形式
powder
质量水平
密度
1.467±0.06 g/cm3 (lit.)
SMILES字符串
C12=CC=CC(C3=C(C4=CC=C5C6=CC=C(C7=CC=C8)C9=C(C%10=C7C8=CC=C%10)C=CC%11C96)C5=C%11C=C3)=C1C4=CC=C2
InChI
1S/C40H22/c1-5-21-6-2-10-24-28-14-18-32-34-20-16-30-26-12-4-8-22-7-3-11-25(36(22)26)29-15-19-33(40(34)38(29)30)31-17-13-27(37(28)39(31)32)23(9-1)35(21)24/h1-20,31,39H
InChI key
BWASZFNXSFVOCT-UHFFFAOYSA-N
应用
A promising candidate for organic electronic applications because it absorbs a broad spectrum of UV and visible light, while possessing excellent thermal and oxidative stability and a low HOMO-LUMO band gap.
- Organic Electronics
- Photovoltaic Components
- Graphene Nanoribbons
- Electroactive Polymers
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
新产品
Ambipolar carrier transport in hetero-layered organic transistors consisting of quaterrylene and N,N'-dioctyl-3,4,9,10-perylenedicarboximide
Hiroshiba et al.
Organic Electronics, 12(8), 1336-1340 (2011)
Synthesis and Photophysics of Quaterrylene Molecules in Single-Walled Carbon Nanotubes: Excitation Energy Transfer between a Nanoscale Cylinder and Encapsulated Molecules
Koyama et al.
The Journal of Physical Chemistry C, 118(37), 21671-21681 (2014)
Rajesh Thamatam et al.
Chemical communications (Cambridge, England), 49(80), 9122-9124 (2013-09-04)
Quaterrylene is prepared in a single reaction and high yield by Scholl-type coupling of perylene, utilizing trifluoromethanesulfonic acid as catalyst and DDQ or molecular oxygen as oxidant. Dissolution in 1 M triflic acid/dichloroethane with sonication yields the aromatic quaterrylene oxidative
On the Way to Graphene: The Bottom-Up Approach to Very Large PAHs Using the Scholl Reaction
Cataldo et al.
Fullerenes, Nanotubes, and Carbon Nanostructures, 19(8), 713-725 (2011)
Exciton dynamics at the heteromolecular interface between N,N'-dioctyl-3,4,9,10-perylenedicarboximide and quaterrylene, studied using time-resolved photoluminescence
Hiroshiba et al.
AIP Advances, 4(6), 067112/1-067112/11 (2014)
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