Gaussian basis sets for use in correlated molecular calculations. I. The atoms boron through neon and hydrogen
Тип публикации: Journal Article
Дата публикации: 1989-01-15
scimago Q1
wos Q2
БС2
SJR: 0.819
CiteScore: 5.3
Impact factor: 3.1
ISSN: 00219606, 10897690
Physical and Theoretical Chemistry
General Physics and Astronomy
Краткое описание
In the past, basis sets for use in correlated molecular calculations have largely been taken from single configuration calculations. Recently, Almlof, 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 i f the exponents of the functions are optimized in atomic correlated calculations, although the primitive (s p) functions for describing correlation effects can be taken from atomic Hartree–Fock calculations i f 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 Almlof 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 c o r r e l a t i o n c o n s i s t e n t b a s i s s e t s, 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.
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Dunning T. H. Gaussian basis sets for use in correlated molecular calculations. I. The atoms boron through neon and hydrogen // Journal of Chemical Physics. 1989. Vol. 90. No. 2. pp. 1007-1023.
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Dunning T. H. Gaussian basis sets for use in correlated molecular calculations. I. The atoms boron through neon and hydrogen // Journal of Chemical Physics. 1989. Vol. 90. No. 2. pp. 1007-1023.
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TY - JOUR
DO - 10.1063/1.456153
UR - https://doi.org/10.1063/1.456153
TI - Gaussian basis sets for use in correlated molecular calculations. I. The atoms boron through neon and hydrogen
T2 - Journal of Chemical Physics
AU - Dunning, Thom H.
PY - 1989
DA - 1989/01/15
PB - AIP Publishing
SP - 1007-1023
IS - 2
VL - 90
SN - 0021-9606
SN - 1089-7690
ER -
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@article{1989_Dunning,
author = {Thom H. Dunning},
title = {Gaussian basis sets for use in correlated molecular calculations. I. The atoms boron through neon and hydrogen},
journal = {Journal of Chemical Physics},
year = {1989},
volume = {90},
publisher = {AIP Publishing},
month = {jan},
url = {https://doi.org/10.1063/1.456153},
number = {2},
pages = {1007--1023},
doi = {10.1063/1.456153}
}
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MLA
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Dunning, Thom H.. “Gaussian basis sets for use in correlated molecular calculations. I. The atoms boron through neon and hydrogen.” Journal of Chemical Physics, vol. 90, no. 2, Jan. 1989, pp. 1007-1023. https://doi.org/10.1063/1.456153.