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Sigma-Aldrich

Coronene

purified by sublimation, 99%

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About This Item

Empirical Formula (Hill Notation):
C24H12
CAS Number:
191-07-1
Molecular Weight:
300.35
Beilstein:
658468
EC Number:
205-881-7
MDL number:
MFCD00004134
UNSPSC Code:
12352103
PubChem Substance ID:
24860308
NACRES:
NA.23

Quality Level

100

Assay

99%

purified by

sublimation

bp

525 °C (lit.)

mp

428 °C (lit.)

SMILES string

c1cc2ccc3ccc4ccc5ccc6ccc1c7c2c3c4c5c67

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

InChI key

VPUGDVKSAQVFFS-UHFFFAOYSA-N

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Application

An n-channel organic semiconductor.
Used to synthesize MBE-grown layered superconductors.

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
0000239164
0000267349
MKBS6209V
MKBR1597V
MKBP2016V

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Jpn J. App. Phys., Part I, 34, 3837-3845 (1995)
Hirofumi Sato et al.
Physical chemistry chemical physics : PCCP, 13(1), 309-313 (2010-11-26)
Coronene (C(24)H(12)) is a flat polyaromatic hydrocarbon consisting of seven peri-fused benzene rings and attracts lots of attention as a fragment of graphene. Using a hybrid method of quantum chemistry and statistical mechanics called RISM-SCF, which is an alternative to
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
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