Photochemical Reduction of Carbon Dioxide to Formic Acid using Ruthenium(II)-Based Catalysts and Visible Light: Difference between revisions

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M  END
M  END
</chemform>
</chemform>
{| class="wikitable"
|+
!Table 1
!2
!3
!4
!5
!6
!7
|-
|cat
|100610
|100607
|100611
|100612
|100608
|100609
|-
|cat c
|0.025
|0.025
|0.025
|0.025
|0.025
|0.025
|-
|PS
|100487
|100487
|100487
|100487
|100487
|100487
|-
|PS c
|0.025
|0.025
|0.025
|0.025
|0.025
|0.025
|-
|e-D
|TEOA (100507)
|TEOA
|TEOA
|TEOA
|TEOA
|TEOA
|-
|Solv A
|NMP (100532)
|NMP
|NMP
|NMP
|NMP
|NMP
|-
|T
|25
|25
|25
|25
|25
|25
|-
|exc
|400 - 700
|400 - 700
|400 - 700
|400 - 700
|400 - 700
|400 - 700
|-
|TON CO
|1
|2
|13
|8
|7
|3
|-
|TON H2
|2
|4
|8
|8
|9
|4
|-
|TON HCOOH
|13
|21
|62
|34
|40
|27
|}
=== Photosensitizer ===
=== Photosensitizer ===
<chemform smiles="C1C2C3C=CC=CC=3~[Ir]3(~C4C=CC=CC=4C4C=CC=CN=4~3)3(~N4=C(C5N~3=CC=CC=5)C=CC=C4)~N=2C=CC=1.P(F)(F)(F)(F)(F)F" inchi="1S/2C11H9N.C10H8N2.F6P.Ir/c2*1-2-6-10(7-3-1)11-8-4-5-9-12-11;1-3-7-11-9(5-1)10-6-2-4-8-12-10;1-7(2,3,4,5)6;/h2*1-9H;1-8H;;" inchikey="YLYRMTZQAOANTD-UHFFFAOYSA-N" height="200px" width="300px" float="none">
<chemform smiles="C1C2C3C=CC=CC=3~[Ir]3(~C4C=CC=CC=4C4C=CC=CN=4~3)3(~N4=C(C5N~3=CC=CC=5)C=CC=C4)~N=2C=CC=1.P(F)(F)(F)(F)(F)F" inchi="1S/2C11H9N.C10H8N2.F6P.Ir/c2*1-2-6-10(7-3-1)11-8-4-5-9-12-11;1-3-7-11-9(5-1)10-6-2-4-8-12-10;1-7(2,3,4,5)6;/h2*1-9H;1-8H;;" inchikey="YLYRMTZQAOANTD-UHFFFAOYSA-N" height="200px" width="300px" float="none">
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M  END
M  END
</chemform>
</chemform>
{| class="wikitable"
|+
test123
!Table 2
!1
!2
!3
!4
!5
!6
!7
!8
!9
!10
!11
!12
!13
|-
|cat
|100610
|100607
|100611
|100612
|100608
|100609
|100611
|100612
|100608
|100611
|100612
|100608
|100609
|-
|cat c
|0.0062
|0.0062
|0.0062
|0.0062
|0.0062
|0.0062
|0.0031
|0.0031
|0.0031
|0.0016
|0.0016
|0.0016
|0.0016
|-
|PS
|100487
|100487
|100487
|100487
|100487
|100487
|100487
|100487
|100487
|100487
|100487
|100487
|100487
|-
|PS c
|0.025
|0.025
|0.025
|0.025
|0.025
|0.025
|0.025
|0.025
|0.025
|0.025
|0.025
|0.025
|0.025
|-
|e-D
|TEOA
|TEOA
|TEOA
|TEOA
|TEOA
|TEOA
|TEOA
|TEOA
|TEOA
|TEOA
|TEOA
|TEOA
|TEOA
|-
|Solv A
|NMP
|NMP
|NMP
|NMP
|NMP
|NMP
|NMP
|NMP
|NMP
|NMP
|NMP
|NMP
|NMP
|-
|T
|25
|25
|25
|25
|25
|25
|25
|25
|25
|25
|25
|25
|25
|-
|exc
|400 - 700
|400 - 700
|400 - 700
|400 - 700
|400 - 700
|400 - 700
|400 - 700
|400 - 700
|400 - 700
|400 - 700
|400 - 700
|400 - 700
|400 - 700
|-
|TON CO
|3
|3
|19
|21
|21
|4
|36
|16
|34
|40
|25
|45
|4
|-
|TON H2
|9
|11
|19
|16
|14
|12
|33
|29
|28
|67
|62
|65
|44
|-
|TON HCOOH
|26
|39
|117
|107
|75
|64
|296
|145
|211
|419
|225
|335
|75
|}
=== Investigations ===
=== Investigations ===
''Kleine Erklärung: Aus der obenstehenden normalen Tabelle 1, wie sie auch im Paper zu finden ist, wird mit dem Investigationform die untenstehende schlaue Tabelle.''
{{#experimentlist:|form=Photocatalytic_CO2_conversion_experiments|name=Table 1}}
 
''Tabelle 2'' ''soll genauso hinzugefügt werden, jede Spalte entspricht einem Experiment im Form.''


''Alle Molekülspalten sollen abfragen, ob es eine Abkürzung gibt und diese dann anzeigen. Idealerweise ist die Abkürzung auch der Link zur Molekülseite. Funktioniert schon bei cat und e-D, noch hinzuzufügen bei PS und Solvent.''{{#experimentlist:|form=Photocatalytic_CO2_conversion_experiments|name=Table 1}}
{{#experimentlist:|form=Photocatalytic_CO2_conversion_experiments|name=Table 2}}

Revision as of 12:08, 20 December 2022

[PRo15]

Catalysts

Photosensitizer

Electron donor

TEOA

Investigations

catcat conc [µM]PSPS conc [mM]e-Dsolvent A.λexc [nm]TON COTON H2TON HCOOH.
1.

Ru(bpy)2Cl2

0.025

[Ir(ppy)2(bpy)][PF6]

0.025

TEOA

NMP

400 - 7001213
2.

Ru(bpy)2CO3

0.025

[Ir(ppy)2(bpy)][PF6]

0.025

TEOA

NMP

400 - 7002421
3.

[Ru(bpy)2ClCO][PF6]

0.025

[Ir(ppy)2(bpy)][PF6]

0.025

TEOA

NMP

400 - 70013862
4.

[Ru(bpy)2HCO][PF6]

0.025

[Ir(ppy)2(bpy)][PF6]

0.025

TEOA

NMP

400 - 7008834
5.

[Ru(bpy)(H2O)(CO)][PF6]

0.025

[Ir(ppy)2(bpy)][PF6]

0.025

TEOA

NMP

400 - 7007940
6.

[Ru(bpy)(AcMe)2][PF6]

0.025

[Ir(ppy)2(bpy)][PF6]

0.025

TEOA

NMP

400 - 7003427
Investigation-Name: Table 1
catcat conc [µM]PSPS conc [mM]e-Dsolvent A.λexc [nm]TON COTON H2TON HCOOH.
1.

Ru(bpy)2Cl2

0.0062

[Ir(ppy)2(bpy)][PF6]

0.025

TEOA

NMP

400 - 7003926
2.

Ru(bpy)2CO3

0.0062

[Ir(ppy)2(bpy)][PF6]

0.025

TEOA

NMP

400 - 70031139
3.

[Ru(bpy)2ClCO][PF6]

0.0062

[Ir(ppy)2(bpy)][PF6]

0.025

TEOA

NMP

400 - 7001919117
4.

[Ru(bpy)2HCO][PF6]

0.0062

[Ir(ppy)2(bpy)][PF6]

0.025

TEOA

NMP

400 - 7002116107
5.

[Ru(bpy)(H2O)(CO)][PF6]

0.0062

[Ir(ppy)2(bpy)][PF6]

0.025

TEOA

NMP

400 - 700211475
6.

[Ru(bpy)(AcMe)2][PF6]

0.0062

[Ir(ppy)2(bpy)][PF6]

0.025

TEOA

NMP

400 - 70041264
7.

[Ru(bpy)2ClCO][PF6]

0.0031

[Ir(ppy)2(bpy)][PF6]

0.025

TEOA

NMP

400 - 7003633296
8.

[Ru(bpy)2HCO][PF6]

0.0031

[Ir(ppy)2(bpy)][PF6]

0.025

TEOA

NMP

400 - 7001629145
9.

[Ru(bpy)(H2O)(CO)][PF6]

0.0031

[Ir(ppy)2(bpy)][PF6]

0.025

TEOA

NMP

400 - 7003428211
10.

[Ru(bpy)2ClCO][PF6]

0.0016

[Ir(ppy)2(bpy)][PF6]

0.025

TEOA

NMP

400 - 7004067419
11.

[Ru(bpy)2HCO][PF6]

0.0016

[Ir(ppy)2(bpy)][PF6]

0.025

TEOA

NMP

400 - 7002562225
12.

[Ru(bpy)(H2O)(CO)][PF6]

0.0016

[Ir(ppy)2(bpy)][PF6]

0.025

TEOA

NMP

400 - 7004565335
13.

[Ru(bpy)(AcMe)2][PF6]

0.0016

[Ir(ppy)2(bpy)][PF6]

0.025

TEOA

NMP

400 - 70044475
Investigation-Name: Table 2

Literature

Investigations