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551112

Sigma-Aldrich

Rubrene

sublimed grade, 99.99% trace metals basis

Synonyme(s) :

5,6,11,12-Tetraphenylnaphthacene

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About This Item

Formule empirique (notation de Hill):
C42H28
Numéro CAS:
517-51-1
Poids moléculaire :
532.67
Numéro Beilstein :
1917339
Numéro CE :
208-242-0
Numéro MDL:
MFCD00003703
Code UNSPSC :
12352103
ID de substance PubChem :
24879199
Nomenclature NACRES :
NA.23

Qualité

sublimed grade

Niveau de qualité

100

Pureté

99.99% trace metals basis

Pf

330-335 °C (lit.)

λmax

299 nm
299 nm

Fluorescence

λem 550 nm in THF

Énergie orbitale

HOMO 5.4 eV 
LUMO 3.2 eV 

Performance des dispositifs OLED

ITO/CuPc/NPD/Alq3:Rubrene (5%): DCM2 (2%)/Alq3/Mg:In

  • Color: red
  • Max. Luminance: 7780 Cd/m2

ITO/PEDOT:PSS/EHCz:Rubrene (1 wt%)/Cs2CO3:ITO
  • Color: red
  • Max. EQE: 0.03 %

Chaîne SMILES 

c1ccc(cc1)-c2c3ccccc3c(-c4ccccc4)c5c(-c6ccccc6)c7ccccc7c(-c8ccccc8)c25

InChI

1S/C42H28/c1-5-17-29(18-6-1)37-33-25-13-14-26-34(33)39(31-21-9-3-10-22-31)42-40(32-23-11-4-12-24-32)36-28-16-15-27-35(36)38(41(37)42)30-19-7-2-8-20-30/h1-28H

Clé InChI

YYMBJDOZVAITBP-UHFFFAOYSA-N

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Description générale

TGA/DSC Lot specific traces available upon request

Application

Organic electronic material useful as OLED dopant (red, λem = 550nm) and as p-type organic semiconductor. Carrier mobilities of 8-20 cm2/ Vs can be achieved in OFETs based on single crystals of sublimed rubrene.
Reagent for chemiluminescence research and for transition metal complex ligation.

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)

Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

Alexander S Bieber et al.
The Journal of chemical physics, 153(8), 084703-084703 (2020-09-03)
Triplet-triplet annihilation-based photon upconversion (UC) using bulk perovskite sensitizers has been previously shown to facilitate efficient UC at low fluences. However, the fabrication of the UC devices has not been fully optimized; thus, there is room for improvement. Here, we
N R Armstrong et al.
Annual review of physical chemistry, 52, 391-422 (2001-04-28)
Electrochemical processes leading to light emission are reviewed, with emphasis on aspects of this subject relevant to the understanding and optimization of electrogenerated luminescence (EL) in organic thin-film materials. The basic energetic requirements of light emission from electrochemically initiated solution
Morpurgo, A. F. et al.
Physica Status Solidi (A): Applied Research, 201, 1302-1302 (2004)
V Podzorov et al.
Physical review letters, 95(22), 226601-226601 (2005-12-31)
We have observed the Hall effect in the field-induced accumulation layer on the surface of single-crystal samples of a small-molecule organic semiconductor rubrene. The Hall mobility muH increases with decreasing temperature in both the intrinsic (high-temperature) and trap-dominated (low-temperature) conduction
Rui M Pinto et al.
Journal of the American Chemical Society, 137(22), 7104-7110 (2015-05-21)
Exciton diffusion is at the heart of most organic optoelectronic devices' operation, and it is currently the most limiting factor to their achieving high efficiency. It is deeply related to molecular organization, as it depends on intermolecular distances and orbital
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