| Weight | 228.294 g/mol |
|---|---|
| Formula | C18H12 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 4 |
| Rotatable Bonds | 0 |
Naphthacene (92-24-0)
tetracene · rubene · 2,3-benzanthrene
Score:
#1969 in Physics
,
#6152 in Chemistry
"What do you need help with?"
LabBot
- Light-emitting field-effect transistor based on a tetracene thin film. (Physical Review Letters, 2003)
- Charge transfer transitions in solid tetracene and pentacene studied by electroabsorption (Chemical Physics, 1981)
- The crystal structure of hexacene, and a revision of the crystallographic data for tetracene (Acta Crystallographica, 1962)
- Synthesis, Crystal Structure, and Transistor Performance of Tetracene Derivatives (Journal of the American Chemical Society, 2004)
- Field-effect transistors on tetracene single crystals (Applied Physics Letters, 2003)
- Mechanism for Singlet Fission in Pentacene and Tetracene: From Single Exciton to Two Triplets (Journal of the American Chemical Society, 2011)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - tetracene
- rubene
- 2,3-benzanthrene
- benz(b)anthracene
- 2,3-benzanthracene
-
SMILESC1=CC=C2C=C3C=C4C=CC=CC4=CC3=CC2=C1
-
InChIKeyIFLREYGFSNHWGE-UHFFFAOYSA-N
- Pubchem - Naphthacene
- Wikipedia - tetracene
Tetracene, also called naphthacene, is a polycyclic aromatic hydrocarbon. It has the appearance of a pale orange powder. Tetracene is the four-ringed member of the series of acenes, the previous one being anthracene (tricene) and the next one being pentacene.
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Naphthacene
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