Formation, characterization, structure and bonding analysis of the metal–carbon bond OM-(η6-C6H6) (M = Sc, Ti) complexes in solid matrix: Infrared spectroscopic and theoretical study

Abstract

The reactions of ScO and TiO molecules with benzene have been studied in solid argon with infrared absorption spectroscopy combining with theoretical calculations. Laser-evaporation of bulk higher oxide targets prepared the scandium and titanium monoxide molecules. The scandium and titanium monoxide molecules reacted with benzene to form the typical transition metal–carbon bond (MCB) complexes, OM-(η6-C6H6) (M = Sc, Ti), which have been identified on the basis of isotopic infrared studies and density functional calculations. The theoretical calculation results illustrate the deformation of the planar carbon skeleton of benzene takes place and the bond lengths of M–O are largely elongated upon OM-(η6-C6H6) (M = Sc, Ti) complexes. The population results illustrate the OM-(η6-C6H6) are determined to have 2A1 and 1A1 electronic ground state both with C2v symmetry arising from 2Δ and 1∑− of excited-state ScO and TiO reaction with benzene, respectively. The OSc-(η6-C6H6) and OTi-(η6-C6H6) are both stable d–pπ coordination compounds and can also not be photoisomerized by UV irradiation under low temperature in solid argon matrix. Natural bond orbital analyses conclude that the OTi-(η6-C6H6) system includes two equivalent Ti–C single bonds with strong binding bond energies.