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A new iron-based metal–organic framework with enhancing catalysis activity for benzene hydroxylation

机译:具有增强的苯羟基化催化活性的新型铁基金属有机框架

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A new Fe-based metal–organic framework (MOF), termed Fe-TBAPy Fe _(2) (OH) _(2) (TBAPy)·4.4H _(2) O, was solvothermally synthesized. Structural analysis revealed that Fe-TBAPy is built from [Fe(OH)(CO _(2) ) _(2) ] _(∞) rod-shaped SBUs (SBUs = secondary building units) and 1,3,6,8-tetrakis( p -benzoate)pyrene (TBAPy ~(4?) ) linker to form the frz topological structure highlighted by 7 ? channels and 3.4 ? narrow pores sandwiching between the pyrene cores of TBAPy ~(4?) . Consequently, Fe-TBAPy was used as a recyclable heterogeneous catalyst for benzene hydroxylation. Remarkably, the catalysis reaction resulted in high phenol yield and selectivity of 64.5% and 92.9%, respectively, which are higher than that of the other Fe-based MOFs and comparable with those of the best-performing heterogeneous catalysts for benzene hydroxylation. This finding demonstrated the potential for the design of MOFs with enhancing catalysis activity for benzene hydroxylation.
机译:溶剂热合成了一种新的铁基金属有机骨架(MOF),称为Fe-TBAPy Fe _(2)(OH)_(2)(TBAPy)·4.4H _(2)O。结构分析表明,Fe-TBAPy是由[Fe(OH)(CO _(2)__(2)] _(∞)杆状SBU(SBU =二级建筑单元)和1,3,6,8建造的-四(对苯甲酸酯)py(TBAPy〜(4?))接头形成frz拓扑结构,由7?突出。频道和3.4吗? TBAPy〜(4?)的the核之间夹着的细孔。因此,Fe-TBAPy用作苯羟基化的可回收非均相催化剂。值得注意的是,催化反应导致苯酚的高收率和选择性分别为64.5%和92.9%,这高于其他基于Fe的MOF的苯酚收率和与苯酚羟基化性能最佳的多相催化剂相当。该发现证明了设计具有增强的苯羟基化催化活性的MOF的潜力。

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