Wang Quanzhong, Xu Baijie, Wang Yingyue, Wang Hui, Hu Xin, Ma Pengtao, Niu Jingyang, Wang Jingping
Henan Key Laboratory of Polyoxometalate Chemistry, College of Chemistry and Chemical Engineering, Henan University, Kaifeng 475004, Henan, P. R. China.
Inorg Chem. 2021 Jun 7;60(11):7753-7761. doi: 10.1021/acs.inorgchem.1c00135. Epub 2021 May 21.
Developing new catalysts for highly efficient and selective oxidation of saturated C-H bonds is significant due to their thermodynamic strength. Via incorporation of PWO, pyridine-2,5-dicarboxylic acids (pydc), and Fe(III) ions into one framework, a new polyoxometalate-based metal-organic framework, [HFeO(HO)(pydc)PWO]·10.5HO (), was successfully prepared by a hydrothermal method. Interestingly, features a three-dimensional porous structure with {FeO} interconnecting with PWO units. displayed excellent performance in the selective oxidation of C-H bonds of alkylbenzenes with high conversion (95.7%) and selectivity (96.6%). As an effective heterogeneous catalyst, demonstrates good reusability and structural stability.
由于饱和碳氢键的热力学强度,开发用于其高效选择性氧化的新型催化剂具有重要意义。通过将磷钨酸(PWO)、吡啶-2,5-二羧酸(pydc)和铁(III)离子引入到一个框架中,采用水热法成功制备了一种新型的基于多金属氧酸盐的金属有机框架[HFeO(HO)(pydc)PWO]·10.5HO()。有趣的是,其具有三维多孔结构,其中{FeO}与PWO单元相互连接。在烷基苯碳氢键的选择性氧化中表现出优异的性能,转化率高(95.7%),选择性好(96.6%)。作为一种有效的非均相催化剂,其具有良好的可重复使用性和结构稳定性。