Bicyclic molecule

The fused ring compound decalin, formally bicyclo[4.4.0]decane.
The bridged bicyclic norbornane, formally bicyclo[2.2.1]heptane.
The spiro compound (spirocyclic compound), spiro[2.2]pentane.
An example of a bicyclic with isolated rings, cyclohexylbenzene.

A bicyclic molecule is a molecule that features just two rings. Bicyclic molecules occur widely in organic and inorganic compounds. Among organic compounds, the two rings can be fully carbocyclic (all atoms in each ring all carbons), or one or both can be heterocyclic (at least one atom in the rings not a carbon atom). Moreover, the two rings can both be aliphatic, or can be aromatic, or a combination of aliphatic and aromatic (cf. decalins and naphthalenes, norbornanes and cyclophanes, aliphatic spiro compounds and spiroaromatics, and biphenyl and cyclohexylbenzene, as aromatic and mixed examples).

Joining of the rings can occur in four ways:

Singly fused rings are the most common, and spiro rings are the least common.

Nomenclature

Bicyclic molecules have a strict nomenclature.[1] On its simplest level the parent hydrocarbon is the equivalent open-carbon alkane. For bridged compounds, the prefix bicyclo is added, followed by, between brackets, separated by periods, and, in descending order, the number of carbon atoms between each of the bridgeheads. For example, in bicyclo[2.2.1]heptane the carbon frame contains a total of 7 atoms, hence the parent name heptane. This molecule has three bridges having 2, 2 and 1 carbon atoms, hence the prefix bicyclo[2.2.1]. For spiro compounds, terms like spiro[2.4] are used, indicating that there are 3- and 5-membered rings meeting at the spiro atom (3 and 5 because the spiro atom itself is not counted).

See also

References

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