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Croatica Chemica Acta, Vol. 82 No. 1, 2009.

Original scientific paper

The Effects of N-Heterocyclic Ligands on the Nature of the Ru–(NO) Bond in Ruthenium Tetraammine Nitrosyl Complexes

Giovanni F. Caramori ; Fachbereich Chemie, Philipps-Universität Marburg, Hans-Meerwein-Strasse, D-35032 Marburg, Germany
Gernot Frenking ; Fachbereich Chemie, Philipps-Universität Marburg, Hans-Meerwein-Strasse, D-35032 Marburg, Germany

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Abstract

Quantum chemical calculations at the DFT level have been carried out to analyze quantitatively the RuII–(NO)+, RuIII–(NO)0 and RuII–(NO)0 bonds in trans-[RuII(NH3)4(L)(NO)]q and trans-[RuII(NH3)4(L)(NO)]q−1 complexes, where L = 4-picoline (4-pic), C-bound imidazole (imC), N-bound imidazole (imN), nicotinamide (nic), pyridine (py), and pyrazine (pz). Equilibrium geometries and the vibrational frequencies are reported for the ground state GS and light-induced metastable states, MS1 and MS2, presenting good agreement with the experimental data. The nature of the RuII–(NO)+ and RuII–(NO)0 bonds was investigated by means of the energy decomposition analysis, EDA. The Ru–(NO) bonding situation has been analyzed in two different situations: prior and after one-electron reduction at the NO+ group. The EDA results for the complexes prior to the reduction of the NO+ indicate that the metalligand π-orbital interactions between NO+ and the [RuII(NH3)4(L)]q−1 are the most important term and that the trans-ligands imN and nic contribute to an increase in the π-donor strength of the metal centre towards NO+. For RuIII–(NO)0 bonds, the smallest values of ΔEint, ΔEPauli, ΔEelstat, and De are observed when L = imC or L = nic, independent of the state under consideration, GS or MS1, indicating that when L = imC or nic the RuIII–(NO)0 bond in GS or in MS1 states is more labile. After the reduction of the NO+ group, the RuII–(NO)0 becomes more labile when the trans-ligand is imC, which agrees with the experimental rate constants of NO0 dissociation.

Keywords

nitric oxide; ruthenium tetraammines; N-heterocyclic ligands; energy decomposition analysis

Hrčak ID:

38648

URI

https://hrcak.srce.hr/38648

Publication date:

30.6.2009.

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