A cyanide-bridged di-manganese carbonyl complex that photochemically reduces CO to CO

Manganese( i ) tricarbonyl complexes such as [Mn(bpy)(CO) 3 L] (L = Br, or CN) are known to be electrocatalysts for CO 2 reduction to CO. However, due to their rapid photodegradation under UV and visible light, these monomeric manganese complexes have not been considered as photocatalysts for CO 2 r...

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Veröffentlicht in:Dalton transactions : an international journal of inorganic chemistry 2019-01, Vol.48 (4), p.1226-1236
Hauptverfasser: Kuo, Hsin-Ya, Lee, Tia S, Chu, An T, Tignor, Steven E, Scholes, Gregory D, Bocarsly, Andrew B
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Zusammenfassung:Manganese( i ) tricarbonyl complexes such as [Mn(bpy)(CO) 3 L] (L = Br, or CN) are known to be electrocatalysts for CO 2 reduction to CO. However, due to their rapid photodegradation under UV and visible light, these monomeric manganese complexes have not been considered as photocatalysts for CO 2 reduction without the use of a photosensitizer. In this paper, we report a cyanide-bridged di-manganese complex, {[Mn(bpy)(CO) 3 ] 2 (μ-CN)}ClO 4 , which is both electrocatalytic and photochemically active for CO 2 reduction to CO. Compared to the [Mn(bpy)(CO) 3 CN] electrocatalyst, our CN-bridged binuclear complex is a more efficient electrocatalyst for CO 2 reduction using H 2 O as a proton source. In addition, we report a photochemical CO 2 reduction to CO using the dimanganese complex under 395 nm irradiation. A cyanide-bridged di-manganese complex, {[Mn(bpy)(CO) 3 ] 2 (μ-CN)} + , is introduced as an efficient electrocatalyst and photochemically active for proton-assisted of CO 2 reduction to CO.
ISSN:1477-9226
1477-9234
DOI:10.1039/c8dt03358g