Metal-free reduction of CO2 to formate using a photochemical organohydride-catalyst recycling strategy

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DOI 10.1038/s41557-023-01157-6
Authors Weibin Xie, Jiasheng Xu, Ubaidah Md Idros, Jouji Katsuhira, Masaaki Fuki, Masahiko Hayashi, Masahiro Yamanaka, Yasuhiro Kobori, Ryosuke Matsubara,
Submitted 23.03.2023
Published online 23.03.2023
Licenses https://www.springernature.com/gp/researchers/text-and-data-mining, https://www.springernature.com/gp/researchers/text-and-data-mining,
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Abstract

Summary

A photochemical reduction of CO2 to CO was shown using the iron complexes (100947), (100948) and (100949) as catalysts in combination with the organic photosensitizer 4CzIPN (100938). Turnover numbers (TONs) of 6320 and a selectivity of 99.4% for CO were reached in DMF/H2O with catalyst (100949). The experiments were conducted under visible-light irradiation (λ = 440 nm) using TEA as sacrificial electron donor (see section SEDs below).

Advances and special progress

Additional remarks

Content of the published article in detail

The article contains results for the reduction of CO2 to CO under visible-light catalysis using the iron complex (100949) as a catalyst. The catalytic system performs best (referring to the TON of CO production) in DMF/H2O.

Catalyst

Photosensitizer

3,6-bis(dimethylamino)-9-phenyl-9H-carbazole (100950)

Investigation

Sacrificial electron donor

In this study, the experiments were done with the sacrificial electron donor ascorbic acid L-ascorbate, sodium (100861). The use of BIH was tested, but found to yield worse results.

Additives

In this study,

Investigations