Photochemical Reduction of Carbon Dioxide to Formic Acid using Ruthenium(II)-Based Catalysts and Visible Light: Difference between revisions
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M V30 37 8 27 25 | M V30 37 8 27 25 | ||
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M END | |||
</chemform><chemform smiles="C1C=CN2[Ru+2](O=C(C)C)(O=C(C)C)3(N4C=CC=CC=4C4C=CC=CN=43)N3=CC=CC=C3C=2C=1.F[P-](F)(F)(F)(F)F.F[P-](F)(F)(F)(F)F" inchi="1S/2C10H8N2.2C3H6O.2F6P.Ru/c2*1-3-7-11-9(5-1)10-6-2-4-8-12-10;2*1-3(2)4;2*1-7(2,3,4,5)6;/h2*1-8H;2*1-2H3;;;/q;;;;2*-1;+2" inchikey="MVHJANUNBKMKDC-UHFFFAOYSA-N" height="200px" width="300px" float="none"> | |||
-INDIGO-08012316532D | |||
0 0 0 0 0 0 0 0 0 0 0 V3000 | |||
M V30 BEGIN CTAB | |||
M V30 COUNTS 47 50 0 0 0 | |||
M V30 BEGIN ATOM | |||
M V30 1 C 4.00985 -3.42507 0.0 0 | |||
M V30 2 C 5.74015 -3.42459 0.0 0 | |||
M V30 3 C 4.87664 -2.92497 0.0 0 | |||
M V30 4 N 5.74015 -4.42553 0.0 0 | |||
M V30 5 C 4.00985 -4.43002 0.0 0 | |||
M V30 6 C 4.87882 -4.92503 0.0 0 | |||
M V30 7 C 6.60641 -2.92499 0.0 0 | |||
M V30 8 C 7.47083 -1.42609 0.0 0 | |||
M V30 9 C 6.60649 -1.92428 0.0 0 | |||
M V30 10 C 8.33778 -1.92638 0.0 0 | |||
M V30 11 N 7.47682 -3.42729 0.0 0 | |||
M V30 12 C 8.3399 -2.92207 0.0 0 | |||
M V30 13 C 3.98485 -6.37507 0.0 0 | |||
M V30 14 N 5.71515 -6.37459 0.0 0 | |||
M V30 15 C 4.85164 -5.87497 0.0 0 | |||
M V30 16 C 5.71515 -7.37553 0.0 0 | |||
M V30 17 C 3.98485 -7.38002 0.0 0 | |||
M V30 18 C 4.85382 -7.87503 0.0 0 | |||
M V30 19 C 6.58166 -7.8747 0.0 0 | |||
M V30 20 C 8.31196 -7.87139 0.0 0 | |||
M V30 21 N 7.44763 -7.37318 0.0 0 | |||
M V30 22 C 8.31359 -8.87233 0.0 0 | |||
M V30 23 C 6.5833 -8.87964 0.0 0 | |||
M V30 24 C 7.45308 -9.37324 0.0 0 | |||
M V30 25 C 9.74199 -6.65 0.0 0 | |||
M V30 26 C 10.608 -6.15 0.0 0 | |||
M V30 27 O 8.87596 -6.15 0.0 0 | |||
M V30 28 C 9.74199 -7.65 0.0 0 | |||
M V30 29 C 9.75 -4.025 0.0 0 | |||
M V30 30 C 9.75 -3.025 0.0 0 | |||
M V30 31 O 8.88398 -4.525 0.0 0 | |||
M V30 32 C 10.616 -4.525 0.0 0 | |||
M V30 33 Ru 7.45618 -5.32553 0.0 0 CHG=2 | |||
M V30 34 F 12.767 -3.05 0.0 0 | |||
M V30 35 P 13.633 -2.55 0.0 0 CHG=-1 | |||
M V30 36 F 14.499 -3.05 0.0 0 | |||
M V30 37 F 13.633 -1.55 0.0 0 | |||
M V30 38 F 12.767 -2.05 0.0 0 | |||
M V30 39 F 14.499 -2.05 0.0 0 | |||
M V30 40 F 13.633 -3.55 0.0 0 | |||
M V30 41 F 13.109 -6.375 0.0 0 | |||
M V30 42 P 13.975 -5.875 0.0 0 CHG=-1 | |||
M V30 43 F 14.841 -6.375 0.0 0 | |||
M V30 44 F 13.975 -4.875 0.0 0 | |||
M V30 45 F 13.109 -5.375 0.0 0 | |||
M V30 46 F 14.841 -5.375 0.0 0 | |||
M V30 47 F 13.975 -6.875 0.0 0 | |||
M V30 END ATOM | |||
M V30 BEGIN BOND | |||
M V30 1 2 3 1 | |||
M V30 2 2 4 2 | |||
M V30 3 1 1 5 | |||
M V30 4 1 2 3 | |||
M V30 5 2 5 6 | |||
M V30 6 1 6 4 | |||
M V30 7 1 2 7 | |||
M V30 8 2 9 7 | |||
M V30 9 2 10 8 | |||
M V30 10 1 7 11 | |||
M V30 11 1 8 9 | |||
M V30 12 2 11 12 | |||
M V30 13 1 12 10 | |||
M V30 14 2 15 13 | |||
M V30 15 2 16 14 | |||
M V30 16 1 13 17 | |||
M V30 17 1 14 15 | |||
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M V30 19 1 18 16 | |||
M V30 20 1 16 19 | |||
M V30 21 2 21 19 | |||
M V30 22 2 22 20 | |||
M V30 23 1 19 23 | |||
M V30 24 1 20 21 | |||
M V30 25 2 23 24 | |||
M V30 26 1 24 22 | |||
M V30 27 1 25 26 | |||
M V30 28 2 25 27 | |||
M V30 29 1 25 28 | |||
M V30 30 1 29 30 | |||
M V30 31 2 29 31 | |||
M V30 32 1 29 32 | |||
M V30 33 10 4 33 | |||
M V30 34 10 33 11 | |||
M V30 35 10 33 14 | |||
M V30 36 10 33 21 | |||
M V30 37 10 33 27 | |||
M V30 38 10 33 31 | |||
M V30 39 1 34 35 | |||
M V30 40 1 35 36 | |||
M V30 41 1 35 37 | |||
M V30 42 1 35 38 | |||
M V30 43 1 35 39 | |||
M V30 44 1 35 40 | |||
M V30 45 1 41 42 | |||
M V30 46 1 42 43 | |||
M V30 47 1 42 44 | |||
M V30 48 1 42 45 | |||
M V30 49 1 42 46 | |||
M V30 50 1 42 47 | |||
M V30 END BOND | M V30 END BOND | ||
M V30 END CTAB | M V30 END CTAB |
Revision as of 15:53, 1 August 2023
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Catalysts
Ru(bpy)2CO3 [Ru(bpy)(H2O)(CO)][PF6] [Ru(bpy)(AcMe)2][PF6]
Photosensitizer
Sacrificial electron donor
Investigations
cat | cat conc [µM] | PS | PS conc [mM] | e-D | solvent A | . | λexc [nm] | TON CO | TON H2 | TON HCOOH | . | |
---|---|---|---|---|---|---|---|---|---|---|---|---|
1. | 0.025 | 0.025 | 400 - 700 | 1 | 2 | 13 | ||||||
2. | 0.025 | 0.025 | 400 - 700 | 2 | 4 | 21 | ||||||
3. | 0.025 | 0.025 | 400 - 700 | 13 | 8 | 62 | ||||||
4. | 0.025 | 0.025 | 400 - 700 | 8 | 8 | 34 | ||||||
5. | 0.025 | 0.025 | 400 - 700 | 7 | 9 | 40 | ||||||
6. | 0.025 | 0.025 | 400 - 700 | 3 | 4 | 27 |
Experiment-Name: Table 1
cat | cat conc [µM] | PS | PS conc [mM] | e-D | solvent A | . | λexc [nm] | TON CO | TON H2 | TON HCOOH | . | |
---|---|---|---|---|---|---|---|---|---|---|---|---|
1. | 0.0062 | 0.025 | 400 - 700 | 3 | 9 | 26 | ||||||
2. | 0.0062 | 0.025 | 400 - 700 | 3 | 11 | 39 | ||||||
3. | 0.0062 | 0.025 | 400 - 700 | 19 | 19 | 117 | ||||||
4. | 0.0062 | 0.025 | 400 - 700 | 21 | 16 | 107 | ||||||
5. | 0.0062 | 0.025 | 400 - 700 | 21 | 14 | 75 | ||||||
6. | 0.0062 | 0.025 | 400 - 700 | 4 | 12 | 64 | ||||||
7. | 0.0031 | 0.025 | 400 - 700 | 36 | 33 | 296 | ||||||
8. | 0.0031 | 0.025 | 400 - 700 | 16 | 29 | 145 | ||||||
9. | 0.0031 | 0.025 | 400 - 700 | 34 | 28 | 211 | ||||||
10. | 0.0016 | 0.025 | 400 - 700 | 40 | 67 | 419 | ||||||
11. | 0.0016 | 0.025 | 400 - 700 | 25 | 62 | 225 | ||||||
12. | 0.0016 | 0.025 | 400 - 700 | 45 | 65 | 335 | ||||||
13. | 0.0016 | 0.025 | 400 - 700 | 4 | 44 | 75 |
Experiment-Name: Table 2
analyte | reduction potential | solvent | electrolyte | . | . | WE | . | . | RE | . | |
---|---|---|---|---|---|---|---|---|---|---|---|
1. | 0,-2.11 | glassy carbon | Ag/AgNO3 in MeCN | ||||||||
2. | 0.45,-1.97 | glassy carbon | Ag/AgNO3 in MeCN | ||||||||
3. | 1.22,-1.75 | glassy carbon | Ag/AgNO3 in MeCN | ||||||||
4. | 1.20,-1.61 | glassy carbon | Ag/AgNO3 in MeCN |
Experiment-Name: Table 3 - CV
Investigations
- CO2 reduction experiments (Molecular process, Photocatalytic CO2 conversion experiments)
- Optimization of concentrations (Molecular process, Photocatalytic CO2 conversion experiments)
- Table 1 (Molecular process, Photocatalytic CO2 conversion experiments)
- Table 2 (Molecular process, Photocatalytic CO2 conversion experiments)
- Table 3 - CV (Assay, Cyclic Voltammetry experiments)