The Journal of Chemical Physics · 1990 · 695 citations · 24 references
Natural SciencesChemistryPhysicsComputational ChemistryQuantum ChemistryTheoretical ChemistryAb Initio MethodsConfiguration InteractionDensity Functional TheoryElectronic StructureMolecular Orbital TheoryAb Initio Molecular CalculationsAtomizationElectron Correlation EffectsElectron Correlation TreatmentGaussian Basis FunctionsGaussian Basis SetsIonizationQuadratic Configuration Interaction
The Gaussian-1 theoretical procedure is extended and tested on compounds containing second-row atoms (Na–Cl). This is a composite procedure based on ab initio molecular orbital theory, utilizing large basis sets (including diffuse-sp, double-d, and f-polarization functions) and treating electron correlation by Mo/ller–Plesset perturbation theory and by quadratic configuration interaction. Total atomization energies for a set of 24 species agree with accurate experimental data to an accuracy of better than 3 kcal/mol in most cases, SO2 being the notable exception. Similar agreement is achieved for ionization energies, electron affinities, and proton affinities. The method is used to assess experimental data for a number of other compounds having less accurate atomization energies.
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Gaussian-1 theory: A general procedure for prediction of molecular energies
John A. Pople, Martin Head‐Gordon, Douglas J. Fox et al. · The Journal of Chemical Physics · 1989 · 1.5K citations
Natural Sciences, Chemistry, Physics +17
JANAF thermochemical tables, 1975 supplement
M. W. Chase, J. L. Curnutt, H. Prophet et al. · Journal of Physical and Chemical Reference Data · 1975 · 612 citations
Natural Sciences, Chemistry, Physics +17