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首页> 外文期刊>Angewandte Chemie >Scorpionate-Type Coordination in MFU-4/ Metal-Organic Frameworks: Small-Molecule Binding and Activation upon the Thermally Activated Formation of Open Metal Sites
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Scorpionate-Type Coordination in MFU-4/ Metal-Organic Frameworks: Small-Molecule Binding and Activation upon the Thermally Activated Formation of Open Metal Sites

机译:MFU-4 /金属有机骨架中的蝎子型配位:小分子结合和开放金属位点的热活化形成后的活化

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摘要

Postsynthetic metal and ligand exchange is a versatile approach towards functionalized MFU-41 frameworks. Upon thermal treatment of MFU-41 formates, coordinatively strongly unsaturated metal centers, such as zinc(II) hydride or cop-per(I) species, are generated selectively. Cu~I-MFU-41 prepared in this way was stable under ambient conditions and showed fully reversible chemisorption of small molecules, such as O2, N2, and H2, with corresponding isosteric heats of adsorption of 53, 42, and 32 kJ mol~(-1), respectively, as determined by gas-sorption measurements and confirmed by DFT calculations. Moreover, Cu'-MFU-4l formed stable complexes with C2H4 and CO. These complexes were characterized by FTIR spectroscopy. The demonstrated hydride transfer to electro-philes and strong binding of small gas molecules suggests these novel, yet robust, metal-organic frameworks with open metal sites as promising catalytic materials comprising earth-abundant metal elements.
机译:合成后金属和配体交换是功能化MFU-41框架的一种通用方法。在对MFU-41晶型进行热处理后,会选择性地生成配位性很强的不饱和金属中心,例如氢化锌(II)或cop-per(I)物种。以此方式制备的Cu〜I-MFU-41在环境条件下稳定,并表现出小分子(如O2,N2和H2)的完全可逆化学吸附,相应的等规吸附热分别为53、42和32 kJ mol〜。 (-1)分别由气体吸收测量确定并由DFT计算确认。此外,Cu'-MFU-4l与C2H4和CO形成稳定的络合物。这些络合物通过FTIR光谱进行表征。氢化物向亲电子试剂的转移以及小气体分子的牢固结合表明,这些新颖但坚固的金属有机骨架具有开放的金属位点,是有前途的催化材料,包括大量地球金属元素。

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