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 |
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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. |
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ISSN: | 1477-9226 1477-9234 |
DOI: | 10.1039/c8dt03358g |