化学
热重分析
吸附
表面改性
水热合成
元素分析
红外光谱学
酰胺
热液循环
结晶学
化学工程
物理化学
无机化学
有机化学
吸附
工程类
作者
Tim Ahnfeldt,Daniel Gunzelmann,Thierry Loiseau,Dunja Hirsemann,Jürgen Senker,Gérard Férey,Norbert Stock
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2009-02-26
卷期号:48 (7): 3057-3064
被引量:372
摘要
Aluminum aminoterephthalate Al(OH)[H(2)N-BDC] x 0.3 (H(2)N-H(2)BDC (denoted MIL-53-NH(2)(as)) was synthesized under hydrothermal conditions. The activation of the compound can be achieved in two steps. The treatment with DMF at 150 degrees C leads to Al(OH)[H(2)N-BDC] x 0.95 DMF (MIL-53-NH(2)(DMF)). In the second step, DMF is thermally removed at 130 degrees C. Upon cooling in air, the hydrated form Al(OH)[H(2)N-BDC] x 0.9 H(2)O (MIL-53-NH(2)(lt)) is obtained. The dehydration leads to a porous compound that exhibits hysteresis behavior in the N(2) sorption experiments. The MIL-53-NH(2)(lt) can be modified by postsynthetic functionalization using formic acid, and the corresponding amide Al(OH)[HC(O)N(H)-BDC] x H(2)O (MIL-53-NHCHO) is formed. All four phases were thoroughly characterized by X-ray powder diffraction, solid-state NMR and IR spectroscopy, and sorption measurements, as well as thermogravimetric and elemental analysis. Based on the refined lattice parameter similar breathing behavior of the framework as found in the unfunctionalized MIL-53 can be deduced. Solid-state NMR spectra unequivocally demonstrate the presence of the guest species, as well as the successful postsynthetic functionalization.
科研通智能强力驱动
Strongly Powered by AbleSci AI