Quantum mechanics study of repulsive π–π interaction and flexibility of phenyl moiety in the iron azodioxide complex

Abstract

In this study, repulsive π–π interactions within iron azodioxide complex Fe[Ph(O)NN(O)Ph]3 were quantum mechanically characterized using DFT, MP2 and CCSD(T) methods. Flexibility of six phenyl moieties in this complex structure was also investigated by structural optimization approach using the DFT methods. Our MP2 and CCSD(T) calculations of the closest pair provided interaction energy of 6.62 and 8.29kcal/mol respectively, which indicate a strongest repulsion among these intra-molecular π–π interactions. Interaction energy of the particular π–π pair calculated from 24 hybrid DFT methods ranges from 4.56kcal/mol from BHandH method to 15.15kcal/mol from O3LYP method. Cares should be exercised when interpreting interaction energy and geometry optimization from DFT simulation of systems containing π–π interaction. Comparison between the DFT results and the benchmark CCSD(T) results shows that the DFT calculations of π–π interaction are reasonable but still need to be interpreted with caution. Furthermore, MP2 interaction energy of −44.69kcal/mol between two substituted π systems/phenyl rings Ph(O)N-moieties suggested that above energetically unfavorable π–π interaction can be compensated by the covalent bond N–N in a single ligand Ph(O)NN(O)Ph, which allows for a reasonable stability across the complex molecules. Optimizations of the entire complex molecule using B3LYP and M06HF methods produced a large variation of π–π distances and orientations, which implied that the complex molecule may perform catalysis at room temperature.