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So for this question I'm considering a chemical to be "similar to azulene" if it obeys the following conditions:

  1. It is aromatic and obeys Hückel's rule,
  2. It is a fused bicyclic compound,
  3. One component ring is aromatic as an anion,
  4. The other ring is aromatic as a cation,
  5. It is not azulene, and
  6. It has been synthesised before and the synthesis has been confirmed.

For instance, I believe bicyclo[3.1.0]hexa-1,3,5-triene should follow all of the previous conditions except possibly the last (but I don't know that it hasn't). Do any chemicals obey all of these conditions?

Gaurang Tandon
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tox123
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2 Answers2

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enter image description here

There is this compound which is I believe the closest to anything which you've asked for. Except the fused part this satisfies all your conditions. In a polar solvent the double bond breaks to form two highly stable aromatic rings(tropylium and dicyclopentene) which act as two separate poles. It also lowers the rotation barrier of this compound. Hence it even becomes soluble. Along with azulene this is as close as an organic compound gets to being ionic.

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OK, so we cannot store the $\ce{C_6H_4}$ compound referred to in the question on a shelf in a lab. But apparently it has been identified as an intermediate species, see here and, for the second page of the article, here.

In summary: a nucleophilic substitution and elimination is carried out on a bicyclic compound, and the most plausible mechanism, backed by other experiments, is via a bicyclo[3.1.0]hexatriene intermediate. Computations indicate that the molecule has a bond through the appropriate diagonal of the hexagon.

Oscar Lanzi
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