Electronic Effects of Substituents on fac-M(bpy-R)(CO)₃ (M = Mn, Re) Complexes for Homogeneous CO₂ Electroreduction

Synthesis and characterization of 14 new 2,2'-bipyridine metal complexes fac-M(bpy-R)(CO)₃X (where M = Mn, X = Br or M = Re, X = Cl and R = -CF₃, -CN, -Ph, -PhOH, -NMe₂) are reported. The complexes have been characterized by NMR, IR spectroscopy and elemental analysis. Single crystal X-Ray diffraction structures have been solved for Re(dpbpy)(CO)₃Cl (dpbpy = 4,6-diphenyl-2,2'-bipyridine) and Re(hpbpy)(CO)₃Cl (hpbpy = 4-(2-hydroxy-phenyl)-6-phenyl-2,2'-bipyridine). Electrochemical behaviors of the complexes in acetonitrile under Ar and their catalytic performances for CO₂ reduction with added water and MeOH have been investigated by cyclic voltammetry and controlled potential electrolysis. The role of the substituents on the electrochemical properties and the related over potentials required for CO₂ transformation have been analyzed. The complexes carrying only electron withdrawing groups like -CF₃, -CN totally lose their catalytic activities toward CO₂ reduction, whereas the symmetric -NMe₂ substituted and push-pull systems (containing both -NMe₂ and -CF₃) still display electrocatalytic current enhancement under CO₂ atmosphere. The complexes carrying a phenyl or a phenol group in position 4 show catalytic behaviors similar to those of simple M-bpy systems. The only detected reduction product by GC analysis is CO: for example, fac-Re (bpy-4,4'-NMe₂)(CO)₃Cl gives CO with high faradic efficiency and a TON of 18 and 31, in absence of external proton source and with 5% MeOH, respectively. DFT calculations were carried out to highlight the electronic properties of the complexes; results are in agreement with experimental electrochemical data.