Cyclooctatetraene

Cyclooctatetraene

Names
IUPAC name 1,3,5,7-cyclooctatetraene
Other names COT, [8]-annulene
Identifiers
CAS Number	629-20-9 Y
ChemSpider	553448 Y
EC Number	211-080-3
Jmol 3D model	Interactive image
RTECS number	CY1400000
InChI InChI=1S/C8H8/c1-2-4-6-8-7-5-3-1/h1-8H/b2-1-,3-1-,4-2-,5-3-,6-4-,7-5-,8-6-,8-7- Y Key: KDUIUFJBNGTBMD-BONZMOEMSA-N Y InChI=1/C8H8/c1-2-4-6-8-7-5-3-1/h1-8H/b2-1-,3-1-,4-2-,5-3-,6-4-,7-5-,8-6-,8-7- Key: KDUIUFJBNGTBMD-BONZMOEMBR
SMILES C1=C\C=C/C=C\C=C1
Properties
Chemical formula	C8H8
Molar mass	104.15 g/mol
Appearance	Clear yellow
Density	0.9250 g/cm3, liquid
Melting point	−5 to −3 °C (23 to 27 °F; 268 to 270 K)
Boiling point	142 to 143 °C (288 to 289 °F; 415 to 416 K)
Solubility in water	immiscible
Vapor pressure	{{{value}}}
Related compounds
Related hydrocarbons	Cyclooctane Tetraphenylene
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

1,3,5,7-Cyclooctatetraene (COT) is an unsaturated derivative of cyclooctane, with the formula C₈H₈. It is also known as [8]annulene. This polyunsaturated hydrocarbon is a colorless to light yellow flammable liquid at room temperature. Because of its stoichiometric relationship to benzene, COT has been the subject of much research and some controversy.

Unlike benzene, C₆H₆, cyclooctatetraene, C₈H₈, is not aromatic, although its dianion, C
₈H²⁻
₈ (cyclooctatetraenide), is. Its reactivity is characteristic of an ordinary polyene, i.e. it undergoes addition reactions. Benzene, by contrast, characteristically undergoes substitution reactions, not additions.

History

1,3,5,7-Cyclooctatetraene was initially synthesized by Richard Willstätter at Munich in 1905:

Willstätter noted that the compound did not exhibit the expected aromaticity. Between 1939 and 1943, chemists throughout the US unsuccessfully attempted to synthesize COT. They rationalized their lack of success with the conclusion that Willstätter had not actually synthesized the compound but instead its isomer, styrene. Willstätter responded to these reviews in his autobiography, where he noted that the American chemists were 'untroubled' by the reduction of his cyclooctatetraene to cyclooctane (a reaction impossible for styrene). During World War 2, Walter Reppe at BASF Ludwigshafen developed a simple, one-step synthesis of cyclooctatetraene from acetylene, providing material identical to that prepared by Willstätter. Any remaining doubts on the accuracy of Willstätter's original synthesis were resolved when Arthur C. Cope and co-workers at MIT reported, in 1947, a complete repetition of the Willstätter synthesis, step by step, using the originally reported techniques. They obtained the same cyclooctatetraene, and they subsequently reported modern spectral characterization of many of the intermediate products, again confirming the accuracy of Willstätter's original work.

Structure and bonding

Cyclooctatetraene in its native "tub-shaped" conformation.

Early studies demonstrated that COT did not display the chemistry of an aromatic compound. Then, early electron diffraction experiments concluded that the C-C bond distances were identical. However, X-ray diffraction data from H. S. Kaufman demonstrated cyclooctatetraene to adopt several conformations and to contain two distinct C–C bond distances. This result indicated that COT is an annulene with fixed alternating single and double C-C bonds.

In its normal state, cyclooctatetraene is non-planar and adopts a tub conformation with angles C=C−C = 126.1° and C=C−H = 117.6°. The point group of cyclooctatetraene is D_2d.

In its planar transition state, D_4h transitional state is more stable than D_8h transitional state due to Jahn–Teller effect.

Synthesis

Richard Willstätter's original synthesis (4 consecutive elimination reactions on a cyclooctane framework) gives relatively low yields. Reppe's synthesis of cyclooctatetraene, which involves treating acetylene at high pressure with a warm mixture of nickel cyanide and calcium carbide, was much better, with chemical yields near 90%:

COT can also be prepared by photolysis of barrelene, one its structural isomers, the reaction proceeding via another isolable isomer, semibullvalene. COT derivatives can also be synthesised by way of semibullvalene intermediates. In the sequence illustrated below, octaethylcyclooctatetraene (C₈Et₈) is formed by thermal isomerisation of octaethylsemibullvalene, itself formed by copper(I) bromide mediated cyclodimerisation of 1,2,3,4-tetraethyl-1,4-dilithio-1,3-butadiene.

Because COT is unstable and easily forms explosive organic peroxides, a small amount of hydroquinone is usually added to commercially available material. Testing for peroxides is advised when using a previously opened bottle; white crystals around the neck of the bottle may be composed of the peroxide, which may explode when mechanically disturbed.

Natural occurrence

Cyclooctatetraene has been isolated from certain fungi.

Reactions

The π bonds in COT react as usual for olefins, rather than as aromatic ring systems. Mono- and polyepoxides can be generated by reaction of COT with peroxy acids or with dimethyldioxirane. Various other addition reactions are also known. Furthermore, polyacetylene can be synthesized via the ring-opening polymerization of cyclooctatetraene. COT itself—and also analogs with side-chains—have been used as metal ligands and in sandwich compounds.

Cyclooctatetraenide as a ligand

Main article: Cyclooctatetraenide anion

File:Cyclooctatetraenide-3D-ball.png

Ball-and-stick model of COT²⁻

COT readily reacts with potassium metal to form the salt K₂COT, which contains the dianion C
₈H²⁻
₈. The dianion is both planar and octagonal in shape and aromatic with a Hückel electron count of 10.

Cyclooctatetraene forms organometallic complexes with some metals, including yttrium and lanthanides. One-dimensional Eu–COT sandwiches have been described as nanowires. The sandwich compounds U(COT)₂ (uranocene), and Fe(COT)₂, are known.

File:Uranocene-3D-vdW.png

Uranocene, a sandwich compound containing two COT²⁻ rings.

The compound Fe(COT)₂, when refluxed in toluene with dimethyl sulfoxide and dimethoxyethane for 5 days, is found to form magnetite and crystalline carbon also containing carbon nanotubes.

Because COT changes conformation between tub-shaped and planar with addition or subtraction of electrons, it could, in principle, be used to construct artificial muscles. Such devices have been contemplated to be makeable by grafting COT derivatives to a backbone of a suitable conducting polymer, which would supply or remove the reducing equivalents.

See also

• Cyclobutadiene
• Pentalene
• Barrelene, structural isomer of cyclooctatetraene
• Heptafulvene, structural isomer of cyclooctatetraene
• Semibullvalene
• Benzene