Sigma and Pi Bonds

Submitted by ChemPRIME Staff on Thu, 12/16/2010 - 12:45

A description of the double bondAttraction between two atoms (nuclei and core electrons) that results from sharing two pairs of electrons between the atoms; a bond with bond order = 2. is the sigma-pi model shown in Fig. 1. In this case only two of the p orbitals on each C atom are involved in the formation of hybrids. Consequently sp2 hybrids are formed, separated by an angle of 120°. Two of these hybrids from each C atom overlap with H 1s orbitals, while the third overlaps with an sp2 hybrid on the other C atom. This overlap directly between the two C atomsThe smallest particle of an element that can be involved in chemical combination with another element; an atom consists of protons and neutrons in a tiny, very dense nucleus, surrounded by electrons, which occupy most of its volume. is called a sigma bondA bond in which the electron density is symmetrically distributed around the line connecting two atomic nuclei; can be formed by the overlap of an s orbital on one atom with any kind of orbital on another atom or by two p orbitals pointing toward each other., and is abbreviated by the Greek letter σ. This orbital has no nodes: electronA negatively charged, sub-atomic particle with charge of 1.602 x 10-19 coulombs and mass of9.109 x 1023 kilograms; electrons have both wave and particle properties; electrons occupy most of the volume of an atom but represent only a tiny fraction of an atom's mass. densityThe ratio of the mass of a sample of a material to its volume. exists continuously from around one atom to the other atom.

Figure 1 The sigma-pi model of a double bond. Three sp2 hybrids around each carbon atom are indicated in color. Two of these overlap directly between the carbon atoms to form the σ bond. Two p orbitals, one on each C atom, are shown in gray. These overlap sideways to form a π bond, also shown in gray.


To view the sigma bonding orbital, select N6. This is actually sigma bonding between C-C and some sigma-like bonding around the Hs as well. Focus on the yellow portion. By selecting N8 HOMO, you can see the pi orbital represented by the two lobes.

The sp2 hybrid orbitals on each carbon atom involve the 2s and two of the 2p orbitals, leaving a single 2p orbital on each carbon atom. A second carbon-carbon bond is formed by the overlap of these two remaining p orbitals. This is called a pi bondA bond in which the electron density lies above and below a plane containing the bonded atoms; formed by combinations such as the overlap of two p orbitals or the overlap of a p orbital and a d orbital., Greek letter π. The pi bond (π bond) has two halves—one above the plane of the molecule, and the other below it. Each of the two electrons in the pi bond (π bond) exists both above and below the plane of the four H atoms and the two C atoms. The pi bond can be thought of as a standing wave with a single node in the plane of the molecule.

If your workstation is enabled for JCE Software, you will see two videos below which compare the behavior of a standing wave with zero nodes versus a standing wave with one node (otherwise, see the drum animation below). The wave with a single node has higher energyA system's capacity to do work.. The sigma bond between the two carbon atoms does not have a node in the plane of the molecule. The pi bond between the two carbon atoms has one node in the plane of the molecule. Thus the pi molecular orbitalAn orbital formed by the overlap of atomic orbitals on at least two different atoms; designated as bonding, non-bonding, or anti-bonding. is higher in energy and is the highest occupied molecular orbital (the HOMO).


(a) No Nodes

(b) Single Node

Standing Waves on a Wave Demonstrator. (a) The lowest energy form of a standing wave has no nodes. This is like the continual electron density in all directions around the sigma bonding orbital. (b) The second lowest energy standing wave has a single node. This node is akin to the shape of the pi bond where there is no electron density along the plane.

Alternatively, we can envision the molecular orbitals with the Drum Model described earlier. Imagine the two atoms opposite one another where a diagonal meets the edge of the drum at extreme left and right points. The m1,0 mode has no nodes, so the maximum amplitude of the standing wave is between the atoms, representing a high electron density sigma bond. The m2,1 mode has a linear node between the atoms, and maximum amplitude in front of, and behind, the node, representing the pi bond. In 3D, this linear node would be a plane, separating the two lobes of high electron density that constitute the pi bond. Because the pi bond has less electron density between the atoms, it is of higher energy in the MO diagram and is weaker than the sigma bond.

Overall this sigma-pi picture of the double bond is reminiscent of a hot dog in a bun. The sigma bond (σ bond) corresponds to the frankfurter, while the pi bond corresponds to the bun on either side of it.

Although the sigma-pi picture is more complexA central metal and the ligands surrounding it; also called coordination complex. than the bent-bond picture of the double bond, it is much used by organicRefers to the branch of chemistry that studies compounds containing carbon, usually in combination with hydrogen and other elements such as O, N, S, and P. Certain small ions and compounds containing carbon (such as carbonate ions and carbon dioxide) are not considered to be organic, but rather are classed as inorganic. chemists (those chemists interested in carbon compounds). The sigma-pi model is especially helpful in understanding what happens when visible light or other radiation is absorbed by a molecule. Further discussion on this topic is found in the sections on Spectra and Structure of Atoms and Molecules.

Figure 2 Dot-density diagrams comparing the sigma-pi and bent-bond models of the double bond. (a) The sigma-pi model. The σ bond is in color and the π bond is in gray. (b) The bent-bond model. One lies above the two nuclei and the other below. Since both diagrams are dot-for-dot the same, they are both describing the same physical reality.

In actual fact the difference between the two models of the double bond (the first model described here and the second found in the section on Orbital Descriptions of Multiple Bonds) is more apparent than real. They are related to each other in much the same way as s and p orbitals are related to sp hybrids. Figure 2 shows two dot-density diagrams for a carbon-carbon double bond in a plane through both carbon nuclei but at right angles to the plane of the molecule. Figure 2a corresponds to a sigma-pi model with the sigma bond (σ bond) in color and the pi bond in gray. Figure 2b shows two bent bonds. Careful inspection reveals that both diagrams are dot-for-dot the same. Only the color coding of the dots is different. Thus the bent-bond and sigma-pi models of the double bond are just two different ways of dividing up the same overall electron density.

A similar situation applies to triple bonds, such as that found in a molecule of ethyne (acetylene), Image:HCCHtriple bond.jpg. As shown in Fig. 3a,we can regard this triple bond as being the result of three overlaps of sp3 hybrids on different carbon atoms forming three bent bonds. Alternatively we can regard it as being composed of one sigma bond and two pi bonds, the sigma bond being due to the overlap of an sp hybrid from each carbon atom. Again both pictures of the bond correspond to the same overall electron density, and hence both are describing the same physical reality. We can use whichever one seems more convenient for the problem under consideration.

Figure 3 Two alternative models for the triple bond in ethyne, Image:HCCHtriple bond.jpg. (a) Three sp3 hybrids from each carbon atom overlap to form three bent bonds. (b) Two sp hybrids overlap to form the sigma bond. Two p orbitals on one carbon overlap with two on the other to form two pi bonds (one in light gray, the other in dark gray). Though these two models appear to be different, the indistinguishability of electrons makes them exactly equivalent.


The orbitals can be viewed by selecting from the orbital menu at right. Again, these orbitals are more easily represented using an MO Cutoff of 0.005. By selecting By selecting N1 you can see the sigma bonding orbital. The two pi bonding orbitals can be viewed by selecting N6 and N7. If you rotate the molecule so that we view the molecule along the H-C-C-H line, you can switch back and forth between N6 and N7 to see the orientation in space.