Dienone

Dibenzylideneacetone is a well known dienone

A dienone is a class of organic compounds with the general formula (R₂C=CR)₂C=O, where R is any substituent, but often H. They are formally "derived from 1,4-diene compounds by conversion of a –CH2– groups into –C(=O)– group .", resulting in "a conjugated structure". They are a kind of enone. The class includes some heterocyclic compounds.

Properties and occurrence

There is no evidence that phenols tautomerizes to a dienone, but such tautomerism is well recognized for resorcinols and some hydroxypyridines.

Being multifunctional, dienones engage in many reactions. They are often good dienophiles. They function as ligands, forming metal-alkene complexes such as tris(dibenzylideneacetone)dipalladium(0).

Cyclic dienones

Extensive work has been reported on cyclic dienones. The parent of the seven-membered ring series is tropone. It is a not only a dienone but a trieneone.

Cyclohexadienones are a significant class of dienones, the premier members being the ortho- and para-quinones. Many cyclohexadienones convert to phenols. In the dienone–phenol rearrangement, they convert to phenols through the dienone–phenol rearrangement:

The parent cyclopentadienone has only a fleeting existence under laboratory conditions, otherwise it dimerizes. The substituted derivative tetraphenylcyclopentadienone is however robust solid.

See also

• Dione
• Penguinone