Abstract
The recently developed DLPNO-CCSD(T) method and seven popular DFT functionals (B3LYP, M06, M06L, PBE, PBE0, TPSS, and TPSSh) with and without an empirical dispersion term have been tested to reproduce 111 gas phase reaction enthalpies involving 11 different transition metals. Our calculations, corrected for both relativistic effects and basis set incompleteness, indicate that most of the methods applied with default settings perform with acceptable accuracy on average. Nevertheless, our calculations also evidenced unexpected and nonsystematic large deviations for specific cases. For group 12 metals (Zn, Cd, Hg), most of the methods provided mean unsigned errors (MUE) less than 5.0 kcal/mol, with DLPNO-CCSD(T) and PBE methods performing excellently (MUE lower 2.0 kcal/mol). Problems started with group 4 metals (Ti and Zr). The best performer for Zr complexes with MUE of 1.8 kcal/mol, PBE0-D3, provides MUE larger than 8 kcal/mol for Ti. DLPNO-CCSD(T) provides a reasonable MUE of 3.3 kcal/mol for Ti reactions but gives MUE a larger than 14.4 kcal/mol for Zr complexes, with all the larger deviations for reactions involving ZrF4. Large and nonsystematic errors have been obtained for group 6 metals (Mo and W), for eight reactions containing Fe, Cu, Nb, and Re complexes. Finally, for the whole set of 111 reactions, the DLPNO-CCSD(T), B3LYP-D3, and PBE0-D3 methods turned out to be the best performers, all providing MUE below 5.0 kcal/mol. Since DFT results cannot be systematically improved and large nonsystematic deviations of 20-30 kcal/mol were obtained even for best performers, our results indicate that current DFT methods are still unable to provide robust predictions in transition metal thermochemistry, at least for the functionals explored in this work. The same conclusion holds for both DLPNO-CCSD(T) and canonical CCSD(T) methods when used entirely as out-of-the-box. However, if careful investigation of core correlation is performed, relativistic effects are properly included and the quality of the reference wave function is properly checked, CCSD(T) methods can still provide good quality results that might even be used to validate DFT methods due to paucity of accurate thermodynamic data for realistic-sized transition metal complexes.