Radialene

are alicyclic organic compounds containing n cross-conjugated exocyclic double bonds. The double bonds are commonly alkene groups but those with a carbonyl (C=O) group are also called radialenes. For some members the unsubstituted parent radialenes are elusive but many substituted derivatives are known.

Radialenes are related to open-chain dendralenes and also to compounds like butadiene and benzene which also consist of a ring of sp² hybridized carbon atoms.

Radialenes are investigated in organic chemistry for their unusual properties and reactivity but have not ventured outside the laboratory. Reported uses are as experimental building blocks for novel organic conductors and ferromagnets. The first radialene called ''hexaethylidencyclohexane'' was synthesised in 1961.

Conformation

and adialenes are expected to have a planar molecular geometry with all carbon atoms in the same plane. This is verified experimentally in ''hexamethyl adialene'' and '. ' has a twist envelope geometry with C₂ symmetry while a chair conformation is calculated for adialene and found experimentally for ''hexa-(ethylidene)cyclohexane''

Due to their specific pi-electron distributions, hydrocarbons such as perylene and triphenylene are not considered radialenes. One study describes a adialene composed of thiophene units:

:

This compound is reported as planar with D_3h symmetry ( X-ray diffraction) but not aromatic: the carbon-carbon bond lengths are unusually long (145 pm vs. 140 pm for benzene) and the calculated NICS value is close to zero.

Synthesis and properties

The parent and adialenes polymerize when in contact with oxygen.

adialenes

adialene or trimethylenecyclopropane was synthesised in 1965. Reported derivatives are triquinocyclopropanes, salts of trimethylenecyclopropane dianions, , and . Phosphorus derivatives (based on ) have also been reported. Phospharadialenes have been investigated as quantum efficiency improvers in solar cells derivatives have been investigated for their low oxidation potentials.

adialenes

The unsubstituted adialene has been prepared in an elimination reaction of ' with sodium methoxide in ethanol.

Hydrogenation with platinum on carbon gives ''cis,cis,cis-tetramethylcyclobutane'' in accordance with the proposed structure. On standing in air at room temperature the compound accepts oxygen and polymerizes.

adialenes

Successful low-temperature synthesis of the parent compound adialene was reported in 2015.

adialenes

The parent adialene is unstable and polymerises immediately on formation. It has been synthesised from 1,5,9-cyclododecatriyne, 1,3,6-tri(chloromethyl)mesitylene and tricyclobutabenzene.

Only substituted adialenes exist as stable compounds. Stable derivatives are the hexamethyl substituted, dodecamethyl substituted and hexabromo substituted radialene.

A trisalkoxy-substituted radialene has also been reported, the central ring adopting a non-planar twist-boat conformation:

:

Uses

Radialenes have been researched as a potential way to access complex synthetic molecules and in polymer synthesis.

References

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Coupling reaction reagent bis(1,5-cyclooctadiene)nickel(0). Equal amount of tetramer formed
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