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,
Subjects -
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Abstract

Summary

A photochemical reduction of CO2 to CO was shown using -missing link parameter- as catalyst in combination with the organic carbazole-based photosensitizer 3,6-bis(dimethylamino)-9-phenyl-9H-carbazole (100950). Turnover numbers (TONs) of 6080 for the catalyst and 8820 for the photosensitizer and an exclusive selectivity for formic acid were reached in MeCN/H2O with catalyst xx. The experiments were conducted under visible-light irradiation (λ = 400 nm) using ascorbic acid 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 HCOO- under visible-light catalysis using as a catalyst. The catalytic system performs best (referring to the TON of formic acid production) in MeCN/H2O.

Catalyst

1,2,3-Trimethylbenzimidazolium iodide (100951)

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, potassium carbonate was added as a base.

Investigations