Photochemical Reduction of Carbon Dioxide to Formic Acid using Ruthenium(II)-Based Catalysts and Visible Light

From ChemWiki
Revision as of 12:11, 12 January 2024 by 127.0.0.1 (talk) (auto-generated)

publication
About
DOI 10.1002/cctc.201500494
Authors Alonso Rosas-Hernández, Henrik Junge, Matthias Beller,
Submitted 26.08.2015
Published online 26.08.2015
Licenses http://doi.wiley.com/10.1002/tdm_license_1.1,
Subjects Inorganic Chemistry, Organic Chemistry, Physical and Theoretical Chemistry, Catalysis
Go to literature page


WikiTemplate chemistry.pngFaulty molecule
A molecule on this page has a mistake in its structure or is missing a part. Please edit the structure or redraw a new molecule using the replace molecule workflow.

Abstract

Summary

A photochemical reduction of CO2 to formic acid was shown using a system containing an iridium-based photosensitizer, ruthenium photocatalyst and triethanolamine as the electron donor. Turnover numbers up to 526 and a selectivity of 80% towards formic acid were observed if the reaction was performed with [Ir(ppy)2(bpy)]PF6 ([Ir(ppy)2(bpy)][PF6] (100784)) as the photosensitizer and [Ru(bpy)2(Cl)(CO)]PF6 ( (100837)) as the catalyst. The experiments were conducted under irradiation with Hg-lamp equipped with a λ=400–700 nm filter.

Advances and special progress

The employed photocatalytic system showed activity for the photoreduction of Na2CO3 to formic acid as well. A TON of 53 was observed after 5h reaction time.

Additional remarks

Experiments using different electron and proton donors such as triethylamine (TEA) and 1-benzyl-1,4-dihydronicotinamide (BNAH) were unsuccessful as the observed activities were lower than those obtained in the presence of TEOA.

Content of the published article in detail

The article contains results for the reduction of CO2 to formic under visible-light catalysis using ruthenium complexes as catalysts, the iridium complex [Ir(ppy)2(bpy)]PF6 ([Ir(ppy)2(bpy)][PF6] (100784)) as a photosensitizer and triethanolamine as the electron donor. The catalytic system performs best (referring to the TON of HCOOH production) with [Ru(bpy)2(Cl)(CO)]PF6 ( (100837)) as photocatalyst.

Catalysts

Ru(bpy)2CO3 (100482)

Photosensitizer

[Ir(ppy)2(bpy)][PF6] (100784)

Investigations

catcat conc [µM]PSPS conc [mM]e-Dsolvent A.λexc [nm]TON COTON H2TON HCOOH..
(edit)1.Ru(bpy)2Cl20.025[Ir(ppy)2(bpy)][PF6]0.025TEOANMP400 - 7001213
(edit)2.Ru(bpy)2CO30.025[Ir(ppy)2(bpy)][PF6]0.025TEOANMP400 - 7002421
(edit)3.[Ru(bpy)2ClCO][PF6]0.025[Ir(ppy)2(bpy)][PF6]0.025TEOANMP400 - 70013862
(edit)4.[Ru(bpy)2HCO][PF6]0.025[Ir(ppy)2(bpy)][PF6]0.025TEOANMP400 - 7008834
(edit)5.[Ru(bpy)(H2O)(CO)][PF6]0.025[Ir(ppy)2(bpy)][PF6]0.025TEOANMP400 - 7007940
(edit)6.[Ru(bpy)(AcMe)2][PF6]0.025[Ir(ppy)2(bpy)][PF6]0.025TEOANMP400 - 7003427

Investigation-Name: Table 1

catcat conc [µM]PSPS conc [mM]e-Dsolvent A.λexc [nm]TON COTON H2TON HCOOH..
(edit)1.Ru(bpy)2Cl20.0062[Ir(ppy)2(bpy)][PF6]0.025TEOANMP400 - 7003926
(edit)2.Ru(bpy)2CO30.0062[Ir(ppy)2(bpy)][PF6]0.025TEOANMP400 - 70031139
(edit)3.[Ru(bpy)2ClCO][PF6]0.0062[Ir(ppy)2(bpy)][PF6]0.025TEOANMP400 - 7001919117
(edit)4.[Ru(bpy)2HCO][PF6]0.0062[Ir(ppy)2(bpy)][PF6]0.025TEOANMP400 - 7002116107
(edit)5.[Ru(bpy)(H2O)(CO)][PF6]0.0062[Ir(ppy)2(bpy)][PF6]0.025TEOANMP400 - 700211475
(edit)6.[Ru(bpy)(AcMe)2][PF6]0.0062[Ir(ppy)2(bpy)][PF6]0.025TEOANMP400 - 70041264
(edit)7.[Ru(bpy)2ClCO][PF6]0.0031[Ir(ppy)2(bpy)][PF6]0.025TEOANMP400 - 7003633296
(edit)8.[Ru(bpy)2HCO][PF6]0.0031[Ir(ppy)2(bpy)][PF6]0.025TEOANMP400 - 7001629145
(edit)9.[Ru(bpy)(H2O)(CO)][PF6]0.0031[Ir(ppy)2(bpy)][PF6]0.025TEOANMP400 - 7003428211
(edit)10.[Ru(bpy)2ClCO][PF6]0.0016[Ir(ppy)2(bpy)][PF6]0.025TEOANMP400 - 7004067419
(edit)11.[Ru(bpy)2HCO][PF6]0.0016[Ir(ppy)2(bpy)][PF6]0.025TEOANMP400 - 7002562225
(edit)12.[Ru(bpy)(H2O)(CO)][PF6]0.0016[Ir(ppy)2(bpy)][PF6]0.025TEOANMP400 - 7004565335
(edit)13.[Ru(bpy)(AcMe)2][PF6]0.0016[Ir(ppy)2(bpy)][PF6]0.025TEOANMP400 - 70044475

Investigation-Name: Table 2

analytereduction potentialsolventelectrolyte..WE..RE.
(edit)1.Ru(bpy)2Cl20,-2.11MeCNTBABF4 glassy carbonAg/AgNO3 in MeCN
(edit)2.Ru(bpy)2CO30.45,-1.97MeCNTBABF4 glassy carbonAg/AgNO3 in MeCN
(edit)3.[Ru(bpy)2ClCO][PF6]1.22,-1.75MeCNTBABF4 glassy carbonAg/AgNO3 in MeCN
(edit)4.[Ru(bpy)2HCO][PF6]1.20,-1.61MeCNTBABF4 glassy carbonAg/AgNO3 in MeCN

Investigation-Name: Table 3 - CV

Sacrificial electron donor

In this study, the experiments were done with the sacrificial electron donor TEOA (100507).

Additives

No additives were used in the described experiments.

Investigations