Butalene
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Butalene is a polycyclic
hydrocarbon In organic chemistry, a hydrocarbon is an organic compound consisting entirely of hydrogen and carbon. Hydrocarbons are examples of group 14 hydrides. Hydrocarbons are generally colourless and hydrophobic, and their odors are usually weak or ex ...
composed of two fused
cyclobutadiene Cyclobutadiene is an organic compound with the formula . It is very reactive owing to its tendency to dimerize. Although the parent compound has not been isolated, some substituted derivatives are robust and a single molecule of cyclobutadiene is ...
rings. A reported possible synthesis of it involves an
elimination reaction An elimination reaction is a type of organic reaction in which two substituents are removed from a molecule in either a one- or two-step mechanism. The one-step mechanism is known as the E2 reaction, and the two-step mechanism is known as the E1 r ...
from a
Dewar benzene Dewar benzene (also spelled ''dewarbenzene'') or bicyclo .2.0exa-2,5-diene is a bicyclic isomer of benzene with the molecular formula C6H6. The compound is named after James Dewar who included this structure in a list of possible C6H6 structures ...
derivative. The structure itself can be envisioned as
benzene Benzene is an organic chemical compound with the molecular formula C6H6. The benzene molecule is composed of six carbon atoms joined in a planar ring with one hydrogen atom attached to each. Because it contains only carbon and hydrogen atoms, ...
with an internal bridge, and calculations indicate it is somewhat less stable than the open
1,4-didehydrobenzene Arynes and benzynes are highly reactive species derived from an aromatic ring by removal of two substituents. Arynes are examples of didehydroarenes (1,2-didehydroarenes in this case), although 1,3- and 1,4-didehydroarenes are also known. Arynes ar ...
biradical, the
valence isomer In organic chemistry, two molecules are valence isomers when they are constitutional isomers that can interconvert through pericyclic reactions. Benzene There are many valence isomers one can draw for the C6H6 formula benzene. Some were originally ...
in which that bridged bond is broken.


Structure and bonding

Ab initio ''Ab initio'' ( ) is a Latin term meaning "from the beginning" and is derived from the Latin ''ab'' ("from") + ''initio'', ablative singular of ''initium'' ("beginning"). Etymology Circa 1600, from Latin, literally "from the beginning", from ab ...
calculations indicate butalene has a planar geometry and, in keeping with a planar structure with 6  π-electron configuration, is
aromatic In chemistry, aromaticity is a chemical property of cyclic ( ring-shaped), ''typically'' planar (flat) molecular structures with pi bonds in resonance (those containing delocalized electrons) that gives increased stability compared to satur ...
. Thus, the most significant π bonding interactions involve
conjugation Conjugation or conjugate may refer to: Linguistics * Grammatical conjugation, the modification of a verb from its basic form * Emotive conjugation or Russell's conjugation, the use of loaded language Mathematics * Complex conjugation, the chang ...
around the periphery of the whole six-atom structure, similar to benzene, rather than cross-ring resonance along the bridging bond. Significant resonance around one or the other four-membered ring alone would be a less-stable
antiaromatic Antiaromaticity is a chemical property of a cyclic molecule with a π electron system that has higher energy, i.e., it is less stable due to the presence of 4n delocalised (π or lone pair) electrons in it, as opposed to aromaticity. Unlike aroma ...
form, as is seen in
cyclobutadiene Cyclobutadiene is an organic compound with the formula . It is very reactive owing to its tendency to dimerize. Although the parent compound has not been isolated, some substituted derivatives are robust and a single molecule of cyclobutadiene is ...
itself.


See also

*
Propalene Propalene or bicyclo .1.0uta-1,3-diene is a polycyclic hydrocarbon composed of two fused cyclopropene rings. Computational studies indicate that the molecule is planar, with the carbon framework forming a parallelogram that has distinctly alter ...
*
Pentalene Pentalene is a polycyclic hydrocarbon composed of two fused cyclopentadiene rings. It has chemical formula . It is antiaromatic, because it has 4''n'' π electrons where ''n'' is any integer. For this reason it dimerizes even at temperatures as ...
*
Heptalene Heptalene is a polycyclic hydrocarbon with chemical formula , composed of two fused cycloheptatriene rings. It is an unstable, non-planar compound which is non-aromatic. The dianion, however, satisfies Hückel's rule In organic chemistry, Hüc ...
*
Octalene Octalene is a polycyclic hydrocarbon composed of two fused cyclooctatetraene rings. Anions Octalene can be readily reduced by lithium to a dianion and, unusually for such a small molecule, a tetraanion .Müllen, K., Oth, J. F. M., Engels, H.-W ...


References

{{PAHs Polycyclic aromatic hydrocarbons Bicyclic compounds Four-membered rings