Multi-configurational self-consistent field

<p>Multi-configurational self-consistent field (MCSCF) is a method in <a href="/facts/Quantum_chemistry/H9AXV0lx">quantum chemistry</a> used to generate qualitatively correct reference states of molecules in cases where <a href="/facts/Hartree%25E2%2580%2593Fock/U9mlRWVR">Hartree–Fock</a> and <a href="/facts/Density_functional_theory/wwz4Gqdg">density functional theory</a> are not adequate (e.g., for molecular ground states which are quasi-degenerate with low-lying excited states or in bond-breaking situations). It uses a linear combination of <a href="/facts/Configuration_state_function/ouDKnRms">configuration state functions</a> (CSF), or configuration determinants, to approximate the exact electronic <a href="/facts/Wavefunction/KgM5ykjY">wavefunction</a> of an atom or molecule. In an MCSCF calculation, the set of coefficients of both the CSFs or determinants and the basis functions in the molecular orbitals are varied to obtain the total electronic wavefunction with the lowest possible energy. This method can be considered a combination between <a href="/facts/Configuration_interaction/CJv3fhYy">configuration interaction</a> (where the molecular orbitals are not varied but the expansion of the wave function is) and Hartree–Fock (where there is only one determinant, but the molecular orbitals are varied).
</p><p>MCSCF wave functions are often used as reference states for <a href="/facts/Multireference_configuration_interaction/Kqydgd5s">multireference configuration interaction</a> (MRCI) or multi-reference perturbation theories like <a href="/facts/Complete_active_space_perturbation_theory/LRmjX1Vj">complete active space perturbation theory</a> (CASPT2). These methods can deal with extremely complex chemical situations and, if computing power permits, may be used to reliably calculate molecular ground and excited states if all other methods fail.
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Multi-configurational self-consistent field open-in-new

Multi-configurational self-consistent field