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R2206

Sigma-Aldrich

Rubrene

powder

Synonym(s):

5,6,11,12-Tetraphenylnaphthacene

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1 G
R$783.00

About This Item

Empirical Formula (Hill Notation):
C42H28
CAS Number:
Molecular Weight:
532.67
Beilstein:
1917339
EC Number:
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.23

R$783.00


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form

powder

Quality Level

mp

330-335 °C (lit.)

λmax

299 nm

OLED Device Performance

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 %

SMILES string

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

InChI key

YYMBJDOZVAITBP-UHFFFAOYSA-N

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Application

Reagent for chemiluminescence research and for transition metal complex ligation.
Reagent for chemiluminescence research[1] and for transition metal complex ligation.[2]

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Inorganic Chemistry, 32, 1078-1078 (1993)
Thorsten Vehoff et al.
Journal of the American Chemical Society, 132(33), 11702-11708 (2010-07-30)
We analyze the relationship among the molecular structure, morphology, percolation network, and charge carrier mobility in four organic crystals: rubrene, indolo[2,3-b]carbazole with CH(3) side chains, and benzo[1,2-b:4,5-b']bis[b]benzothiophene derivatives with and without C(4)H(9) side chains. Morphologies are generated using an all-atom
Surface potential mapping of SAM-functionalized organic semiconductors by Kelvin probe force microscopy.
David J Ellison et al.
Advanced materials (Deerfield Beach, Fla.), 23(4), 502-507 (2011-01-22)
Steffen Duhm et al.
Advanced materials (Deerfield Beach, Fla.), 24(7), 901-905 (2012-03-10)
The hole–phonon coupling of a rubrene monolayer on graphite is measured by means of angle resolved ultraviolet photoelectron spectroscopy. Thus, the charge reorganization energy λ and the small polaron binding energy is determined, which allows insight into the nature of
Organic metal-semiconductor field-effect transistor (OMESFET) fabricated on a rubrene single crystal.
Daniele Braga et al.
Advanced materials (Deerfield Beach, Fla.), 22(3), 424-428 (2010-03-11)

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