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Merck

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
Beilstein:
1917339
EC Number:
208-242-0
MDL number:
MFCD00003703
UNSPSC Code:
12352103
PubChem Substance ID:
24899352
NACRES:
NA.23

Key Documents

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form

powder

Quality Level

100

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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Certificates of Analysis (COA)

Lot/Batch Number
SHBR5025
MKBX2009V
MKBN3145V
MKBJ5267V
MKBF7904V

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Inorganic Chemistry, 32, 1078-1078 (1993)
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
Marina Pivetta et al.
The journal of physical chemistry. B, 113(14), 4578-4581 (2009-04-03)
The growth of rubrene (C(42)H(28), 5,6,11,12-tetraphenylnaphthacene) multilayer islands up to a thickness of six layers on a Au(111) surface has been investigated by scanning tunneling microscopy. The molecules self-organize in parallel twin rows, forming mirror domains of defined local structural
Monolithic complementary inverters based on organic single crystals.
T Uemura et al.
Advanced materials (Deerfield Beach, Fla.), 22(35), 3938-3941 (2010-08-06)
E Dubuisson et al.
Nanotechnology, 20(31), 315301-315301 (2009-07-15)
To develop highly sensitive biosensors, we made directly available to biological aqueous solutions organic nanocrystals previously grown in the pores of sol-gel films. Through the controlled dissolution of the sol-gel surface, we obtained emerging nanocrystals that remained strongly anchored to
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