Pentalene
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Pentalene is a polycyclic hydrocarbon composed of two fused cyclopentadiene rings.[2] It has chemical formula Template:Chem2. It is antiaromatic, because it has 4n π electrons where n is any integer. For this reason it dimerizes even at temperatures as low as −100 °C.[3][4] The derivative 1,3,5-tri-tert-butylpentalene was synthesized in 1973.[5] Because of the tert-butyl substituents this compound is thermally stable. Pentalenes can also be stabilized by benzannulation for example in the compounds benzopentalene and dibenzopentalene.[2]
Dilithium pentalenide was isolated in 1962, long before pentalene itself in 1997.[6] It is prepared from reaction of dihydropentalene (pyrolysis of an isomer of dicyclopentadiene) with n-butyllithium in solution and forms a stable salt. In accordance with its structure proton NMR shows 2 signals in a 2 to 1 ratio. The addition of two electrons removes the antiaromaticity; it becomes a planar 10π-electron aromatic species and is thus a bicyclic analogue of the cyclooctatetraene (COT) dianion Template:Chem2.
The dianion can also be considered as two fused cyclopentadienyl rings, and has been used as a ligand in organometallic chemistry to stabilise many types of mono- and bimetallic complexes, including those containing multiple metal-metal bonds, and anti-bimetallics with extremely high levels of electronic communication between the centers.[7]
See also
References
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