化学
催化作用
微型多孔材料
化学吸附
Knoevenagel冷凝
活动站点
无机化学
多相催化
金属
红外光谱学
有机化学
作者
Pieterjan Valvekens,Matthias Vandichel,Michel Waroquier,Véronique Van Speybroeck,Dirk De Vos
标识
DOI:10.1016/j.jcat.2014.06.006
摘要
The hybrid frameworks M2dobdc (dobdc4− = 2,5-dioxidoterephthalate, M2+ = Mg2+, Co2+, Ni2+, Cu2+ and Zn2+), commonly known as CPO-27 or MOF-74, are shown to be active catalysts in base-catalyzed reactions such as Knoevenagel condensations or Michael additions. Rather than utilizing N-functionalized linkers as a source of basicity, the intrinsic basicity of these materials arises from the presence of the phenolate oxygen atoms coordinated to the metal ions. The overall activity is due to a complex interplay of the basic properties of these structural phenolates and the reactant binding characteristics of the coordinatively unsaturated sites. The nature of the active site and the order of activity between the different M2dobdc materials were rationalized via computational efforts; the most active material, both in theory and in experiment, is the Ni-containing variant. The basicity of Ni2dobdc was experimentally proven by chemisorption of pyrrole and observation by IR spectroscopy.
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