| Weight | 228.294 g/mol |
|---|---|
| Formula | C18H12 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 4 |
| Rotatable Bonds | 0 |
TRIPHENYLENE (217-59-4)
9,10-benzophenanthrene
Score:
#1893 in Physics
,
#5906 in Chemistry
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- Recent developments in the chemistry of triphenylene-based discotic liquid crystals (Liquid Crystals, 2004)
- A systematic study of the photophysical processes in polydentate triphenylene-functionalized Eu3+, Tb3+, Nd3+, Yb3+, and Er3+ complexes (Journal of Physical Chemistry A, 2000)
- Triphenylenebased discotic liquid crystal dimers, oligomers and polymers (Liquid Crystals, 2005)
- The synthesis of triphenylenebased discotic mesogens New and improved routes (Liquid Crystals, 1993)
- The mobility of charge carriers in all four phases of the columnar discotic material hexakis(hexylthio)triphenylene: Combined TOF and PRTRMC results (Advanced Materials, 1996)
- -Complexation of biphenyl, naphthalene, and triphenylene to trimeric perfluoro-ortho-phenylene mercury. Formation of extended binary stacks with unusual luminescent properties (Journal of the American Chemical Society, 2002)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 9,10-benzophenanthrene
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SMILESC1=CC=C2C(=C1)C3=CC=CC=C3C4=CC=CC=C24
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InChIKeySLGBZMMZGDRARJ-UHFFFAOYSA-N
- Pubchem - TRIPHENYLENE
- Wikipedia - triphenylene
In chemistry, the organic compound triphenylene is a flat polycyclic aromatic hydrocarbon (PAH) consisting of four fused benzene rings. Triphenylene can be isolated from coal tar, but it is also made synthetically using benzyne chemistry, as it is a trimer of benzyne. One molecule of triphenylene has delocalized 18--electron systems based on a planar structure.
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TRIPHENYLENE
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