Cyclobutane is a
cycloalkane and
organic compound
Some chemical authorities define an organic compound as a chemical compound that contains a carbon–hydrogen or carbon–carbon bond; others consider an organic compound to be any chemical compound that contains carbon. For example, carbon-co ...
with the formula (CH
2)
4. Cyclobutane is a colourless gas and is commercially available as a
liquefied gas. Derivatives of cyclobutane are called cyclobutanes. Cyclobutane itself is of no commercial or biological significance, but more complex derivatives are important in biology and biotechnology.
Structure
The bond angles between
carbon
Carbon () is a chemical element; it has chemical symbol, symbol C and atomic number 6. It is nonmetallic and tetravalence, tetravalent—meaning that its atoms are able to form up to four covalent bonds due to its valence shell exhibiting 4 ...
atom
Atoms are the basic particles of the chemical elements. An atom consists of a atomic nucleus, nucleus of protons and generally neutrons, surrounded by an electromagnetically bound swarm of electrons. The chemical elements are distinguished fr ...
s are significantly
strained and as such have lower
bond energies than related linear or unstrained hydrocarbons, e.g.
butane
Butane () is an alkane with the formula C4H10. Butane exists as two isomers, ''n''-butane with connectivity and iso-butane with the formula . Both isomers are highly flammable, colorless, easily liquefied gases that quickly vaporize at ro ...
or
cyclohexane
Cyclohexane is a cycloalkane with the molecular formula . Cyclohexane is non-polar. Cyclohexane is a colourless, flammable liquid with a distinctive detergent-like odor, reminiscent of cleaning products (in which it is sometimes used). Cyclohexan ...
. As such, cyclobutane is unstable above about 500 °C.
The four carbon atoms in cyclobutane are not coplanar; instead, the ring typically adopts a folded or "puckered"
conformation.
This implies that the C-C-C angle is less than 90°. One of the carbon atoms makes a 25° angle with the plane formed by the other three carbons. In this way, some of the
eclipsing interactions are reduced. The conformation is also known as a "butterfly". Equivalent puckered conformations interconvert:
:
Cyclobutanes in biology and biotechnology
:

Despite the inherent strain, the cyclobutane motif is indeed found in nature. One example is pentacycloanammoxic acid, which is a
ladderane composed of 5 fused cyclobutane units. The estimated strain in this compound is 3 times that of cyclobutane. The compound is found in bacteria performing the
anammox process where it forms part of a tight and very dense membrane believed to protect the organism from toxic
hydroxylamine and
hydrazine
Hydrazine is an inorganic compound with the chemical formula . It is a simple pnictogen hydride, and is a colourless flammable liquid with an ammonia-like odour. Hydrazine is highly hazardous unless handled in solution as, for example, hydraz ...
involved in the production of nitrogen and water from
nitrite ions and
ammonia
Ammonia is an inorganic chemical compound of nitrogen and hydrogen with the chemical formula, formula . A Binary compounds of hydrogen, stable binary hydride and the simplest pnictogen hydride, ammonia is a colourless gas with a distinctive pu ...
. Some related
fenestranes are also found in nature.
Cyclobutane photo dimers (CPD) are formed by
photochemical reactions that result in the coupling of the C=C double bonds of
pyrimidines.
Thymine dimers (T-T dimers) formed in between two thymines are the most abundant of the CPDs. CPDs are readily repaired by
nucleotide excision repair enzymes. In most organisms, they can also be repaired by photolyases, a light-dependent family of enzymes.
Xeroderma pigmentosum is a genetic disease where this damage can not be repaired, resulting in skin discolouration and tumours induced by exposure to
UV light.
:
Carboplatin is a popular
anticancer drug that is derived from cyclobutane-1,1-dicarboxylic acid.
Preparation
Many methods exist for the preparation of cyclobutanes. Alkenes dimerize upon irradiation with UV-light. 1,4-Dihalobutanes convert to cyclobutanes upon dehalogenation with reducing metals.
Cyclobutane was first synthesized in 1907 by James Bruce and
Richard Willstätter by hydrogenating cyclobutene in the presence of nickel.
See also
*
Butane
Butane () is an alkane with the formula C4H10. Butane exists as two isomers, ''n''-butane with connectivity and iso-butane with the formula . Both isomers are highly flammable, colorless, easily liquefied gases that quickly vaporize at ro ...
*
Octafluorocyclobutane
References
External links
* Datashee
Link
{{Authority control
Cycloalkanes