Novel ruthenium complexes bearing bipyridine-based and N-heterocyclic carbene-supported pyridine (NCN) ligands: the influence of ligands on catalytic transfer hydrogenation of ketones.

Transfer hydrogenation (TH) is a powerful synthetic tool in the production of secondary alcohols from ketones by using a non-H 2 hydrogen source along with metal catalysts. Among homogeneous catalysts, Ru(II) complexes are the most efficient catalysts. In our research, six novel ruthenium(II) complexes bearing bipyridine-based ligands [Ru(L1)Cl 2 ] (1), [Ru(L1)(PPh 3 )Cl]Cl (2) and [Ru(L2)Cl 2 ] (3) and N-heterocyclic carbene-supported pyridine (NCN) ligands [RuCp(L3)]PF 6 (4), [RuCp*(L3)]PF 6 (5), and [Ru( p -cymene)(L3)Cl]PF 6 (6) (where L1 = 6,6'-bis(aminomethyl)-2,2'-bipyridine, L2 = 6,6'-bis(dimethylaminomethyl)-2,2'-bipyridine and L3 = 1,3-bis(2-methylpyridyl)imidazolium bromide) were synthesised and characterised by NMR spectroscopy, HRMS, and X-ray crystallography. The catalytic transfer hydrogenation of 28 ketones in 2-propanol at 80 °C in the presence of KO t Bu (5 mol%) was demonstrated and the effect of ligands is highlighted. The results show that catalyst 1 exhibits improved TH efficiency compared to the commercially available Milstein catalyst and displays higher catalytic activity than 2 due to the steric effect from PPh 3 . From a combination of kinetic data and Eyring analysis, a zero-order dependence on the acetophenone substrate is observed, implying a rate-limiting hydride transfer step, leading to the proposed inner-sphere hydride transfer mechanism.