A triple bond in chemistry is a chemical bond between two chemical elements involving six bonding electrons instead of the usual two in a covalent single bond. The most common triple bond, that between two carbon atoms, can be found in alkynes. Triple bonds are also common with phosphorus atoms.Other functional groups containing a triple bond are cyanides and isocyanides. Some diatomic molecules, such as dinitrogen and carbon monoxide are also triple bonded. In skeletal formula the triple bond is drawn as three parallel lines (≡) between the two connected atoms; in typography, this is accomplished with the identity operator. 
Triple bonds are stronger than single bonds or double bonds and they are also shorter. The bond order is three.
The type of 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° angles and occupy the x-axis (cartesian coordinate system). The p-orbitals are perpendicular on the y-axis and the z-axis. When the carbon atoms approach each other the sp orbitals overlap to form a 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 bent bond theory the triple bond can also formed by the overlapping of three sp3 lobes without the need to invoke a pi-bond.
- ^ March, Jerry (1985), Advanced Organic Chemistry: Reactions, Mechanisms, and Structure (3rd ed.), New York: Wiley, ISBN 0-471-85472-7
- ^ 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