of perylene, it is important not to represent the center ring as a fifth benzene ring. By doing so, this would cause two of the carbons to become sp³ hybridized causing part of the molecule to lose its aromaticity, and therefore its ability to fluoresce. The structure of perylene has been extensively studied by X-ray crystallography. [Donaldson, D. M.; Robertson, J. M.; White, J. G. "The crystal and molecular structure of perylene." "Proc. R. Soc. Lond. A Math. Phys. Sci." 1953, "220", 311–321. [http://links.jstor.org/sici?sici=0080-4630(19531208)220%3A1142%3C311%3ATCAMSO%3E2.0.CO%3B2-F First Page (JSTOR)] ]

References