Ruthenium (II) Complexes of CNC Pincers and Bipyridine in the Photocatalytic CO₂ Reduction Reaction to CO Using Visible Light: Catalysis, Kinetics, and Computational Insights

A series of five ruthenium (II) complexes containing a tridentate CNC pincer ligand, a bidentate 2,2′-bipyridine (bpy) ligand, and a monodentate ligand (chloride, bromide, or acetonitrile) were synthesized. The CNC pincer ligands used imidazole or benzimidazole-derived N-heterocyclic carbenes (NHCs) as the C donors and a 4-methoxy-substituted central pyridyl ring as the N donor. All of the complexes were characterized by analytical, spectroscopic, and single-crystal X-ray diffraction methods. These complexes were used as catalysts for visible-light-driven CO2 reduction in the presence and absence of an external photosensitizer (PS). Notably, complex 4C with a benzimidazole-derived CNC pincer ligand and bromide as the monodentate ligand was the most active catalyst tested for both sensitized and self-sensitized CO2 reduction. Thus, this catalyst was the subject of further mechanistic studies using transient absorption spectroscopy (TAS), absorption spectroelectrochemistry (SEC), and computational studies. A mechanism has been proposed for self-sensitized CO2 reduction involving (1) light excitation of the catalyst, (2) reduction by sacrificial donors, (3) halide loss, and (4) CO2 binding to form [RuCO2]+ as the catalyst resting state. The timeline for these steps and the structures of key intermediates are all supported by experimental observations (including TAS and SEC) and supporting computational studies. Subsequent steps in the cycle past [RuCO2]+ were not experimentally observable, but they are supported by computations. Experiments were also used to explain the differences observed for sensitized catalysis. Catalyst 4C is an unusually active catalyst for both sensitized and self-sensitized CO2 reduction, and thus being able to understand how it functions and which steps are turnover-limiting is an important development facilitating the design of commercially viable catalysts for solar fuel formation

Ruthenium (II) Complexes of CNC Pincers and Bipyridine in the Photocatalytic CO₂ Reduction Reaction to CO Using Visible Light: Catalysis, Kinetics, and Computational Insights

A series of five ruthenium (II) complexes containing a tridentate CNC pincer ligand, a bidentate 2,2′-bipyridine (bpy) ligand, and a monodentate ligand (chloride, bromide, or acetonitrile) were synthesized. The CNC pincer ligands used imidazole or benzimidazole-derived N-heterocyclic carbenes (NHCs) as the C donors and a 4-methoxy-substituted central pyridyl ring as the N donor. All of the complexes were characterized by analytical, spectroscopic, and single-crystal X-ray diffraction methods. These complexes were used as catalysts for visible-light-driven CO2 reduction in the presence and absence of an external photosensitizer (PS). Notably, complex 4C with a benzimidazole-derived CNC pincer ligand and bromide as the monodentate ligand was the most active catalyst tested for both sensitized and self-sensitized CO2 reduction. Thus, this catalyst was the subject of further mechanistic studies using transient absorption spectroscopy (TAS), absorption spectroelectrochemistry (SEC), and computational studies. A mechanism has been proposed for self-sensitized CO2 reduction involving (1) light excitation of the catalyst, (2) reduction by sacrificial donors, (3) halide loss, and (4) CO2 binding to form [RuCO2]+ as the catalyst resting state. The timeline for these steps and the structures of key intermediates are all supported by experimental observations (including TAS and SEC) and supporting computational studies. Subsequent steps in the cycle past [RuCO2]+ were not experimentally observable, but they are supported by computations. Experiments were also used to explain the differences observed for sensitized catalysis. Catalyst 4C is an unusually active catalyst for both sensitized and self-sensitized CO2 reduction, and thus being able to understand how it functions and which steps are turnover-limiting is an important development facilitating the design of commercially viable catalysts for solar fuel formation

Ruthenium (II) Complexes of CNC Pincers and Bipyridine in the Photocatalytic CO₂ Reduction Reaction to CO Using Visible Light: Catalysis, Kinetics, and Computational Insights

A series of five ruthenium (II) complexes containing a tridentate CNC pincer ligand, a bidentate 2,2′-bipyridine (bpy) ligand, and a monodentate ligand (chloride, bromide, or acetonitrile) were synthesized. The CNC pincer ligands used imidazole or benzimidazole-derived N-heterocyclic carbenes (NHCs) as the C donors and a 4-methoxy-substituted central pyridyl ring as the N donor. All of the complexes were characterized by analytical, spectroscopic, and single-crystal X-ray diffraction methods. These complexes were used as catalysts for visible-light-driven CO2 reduction in the presence and absence of an external photosensitizer (PS). Notably, complex 4C with a benzimidazole-derived CNC pincer ligand and bromide as the monodentate ligand was the most active catalyst tested for both sensitized and self-sensitized CO2 reduction. Thus, this catalyst was the subject of further mechanistic studies using transient absorption spectroscopy (TAS), absorption spectroelectrochemistry (SEC), and computational studies. A mechanism has been proposed for self-sensitized CO2 reduction involving (1) light excitation of the catalyst, (2) reduction by sacrificial donors, (3) halide loss, and (4) CO2 binding to form [RuCO2]+ as the catalyst resting state. The timeline for these steps and the structures of key intermediates are all supported by experimental observations (including TAS and SEC) and supporting computational studies. Subsequent steps in the cycle past [RuCO2]+ were not experimentally observable, but they are supported by computations. Experiments were also used to explain the differences observed for sensitized catalysis. Catalyst 4C is an unusually active catalyst for both sensitized and self-sensitized CO2 reduction, and thus being able to understand how it functions and which steps are turnover-limiting is an important development facilitating the design of commercially viable catalysts for solar fuel formation