Conjugated ring systems having 4n π-electrons (e.g. 4, 8, 12 etc. electrons) not only fail to show any aromatic properties, but appear to be less stable and more reactive than expected. As noted above, 1,3,5,7-cyclooctatetraene is non-planar and adopts a tub-shaped conformation. The compound is readily prepared, and undergoes addition reactions typical of alkenes. Catalytic hydrogenation of this tetraene produces cyclooctane. Planar bridged annulenes having 4n π-electrons have proven to be relatively unstable. Examples of 8 and 12-π-electron systems are shown below, together with a similar 10 π-electron aromatic compound.

The simple C₈H₆ hydrocarbon pentalene does not exist as a stable compound, and its hexaphenyl derivative is air sensitive. The 12-π-electron analog heptalene has been prepared, but is also extremely reactive (more so than cyclooctatetraene). On the other hand, azulene is a stable 10-π-electron hydrocarbon that incorporates structural features of both pentalene and heptalene. Azulene is a stable blue crystalline solid that undergoes a number of typical aromatic substitution reactions. The unexpected instability of 4n π-electron annulenes has been termed "antiaromaticity".
Other examples may be cited. Thus, all attempts to isolate 1,3-cyclobutadiene have yielded its dimer, or products from reactions with other compounds introduced into the reaction system. Similarly, cyclopentadienyl cation (4 π-electrons) and cycloheptatrienyl anion (8 π-electrons) show very high reactivity when forced to form.

مواضيع ذات صلة

Organic compounds are more soluble in water as ions

Heterocyclic aromatic compounds

Hückel’s rule tells us if compounds are aromatic

Molecular orbitals and aromaticity

The π molecular orbitals of other conjugated cyclic hydrocarbons

Benzene has six π molecular orbitals

Varying the number of electrons

Heats of hydrogenation of benzene and cyclooctatetraene

? What makes benzene special

Aromaticity

Conjugation and reactivity: looking forward to Chapter 10

The amide group