Density functional study of the Fe-CO bond dissociation energies of Fe(CO)(5)

Fe(CO)(n) (n=1-5) complexes have been studied using density functional theo ry (DFT) methods. Several functionals have been used in the geometry optimi zations, harmonic frequencies computation and calculation of the iron-carbo nyl bond dissociation energies. Coupled-cluster single double (triple) bond dissociation energies have also been computed for the smaller systems. The obtained results show that DFT methods yield reasonable geometries and vib rational frequencies. Regarding the bond dissociation energies, it is shown that the validity of the results depends on whether there is a change in t he atomic state of the metal during the dissociation; When the atomic state is the same for both complexes, the bond dissociation energy computed usin g gradient corrected functionals is within the range of the experimental va lues, while when the atomic state changes, DFT methods overestimate the bon d dissociation energy due to a poor description of the atomic multiplets. ( C) 1999 American Institute of Physics. [S0021-9606(99)31101-6].