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 (100851) and Ru(py)-(MeNdpp)2(CO)2Cl (100852) as catalyst in combination with the ruthenium-based photosensitizer [Ru(bpy)3][PF6] (100808). Turnover numbers (TONs) of 380 for formic acid were reached in dimethylformamide with complex Ru(py)-(MeNdpp)2(CO)2Cl (100852). 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%.

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 (100852) in dimethylformamide.

Catalyst

(100772) [Show R-Groups]

Photosensitizer

[Ru(bpy)3][PF6] (100808)

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.