Otake Ken-Ichi, Cui Yuexing, Buru Cassandra T, Li Zhanyong, Hupp Joseph T, Farha Omar K
Department of Chemistry and Chemical and Biological Engineering , Northwestern University , 2145 Sheridan Road , Evanston , Illinois 60208 , United States.
Department of Chemistry, Faculty of Science , King Abdulaziz University , Jeddah 21589 , Saudi Arabia.
J Am Chem Soc. 2018 Jul 18;140(28):8652-8656. doi: 10.1021/jacs.8b05107. Epub 2018 Jun 29.
We report the syntheses, structures, and oxidation catalytic activities of a single-atom-based vanadium oxide incorporated in two highly crystalline MOFs, Hf-MOF-808 and Zr-NU-1000. These vanadium catalysts were introduced by a postsynthetic metalation, and the resulting materials (Hf-MOF-808-V and Zr-NU-1000-V) were thoroughly characterized through a combination of analytic and spectroscopic techniques including single-crystal X-ray crystallography. Their catalytic properties were investigated using the oxidation of 4-methoxybenzyl alcohol under an oxygen atmosphere as a model reaction. Crystallographic and variable-temperature spectroscopic studies revealed that the incorporated vanadium in Hf-MOF-808-V changes position with heat, which led to improved catalytic activity.
我们报道了负载于两种高度结晶的金属有机框架材料(Hf-MOF-808和Zr-NU-1000)中的单原子钒氧化物的合成、结构及氧化催化活性。这些钒催化剂通过后合成金属化引入,所得材料(Hf-MOF-808-V和Zr-NU-1000-V)通过包括单晶X射线晶体学在内的分析和光谱技术组合进行了全面表征。以氧气气氛下4-甲氧基苄醇的氧化反应作为模型反应,研究了它们的催化性能。晶体学和变温光谱研究表明,Hf-MOF-808-V中负载的钒会随温度变化位置,这导致催化活性提高。