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Pt@MOF-177: Synthesis, Room-Temperature Hydrogen Storage and Oxidation Catalysis

机译:Pt @ MOF-177:合成,室温储氢和氧化催化

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摘要

The gas-phase loading of [Zn4O(btb)(2)](8) (MOF-177: H(3)btb = 1,3,5-benzenetribenzoic acid) with the volatile platinum precursor [Me3PtCp'] (Cp'=methylcyclopentadienyl) was confirmed by solid state C-13 magic angle spinning (MAS)-NMR spectroscopy. Subsequent reduction of the inclusion compound [Me3PtCp'](4)@MOF-177 by hydrogen at 100 bar and 100 degrees C for 24 h was carried out and gave rise to the formation of platinum nanoparticles in a size regime of 2-5 nm embedded in the unchanged MOF-177 host lattice as confirmed by transmission electron microscopy (TEM) micrographs and powder X-ray diffraction (PXRD). The room-temperature hydropen adsorption of Pt@MOF-177 has been followed in it gravimetric fashion (magnetic suspension balance) and shows almost 2.5 wt% in the first cycle. but is decreased down to 0.5 wt% in consecutive cycles. The catalytic activity of Pt@MOF-177 towards the solvent- and base-free room temperature oxidation of alcohols in air has been tested and shows Pt@MOF-177 to be an efficient catalyst in the oxidation of alcohols.
机译:[Zn4O(btb)(2)](8)(MOF-177:H(3)btb = 1,3,5-苯三苯甲酸)的气相负载铂前体[Me3PtCp'](Cp' =甲基环戊二烯基)通过固态C-13魔角旋转(MAS)-NMR光谱确认。随后在100 bar和100摄氏度下用氢气将夹杂化合物[Me3PtCp'](4)@ MOF-177还原24小时,并形成了尺寸为2-5 nm的铂纳米粒子透射电子显微镜(TEM)显微照片和粉末X射线衍射(PXRD)证实,MOF-177嵌入未改变的MOF-177主晶格中。 Pt @ MOF-177的室温加湿笔吸附以重量分析法(磁悬浮平衡)进行,在第一个循环中显示接近2.5 wt%。但在连续循环中降低到0.5 wt%。测试了Pt @ MOF-177对空气中无溶剂和无碱室温下醇类的室温氧化的催化活性,表明Pt @ MOF-177是醇类氧化的有效催化剂。

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