Assessment of model chemistries for noncovalent interactions

In the present study, we report tests of 57 model chemistry methods for calculating binding energies of 31 diverse van der Waals molecules arranged in five databases of noncovalent interaction energies. The model chemistries studied include wave function theory (WFT), density functional theory (DFT), and combined wave function-density-functional-theory (CWFDFT), and they include methods whose computational effort scales (for large systems) as N-7, N-6, N-5, and N-4, where N is the number of atoms. The model chemistries include 2 CWFDFT N-7 models, 4 multilevel WFT N-7 models, 5 single-level WFT N-7 models, 4 CWFDFT N-6 models, 3 multilevel WFT N-6 models, 11 single-level WFT N-6 models, 5 CWFDFT N-5 models, 10 single- level WFT N-5 models, 4 multilevel WFT N-5 models, 4 single-level DFT N-4 models, and 5 single-level WFT N-4 models. We draw the following conclusions based on the mean absolute errors in 31 noncovalent binding energies: (1) MCG3-MPW gives the best performance for predicting the binding energies of these noncovalent complexes. (2) MCQCISD-MPWB and MCQCISD-MPW are the best two N-6 methods. (3) M05-2X is the best single-level method for these noncovalent complexes. These four methods should facilitate useful calculations on a wide variety of practical applications involving hydrogen bonding, charge-transfer complexes, dipole interactions, weak (dispersion-like) interactions, and pi center dot center dot center dot pi stacking. If a user is interested in only a particular type of noncovalent interactions, though, some other methods, may be recommended for especially favorable performance/cost ratios. For example, BMC-CCSD has an outstanding performance for hydrogen bonding, and PWB6K has an outstanding cost-adjusted performance for dipole interaction calculations on very large systems. We also show that M05-2X performs well for interactions of amino acid pair residues.