Photochemical CO2 Reduction Using Rhenium(I) Tricarbonyl Complexes with Bipyridyl-Type Ligands with and without Second Coordination Sphere Effects

The effect of phenyl, phenol, aniline, amino, and CF substituents of the 2,2'-bipyridine ligand in toc-ReCl(L)(CO)(3) (L-2,2'-bipyridine derivative) catalysts on photochemical CO2 reduction in dimethylacetamide is examined, in order to understand the structure-function relationships and to compare the catalytic activities with the previously published electrochemical results. All complexes including ReCl(bpy)(CO)(3) have similar excitedstate lifetimes and emission spectra, but complex 1 with the Ph-NH2 moiety exhibits a significantly larger molar absorption coefficient for its metal-to-ligand charge transfer (MLCT) band. All complexes we tested produce CO with only a negligible amount of H-2 and formate in self-sensitized systems in the presence of triethanolamine (TEOA) and in some cases, BIH (1,3-dimethyl-2-phenyl-2,3-dihydro-1H-benzo[d]-imidazole). The presence of the Ph-NH2 moiety (complex 1) has a beneficial effect on both electrochemical and photochemical activity, allowing a turnover number (TON) of 32 and 120 for photochemical CO production (without and with BIH, respectively). In the case of the Ph-OH group in the second coordination sphere (complexes 4 and 6), these complexes are active for photochemical CO2 reduction, despite the formation of a stable 6-coordinate Re-OPh intermediate via reductive deprotonation as previously observed under electrochemical conditions. Overall, BIH accelerates the rate of formation of the one-electron reduced species (OERS) of the Re catalysts and allows higher turnover frequency (TOF) and TON for CO formation. The X-ray structures of complexes 1 and 4 were determined to have distorted octahedral Re centres, and show pi-pi stacking interactions with neighboring molecules as well as intramolecular hydrogen bonds to the internal chloride ligands. The unusually high absorptivity of the MLCT absorption of complex 1 has been explained by TD-DFT calculations.

Automated summary

The influence of phenyl, phenol, aniline, amino, and CF substituents of the 2,2'-bipyridine ligand on the photochemical CO2 reduction in dimethylacetamide was examined. The presence of Ph-NH2 moiety was found to enhance both electrochemical and photochemical activity, leading to higher turnover numbers for CO production. The complexes with Ph-OH group in the second coordination sphere also showed promising activity in photochemical CO2 reduction, despite the formation of a stable 6-coordinate intermediate under electrochemical conditions.