Iron bispentazole Fe(eta5-N5)2, a theoretically predicted high-energy compound: structure, bonding analysis, metal-ligand bond strength and a comparison with the isoelectronic ferrocene.

Abstract

Quantum-chemical calculations with gradient-corrected (B3LYP) density functional theory have been carried out for iron bispentazole and ferrocene. The calculations predict that Fe(eta5-N5)2 is a strongly bonded complex which has D5d symmetry. The theoretically predicted total bond energy that yields Fe in the 5D ground state and two pentazole ligands is Do = 109.0 kcal mol(-1), which is only 29 kcal mol(-1) less than the calculated bond energy of ferrocene (Do = 138.0 kcal mol(-1); experimental: 158 +/- 2 kcal mol(-1)). The compound Fe(eta5-N5)2 is 260.5 kcal mol(-1) higher in energy than the experimentally known isomer Fe(N2)5, but the bond energy of the latter (Do = 33.7 kcal mol(-1)) is much less. The energy decomposition analyses of Fe(eta5-N5)2 and ferrocene show that the two compounds have similar bonding situations. The metal-ligand bonds are roughly half ionic and half covalent. The covalent bonding comes mainly from (e1g) eta5-N5- --> Fe2+ pi-donation. The previously suggested MO correlation diagram for ferrocene is nicely recovered by the Kohn-Sham orbitals. The calculated vibrational frequencies and IR intensities are reported.