Cyclobutane
Cyclobutane
Cyclobutane
Cyclobutane
Cyclobutane
Names
Preferred IUPAC name
Cyclobutane
Other names
Ethene dimer
Biethylene
Diethylene
Identifiers
3D model (JSmol)
1900183
ChEBI
ChemSpider
ECHA InfoCard 100.005.468 Edit this at Wikidata
EC Number
  • 206-014-5
81684
UNII
UN number 2601
  • InChI=1S/C4H8/c1-2-4-3-1/h1-4H2 checkY
    Key: PMPVIKIVABFJJI-UHFFFAOYSA-N ☒N
  • InChI=1/C4H8/c1-2-4-3-1/h1-4H2
    Key: PMPVIKIVABFJJI-UHFFFAOYAP
  • C1CCC1
Properties
C4H8
Molar mass 56.107 g/mol
Appearance Colorless gas
Density 0.720 g/cm3
Melting point −91 °C (−132 °F; 182 K)
Boiling point 12.5 °C (54.5 °F; 285.6 K)
Hazards
GHS labelling:
GHS02: FlammableGHS04: Compressed Gas
Danger
H220, H280
P210, P377, P381, P403, P410+P403
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 1: Exposure would cause irritation but only minor residual injury. E.g. turpentineFlammability 4: Will rapidly or completely vaporize at normal atmospheric pressure and temperature, or is readily dispersed in air and will burn readily. Flash point below 23 °C (73 °F). E.g. propaneInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
1
4
0
Related compounds
Related alkane
 Butane
Related compounds
 Cyclobutene; Cyclobutadiene; Cyclopropane; Cyclopentane
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 ?)

Cyclobutane is a cycloalkane and organic compound with the formula (CH2)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.[1]

Structure

The bond angles between carbon atoms are significantly strained and as such have lower bond energies than related linear or unstrained hydrocarbons, e.g. butane or cyclohexane. 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.[2] 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

Pentacycloanammoxic acid

Despite the inherent strain, the cyclobutane motif is indeed found in nature. One example is pentacycloanammoxic acid,[3] 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 involved in the production of nitrogen and water from nitrite ions and ammonia.[4] Some related fenestranes are also found in nature.[citation needed]

Cyclobutane photo dimers (CPD) are formed by photochemical reactions that result in the coupling of the C=C double bonds of pyrimidines.[5][6][7] 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.

Photodimers derived from thymine.

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.[8]

See also

References

  1. ^ Zvi Rappoport, Joel F. Liebman, ed. (2005). The Chemistry of Cyclobutanes. PATAI'S Chemistry of Functional Groups. John Wiley & Sons. doi:10.1002/0470864028. ISBN 9780470864029.
  2. ^ "Cyclobutane". Encyclopedia Britannica. Retrieved 8 July 2022.
  3. ^ J. S. Sinninghe Damsté, M. Strous, W. I. C. Rijpstra, E. C. Hopmans, J. A. J. Geenevasen, A. C. T. van Duin, L. A. van Niftrik and M. S. M. Jetten (2002). "Linearly concatenated cyclobutane lipids form a dense bacterial membrane". Nature. 419 (6908): 708–712. Bibcode:2002Natur.419..708S. doi:10.1038/nature01128. PMID 12384695. S2CID 4373854.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  4. ^ Vincent Mascitti and E. J. Corey (2006). "Enantioselective Synthesis of Pentacycloanammoxic Acid". J. Am. Chem. Soc. 128 (10): 3118–9. doi:10.1021/ja058370g. PMID 16522072.Authors state that mode of biosynthesis is quite mysterious
  5. ^ R. B. Setlow (1966). "Cyclobutane-Type Pyrimidine Dimers in Polynucleotides". Science. 153 (3734): 379–386. Bibcode:1966Sci...153..379S. doi:10.1126/science.153.3734.379. PMID 5328566. S2CID 11210761.
  6. ^ Expert reviews in molecular medicine (2 December 2002). "Structure of the major UV-induced photoproducts in DNA" (PDF). Cambridge University Press. Archived from the original (PDF) on 21 March 2005. Retrieved 16 August 2009.
  7. ^ Christopher Mathews; K.E. Van Holde (1990). Biochemistry (2nd ed.). Benjamin Cummings Publication. p. 1168. ISBN 978-0-8053-5015-9.
  8. ^ Richard Willstätter; James Bruce (1907). "Zur Kenntnis der Cyclobutanreihe" [On our knowledge of the cyclobutane series]. Berichte der Deutschen Chemischen Gesellschaft. 40 (4): 3979–3999. doi:10.1002/cber.19070400407.

External links

source: http://en.wikipedia.org/wiki/Cyclobutane