Nickel(II) pincer complexes demonstrate that the remote substituent controls catalytic carbon dioxide reduction

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DOI 10.1039/c7cc09507d
Authors Dalton B. Burks, Shakeyia Davis, Robert W. Lamb, Xuan Liu, Roberta R. Rodrigues, Nalaka P. Liyanage, Yujie Sun, Charles Edwin Webster, Jared H. Delcamp, Elizabeth T. Papish,
Submitted 13.03.2018
Published online 2018
Licenses http://rsc.li/journals-terms-of-use#chorus,
Subjects Materials Chemistry, Metals and Alloys, Surfaces, Coatings and Films, General Chemistry, Ceramics and Composites, Electronic, Optical and Magnetic Materials, Catalysis
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Abstract

Summary

A photochemical reduction of CO2 to CO was shown using the nickel complexes or as catalysts in combination with the iridium-based photosensitizer Ir(ppy)3. Turnover numbers (TONs) of 10.6 for CO with the cobalt complex Ni(4O(-)py)-(MeNHC)2Cl were reached in acetonitrile. The experiments were conducted under visible-light irradiation using BIH and TEA as sacrificial electron donors (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 nickel complexes as catalysts. The catalytic system performs best (referring to the TON of CO production) in acetonitrile with the cobalt catalyst Ni(4O(-)py)-(MeNHC)2Cl.

Catalyst

Ni(4O(-)py)-(MeNHC)2Cl [Ni(py)-(MeNHC)2(MeCN)][PF6]2

Photosensitizer

Ir(ppy)3

Investigation

Investigation-Name: Table 1

Sacrificial Electron Donor

In this study, the experiments were done with the sacrificial electron donors BIH (BIH) and TEA (TEA).

Additives

In this study, TfOH was used as an additive.

Investigations