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Optimization of RI‐MP2 Auxiliary Basis Functions for 6‐31G** and 6‐311G** Basis Sets for First‐, Second‐, and Third‐Row Elements
Author(s) -
Tanaka Masato,
Katouda Michio,
Nagase Shigeru
Publication year - 2013
Publication title -
journal of computational chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.907
H-Index - 188
eISSN - 1096-987X
pISSN - 0192-8651
DOI - 10.1002/jcc.23430
Subject(s) - basis (linear algebra) , basis function , sto ng basis sets , perturbation theory (quantum mechanics) , gaussian , function (biology) , standard basis , computational chemistry , mathematics , basis set , physics , quantum mechanics , chemistry , complete active space , mathematical analysis , combinatorics , density functional theory , geometry , evolutionary biology , biology
Auxiliary basis functions for second‐order Møller–Plesset perturbation theory with resolution‐of‐identity approximation (RI‐MP2) are developed for first‐, second‐, and third‐row elements, which are suitable for Pople‐type 6‐31G** and 6‐311G** basis sets. Atomic‐centered Gaussian functions up to the g ‐type function are used for auxiliary basis functions to obtain higher accuracy for molecules with the accurate description of bonding properties. The performance of the developed auxiliary basis functions were tested and evaluated for 114 small and 23 large molecules. The developed auxiliary basis functions show much smaller energy differences between MP2 and RI‐MP2 than other auxiliary basis functions used for 6‐31G** and 6‐311G** basis sets with similar computational costs. © 2013 Wiley Periodicals, Inc.