Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction: Difference between revisions
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[[Category:Homogeneous photocatalytic CO2 conversion]][[Category:Publication]] | [[Category:Homogeneous photocatalytic CO2 conversion]][[Category:Publication]] | ||
{{BaseTemplate}} | {{BaseTemplate}} | ||
===Abstract=== | |||
[[Category:Publication]] | |||
[[Category:Publication]] | |||
====Summary ==== | |||
A {{Annotation|property=Tag|value=photocatalytic CO2 reduction; voc4cat; voc4cat:0000099|display=photochemical reduction of CO2}} to {{Annotation|property=Tag|value=CO;;|display=CO}} was shown using an Fe2+ and Co2+ complex as catalysts in combination with different photosensitizers. The authors examined the efficiency for photocatalytic CO2RR pending on metal−ligand exchange coupling as an example of charge delocalization. The iron complex {{#moleculelink:|link=YJOFQAAXFUIRKO-UHFFFAOYSA-N|image=false|width=300|height=200}} and cobalt complexes{{#moleculelink:|link=GEWRDVXFGQMHJL-UHFFFAOYSA-N|image=false|width=300|height=200}}, both bearing the redox-active ligand tpyPY2Me were tested in comparison. It was found that the two-electron reduction of the Co(tpyPY2Me)]2+ catalyst {{#moleculelink:|link=GEWRDVXFGQMHJL-UHFFFAOYSA-N|image=false|width=300|height=200}} occurs at potentials 770 mV more negative than the Fe(tpyPY2Me)]2+ analogue{{#moleculelink:|link=YJOFQAAXFUIRKO-UHFFFAOYSA-N|image=false|width=300|height=200}} due to maximizing the exchange coupling in the latter compound. | |||
====Advances and special progress==== | |||
====Additional remarks==== | |||
===Content of the published article in detail=== | |||
===Catalysts tested in this study=== | |||
<chemform smiles="C1C=C2C3C=CC=C4C5C=CC=C6C7(C8C=CC=CN=8[Fe+2](N#CC)(N8C7=CC=CC=8)(N=56)(N=34)N2=CC=1)C" inchi="1S/C27H21N5.C2H3N.Fe/c1-27(24-14-3-6-18-29-24,25-15-4-7-19-30-25)26-16-9-13-23(32-26)22-12-8-11-21(31-22)20-10-2-5-17-28-20;1-2-3;/h2-19H,1H3;1H3;/q;;+2" inchikey="YJOFQAAXFUIRKO-UHFFFAOYSA-N" height="200px" width="300px" float="none"> | |||
-INDIGO-11172400022D | |||
0 0 0 0 0 0 0 0 0 0 0 V3000 | |||
M V30 BEGIN CTAB | |||
M V30 COUNTS 36 44 0 0 0 | |||
M V30 BEGIN ATOM | |||
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M V30 5 C -1.96271 -0.146077 0.0 0 | |||
M V30 6 C -2.82207 -0.160195 0.0 0 | |||
M V30 7 C -1.54526 0.605208 0.0 0 | |||
M V30 8 N -0.685901 0.619325 0.0 0 | |||
M V30 9 C -0.268449 1.37061 0.0 0 | |||
M V30 10 C -0.710354 2.10778 0.0 0 | |||
M V30 11 C -1.56971 2.09366 0.0 0 | |||
M V30 12 C -1.98716 1.34238 0.0 0 | |||
M V30 13 C 0.59091 1.38473 0.0 0 | |||
M V30 14 N 1.03281 0.647561 0.0 0 | |||
M V30 15 C 1.89217 0.661678 0.0 0 | |||
M V30 16 C 2.30963 1.41296 0.0 0 | |||
M V30 17 C 1.86772 2.15013 0.0 0 | |||
M V30 18 C 1.00836 2.13601 0.0 0 | |||
M V30 19 Fe 0.199123 -0.451758 0.0 0 CHG=2 | |||
M V30 20 N 0.225271 -1.81802 0.0 0 | |||
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M V30 23 C 0.263029 -3.46759 0.0 0 | |||
M V30 24 C 0.967873 -3.03885 0.0 0 | |||
M V30 25 C 0.948994 -2.21407 0.0 0 | |||
M V30 26 C 1.66347 -1.86344 0.0 0 | |||
M V30 27 C 2.33535 -2.34218 0.0 0 | |||
M V30 28 N 1.60783 -0.829237 0.0 0 | |||
M V30 29 C 1.90962 -1.59705 0.0 0 | |||
M V30 30 C 2.72547 -1.7196 0.0 0 | |||
M V30 31 C 3.23952 -1.07433 0.0 0 | |||
M V30 32 C 2.93773 -0.306511 0.0 0 | |||
M V30 33 C 2.12188 -0.183966 0.0 0 | |||
M V30 34 N 0.178498 2.35324 0.0 0 | |||
M V30 35 C -0.188361 2.88423 0.0 0 | |||
M V30 36 C -0.771725 3.46759 0.0 0 | |||
M V30 END ATOM | |||
M V30 BEGIN BOND | |||
M V30 1 2 1 2 | |||
M V30 2 1 2 3 | |||
M V30 3 2 3 4 | |||
M V30 4 1 4 5 | |||
M V30 5 2 5 6 | |||
M V30 6 1 6 1 | |||
M V30 7 1 5 7 | |||
M V30 8 2 7 8 | |||
M V30 9 1 8 9 | |||
M V30 10 2 9 10 | |||
M V30 11 1 10 11 | |||
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M V30 13 1 12 7 | |||
M V30 14 1 9 13 | |||
M V30 15 2 13 14 | |||
M V30 16 1 14 15 | |||
M V30 17 2 15 16 | |||
M V30 18 1 16 17 | |||
M V30 19 2 17 18 | |||
M V30 20 1 18 13 | |||
M V30 21 2 20 21 | |||
M V30 22 1 21 22 | |||
M V30 23 2 22 23 | |||
M V30 24 1 23 24 | |||
M V30 25 2 24 25 | |||
M V30 26 1 25 20 | |||
M V30 27 10 4 19 | |||
M V30 28 10 8 19 | |||
M V30 29 10 14 19 | |||
M V30 30 10 20 19 | |||
M V30 31 1 25 26 | |||
M V30 32 1 15 26 | |||
M V30 33 1 26 27 | |||
M V30 34 2 28 29 | |||
M V30 35 1 29 30 | |||
M V30 36 2 30 31 | |||
M V30 37 1 31 32 | |||
M V30 38 2 32 33 | |||
M V30 39 1 33 28 | |||
M V30 40 1 29 26 | |||
M V30 41 10 28 19 | |||
M V30 42 3 34 35 | |||
M V30 43 1 35 36 | |||
M V30 44 10 34 19 | |||
M V30 END BOND | |||
M V30 END CTAB | |||
M END | |||
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-INDIGO-11172400032D | |||
0 0 0 0 0 0 0 0 0 0 0 V3000 | |||
M V30 BEGIN CTAB | |||
M V30 COUNTS 36 44 0 0 0 | |||
M V30 BEGIN ATOM | |||
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M V30 2 C -2.79762 -1.64865 0.0 0 | |||
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M V30 4 N -1.52081 -0.883244 0.0 0 | |||
M V30 5 C -1.96271 -0.146077 0.0 0 | |||
M V30 6 C -2.82207 -0.160195 0.0 0 | |||
M V30 7 C -1.54526 0.605208 0.0 0 | |||
M V30 8 N -0.685901 0.619325 0.0 0 | |||
M V30 9 C -0.268449 1.37061 0.0 0 | |||
M V30 10 C -0.710354 2.10778 0.0 0 | |||
M V30 11 C -1.56971 2.09366 0.0 0 | |||
M V30 12 C -1.98716 1.34238 0.0 0 | |||
M V30 13 C 0.59091 1.38473 0.0 0 | |||
M V30 14 N 1.03281 0.647561 0.0 0 | |||
M V30 15 C 1.89217 0.661678 0.0 0 | |||
M V30 16 C 2.30963 1.41296 0.0 0 | |||
M V30 17 C 1.86772 2.15013 0.0 0 | |||
M V30 18 C 1.00836 2.13601 0.0 0 | |||
M V30 19 Co 0.199123 -0.451758 0.0 0 CHG=2 | |||
M V30 20 N 0.225271 -1.81802 0.0 0 | |||
M V30 21 C -0.479574 -2.24676 0.0 0 | |||
M V30 22 C -0.460695 -3.07155 0.0 0 | |||
M V30 23 C 0.263029 -3.46759 0.0 0 | |||
M V30 24 C 0.967873 -3.03885 0.0 0 | |||
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M V30 26 C 1.66347 -1.86344 0.0 0 | |||
M V30 27 C 2.33535 -2.34218 0.0 0 | |||
M V30 28 N 1.60783 -0.829237 0.0 0 | |||
M V30 29 C 1.90962 -1.59705 0.0 0 | |||
M V30 30 C 2.72547 -1.7196 0.0 0 | |||
M V30 31 C 3.23952 -1.07433 0.0 0 | |||
M V30 32 C 2.93773 -0.306511 0.0 0 | |||
M V30 33 C 2.12188 -0.183966 0.0 0 | |||
M V30 34 N 0.178498 2.35324 0.0 0 | |||
M V30 35 C -0.188361 2.88423 0.0 0 | |||
M V30 36 C -0.771725 3.46759 0.0 0 | |||
M V30 END ATOM | |||
M V30 BEGIN BOND | |||
M V30 1 2 1 2 | |||
M V30 2 1 2 3 | |||
M V30 3 2 3 4 | |||
M V30 4 1 4 5 | |||
M V30 5 2 5 6 | |||
M V30 6 1 6 1 | |||
M V30 7 1 5 7 | |||
M V30 8 2 7 8 | |||
M V30 9 1 8 9 | |||
M V30 10 2 9 10 | |||
M V30 11 1 10 11 | |||
M V30 12 2 11 12 | |||
M V30 13 1 12 7 | |||
M V30 14 1 9 13 | |||
M V30 15 2 13 14 | |||
M V30 16 1 14 15 | |||
M V30 17 2 15 16 | |||
M V30 18 1 16 17 | |||
M V30 19 2 17 18 | |||
M V30 20 1 18 13 | |||
M V30 21 2 20 21 | |||
M V30 22 1 21 22 | |||
M V30 23 2 22 23 | |||
M V30 24 1 23 24 | |||
M V30 25 2 24 25 | |||
M V30 26 1 25 20 | |||
M V30 27 10 4 19 | |||
M V30 28 10 8 19 | |||
M V30 29 10 14 19 | |||
M V30 30 10 20 19 | |||
M V30 31 1 25 26 | |||
M V30 32 1 15 26 | |||
M V30 33 1 26 27 | |||
M V30 34 2 28 29 | |||
M V30 35 1 29 30 | |||
M V30 36 2 30 31 | |||
M V30 37 1 31 32 | |||
M V30 38 2 32 33 | |||
M V30 39 1 33 28 | |||
M V30 40 1 29 26 | |||
M V30 41 10 28 19 | |||
M V30 42 3 34 35 | |||
M V30 43 1 35 36 | |||
M V30 44 10 34 19 | |||
M V30 END BOND | |||
M V30 END CTAB | |||
M END | |||
</chemform> | |||
=== Photosensitizer === | |||
<chemform smiles="N12[Ru+2](N3=CC=CC=C3C1=CC=CC=2)1(N2C(C3N1=CC=CC=3)=CC=CC=2)1N2C=CC=CC=2C2=N1C=CC=C2" inchi="1S/3C10H8N2.Ru/c3*1-3-7-11-9(5-1)10-6-2-4-8-12-10;/h3*1-8H;/q;;;+2" inchikey="HNVRWFFXWFXICS-UHFFFAOYSA-N" height="200px" width="300px" float="none"> | |||
-INDIGO-02142311402D | |||
0 0 0 0 0 0 0 0 0 0 0 V3000 | |||
M V30 BEGIN CTAB | |||
M V30 COUNTS 37 45 0 0 0 | |||
M V30 BEGIN ATOM | |||
M V30 1 N 10.4686 -4.89367 0.0 0 | |||
M V30 2 C 9.86013 -3.35178 0.0 0 | |||
M V30 3 C 9.7559 -4.32845 0.0 0 | |||
M V30 4 C 10.5812 -2.93696 0.0 0 | |||
M V30 5 C 11.2912 -4.28715 0.0 0 | |||
M V30 6 C 11.2672 -3.32813 0.0 0 | |||
M V30 7 C 11.926 -4.59035 0.0 0 | |||
M V30 8 C 13.407 -4.41796 0.0 0 | |||
M V30 9 C 12.6927 -4.07702 0.0 0 | |||
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M V30 13 N 12.1907 -7.31984 0.0 0 | |||
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M V30 15 C 13.0884 -6.97298 0.0 0 | |||
M V30 16 C 13.8688 -8.43063 0.0 0 | |||
M V30 17 C 12.3039 -8.35398 0.0 0 | |||
M V30 18 C 13.1498 -8.81725 0.0 0 | |||
M V30 19 C 11.6693 -8.71536 0.0 0 | |||
M V30 20 C 11.0428 -10.0631 0.0 0 | |||
M V30 21 C 11.7283 -9.63489 0.0 0 | |||
M V30 22 C 10.2824 -9.6709 0.0 0 | |||
M V30 23 N 10.7291 -8.179 0.0 0 | |||
M V30 24 C 10.1211 -8.72059 0.0 0 | |||
M V30 25 C 7.40786 -6.05302 0.0 0 | |||
M V30 26 C 7.41674 -5.26498 0.0 0 | |||
M V30 27 C 8.98334 -5.17125 0.0 0 | |||
M V30 28 C 8.22399 -6.45531 0.0 0 | |||
M V30 29 N 9.14653 -5.94372 0.0 0 | |||
M V30 30 C 8.17252 -7.17954 0.0 0 | |||
M V30 31 C 8.93917 -8.5102 0.0 0 | |||
M V30 32 N 9.12933 -7.59242 0.0 0 | |||
M V30 33 C 8.01894 -8.86654 0.0 0 | |||
M V30 34 C 7.37472 -7.63591 0.0 0 | |||
M V30 35 C 7.32652 -8.42014 0.0 0 | |||
M V30 36 C 8.11795 -4.83872 0.0 0 | |||
M V30 37 Ru 10.613 -6.61608 0.0 0 CHG=2 | |||
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 5 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 | |||
M V30 18 2 17 18 | |||
M V30 19 1 18 16 | |||
M V30 20 1 17 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 2 26 25 | |||
M V30 28 1 25 28 | |||
M V30 29 2 28 29 | |||
M V30 30 1 29 27 | |||
M V30 31 1 28 30 | |||
M V30 32 2 32 30 | |||
M V30 33 2 33 31 | |||
M V30 34 1 30 34 | |||
M V30 35 1 31 32 | |||
M V30 36 2 34 35 | |||
M V30 37 1 35 33 | |||
M V30 38 2 27 36 | |||
M V30 39 1 36 26 | |||
M V30 40 10 29 37 | |||
M V30 41 10 32 37 | |||
M V30 42 10 23 37 | |||
M V30 43 10 13 37 | |||
M V30 44 10 11 37 | |||
M V30 45 10 1 37 | |||
M V30 END BOND | |||
M V30 END CTAB | |||
M END | |||
</chemform><chemform smiles="NC1C=C2[N+](=C3C(=CC2=CC=1)C=CC(N)=C3)C" inchi="1S/C14H13N3/c1-17-13-7-11(15)4-2-9(13)6-10-3-5-12(16)8-14(10)17/h2-8H,1H3,(H3,15,16)/p+1" inchikey="XSIOKTWDEOJMGG-UHFFFAOYSA-O" height="200px" width="300px" float="none"> | |||
-INDIGO-11172411382D | |||
0 0 0 0 0 0 0 0 0 0 0 V3000 | |||
M V30 BEGIN CTAB | |||
M V30 COUNTS 17 19 0 0 0 | |||
M V30 BEGIN ATOM | |||
M V30 1 N -2.59808 -0.5 0.0 0 | |||
M V30 2 C -1.73205 0.0 0.0 0 | |||
M V30 3 C -1.73205 1.0 0.0 0 | |||
M V30 4 C -0.866025 1.5 0.0 0 | |||
M V30 5 C 0.0 1.0 0.0 0 | |||
M V30 6 C 0.0 0.0 0.0 0 | |||
M V30 7 N 0.866026 -0.5 0.0 0 CHG=1 | |||
M V30 8 C 0.866025 -1.5 0.0 0 | |||
M V30 9 C 1.73205 0.0 0.0 0 | |||
M V30 10 C 2.59808 -0.5 0.0 0 | |||
M V30 11 C 3.4641 0.0 0.0 0 | |||
M V30 12 N 4.33013 -0.5 0.0 0 | |||
M V30 13 C 3.4641 1 0.0 0 | |||
M V30 14 C 2.59808 1.5 0.0 0 | |||
M V30 15 C 1.73205 1 0.0 0 | |||
M V30 16 C 0.866026 1.5 0.0 0 | |||
M V30 17 C -0.866025 -0.5 0.0 0 | |||
M V30 END ATOM | |||
M V30 BEGIN BOND | |||
M V30 1 1 1 2 | |||
M V30 2 2 2 3 | |||
M V30 3 1 3 4 | |||
M V30 4 2 4 5 | |||
M V30 5 1 5 6 | |||
M V30 6 1 6 7 | |||
M V30 7 1 7 8 | |||
M V30 8 2 7 9 | |||
M V30 9 1 9 10 | |||
M V30 10 2 10 11 | |||
M V30 11 1 11 12 | |||
M V30 12 1 11 13 | |||
M V30 13 2 13 14 | |||
M V30 14 1 9 15 | |||
M V30 15 1 15 14 | |||
M V30 16 2 15 16 | |||
M V30 17 1 16 5 | |||
M V30 18 2 6 17 | |||
M V30 19 1 17 2 | |||
M V30 END BOND | |||
M V30 END CTAB | |||
M END | |||
</chemform> <chemform smiles="[Ir+]1(N2C=C(C=CC=2C2=C(F)C=C(F)C=C21)C(F)(F)F)1(C2C=C(F)C=C(F)C=2C2N1=CC(=CC=2)C(F)(F)F)1N2C=CC(C(C)(C)C)=CC=2C2=CC(C(C)(C)C)=CC=N21" inchi="1S/C18H24N2.2C12H5F5N.Ir/c1-17(2,3)13-7-9-19-15(11-13)16-12-14(8-10-20-16)18(4,5)6;2*13-8-2-3-9(10(14)5-8)11-4-1-7(6-18-11)12(15,16)17;/h7-12H,1-6H3;2*1-2,4-6H;/q;;;+1" inchikey="OZUQNBMGKZFLJQ-UHFFFAOYSA-N" height="200px" width="300px" float="none"> | |||
-INDIGO-11172411402D | |||
0 0 0 0 0 0 0 0 0 0 0 V3000 | |||
M V30 BEGIN CTAB | |||
M V30 COUNTS 57 65 2 0 0 | |||
M V30 BEGIN ATOM | |||
M V30 1 Ir -0.352408 -0.02048 0.0 0 CHG=1 | |||
M V30 2 C -3.22713 1.53262 0.0 0 | |||
M V30 3 C -3.23259 0.70764 0.0 0 | |||
M V30 4 C -2.52086 0.290423 0.0 0 | |||
M V30 5 C -1.80368 0.698189 0.0 0 | |||
M V30 6 C -1.79822 1.52317 0.0 0 | |||
M V30 7 C -2.50995 1.94039 0.0 0 | |||
M V30 8 C -1.08104 1.93094 0.0 0 | |||
M V30 9 N -0.369308 1.51372 0.0 0 | |||
M V30 10 C 0.347875 1.92148 0.0 0 | |||
M V30 11 C 0.353331 2.74647 0.0 0 | |||
M V30 12 C -0.358395 3.16368 0.0 0 | |||
M V30 13 C -1.07558 2.75592 0.0 0 | |||
M V30 14 C 2.50507 1.62732 0.0 0 | |||
M V30 15 C 1.78864 2.03641 0.0 0 | |||
M V30 16 C 1.07615 1.62049 0.0 0 | |||
M V30 17 N 1.08009 0.795504 0.0 0 | |||
M V30 18 C 1.79652 0.386423 0.0 0 | |||
M V30 19 C 2.50901 0.802334 0.0 0 | |||
M V30 20 C 1.80047 -0.438567 0.0 0 | |||
M V30 21 N 1.08798 -0.854477 0.0 0 | |||
M V30 22 C 1.09192 -1.67947 0.0 0 | |||
M V30 23 C 1.80835 -2.08855 0.0 0 | |||
M V30 24 C 2.52084 -1.67264 0.0 0 | |||
M V30 25 C 2.5169 -0.847647 0.0 0 | |||
M V30 26 C -2.47922 -0.244491 0.0 0 | |||
M V30 27 C -3.19695 -0.65131 0.0 0 | |||
M V30 28 C -3.20349 -1.47628 0.0 0 | |||
M V30 29 C -2.49231 -1.89444 0.0 0 | |||
M V30 30 C -1.77459 -1.48762 0.0 0 | |||
M V30 31 C -1.76805 -0.662645 0.0 0 | |||
M V30 32 C -1.06342 -1.90577 0.0 0 | |||
M V30 33 C -1.06996 -2.73075 0.0 0 | |||
M V30 34 C -0.358784 -3.1489 0.0 0 | |||
M V30 35 C 0.358936 -2.74208 0.0 0 | |||
M V30 36 C 0.365481 -1.91711 0.0 0 | |||
M V30 37 N -0.345696 -1.49895 0.0 0 | |||
M V30 38 C 3.21756 2.04324 0.0 0 | |||
M V30 39 C 3.23728 -2.08172 0.0 0 | |||
M V30 40 F -2.50449 2.76537 0.0 0 | |||
M V30 41 F -3.94977 0.299875 0.0 0 | |||
M V30 42 F -3.90812 -0.233155 0.0 0 | |||
M V30 43 F -2.49886 -2.71941 0.0 0 | |||
M V30 44 C 3.21362 2.86823 0.0 0 | |||
M V30 45 C 3.934 1.63416 0.0 0 | |||
M V30 46 C 3.93005 2.45915 0.0 0 | |||
M V30 47 C 3.24122 -2.90671 0.0 0 | |||
M V30 48 C 3.94977 -1.66581 0.0 0 | |||
M V30 49 C 3.23334 -1.25673 0.0 0 | |||
M V30 50 C 1.07052 3.15423 0.0 0 | |||
M V30 51 F 1.47828 2.43705 0.0 0 | |||
M V30 52 F 1.7877 3.562 0.0 0 | |||
M V30 53 F 0.66275 3.87141 0.0 0 | |||
M V30 54 C 1.07011 -3.16024 0.0 0 | |||
M V30 55 F 0.651958 -3.87141 0.0 0 | |||
M V30 56 F 1.78129 -3.57839 0.0 0 | |||
M V30 57 F 1.48827 -2.44906 0.0 0 | |||
M V30 END ATOM | |||
M V30 BEGIN BOND | |||
M V30 1 1 50 51 | |||
M V30 2 1 50 52 | |||
M V30 3 1 50 53 | |||
M V30 4 1 11 50 | |||
M V30 5 1 54 55 | |||
M V30 6 1 54 56 | |||
M V30 7 1 54 57 | |||
M V30 8 1 35 54 | |||
M V30 9 2 2 3 | |||
M V30 10 1 3 4 | |||
M V30 11 2 4 5 | |||
M V30 12 1 5 6 | |||
M V30 13 2 6 7 | |||
M V30 14 1 7 2 | |||
M V30 15 1 6 8 | |||
M V30 16 2 8 9 | |||
M V30 17 1 9 10 | |||
M V30 18 2 10 11 | |||
M V30 19 1 11 12 | |||
M V30 20 2 12 13 | |||
M V30 21 1 13 8 | |||
M V30 22 2 14 15 | |||
M V30 23 1 15 16 | |||
M V30 24 2 16 17 | |||
M V30 25 1 17 18 | |||
M V30 26 2 18 19 | |||
M V30 27 1 19 14 | |||
M V30 28 1 18 20 | |||
M V30 29 2 20 21 | |||
M V30 30 1 21 22 | |||
M V30 31 2 22 23 | |||
M V30 32 1 23 24 | |||
M V30 33 2 24 25 | |||
M V30 34 1 25 20 | |||
M V30 35 2 26 27 | |||
M V30 36 1 27 28 | |||
M V30 37 2 28 29 | |||
M V30 38 1 29 30 | |||
M V30 39 2 30 31 | |||
M V30 40 1 31 26 | |||
M V30 41 1 30 32 | |||
M V30 42 2 32 33 | |||
M V30 43 1 33 34 | |||
M V30 44 2 34 35 | |||
M V30 45 1 35 36 | |||
M V30 46 2 36 37 | |||
M V30 47 1 37 32 | |||
M V30 48 10 17 1 | |||
M V30 49 10 21 1 | |||
M V30 50 10 37 1 | |||
M V30 51 1 31 1 | |||
M V30 52 1 14 38 | |||
M V30 53 1 24 39 | |||
M V30 54 1 7 40 | |||
M V30 55 1 3 41 | |||
M V30 56 1 27 42 | |||
M V30 57 1 29 43 | |||
M V30 58 1 38 44 | |||
M V30 59 1 38 45 | |||
M V30 60 1 38 46 | |||
M V30 61 1 39 47 | |||
M V30 62 1 39 48 | |||
M V30 63 1 39 49 | |||
M V30 64 1 5 1 | |||
M V30 65 10 9 1 | |||
M V30 END BOND | |||
M V30 BEGIN SGROUP | |||
M V30 1 SUP 1 ATOMS=(4 50 51 52 53) BRKXYZ=(9 0.000000 0.000000 0.000000 0.0- | |||
M V30 00000 0.000000 0.000000 0.000000 0.000000 0.000000) BRKXYZ=(9 0.000000- | |||
M V30 0.000000 0.000000 0.000000 0.000000 0.000000 0.000000 0.000000 0.0000- | |||
M V30 00) LABEL=CF3 | |||
M V30 2 SUP 2 ATOMS=(4 54 55 56 57) BRKXYZ=(9 0.000000 0.000000 0.000000 0.0- | |||
M V30 00000 0.000000 0.000000 0.000000 0.000000 0.000000) BRKXYZ=(9 0.000000- | |||
M V30 0.000000 0.000000 0.000000 0.000000 0.000000 0.000000 0.000000 0.0000- | |||
M V30 00) LABEL=CF3 | |||
M V30 END SGROUP | |||
M V30 END CTAB | |||
M END | |||
</chemform> <chemform smiles="" inchi="" inchikey="NSABRUJKERBGOU-UHFFFAOYSA-N" height="200px" width="300px" float="none"></chemform> | |||
=== Investigation === | |||
General details for the experimental setup: Conducted inside a 25 mL borosilicate culture tube with a stir bar, a rubber septum, and an aluminum crimped top. The reaction vessel contained 5 mL of CH3CN, 2 μM of the catalyst, 200 μM of the photosensitizer, 100 mM BIH (112 mg), and 1 M phenol (470 mg). The reaction tubes were sparged with CO2 for 10 min, followed by injection of a gaseous internal standard (0.1 mL of C2H6). The reactions were placed on a stirplate 13 cm from two Kessil blue LED lamps (440 nm) for 15 or 30 min at a time and maintained at ambient temperature using a fan. Analysis of the headspace by Gas Chromatography (GC).{{#experimentlist:|form=Photocatalytic_CO2_conversion_experiments|name=CO2 Reduction under diverse conditions with diverse sensitizers|importFile=Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction_2.xlsx}} | |||
The values in Table 2 include TOF numbers given in TON/h | |||
{{#experimentlist:|form=Photocatalytic_CO2_conversion_experiments|name=Table 2 Co catalyst testing|importFile=Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction_Table2.xlsx}} | |||
=== Further Information === | |||
The results for the catalytic activity of the Co2+ compound {{#moleculelink:|link=GEWRDVXFGQMHJL-UHFFFAOYSA-N|image=false|width=300|height=200}} in Table 2 were gained from the Supporting Information. | |||
====Sacrificial electron donor==== | |||
In this study, the experiments were done with the sacrificial electron donor BIH ([[Molecule:100508|100508]]). | |||
====Additives==== | |||
Different sources of protons were used, e.g. {{#moleculelink:|link=ISWSIDIOOBJBQZ-UHFFFAOYSA-N|image=false|width=300|height=200}}, {{#moleculelink:|link=RHQDFWAXVIIEBN-UHFFFAOYSA-N|image=false|width=300|height=200}} and {{#moleculelink:|link=WXNZTHHGJRFXKQ-UHFFFAOYSA-N|image=false|width=300|height=200}} |
Latest revision as of 23:47, 17 November 2024
Abstract[edit | edit source]
Summary[edit | edit source]
A photochemical reduction of CO2 to CO was shown using an Fe2+ and Co2+ complex as catalysts in combination with different photosensitizers. The authors examined the efficiency for photocatalytic CO2RR pending on metal−ligand exchange coupling as an example of charge delocalization. The iron complex 100968 and cobalt complexes100969, both bearing the redox-active ligand tpyPY2Me were tested in comparison. It was found that the two-electron reduction of the Co(tpyPY2Me)]2+ catalyst 100969 occurs at potentials 770 mV more negative than the Fe(tpyPY2Me)]2+ analogue100968 due to maximizing the exchange coupling in the latter compound.
Advances and special progress[edit | edit source]
Additional remarks[edit | edit source]
Content of the published article in detail[edit | edit source]
Catalysts tested in this study[edit | edit source]
Photosensitizer[edit | edit source]
Ru(bpy)3 3,6-Diamino-10-methylacridinium 100971 Ir(ppy)3
Investigation[edit | edit source]
General details for the experimental setup: Conducted inside a 25 mL borosilicate culture tube with a stir bar, a rubber septum, and an aluminum crimped top. The reaction vessel contained 5 mL of CH3CN, 2 μM of the catalyst, 200 μM of the photosensitizer, 100 mM BIH (112 mg), and 1 M phenol (470 mg). The reaction tubes were sparged with CO2 for 10 min, followed by injection of a gaseous internal standard (0.1 mL of C2H6). The reactions were placed on a stirplate 13 cm from two Kessil blue LED lamps (440 nm) for 15 or 30 min at a time and maintained at ambient temperature using a fan. Analysis of the headspace by Gas Chromatography (GC).
cat | cat conc [µM] | PS | PS conc [mM] | e-D | e-D conc [M] | . | . | solvent A | additives | . | . | TON CO | TON H2 | . | . | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1. | 2 | 0.2 | 0.1 | 15520 | 86 | |||||||||||
2. | 0.2 | 0.2 | 0.1 | 30349 | 1013 | |||||||||||
3. | 0.2 | 0.1 | 43 | 52 | ||||||||||||
4. | 2 | 0.1 | 112 | 0 | ||||||||||||
5. | 2 | 0.2 | 150 | 0 | ||||||||||||
6. | 2 | 0.2 | 0.1 | 6 | 0 | |||||||||||
7. | 2 | 0.2 | 0.1 | Ar | 0 | 222 | ||||||||||
8. | 2 | 0.2 | 0.1 | 12749 | 163 | |||||||||||
9. | 0.2 | 0.2 | 0.1 | 28712 | 6527 | |||||||||||
10. | 2 | 0.2 | 0.1 | 18502 | 141 | |||||||||||
11. | 2 | 0.2 | 0.1 | 6710 | 0 |
The values in Table 2 include TOF numbers given in TON/h
cat | cat conc [µM] | PS | PS conc [mM] | e-D | e-D conc [M] | . | . | solvent A | . | . | . | . | . | . | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1. | 2 | 0.2 | 0.1 | ||||||||||||
2. | 2 | 0.2 | 0.1 | ||||||||||||
3. | 2 | 0.2 | 0.05 | ||||||||||||
4. | 2 | 0.2 | 0.05 | ||||||||||||
5. | 2 | 0.2 | 0.05 | ||||||||||||
6. | 2 | 0.2 | 0.05 | ||||||||||||
7. | 2 | 0.2 | 0.05 | ||||||||||||
8. | 2 | 0.2 | 0.05 | ||||||||||||
9. | 2 | 0.2 | 0.05 |
Further Information[edit | edit source]
The results for the catalytic activity of the Co2+ compound 100969 in Table 2 were gained from the Supporting Information.
Sacrificial electron donor[edit | edit source]
In this study, the experiments were done with the sacrificial electron donor BIH (100508).
Additives[edit | edit source]
Different sources of protons were used, e.g. PhOH, TFE and 4-CHLOROPHENOL
Investigations
- CO2 Reduction under diverse conditions with diverse sensitizers (Molecular process, Photocatalytic CO2 conversion experiments)
- Iron-Catalyzed Photochemical CO2 Reduction under diverse conditions (Molecular process, Photocatalytic CO2 conversion experiments)
- Iron-Catalyzed Photochemical CO2 Reduction under diverse conditions error (Molecular process, Photocatalytic CO2 conversion experiments)
- Table 2 Co catalyst testing (Molecular process, Photocatalytic CO2 conversion experiments)
- Table 2 Conversion with Co catalyst (Molecular process, Photocatalytic CO2 conversion experiments)
- Table 2 conversion with Co catalyst (Molecular process, Photocatalytic CO2 conversion experiments)