Coronene

Coronene (also known as superbenzene and cyclobenzene) is a polycyclic aromatic hydrocarbon (PAH) comprising seven peri-fused benzene rings.

[12] The presence of coronene putatively formed from contact of magma with fossil fuel deposits has been used to argue that Permian-Triassic “Great Dying” event was caused by a greenhouse gas warming episode triggered by large-scale Siberian vulcanism.

[13] Coronene is produced in the petroleum-refining process of hydrocracking, where it can dimerize to a fifteen ring PAH, trivially named "dicoronylene" .

1 Tesla)[8] or by phase transition from γ decreasing the temperature below 158 K.[14] The structure containing two C-H groups on one benzene ring, so-called DUO, was analyzed by infrared spectroscopy.

For example, coronene molecules evaporated onto a copper surface at 1000 degrees Celsius will form a graphene lattice which can then be transferred onto another substrate.

NFPA 704 four-colored diamond Health 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g. chloroform Flammability 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g. canola oil Instability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogen Special hazards (white): no code
Carpathite
Crystals of β and γ coronene under daylight (left) and UV light (right). [ 8 ]
Structure and electron micrograph of a coronene-based metal–organic framework