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 complex Ni(4O(-)py)-(MeNHC)2Cl (100823) in comparison to the inactive derivative [Ni(py)-(MeNHC)2(MeCN)][PF6]2 (100827) as catalyst in combination with the iridium-based photosensitizer Ir(ppy)3 (100843). Turnover numbers (TONs) of 10.6 for CO with the cobalt complex Ni(4O(-)py)-(MeNHC)2Cl (100823) 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

The authors showed the importance of remote substituents by a drastic change in activity through a change in a remote substituent.

Additional remarks

The designed photocatalyst could be turned on and off via (de)protonation.

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 (100823).

Catalyst

Ni(4O(-)py)-(MeNHC)2Cl (100823) [Ni(py)-(MeNHC)2(MeCN)][PF6]2 (100827)

Photosensitizer

Ir(ppy)3 (100843)

Investigation

catcat conc [µM]PSPS conc [mM]e-De-D conc [M]solvent Aadditivesλexc [nm]TON CO..
(edit)1.Ni(4O(-)py)-(MeNHC)2Cl0.1Ir(ppy)30.1BIH0.011MeCNTEAsolar spectrum10.6
(edit)2.[Ni(py)-(MeNHC)2(MeCN)][PF6]20.1Ir(ppy)30.1BIH0.011MeCNTEAsolar spectrum0.1
(edit)3.Ni(4O(-)py)-(MeNHC)2Cl0.1Ir(ppy)30.1BIH0.011DMFTEAsolar spectrum9
(edit)4.[Ni(py)-(MeNHC)2(MeCN)][PF6]20.1Ir(ppy)30.1BIH0.011DMFTEAsolar spectrum0.5
(edit)5.Ni(4O(-)py)-(MeNHC)2Cl0.1Ir(ppy)30.1BIH0.011MeCNsolar spectrum1.8
(edit)6.Ni(4O(-)py)-(MeNHC)2Cl0.1Ir(ppy)30.1BIH0.011MeCNproton spongesolar spectrum5.6
(edit)7.Ni(4O(-)py)-(MeNHC)2Cl0.1Ir(ppy)30.1BIH0.011MeCNTfOHsolar spectrum0.9
(edit)8.Ni(4O(-)py)-(MeNHC)2Cl0.1BIH0.011MeCNTEAsolar spectrum0.6
(edit)9.Ni(4O(-)py)-(MeNHC)2Cl0.1Ir(ppy)30.1MeCNTEAsolar spectrum0.3
(edit)10.Ni(4O(-)py)-(MeNHC)2Cl0.1Ir(ppy)30.1BIH0.011MeCNN2solar spectrum0.2

Investigation-Name: Photocatalytic CO2 reduction under varied conditions

Sacrificial Electron Donor

In this study, the experiments were done with the sacrificial electron donors BIH (BIH (100508)) and TEA (TEA (100505)).

Additives

In this study, TfOH (100744) and proton sponge were used as additives to (de)protonate the catalytically active nickel complex. Moreover, a control experiment under nitrogen atmosphere was conducted.

Investigations