In quantum chemistry, the computation of the energy and wavefunction of an average-size molecule is a formidable task that is alleviated by the **Bornâ€“Oppenheimer (BO) approximation**, named after Max Born and J. Robert Oppenheimer. For instance the benzene molecule consists of 12 nuclei and 42 electrons. The time independent SchrÃ¶dinger equation, which must be solved to obtain the energy and molecular wavefunction of this molecule, is a partial differential eigenvalue equation in 162 variablesâ€”the spatial coordinates of the electrons and the nuclei. The **BO approximation** makes it possible to compute the wavefunction in two less complicated consecutive steps. This approximation was proposed in 1927, in the early period of quantum mechanics, by Born and Oppenheimer and is still indispensable in quantum chemistry.

In basic terms, it allows the wavefunction of a molecule to be broken into its electronic and nuclear (vibrational, rotational) components.

In the first step of the **BO approximation** the electronic SchrÃ¶dinger equation is solved, yielding the wavefunction Ïˆelectronic depending on electrons only. For benzene this wavefunction depends on 126 electronic coordinates. During this solution the nuclei are fixed in a certain configuration, very often the equilibrium configuration. If the effects of the quantum mechanical nuclear motion are to be studied, for instance because a vibrational spectrum is required, this electronic computation must be in nuclear coordinates. In the second step of the **BO approximation** this function serves as a potential in a SchrÃ¶dinger equation containing only the nucleiâ€”for benzene an equation in 36 variables.

The success of the **BO approximation** is due to the high ratio between nuclear and electronic masses. The approximation is an important tool of quantum chemistry; without it only the lightest molecule, H_{2}, could be handled, and all computations of molecular wavefunctions for larger molecules make use of it. Even in the cases where the **BO approximation** breaks down, it is used as a point of departure for the computations.

The electronic energies, constituting the nuclear potential, consist of kinetic energies, __interelectronic repulsions__ and __electronâ€“nuclear attractions__. In a handwaving manner the nuclear potential is taken to be an averaged electronâ€“nuclear attraction. The BO approximation follows from the inertia of electrons being considered to be negligible in comparison to the atom to which they are bound. wikipedia - Born Oppenheimer approximation underline added, see repulsion, attraction

See Also

**12.11 - Eighteen Attributes or Dimensions**
**Angular Momentum coupling**
**magnetic moment**
**Quantum coupling**
**Renner-Teller Effect**
**Rotational-vibrational coupling**
**rovibronic coupling**
**spin-orbit coupling**
**spintronics**