Exploring the Full Potential of Photocatalytic Carbon Dioxide Reduction Using a Dinuclear Re2Cl2 Complex Assisted by Various Photosensitizers: Difference between revisions

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DOI 10.1002/cptc.202100034
Authors Robin Giereth, Martin Obermeier, Lukas Forschner, Michael Karnahl, Matthias Schwalbe, Stefanie Tschierlei,
Submitted 17.03.2021
Published online 02.05.2021
Licenses http://creativecommons.org/licenses/by-nc-nd/4.0/, http://doi.wiley.com/10.1002/tdm_license_1.1,
Subjects Organic Chemistry, Physical and Theoretical Chemistry, Analytical Chemistry
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==== Additional remarks ====
==== Additional remarks ====
The experiments were preformed using the rhenium complex (50 μM in DMF) as the catalyst in combination with different loadings of the sensitizers and sacrificial electron donors under 4 h of irradiation with λ > 400 nm.
The experiments were performed using the rhenium complex (50 μM in DMF) as the catalyst in combination with different loadings of the sensitizers and sacrificial electron donors under 4 h of irradiation with λ > 400 nm.


===Content of the published article in detail===
===Content of the published article in detail===

Latest revision as of 09:33, 10 May 2024


Abstract[edit | edit source]

Summary[edit | edit source]

A photochemical reduction of CO2 to CO was shown using the dirhenium complex (tBuxant)-(Re(bpy)(CO)3Cl)2 in combination with the ruthenium and copper photosensitizers Ir(fppy)3 and [Cu(bcp)(xant)][PF6]. Turnover numbers (TONs) of up to 270 were reached after 4 h of irradiation (λ > 400 nm) in DMF.

Advances and special progress[edit | edit source]

One of very few studies where a dinuclear catalytic system able to activate CO2 is used in combination with photosensitizers.

Additional remarks[edit | edit source]

The experiments were performed using the rhenium complex (50 μM in DMF) as the catalyst in combination with different loadings of the sensitizers and sacrificial electron donors under 4 h of irradiation with λ > 400 nm.

Content of the published article in detail[edit | edit source]

The article contains results of a detailed study on the influence of additional photosensitizers on the catalytic performance of the dinuclear rhenium catalyst (tBuxant)-(Re(bpy)(CO)3Cl)2 for the reduction of CO2 to CO. The catalytic system performs best (referring to the TON of CO production) for the combination of the above mentioned catalyst with the iridium complex Ir(fppy)3 as the photosensitizer in the presence of BIH/TEA as sacrificial electron donors.

Catalyst[edit | edit source]

(tBuxant)-(Re(bpy)(CO)3Cl)2

Photosensitizer[edit | edit source]

Ir(fppy)3 [Cu(bcp)(xant)][PF6]

Investigation[edit | edit source]

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

(tBuxant)-(Re(bpy)(CO)3Cl)2

0.05

Ir(fppy)3

0.05

TEA

0.36

DMF

> 40052
2.

(tBuxant)-(Re(bpy)(CO)3Cl)2

0.05

Ir(fppy)3

0.05

BIH

0.005

DMF

TEA> 40078
3.

(tBuxant)-(Re(bpy)(CO)3Cl)2

0.05

Ir(fppy)3

0.05

BIH

0.01

DMF

TEA> 400195
4.

(tBuxant)-(Re(bpy)(CO)3Cl)2

0.05

Ir(fppy)3

0.05

BIH

0.01

DMF

TEA> 400154
5.

(tBuxant)-(Re(bpy)(CO)3Cl)2

0.05

Ir(fppy)3

0.05

BIH

0.01

DMF

TEA> 400131
6.

(tBuxant)-(Re(bpy)(CO)3Cl)2

0.05

Ir(fppy)3

0.05

BIH

0.02

DMF

TEA> 400134
7.

(tBuxant)-(Re(bpy)(CO)3Cl)2

0.05

Ir(fppy)3

0.05

BIH

0.02

DMF

TEA> 400193
8.

(tBuxant)-(Re(bpy)(CO)3Cl)2

0.05

Ir(fppy)3

0.05

BIH

0.5

DMF

TEA> 400255
9.

(tBuxant)-(Re(bpy)(CO)3Cl)2

0.05


BIH

0.01

DMF

TEA> 40063
10.

(tBuxant)-(Re(bpy)(CO)3Cl)2

0.05

Ir(fppy)3

0.005

BIH

0.01

DMF

TEA> 400124
11.

(tBuxant)-(Re(bpy)(CO)3Cl)2

0.05

Ir(fppy)3

0.0125

BIH

0.01

DMF

TEA> 400144
12.

(tBuxant)-(Re(bpy)(CO)3Cl)2

0.05

Ir(fppy)3

0.025

BIH

0.01

DMF

TEA> 400149
13.

(tBuxant)-(Re(bpy)(CO)3Cl)2

0.05

Ir(fppy)3

0.1

BIH

0.05

DMF

TEA> 400270
14.

(tBuxant)-(Re(bpy)(CO)3Cl)2

0.05

[Cu(bcp)(xant)][PF6]

0.05

BIH

0.01

DMF

TEA> 400169
Investigation-Name: Optimizations of the conditions

Sacrificial electron donor[edit | edit source]

In this study, TEA (TEA) and BIH (BIH) were used as sacrificial electron donors.

Investigations