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Gaussian-3 theory using reduced Mo/ller-Plesset order

Larry A. CurtissChemistry and Materials Science Divisions, Argonne National Laboratory, Argonne, Illinois 60439Paul C. RedfernChemistry and Materials Science Divisions, Argonne National Laboratory, Argonne, Illinois 60439Krishnan RaghavachariVitaly A. RassolovDepartment of Chemistry, Northwestern University, Evanston, Illinois 60208John A. PopleDepartment of Chemistry, Northwestern University, Evanston, Illinois 60208
1999en
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A variation of Gaussian-3 (G3) theory is presented in which the basis set extensions are obtained at the second-order Mo/ller–Plesset level. This method, referred to as G3(MP2) theory, is assessed on 299 energies from the G2/97 test set [J. Chem. Phys. 109, 42 (1998)]. The average absolute deviation from experiment of G3(MP2) theory for the 299 energies is 1.30 kcal/mol and for the subset of 148 neutral enthalpies it is 1.18 kcal/mol. This is a significant improvement over the related G2(MP2) theory [J. Chem. Phys. 98, 1293 (1993)], which has an average absolute deviation of 1.89 kcal/mol for all 299 energies and 2.03 kcal/mol for the 148 neutral enthalpies. The corresponding average absolute deviations for full G3 theory are 1.01 and 0.94 kcal/mol, respectively. The new method provides significant savings in computational time compared to G3 theory and, also, G2(MP2) theory.

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