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 10.1021/jacs.8b10619
Authors Hiroyuki Takeda, Hiroko Kamiyama, Kouhei Okamoto, Mina Irimajiri, Toshihide Mizutani, Kazuhide Koike, Akiko Sekine, Osamu Ishitani,
Submitted 27.11.2018
Published online 27.11.2018
Licenses http://pubs.acs.org/page/policy/authorchoice_termsofuse.html,
Subjects Colloid and Surface Chemistry, Biochemistry, General Chemistry, Catalysis
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{{#doiinfobox: 10.1021/jacs.8b10619}}
{{DOI|doi=10.1021/jacs.8b10619}}
[[Category:Photocatalytic CO2 conversion to HCOOH]]
[[Category:Photocatalytic CO2 conversion to HCOOH]]
{{BaseTemplate}}
{{BaseTemplate}}


{{MissingMolecule
===Abstract===
|date=2023-03-10
==== Summary====
|author=ChN
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.


==== Investigation ====
==== Additional remarks====
{{#experimentlist:|form=Photocatalytic_CO2_conversion_experiments|name=Table 1}}
The authors could show that the substituents on the manganese complexes largely influenced the photocatalytic efficiency and product selectivity.


==== Catalyst ====
===Content of the published article in detail===
<chemform smiles="C([*])1C=C2C3N([Mn+](C#O)(C#O)(C#O)([Br-])N2=CC=1)=CC=C([*])C=3" inchi="" inchikey="" height="200px" width="300px" float="none" r1="H,OMe">
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.
   -INDIGO-02132315572D
==== Catalyst====
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   -INDIGO-05052316132D


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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 Br 7.55 -4.475 0.0 0 CHG=-1
M  V30 14 C 8.41603 -4.975 0.0 0 CHG=-1
M  V30 15 C 8.41603 -4.975 0.0 0
M  V30 15 C 8.41603 -5.975 0.0 0 CHG=-1
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M  V30 16 C 7.55 -6.475 0.0 0 CHG=-1
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M  V30 22 Br 7.525 -3.3 0.0 0 CHG=-1
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M  V30 END ATOM
M  V30 BEGIN BOND
M  V30 BEGIN BOND
Line 61: Line 64:
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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)(~Br)N2=C(C2C(C)=CC(C)=CC=2C)C=1" inchi="1S/C28H28N2.2CHO.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;2*1H;1H;/q;;;;+1/p-1" inchikey="LAJRVYLSNAAJQU-UHFFFAOYSA-M" height="200px" width="300px" float="none">
</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-03102311002D
   -INDIGO-01102416202D


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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 150: Line 153:
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Line 160: 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
 
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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]

[Cu(phen)-(dPPh-Bu)2]2[PF6]2

Investigation[edit | edit source]

catcat conc [µM]PSPS conc [mM]e-De-D conc [M]solvent A..λexc [nm].TON CO.TON H2TON HCOOH...
1.

Mn(bpy)(CO)3Br

0.05

[Cu(phen)-(dPPh-Bu)2]2[PF6]2

0.25

BIH

0.01

MeCN

436504157
2.

Molecule:100845

0.05

[Cu(phen)-(dPPh-Bu)2]2[PF6]2

0.25

BIH

0.01

MeCN

436164165
3.

Mn(oMesbpy)(CO)2Br

0.05

[Cu(phen)-(dPPh-Bu)2]2[PF6]2

0.25

BIH

0.01

MeCN

4362080.55
catcat conc [µM]PSPS conc [mM]e-De-D conc [M]solvent A..λexc [nm].TON COTON H2TON HCOOH.
1.

Molecule:100845

0.05

[Cu(phen)-(dPPh-Bu)2]2[PF6]2

0.25

BIH

0.1

MeCN

436 nm100468310
Investigation-Name: Durability test

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