Gaussian basis sets for use in correlated molecular calculations. I. The atoms boron through neon and hydrogen

1989 The Journal of Chemical Physics 30,931 citations

Abstract

In the past, basis sets for use in correlated molecular calculations have largely been taken from single configuration calculations. Recently, Almlöf, Taylor, and co-workers have found that basis sets of natural orbitals derived from correlated atomic calculations (ANOs) provide an excellent description of molecular correlation effects. We report here a careful study of correlation effects in the oxygen atom, establishing that compact sets of primitive Gaussian functions effectively and efficiently describe correlation effects if the exponents of the functions are optimized in atomic correlated calculations, although the primitive (sp) functions for describing correlation effects can be taken from atomic Hartree–Fock calculations if the appropriate primitive set is used. Test calculations on oxygen-containing molecules indicate that these primitive basis sets describe molecular correlation effects as well as the ANO sets of Almlöf and Taylor. Guided by the calculations on oxygen, basis sets for use in correlated atomic and molecular calculations were developed for all of the first row atoms from boron through neon and for hydrogen. As in the oxygen atom calculations, it was found that the incremental energy lowerings due to the addition of correlating functions fall into distinct groups. This leads to the concept of correlation consistent basis sets, i.e., sets which include all functions in a given group as well as all functions in any higher groups. Correlation consistent sets are given for all of the atoms considered. The most accurate sets determined in this way, [5s4p3d2f1g], consistently yield 99% of the correlation energy obtained with the corresponding ANO sets, even though the latter contains 50% more primitive functions and twice as many primitive polarization functions. It is estimated that this set yields 94%–97% of the total (HF+1+2) correlation energy for the atoms neon through boron.

Keywords

NeonBasis setBasis (linear algebra)STO-nG basis setsGaussianMolecular orbitalAtom (system on chip)ChemistryAtomic orbitalElectronic correlationAtomic physicsBasis functionCorrelationMoleculeComputational chemistryPhysicsQuantum mechanicsMathematicsLinear combination of atomic orbitalsDensity functional theoryArgonGeometry

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Year
1989
Type
article
Volume
90
Issue
2
Pages
1007-1023
Citations
30931
Access
Closed

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Thom H. Dunning (1989). Gaussian basis sets for use in correlated molecular calculations. I. The atoms boron through neon and hydrogen. The Journal of Chemical Physics , 90 (2) , 1007-1023. https://doi.org/10.1063/1.456153

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DOI
10.1063/1.456153