Visible-Light Photocatalytic Reduction of CO2 to Formic Acid with a Ru Catalyst Supported by N,N’- Bis(diphenylphosphino)-2,6-diaminopyridine Ligands: Difference between revisions

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DOI 10.1002/cssc.201901326
Authors Yasmeen Hameed, Gyandshwar Kumar Rao, Jeffrey S. Ovens, Bulat Gabidullin, Darrin Richeson,
Submitted 11.06.2019
Published online 03.07.2019
Licenses http://onlinelibrary.wiley.com/termsAndConditions#vor, http://doi.wiley.com/10.1002/tdm_license_1.1,
Subjects General Energy, General Materials Science, General Chemical Engineering, Environmental Chemistry
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===Abstract===
===Abstract===
====Summary====
====Summary====
A photochemical reduction of CO<sub>2</sub> to formic acid was shown using the ruthenium pincer complexes {{#moleculelink:|link=RQVVTEHURKEOIA-UHFFFAOYSA-M|image=false|width=300|height=200}} and {{#moleculelink:|link=XNTONGVEYKVCNE-UHFFFAOYSA-M|image=false|width=300|height=200}} as catalyst in combination with the ruthenium-based photosensitizer {{#moleculelink:|link=KLDYQWXVZLHTKT-UHFFFAOYSA-N|image=false|width=300|height=200}}. Turnover numbers (TONs) of 380 for formic acid were reached in dimethylformamide with complex {{#moleculelink:|link=XNTONGVEYKVCNE-UHFFFAOYSA-M|image=false|width=300|height=200}}. The experiments were conducted under visible-light irradiation (λ = 405 nm) using TEOA as sacrificial electron donor (see section SEDs below).
A photochemical reduction of CO<sub>2</sub> to formic acid was shown using the ruthenium pincer complexes {{#moleculelink: |link=RQVVTEHURKEOIA-UHFFFAOYSA-M|image=false|width=300|height=200}} and {{#moleculelink:|link=XNTONGVEYKVCNE-UHFFFAOYSA-M|image=false|width=300|height=200}} as catalyst in combination with the ruthenium-based photosensitizer {{#moleculelink:|link=KLDYQWXVZLHTKT-UHFFFAOYSA-N|image=false|width=300|height=200}}. Turnover numbers (TONs) of 380 for formic acid were reached in dimethylformamide with complex {{#moleculelink:|link=XNTONGVEYKVCNE-UHFFFAOYSA-M|image=false|width=300|height=200}}. 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====
====Advances and special progress====
The authors report a novel molecular architecture for a ruthenium photocatalyst active in the reduction of CO<sub>2</sub> to formic acid, displaying competitive TONs and quantum yields up to 14%.
The authors report a novel molecular architecture for a ruthenium photocatalyst active in the reduction of CO<sub>2</sub> to formic acid, displaying competitive TONs and quantum yields up to 14%.

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

Additional remarks

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 in dimethylformamide.

Catalyst

100772 [Show R-Groups]

Photosensitizer

[Ru(bpy)3][PF6]

Investigation

Investigation-Name: Table 1

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.

Investigations

  • Table 1 (Molecular process, Photocatalytic CO2 conversion experiments)