Bimetallic Carbonyl Complexes Based on Iridium and Rhodium: Useful Tools for Hydrodefluorination Reactions

Abstract

AbstractA set of bimetallic complexes based on iridium and rhodium with bis(diphenylphosphino)methane, bis(di‐iso‐propylphosphino)methane, diphenyl‐2‐pyridylphosphine and 2‐(di‐iso‐propylphosphino)imidazole bridging ligands was prepared. The complexes were characterized by NMR and IR spectroscopy and studied quantum‐chemically using DFT methods. The bimetallic systems succeeded in catalytic hydrodefluorination reactions of lower fluorinated aryl fluorides using molecular hydrogen and sodiumtert‐butoxide as a base. Effects of (i) ligand variation, (ii) mono‐ vs bimetallic nuclearity, and (iii) Ir vs Rh metal identity were studied and rationalized en route to achieve an effective hydrodefluorination.