Metal−Ligand Bond Distances in First-Row Transition Metal Coordination Compounds: Coordination Number, Oxidation State, and Specific Ligand Effects

Abstract

Mean metal−ligand bond distances for the coordination ligands isothiocyanate, pyridine, imidazole, water, and chloride, bound to the transition metals Mn, Fe, Co, Ni, Cu, and Zn in their 2+ oxidation states, were collected from searches the Cambridge Structure Database. The metal−ligand bond distances were converted to bond orders through the bond distance-bond order technique, as suggested by Pauling. The mean bond order sums at the 2+ metal centers were found to be independent of coordination number or geometry and to be strongly ligand-dependent; the values (by ligand) are as follows: isothiocyanate = 2.56 ± 0.13; imidazole = 2.13 ± 0.04; chloride = 2.12 ± 0.07; pyridine 1.95 ± 0.10; water = 1.88 ± 0.10. The bond order sum for Fe(III) bound to chloride was found to be 3.09, approximately one bond order unit larger than for the 2+ metal centers bound to chloride. Division of the ligand-specific bond order sums by coordination number allows prediction of the M−L bond distance to within 0.017 Å, regardless of the specific coordination geometry. The physical basis for the ligand-specific variation in bond order sum is also discussed.