Visible-Light Photocatalytic Reduction of CO2 to Formic Acid with a Ru Catalyst Supported by N,N’- Bis(diphenylphosphino)-2,6-diaminopyridine Ligands
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Abstract
Summary
A photochemical reduction of CO2 to formic acid was shown using the ruthenium pincer complexes Ru(py)-(HNdpp)2(CO)2Cl and Ru(py)-(MeNdpp)2(CO)2Cl as catalyst in combination with the ruthenium-based photosensitizer [Ru(bpy)3][PF6]. Turnover numbers (TONs) of 380 for formic acid were reached in dimethylformamide with complex Ru(py)-(MeNdpp)2(CO)2Cl. The experiments were conducted under visible-light irradiation (λ = 405 nm) using TEOA as sacrificial electron donor (see section SEDs below).
Advances and special progress
The authors report a novel molecular architecture for a ruthenium photocatalyst active in the reduction of CO2 to formic acid, displaying competitive TONs and quantum yields up to 14%.
Additional remarks
Content of the published article in detail
The article contains results for the reduction of CO2 to formic acid under visible-light catalysis using ruthenium complexes as catalysts. The catalytic system performs best (referring to the TON of formic acid production) with complex Ru(py)-(MeNdpp)2(CO)2Cl in dimethylformamide.
Catalyst
Photosensitizer
Investigation
Experiment 'Visible-Light Photocatalytic Reduction of CO2 to Formic Acid with a Ru Catalyst Supported by N,N’- Bis(diphenylphosphino)-2,6-diaminopyridine Ligands/Best photocatalytic results' does not exist.
Sacrificial electron donor
In this study, the experiments were done with the sacrificial electron donors TEOA (100507).
Additives
In this study, no additives were tested.
Investigations
- Table 1 (Molecular process, Photocatalytic CO2 conversion experiments)