A triple bond in chemistry is a chemical bond between two atoms involving six bonding electrons instead of the usual two in a covalent single bond. Triple bonds are stronger than the equivalent single bonds or double bonds, with a bond order of three. The most common triple bond is in a nitrogen N2 molecule; the second most common is that between two carbon atoms, which can be found in alkynes. Other functional groups containing a triple bond are cyanides and isocyanides. Some diatomic molecules, such as diphosphorus[1] and carbon monoxide, are also triple bonded. In skeletal formulae the triple bond is drawn as three parallel lines (≡) between the two connected atoms.[2][3][4]
|
|
|
| acetylene, H−C≡C−H | cyanogen, N≡C−C≡N | carbon monoxide, C≡O |
Bonding
editTriple bonding can be explained in terms of orbital hybridization. In the case of acetylene, each carbon atom has two sp-orbitals and two p-orbitals. The two sp-orbitals are linear, with 180° bond angles, and occupy the x-axis in the cartesian coordinate system. The p-orbitals are perpendicular to the sp-orbitals on the y-axis and the z-axis. When the atoms approach each other, the sp orbitals overlap to form an sp-sp sigma bond. At the same time the pz-orbitals approach and together they form a pz-pz pi-bond. Likewise, the other pair of py-orbitals form a py-py pi-bond. The result is formation of one sigma bond and two pi bonds.
In the bent bond model, the triple bond can also formed by the overlapping of three sp3 lobes without the need to invoke a pi-bond.[5]
Triple bonds between elements heavier than oxygen
editMany elements beyond oxygen can form triple bonds. These bonds are common in some transition metals. Hexa(tert-butoxy)ditungsten(III) and Hexa(tert-butoxy)dimolybdenum(III) are well known examples, in which the metal-metal bond distance is about 233 pm.[6] Hexa(tert-butoxy)ditungsten(III) has attracted particular attention for its reactions with alkynes, leading to metal-carbon triple bonded compounds of the formula RC≡W(OBut)3[7]
Additionally, phosphorus can exist as the highly reactive diatomic molecule diphosphorus, which has roughly half the bond-dissociation energy of dinitrogen.[1]
References
edit- ^ a b Huber, K. P.; Herzberg, G. (1979). Molecular Spectra and Molecular Structure IV. Constants of Diatomic Molecules. New York: Van Nostrand. ISBN 978-0442233945.
- ^ March, Jerry (1985), Advanced Organic Chemistry: Reactions, Mechanisms, and Structure, 3rd edition, New York: Wiley, ISBN 9780471854722, OCLC 642506595
- ^ Organic Chemistry 2nd Ed. John McMurry
- ^ Pyykkö, Pekka; Riedel, Sebastian; Patzschke, Michael (2005). "Triple-Bond Covalent Radii". Chemistry: A European Journal. 11 (12): 3511–20. doi:10.1002/chem.200401299. PMID 15832398.
- ^ Advanced Organic Chemistry Carey, Francis A., Sundberg, Richard J. 5th ed. 2007
- ^ Chisholm, Malcolm H.; Gallucci, Judith C.; Hollandsworth, Carl B. (2006). "Crystal and molecular structure of W2(OBut)6 and electronic structure calculations on various conformers of W2(OMe)6". Polyhedron. 25 (4): 827–833. doi:10.1016/j.poly.2005.07.010.
- ^ .Listemann, Mark L.; Schrock, Richard R. (1985). "Multiple metal carbon Bonds. 35. A General Route to tri-tert-Butoxytungsten Alkylidyne complexes. Scission of Acetylenes by Ditungsten Hexa-tert-butoxide". Organometallics. 4: 74–83. doi:10.1021/om00120a014.