Coronene
Coronene is a polycyclic aromatic hydrocarbon comprising seven peri-fused benzene rings. Its chemical formula is. It is a yellow material that dissolves in common solvents including benzene, toluene, and dichloromethane. Its solutions emit blue light fluorescence under UV light. It has been used as a solvent probe, similar to pyrene.
The compound is of theoretical interest to organic chemists because of its aromaticity. It can be described by 20 resonance structures or by a set of three mobile Clar sextets. In the Clar sextet case, most stable structure for coronene has only three isolated outer sextets as fully aromatic although superaromaticity would still be possible when these sextets are able to migrate into next ring.
Occurrence and synthesis
Coronene occurs naturally as the very rare mineral carpathite, characterized by flakes of pure coronene embedded in sedimentary rock. This mineral may be created from ancient hydrothermal vent activity. In earlier times this mineral was also called karpatite or pendletonite.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.
Coronene is produced in the petroleum-refining process of hydrocracking, where it can dimerize to a fifteen ring PAH, trivially named "dicoronylene". Centimeter-long crystals can be grown from a supersaturated solution of molecules in toluene, which is slowly cooled from 328 K to 298 K over a period of 12 hours.