Mn-carbonyl molecular catalysts containing a redox-active phenanthroline-5,6-dione for selective electro- and photoreduction of CO2 to CO or HCOOH: Difference between revisions
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===Abstract=== | ===Abstract=== | ||
==== Summary==== | ==== Summary==== | ||
A photochemical reduction of CO<sub>2</sub> to CO was shown using the manganese complexes as catalyst in combination with the ruthenium-based photosensitizer {{#moleculelink:|link=SJFYGUKHUNLZTK-UHFFFAOYSA-L|image=false|width=300|height=200}}. Turnover numbers (TONs) | A photochemical reduction of CO<sub>2</sub> to CO or formic acid was shown using the manganese complexes as catalyst in combination with the ruthenium-based photosensitizer {{#moleculelink:|link=SJFYGUKHUNLZTK-UHFFFAOYSA-L|image=false|width=300|height=200}}. Turnover numbers (TONs) of 58 for formic acid were reached in xx. The experiments were conducted under visible-light irradiation (λ = xx nm) using TEOA and BNAH as sacrificial electron donors (see section SEDs below). | ||
====Advances and special progress==== | ====Advances and special progress==== | ||
====Additional remarks==== | ====Additional remarks==== | ||
In electrochemical CO<sub>2</sub> reduction experiments, a selectivity for CO formation was observed, contrary to the preferential formation of formic acid in the photocatalytic CO<sub>2</sub> reduction. | |||
===Content of the published article in detail=== | ===Content of the published article in detail=== | ||
The article contains results for the reduction of CO<sub>2</sub> to | The article contains results for the reduction of CO<sub>2</sub> to formic acid under visible-light catalysis using manganese complexes as catalysts. The catalytic system performs best (referring to the TON of formic acid production) in xx using catalyst xx. | ||
==== Catalyst==== | ==== Catalyst==== | ||
<chemform smiles="C1C=CN2[Mn+]([Br-])([C-]#[O+])([C-]#[O+])([C-]#[O+])N3=CC=CC4C(=O)C(=O)C=1C=2C=43" inchikey="KOYXLRUHHLMCRS-UHFFFAOYSA-M" inchi="1S/C12H6N2O2.3CO.BrH.Mn/c15-11-7-3-1-5-13-9(7)10-8(12(11)16)4-2-6-14-10;3*1-2;;/h1-6H;;;;1H;/q;;;;;+1/p-1" float="none" width="200" height="200"> | <chemform smiles="C1C=CN2[Mn+]([Br-])([C-]#[O+])([C-]#[O+])([C-]#[O+])N3=CC=CC4C(=O)C(=O)C=1C=2C=43" inchikey="KOYXLRUHHLMCRS-UHFFFAOYSA-M" inchi="1S/C12H6N2O2.3CO.BrH.Mn/c15-11-7-3-1-5-13-9(7)10-8(12(11)16)4-2-6-14-10;3*1-2;;/h1-6H;;;;1H;/q;;;;;+1/p-1" float="none" width="200" height="200"> | ||
Revision as of 16:37, 18 January 2024
Abstract
Summary
A photochemical reduction of CO2 to CO or formic acid was shown using the manganese complexes as catalyst in combination with the ruthenium-based photosensitizer Ru(bpy)3Cl2. Turnover numbers (TONs) of 58 for formic acid were reached in xx. The experiments were conducted under visible-light irradiation (λ = xx nm) using TEOA and BNAH as sacrificial electron donors (see section SEDs below).
Advances and special progress
Additional remarks
In electrochemical CO2 reduction experiments, a selectivity for CO formation was observed, contrary to the preferential formation of formic acid in the photocatalytic CO2 reduction.
Content of the published article in detail
The article contains results for the reduction of CO2 to formic acid under visible-light catalysis using manganese complexes as catalysts. The catalytic system performs best (referring to the TON of formic acid production) in xx using catalyst xx.
Catalyst
Mn(phdk)(CO)3Br
Mn(phdk)(CO)3(MeCN)
Mn(phen)(CO)3Br
Mn(bpy)(CO)3Br
Photosensitizer
Investigation
| cat | cat conc [µM] | PS | PS conc [mM] | e-D | e-D conc [M] | solvent A | . | . | . | additives | λexc [nm] | . | TON CO | TON HCOOH | . | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 1. | 100 | 0.1 | 480 | 8 | 52 | |||||||||||
| 2. | 100 | 0.1 | 480 | 15 | 58 | |||||||||||
| 3. | 100 | 0.1 | 480 | 9 | 48 | |||||||||||
| 4. | 100 | 0.1 | 480 | 47 | 15 | |||||||||||
| 5. | 100 | 0.1 | 500 | 7 | 40 | |||||||||||
| 6. | 100 | 0.1 | 457 | 7 | 34 | |||||||||||
| 7. | 2 | 100 | 0.1 | 480 | 5 | 18 | ||||||||||
| 8. | 200 | 0.1 | 480 | 8 | 52 | |||||||||||
| 9. | 100 | 0.1 | 480 | |||||||||||||
| 10. | 100 | 0.1 | 500 | |||||||||||||
| 11. | 100 | 480 | 3 | |||||||||||||
| 12. | 0.1 | 500 | ||||||||||||||
| 13. | 100 | 0.1 | Argon gas | 480 | ||||||||||||
| 14. | 100 | 0.1 | 480 | |||||||||||||
| 15. | 100 | 0.1 | 480 | |||||||||||||
| 16. | 100 | 0.1 | 480 | 21 | 22 | |||||||||||
| 17. | 100 | 0.1 | 480 | 2 | ||||||||||||
| 18. | 100 | 480 | 9 | 13 | ||||||||||||
| 19. | 100 | 0.1 | 480 | 17 | 4 | |||||||||||
| 20. | 100 | 0.1 | 480 | 6 | 39 | |||||||||||
| 21. | 100 | ascorbic acid/NaA | 480 | |||||||||||||
| 22. | 100 | ascorbic acid/NaA | 500 |
Sacrificial electron donor
In this study, the experiments were done with the sacrificial electron donors TEOA (100507) and BNAH (BNAH).
Additives
In this study, ascorbic acid was tested as an additive and control experiments under argon atmosphere were performed.
Investigations
- Table 1 (Molecular process, Photocatalytic CO2 conversion experiments)
