丙烯
丙炔
化学
路易斯酸
吸附
无机化学
介孔材料
丙烷
傅里叶变换红外光谱
红外光谱学
金属
吡啶
分子
催化作用
金属有机骨架
等温微量热法
药物化学
物理化学
光化学
有机化学
化学工程
焓
量子力学
工程类
物理
作者
Hervé Leclerc,Alexandré Vimont,Jean‐Claude Lavalley,Marco Daturi,Andrew D. Wiersum,Philip L. Llwellyn,Patricia Horcajada,Gérard Férey,Christian Serre
摘要
The present study illustrates the importance of the oxidation state of iron within the mesoporous iron trimesate [{Fe(3)O(H(2)O)(2)F(0.81)(OH)(0.19)}{C(6)H(3)(CO(2))(3)}(2)] denoted MIL-100(Fe) (MIL= Material from Institut Lavoisier) during adsorption of molecules that can interact with the accessible metal sites through π-back donation. Adsorption of CO has been first followed by FTIR spectroscopy to quantify the Lewis acid sites in the dehydrated Fe(III) sample, outgassed at 150 °C, and on the partially reduced Fe(II/III), outgassed at 250 °C. The exposure of MIL-100(Fe) to CO(2), propane, propene and propyne has then been studied by FTIR spectroscopy and microcalorimetry. It appears that π-back donating molecules are strongly adsorbed on reduced iron(II) sites despite the weaker Lewis acidity of cus Fe(2+) sites compared to that of Fe(3+) ones, as shown by pyridine adsorption.
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