The Journal of Chemical Physics · 2002 · 372 citations · 81 references
Natural SciencesChemistryPhysicsComputational ChemistryQuantum ChemistryQuantum MechanicsAb Initio MethodsCoupled Cluster TheoryHartree-fock TheoryMolecular Orbital TheoryMultireference MethodsStrongly Correlated Electron SystemsCoupled-cluster ApproximationElectron Correlation EffectsHigh-spin ConfigurationsHigh-spin StatesOpen-shell ConfigurationsOpen-shell Singlet StatesSpin StatesTriplet States
The spin-flip approach has been applied to calculate vertical and adiabatic energy separations between low-lying singlet and triplet states in diradicals. The spin-flip model describes both closed- and open-shell singlet and (low-spin) triplet states within a single reference formalism as spin-flipping, e.g., α→β, excitations from a high-spin triplet (Ms=1) reference state. Since both dynamical and nondynamical correlation effects are much smaller for the high-spin triplet states than for the corresponding singlet states, the spin-flip models yield systematically more accurate results than their traditional (non-spin-flip) counterparts. For all the diradicals studied in this work, the spin-flip variant of the coupled-cluster model with double excitations yields energy separations which are within less than 3 kcal/mol of the experimental or the highly accurate multireference values. In most cases the errors are about 1 kcal/mol.
81
General atomic and molecular electronic structure system
Michael W. Schmidt, Kim K. Baldridge, Jerry A. Boatz et al. · Journal of Computational Chemistry · 1993 · 20.2K citations
Natural Sciences, Chemistry, Physics +17