335355
Coronene
purified by sublimation, 99%
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About This Item
Empirical Formula (Hill Notation):
C24H12
CAS Number:
Molecular Weight:
300.35
UNSPSC Code:
12352103
NACRES:
NA.23
PubChem Substance ID:
EC Number:
205-881-7
Beilstein/REAXYS Number:
658468
MDL number:
Product Name
Coronene, purified by sublimation, 99%
InChI key
VPUGDVKSAQVFFS-UHFFFAOYSA-N
InChI
1S/C24H12/c1-2-14-5-6-16-9-11-18-12-10-17-8-7-15-4-3-13(1)19-20(14)22(16)24(18)23(17)21(15)19/h1-12H
SMILES string
c1cc2ccc3ccc4ccc5ccc6ccc1c7c2c3c4c5c67
assay
99%
purified by
sublimation
bp
525 °C (lit.)
mp
428 °C (lit.)
Quality Level
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Related Categories
Application
An n-channel organic semiconductor.
Used to synthesize MBE-grown layered superconductors.
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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Jpn J. App. Phys., Part I, 34, 3837-3845 (1995)
Long Chen et al.
Journal of the American Chemical Society, 134(43), 17869-17872 (2012-10-16)
Here we report hexathienocoronenes (HTCs), fully thiophene-annelated coronenes in which six double bonds in the periphery are thieno-fused. The derivatives tetrasubstituted with hexyl and dodecyl chains show a phase formation that strongly depends on the chain length. HTCs are remarkably
Anna M Hiszpanski et al.
ACS nano, 7(1), 294-300 (2012-12-12)
The structuring in organic electrically active thin films critically influences the performance of devices comprising them. Controlling film structure, however, remains challenging and generally requires stringent deposition conditions or modification of the substrate. To this end, we have developed post-deposition
Seok Ju Kang et al.
Angewandte Chemie (International ed. in English), 51(34), 8594-8597 (2012-07-19)
"Ball and socket" motif: The contorted dibenzotetrathienocoronene (6-DBTTC) forms a complex with the C(70) fullerene PC(70) BM embedded in an amorphous phase of PC(70) BM. The materials are processable into organic solar cells in solution. The power conversion efficiency is
Di Wu et al.
The Journal of organic chemistry, 77(24), 11319-11324 (2012-11-29)
The construction of coronenes using simple building blocks is a challenging task. In this work, triphenylene was used as a building block to construct functionalized coronenes, and their solid structures and optoelectronic properties were investigated. The single crystal structures showed
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