Bullvalene

Bullvalene

File:Bullvalene.svg File:Bullvalene-from-xtal-3D-balls.png
Names
Preferred IUPAC name Tricyclo[3.3.2.02,8]deca-3,6,9-triene
Other names Bullvalen
Identifiers
CAS Number	1005-51-2 checkY
3D model (JSmol)	Interactive image
ChemSpider	120549 checkY
ECHA InfoCard
E number
PubChem CID	136796
UNII	ZQZ1X09E2B checkY
CompTox Dashboard (EPA)	{{#property:P3117}}
InChI InChI=1S/C10H10/c1-4-8-9-5-2-7(1)3-6-10(8)9/h1-10H checkY Key: UKFBVTJTKMSPMI-UHFFFAOYSA-N checkY InChI=1/C10H10/c1-4-8-9-5-2-7(1)3-6-10(8)9/h1-10H Key: UKFBVTJTKMSPMI-UHFFFAOYAK
SMILES C\2=C\C/1\C=C/C3C(\C=C\1)C/23
Properties
Chemical formula	C10H10
Molar mass	130.19 g/mol
Melting point	96 °C (205 °F; 369 K)
Boiling point	decomposition at about 400 °C (752 °F; 673 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). ☒N verify (what is checkY☒N ?) Infobox references

Bullvalene is a hydrocarbon with the chemical formula C₁₀H₁₀. The molecule has a cage-like structure formed by the fusion of one cyclopropane and three cyclohepta-1,4-diene rings. Bullvalene is unusual as an organic molecule due to the C−C and C=C bonds forming and breaking rapidly through Cope rearrangements; this property makes it a fluxional molecule.

Stereodynamics

The bullvalene molecule is a cyclopropane platform with three vinylene arms conjoined at a methine group. This arrangement enables a degenerate Cope rearrangement with the result that all carbon atoms and hydrogen atoms appear equivalent on the NMR timescale. At room temperature the ¹H NMR signals average to a rounded peak at 5.76 ppm. At lower temperatures the peak broadens into a mound-like appearance, and at very low temperatures the fluxional behavior of bullvalene is reduced, allowing for 4 total signals to be seen. This pattern is consistent with an exchange process whose rate k is close to the frequency separation of the four contributing resonances. The number of possible valence tautomers of a bullvalene depends on the number of unique substituents. The number of isomers with ten distinguishable substituents is 10!/3 = 1,209,600.

File:Bullvalene Cope.svg

Synthesis

In 1963, G. Schröder produced bullvalene by photolysis of a dimer of cyclooctatetraene. The reaction proceeds with expulsion of benzene.

In 1966 W. von Eggers Doering and Joel W. Rosenthal synthesized it by the photochemical rearrangement of cis-9,10-dihydronaphthalene.

Related compounds

Bullvalones

In bullvalones one vinyl group in one of the arms in bullvalene is replaced by a keto group on a methylene bridge. In this way it is possible to activate the fluxional state by adding base and deactivate it again by removing the base:

File:Bullvalone.png

Scheme 2. A bullvalone

Compound 1 in scheme 2 is not a fluxional molecule but by adding base (sodium methoxide in methanol) the ketone converts to the enolate 2 and the fluxional state is switched on. Deuterium labeling is possible forming first 3 a then a complex mixture with up to 7 deuterium atoms, compound 4 being just one of them.

Semibullvalene

In semibullvalene (C₈H₈), one ethylene arm is replaced by a single bond. The compound was first prepared by photolysis of barrelene in isopentane with acetone as a photosensitizer in 1966.

File:Semibullvalene synthesis.svg

Scheme 3. Semibullvalene synthesis

Semibullvalene exists only as two valence tautomers (2a and 2b in scheme 3) but in this molecule the Cope rearrangement takes place even at -110 °C, a temperature at which this type of reaction is ordinarily not possible.

One insight into the reaction mechanism for this photoreaction is given by an isotope scrambling experiment. The 6 vinylic protons in barrelene 1 are more acidic than the two bridgehead protons and therefore they can be replaced by deuterium with N-deuteriocyclohexylamide. Photolysis of 2 results in the initial formation of a biradical intermediate with a cyclopropane ring formed. This product rearranges to a second intermediate with a more favorable allylic radical as two mesomers. Intersystem crossing and radical recombination results in equal quantities of semibullvalenes 3 and 4. The new proton distribution with allylic, vinylic and cyclopropanyl protons determined with proton NMR confirms this model. As noted, the conversion of barrelene to semibullvalene is a di-π-methane rearrangement.

File:Semibullvalene mechanism.png

Scheme 4. Barrelene photolysis mechanism

A synthetic procedure for alkylated semibullvalenes published in 2006 is based on cyclodimerisation of a substituted 1,4-dilithio-1,3-butadiene with copper(I) bromide. At 140 °C the ethylated semibullvalene isomerises to the cyclooctatetraene derivative.

File:NewSemibullvaleneSynthesis.png

Scheme 5. New semibullvalene synthesis

Barbaralane

In barbaralane, one ethylene arm is replaced by a methylene bridge and the dynamics are comparable to that of semibullvalene. There is also an intermediate ketone in bullvalene synthesis called "barbaralone". Both are named after Barbara M. Ferrier, (1932–2006) professor of the Department of Biochemistry and Biomedical Sciences at McMaster University.

Origin of the name

The name bullvalene is derived from the nickname of one of the scientists who predicted its properties in 1963 and the underlying concept of valence tautomerism, William "Bull" Doering. According to Klärner in 2011, the weekly seminars organised by Doering were secretly called "Bull sessions" by PhD students and postdocs and "were feared by those who were poorly prepared". The name was bestowed on the molecule, in 1961, by two of Doering's Yale graduate students, Maitland Jones Jr and Ron Magid. The name celebrates Bill Doering's well-known nickname and was chosen to rhyme with fulvalene, a molecule of great interest to the research group.