Structure and bonding of the transition-metal carbonyl complexes M(CO)(5)L (M=Cr, Mo, W) and M(CO)(3)L (M=Ni, Pd, Pt; L=CO, SiO, CS, N-2, NO+, CN-, NC-, HCCH, CCH2, CH2, CF2, H-2)

Quantum mechanical ab initio calculations at the MP2 and CCSD(T) level of theory using effective core potentials (ECP) for the metals with a valence basis set of DZP quality and a 6-31G(d) all-electron basis set for the other elements are reported for the complexes M(CO)(5)L (M = Cr, Mo, W) and M(CO)(3)L (M = Ni, Pd, Pt) with ligands L = CO, SiO, CS, N-2, NO+, CN-, NC-, HCCH, CCH2, CH2, CF2, and H-2. The optimized geometries at MP2/II are in very good agreement with experiment. The theoretically predicted (CO)(n)M-L bond dissociation energies at CCSD(T)II using MP2/II optimized geometries also agree quite well with experimental data. The (CO)(n)M-L bond is investigated using the charge decomposition analysis (CDA), which gives an interpretation of the donor-acceptor complexes in terms of charge donation, back-donation and repulsive polarization. The CDA results, which may be considered as a quantitative expression of the Dewar-Chatt-Duncanson model, are in agreement with the standard classification of the ligands.