Metal-free reduction of CO2 to formate using a photochemical organohydride-catalyst recycling strategy

Abstract

Summary

A photochemical reduction of CO₂ to formic acid was shown using 1,2,3-Trimethylbenzimidazolium iodide (100951) as catalyst in combination with the organic carbazole-based photosensitizer 3,6-bis(dimethylamino)-9-phenyl-9H-carbazole (100950). Turnover numbers (TONs) of 6080 for the catalyst and 8820 for the photosensitizer and an exclusive selectivity for formic acid were reached in MeCN/H₂O. The experiments were conducted under visible-light irradiation (λ = 400 nm) using ascorbic acid as sacrificial electron donor (see section SEDs below) and potassium carbonate as a base.

Advances and special progress

A transition-metal free process for the efficient photocatalytic reduction of CO₂ to formic acid was described. The use of an organohydride catalyst allowed for a high selectivity for formate without noteworthy formation of H₂ or CO.

Additional remarks

Derivatives in which the carbazole and benzimidazolium moieties were covalently connected were tested as a combined catalyst/photosensitizer, but showed a lower activity in catalyzing CO₂ reduction.

Content of the published article in detail

The article contains results for the reduction of CO₂ to HCOO^- under visible-light catalysis using 1,2,3-Trimethylbenzimidazolium iodide (100951) as a catalyst. The catalytic system performs best (referring to the TON of formic acid production) in MeCN/H₂O with photosensitizer 3,6-bis(dimethylamino)-9-phenyl-9H-carbazole (100950).

Catalyst

1,2,3-Trimethylbenzimidazolium iodide (100951) BIH (100508)

Photosensitizer

3,6-bis(dimethylamino)-9-phenyl-9H-carbazole (100950) 3,6-bis(dimethylamino)carbazole (100952) 3,6-Bis(diphenylamino)-9-phenyl-9H-carbazole (100953) Ir(ppy)3 (100843)

Investigation

		cat	cat conc [µM]	PS	PS conc [mM]	e-D	e-D conc [M]	solvent A	.	.	.	λexc [nm]	.	TON CO	.	.	.	.
(edit)	1.	Molecule:100951	2.5	Molecule:100952	0.005	Molecule:100861	0.05	MeCN				400		2750
(edit)	2.	Molecule:100951	2.5	Molecule:100950	0.005	Molecule:100861	0.05	MeCN				400		6510
(edit)	3.	Molecule:100951	2.5	Molecule:100953	0.005	Molecule:100861	0.05	MeCN				400		8820
(edit)	4.	Molecule:100951	2.5	Ir(ppy)3	0.005	Molecule:100861	0.05	MeCN				400		7380
(edit)	5.	Molecule:100951	2.5			Molecule:100861	0.05	MeCN				400		0
(edit)	6.	Molecule:100951	0.05	Molecule:100950	0.5	Molecule:100861	0.05	MeCN				400		61
(edit)	7.			Molecule:100950	0.5	Molecule:100861	0.05	MeCN				400		0
(edit)	8.	Molecule:100951	0.05	Molecule:100950	0.05	Molecule:100861	0.05	MeCN				400		710
(edit)	9.	Molecule:100951	0.05	Molecule:100950	0.005	Molecule:100861	0.05	MeCN				400		860
(edit)	10.	Molecule:100951	0.005	Molecule:100950	0.005	Molecule:100861	0.05	MeCN				400		0

Investigation-Name: photocatalytic CO2 conversion under different conditions

Sacrificial electron donor

In this study, the experiments were done with the sacrificial electron donor ascorbic acid L-ascorbate, sodium (100861). The use of BIH was tested, but found to yield worse results.

Additives

In this study, potassium carbonate was added as a base. Control experiments under argon and with other bases were performed.