Laboratoire Chimie Provence, Université Aix-Marseille I-CNRS, UMR 6264, Centre de Saint Jérôme, 13397 Marseille, France.
J Am Chem Soc. 2009 Sep 16;131(36):13002-8. doi: 10.1021/ja902740r.
This investigation is based on a combination of experimental tools completed by a computational approach to deeply characterize the unusual adsorption behavior of the flexible MIL-53(Fe) in the presence of short linear alkanes. In contrast to the aluminum or chromium analogues we previously reported, the iron MIL-53 solid, which initially exhibits a closed structure in the dry state, shows more complex adsorption isotherms with multisteps occurring at pressures that depend on the nature of the alkane. This behavior has been attributed to the existence of four discrete pore openings during the whole adsorption process. Molecular simulations coupled with in situ X-ray powder diffraction were able to uncover these various structural states.
这项研究基于实验工具的结合,并采用计算方法对柔性 MIL-53(Fe) 在短链烷烃存在下的异常吸附行为进行深入表征。与我们之前报道的铝或铬类似物不同,铁 MIL-53 固体在干燥状态下最初呈现封闭结构,但在压力下表现出更复杂的吸附等温线,其中多步吸附取决于烷烃的性质。这种行为归因于在整个吸附过程中存在四个离散的孔口。分子模拟与原位 X 射线粉末衍射相结合,能够揭示这些不同的结构状态。