Sigma bond
In chemistry, sigma bonds (σ bonds) are the strongest type of covalent chemical bond.[1] They are formed by head-on overlapping between atomic orbitals. Sigma bonding is most simply defined for diatomic molecules using the language and tools of symmetry groups. In this formal approach, a σ-bond is symmetrical with respect to rotation about the bond axis. By this definition, common forms of sigma bonds are s+s, pz+pz, s+pz and dz2+dz2 (where z is defined as the axis of the bond).[2] Quantum theory also indicates that molecular orbitals (MO) of identical symmetry actually mix or hybridize. As a practical consequence of this mixing of diatomic molecules, the wavefunctions s+s and pz+pz molecular orbitals become blended. The extent of this mixing (or hybridization or blending) depends on the relative energies of the MO's of like symmetry.
For homodiatomics, bonding σ orbitals have no nodal planes at which the wavefunction is zero, either between the bonded atoms or passing through the bonded atoms. The corresponding antibonding, or σ* orbital, is defined by the presence of one nodal plane between the two bonded atoms.
Sigma bonds are the strongest type of covalent bonds due to the direct overlap of orbitals, and the electrons in these bonds are sometimes referred to as sigma electrons.[3]
The symbol σ is the Greek letter sigma. When viewed down the bond axis, a σ MO has a circular symmetry, hence resembling a similarly sounding "s" atomic orbital.
Typically, a single bond is a sigma bond while a multiple bond is composed of one sigma bond together with pi or other bonds. A double bond has one sigma plus one pi bond, and a triple bond has one sigma plus two pi bonds.
| —— | ———————————————— | ————— |
Atomic orbitals |
 | |
| Symmetric (s–s and p–p) sigma bonds between atomic orbitals |
A pi bond, for comparison | |
| —— | ———————————————— | ————— |
 σs–hybrid |
 σs–p | |
Polyatomic molecules
Sigma bonds are obtained by head-on overlapping of atomic orbitals. The concept of sigma bonding is extended to describe bonding interactions involving overlap of a single lobe of one orbital with a single lobe of another. For example, propane is described as consisting of ten sigma bonds, one each for the two C−C bonds and one each for the eight C−H bonds.
Multiple-bonded complexes
Transition metal complexes that feature multiple bonds, such as the dihydrogen complex, have sigma bonds between the multiple bonded atoms. These sigma bonds can be supplemented with other bonding interactions, such as π-back donation, as in the case of W(CO)3(PCy3)2(H2), and even δ-bonds, as in the case of chromium(II) acetate.[4]
Organic molecules
Organic molecules are often cyclic compounds containing one or more rings, such as benzene, and are often made up of many sigma bonds along with pi bonds. According to the sigma bond rule, the number of sigma bonds in a molecule is equivalent to the number of atoms plus the number of rings minus one.
- Nσ = Natoms + Nrings − 1
A molecule with no rings can be represented as a tree with a number of bonds equal to the number of atoms minus one (as in dihydrogen, H2, with only one sigma bond, or ammonia, NH3, with 3 sigma bonds). There is no more than 1 sigma bond between any two atoms.
Molecules with rings have additional sigma bonds, such as benzene rings, which have 6 C−C sigma bonds within the ring for 6 carbon atoms. The anthracene molecule, C14H10, has three rings so that the rule gives the number of sigma bonds as 24 + 3 − 1 = 26. In this case there are 16 C−C sigma bonds and 10 C−H bonds.
See also
References
- ↑ Moore, John; Stanitski, Conrad L.; Jurs, Peter C. Principles of Chemistry: The Molecular Science.
- ↑ Clayden, Jonathan; Greeves, Nick; Warren, Stuart (March 2012) [2002]. Organic Chemistry (2nd ed.). Oxford: OUP Oxford. pp. 101–136. ISBN 978-0199270293.
- ↑ Keeler, James; Wothers, Peter (May 2008). Chemical Structure and Reactivity (1st ed.). Oxford: OUP Oxford. pp. 27–46. ISBN 978-0199289301.
- ↑ Kubas, Gregory (2002). "Metal Dihydrogen and σ-Bond Complexes: Structure, Theory, and Reactivity". JCAS 14: 3799–3800. doi:10.1021/ja0153417.
External links
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