Assessment of the OLYP and O3LYP density functionals for first-row transition metals

• Published in: Journal of computational chemistry Vol. 24; no. 10; pp. 1184 - 1191
• Main Authors: Baker, Jon, Pulay, Peter
• Format: Journal Article
• Language: English
• Published: Hoboken Wiley Subscription Services, Inc., A Wiley Company 30-07-2003
• Subjects: BLYP/B3LYP functionals; density functional theory; OLYP/O3LYP functionals; transition metals
• ISSN: 0192-8651; 1096-987X
• DOI: 10.1002/jcc.10280

We have investigated the performance of the OLYP and O3LYP density functionals for predicting atomic excitation energies and ionization potentials, and bond dissociation energies, geometries, and vibrational frequencies for selected first‐row transition metal compounds, including hydrides (MH) and singly charged methylene and methyl cations. The OLYP and O3LYP functionals are similar to the well‐known BLYP and B3LYP functionals, respectively, but use a new optimized exchange functional (OPTX) developed by Handy and Cohen (Mol Phys 2001, 99, 403) in place of the standard B88 exchange. A previous study by us on organic reactions (J Chem Phys 2002, 117, 1331) indicated that both OLYP and O3LYP gave results for heats of reaction and barrier heights that were overall superior to those using the popular B3LYP functional. For transition metals, however, although OLYP is overall superior to BLYP for molecular calculations, it is inferior to B3LYP. O3LYP provides results for molecules of about the same quality as B3LYP. For atomic excitation and 4s ionization energies, unless relativistic effects are included, OLYP and O3LYP are clearly worse than both BLYP and B3LYP. There is thus no real incentive to use either OLYP or O3LYP in place of B3LYP for calculations involving first‐row transition metals. © 2003 Wiley Periodicals, Inc. J Comput Chem 24: 1184–1191, 2003