Klopman-Salem equation

In modern form,[3] the Klopman-Salem equation is commonly given as

${\displaystyle \Delta E={\Big (}-\sum _{a,b}(q_{a}+q_{b})\beta _{ab}S_{ab}{\Big )}+{\Big (}\sum _{k<\ell }{\frac {Q_{k}Q_{\ell }}{\varepsilon R_{k\ell }}}{\Big )}+{\Big (}\sum _{r}^{\mathrm {occ.} }\sum _{s}^{\mathrm {unocc.} }-\sum _{s}^{\mathrm {occ.} }\sum _{r}^{\mathrm {unocc.} }{\frac {2(\sum _{a,b}c_{ra}c_{sb}\beta _{ab})^{2}}{E_{r}-E_{s}}}{\Big )}}$,

where

${\displaystyle q_{a}}$ is the electron population in atomic orbital a,

${\displaystyle \beta _{ab}}$, ${\displaystyle S_{ab}}$ are the resonance and overlap integrals for the interaction of atomic orbitals a and b,

${\displaystyle Q_{k}}$ is the total charge on atom k,

${\displaystyle \varepsilon }$ is the local dielectric constant,

${\displaystyle R_{k\ell }}$ is the distance between the nuclei of atoms k and l,

${\displaystyle c_{ra}}$ is the coefficient of atomic orbital a in molecular orbital r,

and ${\displaystyle E_{r}}$ is the energy of molecular orbital r.

Broadly speaking, the first term describes the closed-shell repulsion of the occupied molecular orbitals of the reactants (four-electron filled-filled interactions, steric effects[4]). The second term describes the Coulombic attraction or repulsion between the atoms of the reactants (ionic contribution, electrostatic effects). Finally, the third term accounts for all possible interactions between the occupied and unoccupied molecular orbitals of the reactants (two-electron filled-unfilled interactions, stereoelectronic effects[5]). Although conceptually useful, the Klopman-Salem equation seldom serves as the basis for energetic analysis in modern quantum chemical calculations.

Because of the difference in MO energies appearing in the denominator of the third term, energetically close orbitals make the biggest contribution. Hence, approximately speaking, analysis can often be simplified by considering only the highest occupied and lowest unoccupied molecular orbitals of the reactants (the HOMO-LUMO interaction in frontier molecular orbital theory).[6] The relative contributions of the second (ionic) and third (covalent) terms play an important role in justifying hard soft acid base theory (HSAB), with hard-hard interactions governed by the ionic term and soft-soft interactions governed by the covalent term.[7]