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Merck
CN

R2206

Rubrene

powder

Synonym(s):

5,6,11,12-Tetraphenylnaphthacene

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About This Item

Empirical Formula (Hill Notation):
C42H28
CAS Number:
517-51-1
Molecular Weight:
532.67
UNSPSC Code:
12352103
NACRES:
NA.23
PubChem Substance ID:
24899352
EC Number:
208-242-0
Beilstein/REAXYS Number:
1917339
MDL number:
MFCD00003703

Key Documents

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InChI key

YYMBJDOZVAITBP-UHFFFAOYSA-N

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

SMILES string

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

form

powder

mp

330-335 °C (lit.)

Quality Level

100

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 %

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Related Categories

Application

Reagent for chemiluminescence research and for transition metal complex ligation.
Reagent for chemiluminescence research and for transition metal complex ligation.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
SHBT0876
SHBR5025
MKBX2009V
MKBN3145V
MKBJ5267V

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Inorganic Chemistry, 32, 1078-1078 (1993)
Motonobu Murakami et al.
The journal of physical chemistry. A, 112(4), 635-642 (2008-01-05)
The investigations were made on photoinduced electron transfer (ET) from the singlet excited state of rubrene (1RU*) to p-benzoquinone derivatives (duroquinone, 2,5-dimethyl-p-benzoquinone, p-benzoquinone, 2,5-dichloro-p-benzoquinone, and p-chloranil) in benzonitrile (PhCN) by using the steady state and time-resolved spectroscopies. The photoinduced ET
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)
Robert J Thompson et al.
Physical chemistry chemical physics : PCCP, 15(14), 5202-5207 (2013-03-05)
To address the question of surface oxidation in organic electronics the chemical composition at the surface of single crystalline rubrene is spatially profiled and analyzed using Time of Flight - Secondary Ion Mass Spectroscopy (ToF-SIMS). It is seen that a
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)
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