催化作用
反应性(心理学)
分解
可见光谱
辐照
化学
光化学
药物化学
材料科学
有机化学
物理
光电子学
医学
病理
核物理学
替代医学
作者
Sara Realista,Janaína C. Almeida,Sofia A. Milheiro,Nuno A. G. Bandeira,Luís G. Alves,Filipe Madeira,Maria José Calhorda,Paulo N. Martinho
标识
DOI:10.1002/chem.201901806
摘要
Three CoII octaazacryptates, with different substituents on the aromatic rings (Br, NO2 , CCH), were synthesised and characterised. These and the already published non-substituted cryptate catalysed CO2 photoreduction to CO and CH4 under blue visible light at room temperature. Although CO was observed after short irradiation times and a large range of catalyst concentrations, CH4 was only observed after longer irradiation periods, such as 30 h, but with a small catalyst concentration (25 nm). Experiments with 13 C labelled CO2 showed that CO is formed and reacts further when the reaction time is long. The CCH catalyst is deactivated faster than the others and the more efficient catalyst for CH4 production is the one with Br. This reactivity trend was explained by an energy decomposition analysis based on DFT calculations.
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