Homogeneous photocatalytic CO2 conversion

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Revision as of 14:09, 14 July 2023 by ChN (talk | contribs)

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Scope of this topic and related important content

The content of this topic page covers information on homogeneous approaches that are relevant for the reduction of CO2. Currently, the information on this page is limited to information on the conversion of CO2 to CO, CH4 and CHOOH, further extension of the content is planned in the future. To get the right context and preceding information, reading the higher level topics CO2 conversion and Photocatalytic CO2 conversion might be helpful.

Distinction from other articles within the topic >Photocatalytic CO2 conversion

>Photocatalytic CO2 conversion can be formally split into processes using homogeneous catalysis or heterogeneous catalysis for the conversion of the starting material CO2. In this article, we focus on the homogeneous catalysis which involves a catalyst that is in the same phase (usually liquid or gas) as the reactants. In this case, the catalyst and the reactants are well-mixed and form a single phase throughout the reaction. The catalyst interacts directly with the reactants, forming an intermediate complex, which then undergoes a reaction to form the desired products. Homogeneous catalysis often involves the use of transition metal complexes or organocatalysts. One advantage of homogeneous catalysis is that the catalyst can be precisely tuned and controlled to promote specific reactions.

The related topic >Heterogeneous photocatalytic CO2 conversion refers to reactions that involve a catalyst that is in a different phase (typically solid) from the reactants. The reactants are in a different phase (liquid or gas) and come into contact with the solid catalyst, which is usually in the form of a powder or a material such as a modified surface or material in general. The reactants adsorb onto the surface of the catalyst, where the catalytic reaction occurs.

Important aspects of homogeneous photocatalytic CO2 conversion

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Summary of selected scientific progress

Table of all experiments that have a turnover number for one of the products CO, CH4, HCOOH, H2 or MeOH over 100. This table is sorted by catalyst.

TON CO, CH4, HCOOH, H2, MeOH >100, sorted by catalyst

catcat conc [µM]PSPS conc [mM]e-De-D conc [M]..solvent A..additives.....TON CO.TON CH4TON H2.TON HCOOH....
1.Ru(dtBubpy)(CO)2Cl20.05Molecule:100877 0.05BI(OH)H0.03DMF1649280
2.Ru(dtBubpy)(CO)2Cl20.05Molecule:100877 0.05DMF2072290
3.[MoO(qpdt)2][NBu4]20.05Ru(bpy)3Cl20.5BIH0.1MeCN7367080
4.Ni(pbi)(pyS)20.004Eosin Y2TEOA0.4H2O14000
5.Ni(pbt)(pyS)20.004Eosin Y2TEOA0.4H2O13100
6.Fe(DHPP)Cl0.002Ir(ppy)30.2TEA0.05MeCN1392615
7.Fe(DHPP)Cl0.0002[Cu(PP)2][TBA]20.1BIH0.1DMF16109843
8.Fe(DHPP)Cl0.002Ir(ppy)30.2TEA0.36MeCN140
9.Fe(DHPP)Cl0.0006Molecule:100932 0.02BIH0.06DMF21616
10.Fe(DHPP)Cl0.0002[Cu(PP)2][TBA]20.1BIH0.01DMF4779270
11.Mn(oMesbpy)(CO)2Br0.05[Cu(phen)-(dPPh-Bu)2]2[PF6]20.25BIH0.01MeCN2080.55
12.Mn(CN)(bpy)(CO)30.1[Ru(dmb)3][PF6]20.5BNAH0.1DMF9.11.2130
13.Mn(CN)(bpy)(CO)30.1[Ru(dmb)3][PF6]21BNAH0.1DMF7.11.6130
14.Mn(bpy)(CO)3Br0.05[Ru(dmb)3][PF6]20.05BNAH0.1DMF1214149
15.Mn(bpy)(CO)3Br2ZnTPP0.5TEA0.1MeCN11919
16.Mn(bpy)(CO)3Br0.05[Cu(phen)-(dPPh-Bu)2]2[PF6]20.25BIH0.01MeCN504157
17.Mn(bpy)(CO)3Br0.05Ru(bpy)30.05BNAH0.1DMF128157
18.[Ir(mesbpy-(PCy2)2)][BPh4]0.02BIH0.2DMA470152080
19.[Co(pabop)][ClO4]20.05Ir(ppy)30.2TEAMeCN270
20.[Re(bpy)2(CO)2][OTf]0.01[Ru(bpy)3][PF6]1TEOADMA3752750
21.[Re(bpy)2(CO)2][OTf]0.5[Ru(bpy)3][PF6]1TEOADMA15115
22.[Re(bpy)2(CO)2][OTf]0.2[Ru(bpy)3][PF6]1TEOADMA24275
23.[Re(bpy)2(CO)2][OTf]0.1[Ru(bpy)3][PF6]1TEOADMA38428
24.[Re(bpy)2(CO)2][OTf]0.05[Ru(bpy)3][PF6]1TEOADMA50535
further results hidden...

Table of all experiments that have a turnover number for one of the products CO, CH4, HCOOH, H2 or MeOH less than 100. This table is sorted by the turnover number of H2 in descending order.

TON CO, CH4, HCOOH, H2, MeOH >100, sorted by TON H2 descending

catcat conc [µM]PSPS conc [mM]e-De-D conc [M]..solvent A..additives....TON CO.TON CH4TON H2.TON HCOOH....
1.[Ni(bpy)-(MeNHC)2][PF6]22.0E-6Ir(ppy)30.1TEAMeCN130000290004900000
2.[Ni(bpy)-(MeNHC)2][PF6]22.0E-6Ir(ppy)30.1BIH0.01MeCNTEA, H2O31000320000
3.[Ni(bpy)-(MeNHC)2][PF6]22.0E-6Ir(ppy)30.1BIH0.01MeCNTEA1080004000278000
4.[Ni(bpy)-(MeNHC)2][PF6]22.0E-6Ir(ppy)30.1BIH0.01MeCNTEA 5% (v/v), H2O 2% (v/v)1000058000
5.[Ni(bpy-bNHCEt)][PF6]22.0E-6Ir(ppy)30.1TEAMeCN900036000
6.[Ni(bpy-bNHCMe)][PF6]22.0E-6Ir(ppy)30.1BIH0.01MeCNTEA, H2O8000500034000
7.[Ni(bpy-bNHCEt)][PF6]22.0E-6Ir(ppy)30.1BIH0.01MeCNTEA31000033000
8.[Ni(bpy-bNHCEt)][PF6]22.0E-6Ir(ppy)30.1BIH0.01MeCNTEA, H2O1750001900029000
9.[Ni(bpy-bNHCMe)][PF6]22.0E-6Ir(ppy)30.1BIH0.01MeCNTEA7600017000
10.[Ni(bpy-bNHCMe)][PF6]22.0E-6Ir(ppy)30.1TEAMeCN5000100015000
11.Molecule:100968 0.2Molecule:100971 0.2BIH0.1MeCN287126527
12.Molecule:100968 0.2Molecule:100971 0.2BIH0.1MeCN287126527
13.[Ru(bpy)(py)-(MeNHC)2CO][PF6]20.01[Ru(dmb)3][PF6]20.05BI(OH)H0.1DMA30018975634
14.[Ru(bpy)(py)-(MeNHC)2(MeCN)][PF6]20.01[Ru(dmb)3][PF6]20.05BI(OH)H0.1DMA22414384593
15.Molecule:100968 0.2Ru(bpy)30.2BIH0.1MeCN303491013
16.Molecule:100968 0.2Ru(bpy)30.2BIH0.1MeCN303491013
17.Molecule:100968 0.2Ru(bpy)30.2BIH0.1MeCN303491013
18.Fe(DHPP)Cl0.0002[Cu(PP)2][TBA]20.1BIH0.1DMF16109843
19.[MoO(qpdt)2][NBu4]20.05Ru(bpy)3Cl20.5BIH0.1MeCN7367080
20.[Ru(bpy)(py)-(tBuNHC)2(MeCN)][PF6]20.01[Ru(dmb)3][PF6]20.05BI(OH)H0.1DMA1295563296
21.[Ru(bpy)(py)-(tBuNHC)2CO][PF6]20.01[Ru(dmb)3][PF6]20.05BI(OH)H0.1DMA1295053792
22.[Re(bpy)2(CO)2][OTf]0.01[Ru(bpy)3][PF6]1TEOADMA3752750
23.Molecule:100776 2.5E-5[Ru(phen)3][PF6]20.4TEOA300MeCN16896368
24.Molecule:100941 0.01Molecule:100940 1BIH0.02MeCN576287
further results hidden...


Dear reader, I am a test molecule called phenol PhOH (100617), you can call me also benzenol PhOH (100617).

Subtopics of "Homogeneous photocatalytic CO2 conversion"

This topic has the following 3 subtopics, out of 3 total.