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经验公式(希尔记法):
C42H28
化学文摘社编号:
分子量:
532.67
UNSPSC Code:
12352103
NACRES:
NA.23
PubChem Substance ID:
EC Number:
208-242-0
Beilstein/REAXYS Number:
1917339
MDL number:
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
λmax
299 nm
OLED device performance
ITO/CuPc/NPD/Alq3:Rubrene (5%): DCM2 (2%)/Alq3/Mg:In
, ITO/PEDOT:PSS/EHCz:Rubrene (1 wt%)/Cs2CO3:ITO
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Application
用于化学发光研究和过渡金属络合物形成的试剂。
用于化学发光研究和过渡金属络合物形成的试剂。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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
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
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
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
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