| Weight | 152.196 g/mol |
|---|---|
| Formula | C12H8 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
BIPHENYLENE (259-79-0)
Score:
#309 in Materials science
,
#1990 in Physics
,
#6221 in Chemistry
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LabBot
- Self-assembly of biphenylene-bridged hybrid mesoporous solid with molecular-scale periodicity in the pore walls. (Journal of the American Chemical Society, 2002)
- Nickel(0) Complexes of N-Alkyl-Substituted N-Heterocyclic Carbenes and Their Use in the Catalytic CarbonCarbon Bond Activation of Biphenylene (Organometallics, 2006)
- A refinement of the structure of biphenylene (Acta Crystallographica, 1966)
- Organic chemistry of subvalent transition complexes. 9. Oxidative addition of nickel(0) complexes to carbon-carbon bonds in biphenylene: formation of nickelole and 1,2-dinickelecin intermediates (Organometallics, 1985)
- Cleavage of the carboncarbon bond in biphenylene using transition metals (Journal of Molecular Catalysis A-chemical, 2002)
- Color lightness and highly organosoluble fluorinated polyamides, polyimides and poly(amideimide)s based on noncoplanar 2,2-dimethyl-4,4-biphenylene units (Polymer, 2006)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C2C(=C1)C3=CC=CC=C23
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InChIKeyIFVTZJHWGZSXFD-UHFFFAOYSA-N
- Pubchem - BIPHENYLENE
- Wikipedia - biphenylene
Biphenylene is an alternant, polycyclic hydrocarbon composed of two benzene rings joined together by a pair of mutual attachments (as opposed to a normal ring fusion), thus forming a 6-4-6 arene system. The resulting planar structure was one of the first pi-electronic hydrocarbon systems discovered to show evidence of antiaromaticity.
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BIPHENYLENE
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