Highly Efficient and Robust Photocatalytic Systems for CO2 Reduction Consisting of a Cu(I) Photosensitizer and Mn(I) Catalysts: Difference between revisions
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{{ | {{DOI|doi=10.1021/jacs.8b10619}} | ||
[[Category:Photocatalytic CO2 conversion to HCOOH]] | [[Category:Photocatalytic CO2 conversion to HCOOH]] | ||
{{BaseTemplate}} | {{BaseTemplate}} | ||
==== | ===Abstract=== | ||
{{# | ==== Summary==== | ||
A photochemical reduction of CO<sub>2</sub> to CO or formic acid was shown using the manganese complexes {{#moleculelink:|link=ZUZWBGQHMPVNDY-UHFFFAOYSA-M|image=false|width=300|height=200}}, {{#moleculelink:|link=AQJGHJDFPVIJPY-UHFFFAOYSA-M|image=false|width=300|height=200}} or {{#moleculelink:|link=MMWVUSACGPQHBP-UHFFFAOYSA-M|image=false|width=300|height=200}} as catalyst in combination with the copper-based photosensitizer {{#moleculelink:|link=LRXMZDJKCHDVRC-UHFFFAOYSA-N|image=false|width=300|height=200}}. Turnover numbers (TONs) over 1300 for CO were reached in dimethylacetamide/TEOA for complex {{#moleculelink:|link=AQJGHJDFPVIJPY-UHFFFAOYSA-M|image=false|width=300|height=200}}. The highest selectivity for CO (96%) was obtained for catalyst {{#moleculelink:|link=MMWVUSACGPQHBP-UHFFFAOYSA-M|image=false|width=300|height=200}} while catalyst {{#moleculelink:|link=ZUZWBGQHMPVNDY-UHFFFAOYSA-M|image=false|width=300|height=200}} allowed for the reduction of CO<sub>2</sub> to formic acid with a selectivity of 74%. The experiments were conducted under visible-light irradiation (λ = 436 nm) using BIH as sacrificial electron donor (see section SEDs below). | |||
==== Advances and special progress ==== | |||
Employing catalyst {{#moleculelink:|link=AQJGHJDFPVIJPY-UHFFFAOYSA-M|image=false|width=300|height=200}}, the highest quantum yield for CO<sub>2</sub> reduction using abundant elements (57%) at that time was achieved. The authors also demonstrated the stability of their catalyst over a 36 h experiment, where it was shown that BIH was the limiting factor, even in large amounts. | |||
==== Catalyst ==== | ==== Additional remarks==== | ||
<chemform smiles="C([*])1C=C2C3N([Mn+]( | The authors could show that the substituents on the manganese complexes largely influenced the photocatalytic efficiency and product selectivity. | ||
-INDIGO- | |||
===Content of the published article in detail=== | |||
The article contains results for the reduction of CO<sub>2</sub> to CO and formic acid under visible-light catalysis using manganese complexes as catalysts. The catalytic system performs best (referring to the TON of CO production) in DMA/TEOA. | |||
==== Catalyst==== | |||
<chemform smiles="C([*])1C=C2C3N([Mn+]([Br-])([C-]#[O+])([C-]#[O+])([C-]#[O+])N2=CC=1)=CC=C([*])C=3" inchi="" inchikey="" height="200px" width="300px" float="none" r1="H,OMe"> | |||
-INDIGO-05052316132D | |||
0 0 0 0 0 0 0 0 0 0 0 V3000 | 0 0 0 0 0 0 0 0 0 0 0 V3000 | ||
Line 35: | Line 35: | ||
M V30 12 C 5.62882 -7.92503 0.0 0 | M V30 12 C 5.62882 -7.92503 0.0 0 | ||
M V30 13 Mn 7.55 -5.475 0.0 0 CHG=1 | M V30 13 Mn 7.55 -5.475 0.0 0 CHG=1 | ||
M V30 14 | M V30 14 C 8.41603 -4.975 0.0 0 CHG=-1 | ||
M V30 15 C 8.41603 - | M V30 15 C 8.41603 -5.975 0.0 0 CHG=-1 | ||
M V30 16 | M V30 16 C 7.55 -6.475 0.0 0 CHG=-1 | ||
M V30 17 O 7.55 -7.475 0.0 0 CHG=1 | |||
M V30 | M V30 18 O 9.28205 -6.475 0.0 0 CHG=1 | ||
M V30 | M V30 19 O 9.28205 -4.475 0.0 0 CHG=1 | ||
M V30 | M V30 20 R# 3.89382 -2.97507 0.0 0 RGROUPS=(1 1) | ||
M V30 | M V30 21 R# 3.89382 -7.93002 0.0 0 RGROUPS=(1 1) | ||
M V30 | M V30 22 Br 7.525 -3.3 0.0 0 CHG=-1 | ||
M V30 END ATOM | M V30 END ATOM | ||
M V30 BEGIN BOND | M V30 BEGIN BOND | ||
Line 64: | Line 64: | ||
M V30 17 10 13 15 | M V30 17 10 13 15 | ||
M V30 18 10 13 16 | M V30 18 10 13 16 | ||
M V30 19 | M V30 19 3 16 17 | ||
M V30 20 3 | M V30 20 3 15 18 | ||
M V30 21 3 | M V30 21 3 14 19 | ||
M V30 22 | M V30 22 1 1 20 | ||
M V30 23 1 | M V30 23 1 11 21 | ||
M V30 24 | M V30 24 10 13 22 | ||
M V30 END BOND | M V30 END BOND | ||
M V30 END CTAB | M V30 END CTAB | ||
M END | M END | ||
</chemform><chemform smiles="C1C=C2C3C=CC=C(C4C(C)=CC(C)=CC=4C)N=3[Mn](C#O)(C#O)( | </chemform><chemform smiles="C1C=C2C3C=CC=C(C4C(C)=CC(C)=CC=4C)N=3[Mn+]([C-]#[O+])([C-]#[O+])([Br-])N2=C(C2C(C)=CC(C)=CC=2C)C=1" inchikey="MMWVUSACGPQHBP-UHFFFAOYSA-M" inchi="1S/C28H28N2.2CO.BrH.Mn/c1-17-13-19(3)27(20(4)14-17)25-11-7-9-23(29-25)24-10-8-12-26(30-24)28-21(5)15-18(2)16-22(28)6;2*1-2;;/h7-16H,1-6H3;;;1H;/q;;;;+1/p-1" float="none" width="200" height="200"> | ||
-INDIGO- | -INDIGO-01102416202D | ||
0 0 0 0 0 0 0 0 0 0 0 V3000 | 0 0 0 0 0 0 0 0 0 0 0 V3000 | ||
Line 110: | Line 110: | ||
M V30 29 C 6.47682 -8.98054 0.0 0 | M V30 29 C 6.47682 -8.98054 0.0 0 | ||
M V30 30 C 9.93819 -8.97039 0.0 0 | M V30 30 C 9.93819 -8.97039 0.0 0 | ||
M V30 31 Mn | M V30 31 Mn 9.55 -5.025 0.0 0 CHG=1 | ||
M V30 32 Br | M V30 32 Br 9.55 -3.675 0.0 0 CHG=-1 | ||
M V30 33 C | M V30 33 C 10.741 -4.3 0.0 0 CHG=-1 | ||
M V30 34 C | M V30 34 C 10.741 -5.75 0.0 0 CHG=-1 | ||
M V30 35 O | M V30 35 O 11.607 -3.8 0.0 0 CHG=1 | ||
M V30 36 O | M V30 36 O 11.607 -6.25 0.0 0 CHG=1 | ||
M V30 END ATOM | M V30 END ATOM | ||
M V30 BEGIN BOND | M V30 BEGIN BOND | ||
Line 153: | Line 153: | ||
M V30 34 10 4 31 | M V30 34 10 4 31 | ||
M V30 35 10 9 31 | M V30 35 10 9 31 | ||
M V30 36 | M V30 36 10 31 32 | ||
M V30 37 10 31 33 | M V30 37 10 31 33 | ||
M V30 38 10 31 34 | M V30 38 10 31 34 | ||
Line 163: | Line 163: | ||
</chemform> | </chemform> | ||
==== Photosensitizer ==== | ====Photosensitizer ==== | ||
<chemform smiles="" inchi="" inchikey="" height="200px" width="300px" float="none"></chemform> | <chemform smiles="C(C1C=CC=CC=1)1C2C=CC3C(C4C=CC=CC=4)=CC4CCCCP(C5C=CC=CC=5)(C5C=CC=CC=5)[Cu+]56N7C8C9N5=C(CCCCP6(C5C=CC=CC=5)C5C=CC=CC=5)C=C(C5C=CC=CC=5)C=9C=CC=8C(C5C=CC=CC=5)=CC=7CCCCP(C5C=CC=CC=5)(C5C=CC=CC=5)[Cu+]56P(C7C=CC=CC=7)(C7C=CC=CC=7)CCCCC(C=1)=N5C=2C=3N=46.F[P-](F)(F)(F)(F)F.F[P-](F)(F)(F)(F)F" inchi="1S/2C56H50N2P2.2Cu.2F6P/c2*1-7-23-43(24-8-1)53-41-45(27-19-21-39-59(47-29-11-3-12-30-47)48-31-13-4-14-32-48)57-55-51(53)37-38-52-54(44-25-9-2-10-26-44)42-46(58-56(52)55)28-20-22-40-60(49-33-15-5-16-34-49)50-35-17-6-18-36-50;;;2*1-7(2,3,4,5)6/h2*1-18,23-26,29-38,41-42H,19-22,27-28,39-40H2;;;;/q;;2*+1;2*-1" inchikey="LRXMZDJKCHDVRC-UHFFFAOYSA-N" height="200px" width="300px" float="none"> | ||
-INDIGO-11282314582D | |||
0 0 0 0 0 0 0 0 0 0 0 V3000 | |||
M V30 BEGIN CTAB | |||
M V30 COUNTS 136 156 0 0 0 | |||
M V30 BEGIN ATOM | |||
M V30 1 C 3.88485 -2.97507 0.0 0 | |||
M V30 2 C 5.61515 -2.97459 0.0 0 | |||
M V30 3 C 4.75164 -2.47497 0.0 0 | |||
M V30 4 N 5.61515 -3.97553 0.0 0 | |||
M V30 5 C 3.88485 -3.98002 0.0 0 | |||
M V30 6 C 4.75382 -4.47503 0.0 0 | |||
M V30 7 C 4.75895 -5.47202 0.0 0 | |||
M V30 8 C 3.89572 -5.97743 0.0 0 | |||
M V30 9 C 3.01817 -4.48745 0.0 0 | |||
M V30 10 C 3.03003 -5.48682 0.0 0 | |||
M V30 11 N 5.62527 -5.96593 0.0 0 | |||
M V30 12 C 5.63165 -6.96644 0.0 0 | |||
M V30 13 C 3.90212 -6.98194 0.0 0 | |||
M V30 14 C 4.77387 -7.47121 0.0 0 | |||
M V30 15 C 13.5598 -4.82507 0.0 0 | |||
M V30 16 C 15.2902 -4.82459 0.0 0 | |||
M V30 17 C 14.4266 -4.32497 0.0 0 | |||
M V30 18 C 15.2902 -5.82553 0.0 0 | |||
M V30 19 N 13.5598 -5.83002 0.0 0 | |||
M V30 20 C 14.4288 -6.32503 0.0 0 | |||
M V30 21 C 16.1504 -6.32074 0.0 0 | |||
M V30 22 C 16.1526 -7.31665 0.0 0 | |||
M V30 23 C 14.431 -7.32493 0.0 0 | |||
M V30 24 C 15.2967 -7.81554 0.0 0 | |||
M V30 25 C 15.304 -8.8075 0.0 0 | |||
M V30 26 C 14.4462 -9.31227 0.0 0 | |||
M V30 27 N 13.5698 -7.83171 0.0 0 | |||
M V30 28 C 13.5838 -8.82603 0.0 0 | |||
M V30 29 C 3.04076 -7.48994 0.0 0 | |||
M V30 30 C 16.1739 -9.30071 0.0 0 | |||
M V30 31 C 16.1564 -4.32499 0.0 0 | |||
M V30 32 C 2.17704 -8.98925 0.0 0 | |||
M V30 33 C 3.04115 -8.49065 0.0 0 | |||
M V30 34 C 1.30986 -8.48936 0.0 0 | |||
M V30 35 C 2.17012 -6.98805 0.0 0 | |||
M V30 36 C 1.30728 -7.49367 0.0 0 | |||
M V30 37 C 17.9042 -9.29906 0.0 0 | |||
M V30 38 C 17.0404 -8.80002 0.0 0 | |||
M V30 39 C 17.9049 -10.3 0.0 0 | |||
M V30 40 C 16.1746 -10.3057 0.0 0 | |||
M V30 41 C 17.0439 -10.8001 0.0 0 | |||
M V30 42 C 17.0201 -2.82569 0.0 0 | |||
M V30 43 C 16.156 -3.32428 0.0 0 | |||
M V30 44 C 17.8873 -3.32558 0.0 0 | |||
M V30 45 C 17.0271 -4.82688 0.0 0 | |||
M V30 46 C 17.8899 -4.32126 0.0 0 | |||
M V30 47 C 3.01882 -2.47507 0.0 0 | |||
M V30 48 C 1.28852 -2.47672 0.0 0 | |||
M V30 49 C 2.15237 -2.97576 0.0 0 | |||
M V30 50 C 1.28785 -1.47578 0.0 0 | |||
M V30 51 C 3.01815 -1.47013 0.0 0 | |||
M V30 52 C 2.14885 -0.975699 0.0 0 | |||
M V30 53 Cu 7.35 -5.075 0.0 0 CHG=1 | |||
M V30 54 Cu 12.175 -6.8 0.0 0 CHG=1 | |||
M V30 55 P 10.925 -7.925 0.0 0 | |||
M V30 56 P 8.925 -6.875 0.0 0 | |||
M V30 57 P 8.3 -3.175 0.0 0 | |||
M V30 58 C 12.7429 -8.45985 0.0 0 | |||
M V30 59 C 12.6841 -9.4508 0.0 0 | |||
M V30 60 C 11.902 -8.86867 0.0 0 | |||
M V30 61 C 11.4111 -9.37749 0.0 0 | |||
M V30 62 C 6.59757 -6.70762 0.0 0 | |||
M V30 63 C 6.85639 -7.67355 0.0 0 | |||
M V30 64 C 7.35639 -6.80752 0.0 0 | |||
M V30 65 C 8.22242 -7.30752 0.0 0 | |||
M V30 66 C 6.32226 -2.26748 0.0 0 | |||
M V30 67 C 6.58108 -3.23341 0.0 0 | |||
M V30 68 C 7.28818 -2.5263 0.0 0 | |||
M V30 69 C 7.78818 -3.39233 0.0 0 | |||
M V30 70 P 11.1 -4.55 0.0 0 | |||
M V30 71 C 13.301 -3.85915 0.0 0 | |||
M V30 72 C 12.5939 -4.56626 0.0 0 | |||
M V30 73 C 12.3351 -3.60033 0.0 0 | |||
M V30 74 C 11.9351 -4.62533 0.0 0 | |||
M V30 75 C 6.56618 -0.859074 0.0 0 | |||
M V30 76 C 8.54818 -0.676982 0.0 0 | |||
M V30 77 C 11.0504 -2.3253 0.0 0 | |||
M V30 78 C 12.9496 -1.9497 0.0 0 | |||
M V30 79 C 11.2162 -10.7659 0.0 0 | |||
M V30 80 C 9.98397 -9.55 0.0 0 | |||
M V30 81 C 6.575 -8.99102 0.0 0 | |||
M V30 82 C 7.75 -10.325 0.0 0 | |||
M V30 83 C 6.12875 -10.6628 0.0 0 | |||
M V30 84 C 6.83437 -9.95754 0.0 0 | |||
M V30 85 C 5.16174 -10.4044 0.0 0 | |||
M V30 86 C 5.60412 -8.73158 0.0 0 | |||
M V30 87 C 4.90155 -9.44329 0.0 0 | |||
M V30 88 C 8.19942 -11.9959 0.0 0 | |||
M V30 89 C 8.45788 -11.0323 0.0 0 | |||
M V30 90 C 7.23276 -12.2556 0.0 0 | |||
M V30 91 C 6.77947 -10.5857 0.0 0 | |||
M V30 92 C 6.52688 -11.5534 0.0 0 | |||
M V30 93 C 9.98562 -11.2803 0.0 0 | |||
M V30 94 C 10.4847 -10.4165 0.0 0 | |||
M V30 95 C 8.98468 -11.281 0.0 0 | |||
M V30 96 C 8.97903 -9.55067 0.0 0 | |||
M V30 97 C 8.4846 -10.42 0.0 0 | |||
M V30 98 C 12.4409 -11.9883 0.0 0 | |||
M V30 99 C 12.1829 -11.0246 0.0 0 | |||
M V30 100 C 11.7336 -12.6965 0.0 0 | |||
M V30 101 C 10.5061 -11.477 0.0 0 | |||
M V30 102 C 10.7711 -12.4413 0.0 0 | |||
M V30 103 C 12.9479 -0.219397 0.0 0 | |||
M V30 104 C 12.4489 -1.08325 0.0 0 | |||
M V30 105 C 13.9489 -0.218726 0.0 0 | |||
M V30 106 C 13.9545 -1.94902 0.0 0 | |||
M V30 107 C 14.4489 -1.07972 0.0 0 | |||
M V30 108 C 10.1839 -0.82764 0.0 0 | |||
M V30 109 C 10.1836 -1.82528 0.0 0 | |||
M V30 110 C 11.0504 -0.326587 0.0 0 | |||
M V30 111 C 11.9204 -1.82225 0.0 0 | |||
M V30 112 C 11.9139 -0.822192 0.0 0 | |||
M V30 113 C 5.06687 0.00465143 0.0 0 | |||
M V30 114 C 5.56547 -0.859457 0.0 0 | |||
M V30 115 C 5.56676 0.871829 0.0 0 | |||
M V30 116 C 7.06807 0.011571 0.0 0 | |||
M V30 117 C 6.56245 0.874412 0.0 0 | |||
M V30 118 C 7.6816 0.82068 0.0 0 | |||
M V30 119 C 7.68134 -0.176956 0.0 0 | |||
M V30 120 C 8.54811 1.32173 0.0 0 | |||
M V30 121 C 9.41815 -0.173926 0.0 0 | |||
M V30 122 C 9.41169 0.826128 0.0 0 | |||
M V30 123 F 18.1295 -1.33125 0.0 0 | |||
M V30 124 P 18.9955 -0.83125 0.0 0 CHG=-1 | |||
M V30 125 F 19.8615 -1.33125 0.0 0 | |||
M V30 126 F 18.9955 0.16875 0.0 0 | |||
M V30 127 F 19.8615 -0.33125 0.0 0 | |||
M V30 128 F 18.9955 -1.83125 0.0 0 | |||
M V30 129 F 18.1295 -0.33125 0.0 0 | |||
M V30 130 F 19.134 -4.3625 0.0 0 | |||
M V30 131 P 20.0 -3.8625 0.0 0 CHG=-1 | |||
M V30 132 F 20.866 -4.3625 0.0 0 | |||
M V30 133 F 20.0 -2.8625 0.0 0 | |||
M V30 134 F 20.866 -3.3625 0.0 0 | |||
M V30 135 F 20.0 -4.8625 0.0 0 | |||
M V30 136 F 19.134 -3.3625 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 2 8 7 | |||
M V30 8 1 5 9 | |||
M V30 9 1 7 6 | |||
M V30 10 2 9 10 | |||
M V30 11 1 10 8 | |||
M V30 12 2 12 11 | |||
M V30 13 1 8 13 | |||
M V30 14 1 11 7 | |||
M V30 15 2 13 14 | |||
M V30 16 1 14 12 | |||
M V30 17 1 17 15 | |||
M V30 18 1 18 16 | |||
M V30 19 2 15 19 | |||
M V30 20 2 16 17 | |||
M V30 21 1 19 20 | |||
M V30 22 2 20 18 | |||
M V30 23 2 22 21 | |||
M V30 24 1 20 23 | |||
M V30 25 1 21 18 | |||
M V30 26 2 23 24 | |||
M V30 27 1 24 22 | |||
M V30 28 2 26 25 | |||
M V30 29 1 23 27 | |||
M V30 30 1 25 24 | |||
M V30 31 2 27 28 | |||
M V30 32 1 28 26 | |||
M V30 33 1 13 29 | |||
M V30 34 1 25 30 | |||
M V30 35 1 16 31 | |||
M V30 36 2 33 29 | |||
M V30 37 2 34 32 | |||
M V30 38 1 29 35 | |||
M V30 39 1 32 33 | |||
M V30 40 2 35 36 | |||
M V30 41 1 36 34 | |||
M V30 42 2 38 30 | |||
M V30 43 2 39 37 | |||
M V30 44 1 30 40 | |||
M V30 45 1 37 38 | |||
M V30 46 2 40 41 | |||
M V30 47 1 41 39 | |||
M V30 48 2 43 31 | |||
M V30 49 2 44 42 | |||
M V30 50 1 31 45 | |||
M V30 51 1 42 43 | |||
M V30 52 2 45 46 | |||
M V30 53 1 46 44 | |||
M V30 54 1 1 47 | |||
M V30 55 2 49 47 | |||
M V30 56 2 50 48 | |||
M V30 57 1 47 51 | |||
M V30 58 1 48 49 | |||
M V30 59 2 51 52 | |||
M V30 60 1 52 50 | |||
M V30 61 1 28 58 | |||
M V30 62 1 58 59 | |||
M V30 63 1 59 60 | |||
M V30 64 1 60 61 | |||
M V30 65 1 61 55 | |||
M V30 66 1 12 62 | |||
M V30 67 1 62 63 | |||
M V30 68 1 63 64 | |||
M V30 69 1 64 65 | |||
M V30 70 1 65 56 | |||
M V30 71 1 2 66 | |||
M V30 72 1 66 67 | |||
M V30 73 1 67 68 | |||
M V30 74 1 68 69 | |||
M V30 75 1 69 57 | |||
M V30 76 1 15 71 | |||
M V30 77 1 71 72 | |||
M V30 78 1 72 73 | |||
M V30 79 1 73 74 | |||
M V30 80 1 74 70 | |||
M V30 81 10 4 53 | |||
M V30 82 10 11 53 | |||
M V30 83 10 57 53 | |||
M V30 84 10 56 54 | |||
M V30 85 10 70 53 | |||
M V30 86 10 55 54 | |||
M V30 87 10 27 54 | |||
M V30 88 10 19 54 | |||
M V30 89 1 57 75 | |||
M V30 90 1 70 77 | |||
M V30 91 1 70 78 | |||
M V30 92 1 55 79 | |||
M V30 93 1 55 80 | |||
M V30 94 1 56 81 | |||
M V30 95 1 56 82 | |||
M V30 96 2 84 81 | |||
M V30 97 2 85 83 | |||
M V30 98 1 81 86 | |||
M V30 99 1 83 84 | |||
M V30 100 2 86 87 | |||
M V30 101 1 87 85 | |||
M V30 102 2 89 82 | |||
M V30 103 2 90 88 | |||
M V30 104 1 82 91 | |||
M V30 105 1 88 89 | |||
M V30 106 2 91 92 | |||
M V30 107 1 92 90 | |||
M V30 108 2 94 80 | |||
M V30 109 2 95 93 | |||
M V30 110 1 80 96 | |||
M V30 111 1 93 94 | |||
M V30 112 2 96 97 | |||
M V30 113 1 97 95 | |||
M V30 114 2 99 79 | |||
M V30 115 2 100 98 | |||
M V30 116 1 79 101 | |||
M V30 117 1 98 99 | |||
M V30 118 2 101 102 | |||
M V30 119 1 102 100 | |||
M V30 120 2 104 78 | |||
M V30 121 2 105 103 | |||
M V30 122 1 78 106 | |||
M V30 123 1 103 104 | |||
M V30 124 2 106 107 | |||
M V30 125 1 107 105 | |||
M V30 126 2 109 77 | |||
M V30 127 2 110 108 | |||
M V30 128 1 77 111 | |||
M V30 129 1 108 109 | |||
M V30 130 2 111 112 | |||
M V30 131 1 112 110 | |||
M V30 132 2 114 75 | |||
M V30 133 2 115 113 | |||
M V30 134 1 75 116 | |||
M V30 135 1 113 114 | |||
M V30 136 2 116 117 | |||
M V30 137 1 117 115 | |||
M V30 138 2 119 76 | |||
M V30 139 2 120 118 | |||
M V30 140 1 76 121 | |||
M V30 141 1 118 119 | |||
M V30 142 2 121 122 | |||
M V30 143 1 122 120 | |||
M V30 144 1 76 57 | |||
M V30 145 1 123 124 | |||
M V30 146 1 124 125 | |||
M V30 147 1 124 126 | |||
M V30 148 1 124 127 | |||
M V30 149 1 124 128 | |||
M V30 150 1 124 129 | |||
M V30 151 1 130 131 | |||
M V30 152 1 131 132 | |||
M V30 153 1 131 133 | |||
M V30 154 1 131 134 | |||
M V30 155 1 131 135 | |||
M V30 156 1 131 136 | |||
M V30 END BOND | |||
M V30 END CTAB | |||
M END | |||
</chemform> | |||
====Investigation==== | |||
{{#experimentlist: |form=Photocatalytic_CO2_conversion_experiments|name=Results for photocatalytic reduction of CO2}} | |||
{{#experimentlist:|form=Photocatalytic_CO2_conversion_experiments|name=Durability test|importFile=}} | |||
====Sacrificial electron donor==== | |||
In this study, the experiments were done with the sacrificial electron donors TEOA ([[Molecule:100507|100507]]) and BIH ([[Molecule:100508|100508]]). | |||
====Additives==== | |||
In this study, no additives were tested.[[Category:Publication]] |
Latest revision as of 10:37, 11 April 2024
Abstract[edit | edit source]
Summary[edit | edit source]
A photochemical reduction of CO2 to CO or formic acid was shown using the manganese complexes Mn(bpy)(CO)3Br, 100845 or Mn(oMesbpy)(CO)2Br as catalyst in combination with the copper-based photosensitizer [Cu(phen)-(dPPh-Bu)2]2[PF6]2. Turnover numbers (TONs) over 1300 for CO were reached in dimethylacetamide/TEOA for complex 100845. The highest selectivity for CO (96%) was obtained for catalyst Mn(oMesbpy)(CO)2Br while catalyst Mn(bpy)(CO)3Br allowed for the reduction of CO2 to formic acid with a selectivity of 74%. The experiments were conducted under visible-light irradiation (λ = 436 nm) using BIH as sacrificial electron donor (see section SEDs below).
Advances and special progress[edit | edit source]
Employing catalyst 100845, the highest quantum yield for CO2 reduction using abundant elements (57%) at that time was achieved. The authors also demonstrated the stability of their catalyst over a 36 h experiment, where it was shown that BIH was the limiting factor, even in large amounts.
Additional remarks[edit | edit source]
The authors could show that the substituents on the manganese complexes largely influenced the photocatalytic efficiency and product selectivity.
Content of the published article in detail[edit | edit source]
The article contains results for the reduction of CO2 to CO and formic acid under visible-light catalysis using manganese complexes as catalysts. The catalytic system performs best (referring to the TON of CO production) in DMA/TEOA.
Catalyst[edit | edit source]
100751 [Show R-Groups] Mn(oMesbpy)(CO)2Br
Photosensitizer[edit | edit source]
Investigation[edit | edit source]
cat | cat conc [µM] | PS | PS conc [mM] | e-D | e-D conc [M] | solvent A | . | . | λexc [nm] | . | TON CO | . | TON H2 | TON HCOOH | . | . | . | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1. | 0.05 | 0.25 | 0.01 | 436 | 50 | 4 | 157 | |||||||||||
2. | 0.05 | 0.25 | 0.01 | 436 | 164 | 1 | 65 | |||||||||||
3. | 0.05 | 0.25 | 0.01 | 436 | 208 | 0.5 | 5 |
cat | cat conc [µM] | PS | PS conc [mM] | e-D | e-D conc [M] | solvent A | . | . | λexc [nm] | . | TON CO | TON H2 | TON HCOOH | . | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1. | 0.05 | 0.25 | 0.1 | 436 nm | 1004 | 68 | 310 |
Sacrificial electron donor[edit | edit source]
In this study, the experiments were done with the sacrificial electron donors TEOA (100507) and BIH (100508).
Additives[edit | edit source]
In this study, no additives were tested.
Investigations
- Durability test (Molecular process, Photocatalytic CO2 conversion experiments)
- Results for photocatalytic reduction of CO2 (Molecular process, Photocatalytic CO2 conversion experiments)