Li Feng-Cai, Tan Li-Kun, Li Xi-Li, Kong Hua-Jie, Ge Li-Ming, Yue Ling-Yu, Han Li-Feng
Henan Provincial Key Laboratory of Surface and Interface Science, Zhengzhou University of Light Industry, Zhengzhou 450002, PR China.
Dalton Trans. 2019 Apr 23;48(17):5831-5841. doi: 10.1039/c9dt00499h.
Herein, two novel Evans-Showell-type polyoxometalate (POM)-based metal-organic complexes, namely, {[Cu(L)(H2O)3][Cu(L)0.5(H2O)][Cu(L)0.5(H2O)4][Co2Mo10H4O38]}·5H2O (1) and [(H2L)0.5]2{[Zn(L)0.5(H2O)4]2[Co2Mo10H4O38]}·2H2O (2) (L = N,N'-bis(3-pyridinecarboxamide)-piperazine), were hydrothermally synthesized using a semi-rigid bis-pyridyl-bis-amide ligand and structurally characterized via single-crystal X-ray diffraction, elemental analysis, IR spectroscopy, powder X-ray diffraction (PXRD) and thermogravimetric analyses (TGA). The single-crystal X-ray diffraction analysis shows that complex 1 is a 3D Evans-Showell-type POM-based metal-organic network. In complex 1, the 1D infinite double chain structure constructed from {{Cu[Co2Mo10H4O38]}4-L} units and the μ4-bridging L ligand are linked by quadrate Cu2L2 loops to form a 2D layer, which is further connected by μ2-bridging L ligands, forming a 3D (2,3,4)-connected metal-organic framework. Complex 2 displays 3D supramolecular networks based on 1D {[Co2Mo10H4O38]-Zn-L}n infinite chains, which are constructed from Evans-Showell-type polyoxoanions and μ2-bridging 3-bpfp ligands (via ligation of pyridyl nitrogen atoms). The different coordination modes of the POM polyanions, bis(pyridylformyl)piperazine ligands and ratios play key roles in the construction of the title complexes. Significantly, the ligand L shows a μ4-bridging coordination mode in complex 1, which is observed for the first time in a POM system. Compounds 1 and 2 represent the first examples of metal-organic complexes based on Evans-Showell-type polyoxoanion and transition metal-bis-pyrazine-bis-amide coordination complexes. The fluorescence properties of the title complexes are reported herein. In addition, the title complexes act as heterogeneous Lewis acid catalysts for the oxidation of benzyl alcohol, and can also be recovered and reused without any significant loss in activity. Significantly, compound 1 with a 3D metal-organic framework showed higher catalytic performance with 99.4% conversion and 98.8% selectivity for benzoic acid at 10 h than compound 2 with 3D supramolecular networks.
在此,使用半刚性双吡啶双酰胺配体水热合成了两种新型的基于埃文斯-肖韦尔型多金属氧酸盐(POM)的金属有机配合物,即{[Cu(L)(H₂O)₃][Cu(L)₀.₅(H₂O)][Cu(L)₀.₅(H₂O)₄][Co₂Mo₁₀H₄O₃₈]}·5H₂O(1)和[(H₂L)₀.₅]₂{[Zn(L)₀.₅(H₂O)₄]₂[Co₂Mo₁₀H₄O₃₈]}·2H₂O(2)(L = N,N'-双(3-吡啶甲酰胺)-哌嗪),并通过单晶X射线衍射、元素分析、红外光谱、粉末X射线衍射(PXRD)和热重分析(TGA)对其结构进行了表征。单晶X射线衍射分析表明,配合物1是一种三维埃文斯-肖韦尔型基于POM的金属有机网络。在配合物1中,由{{Cu[Co₂Mo₁₀H₄O₃₈]}₄-L}单元构建的一维无限双链结构和μ₄-桥连L配体通过方形Cu₂L₂环连接形成二维层,该二维层通过μ₂-桥连L配体进一步连接,形成三维(2,3,4)连接的金属有机骨架。配合物2展示了基于一维{[Co₂Mo₁₀H₄O₃₈]-Zn-L}n无限链的三维超分子网络,这些无限链由埃文斯-肖韦尔型多氧阴离子和μ₂-桥连3-bpfp配体(通过吡啶氮原子的配位)构建而成。POM多阴离子、双(吡啶甲酰基)哌嗪配体的不同配位模式和比例在标题配合物的构建中起关键作用。值得注意的是,配体L在配合物1中显示出μ₄-桥连配位模式,这在POM体系中是首次观察到。化合物1和2代表了基于埃文斯-肖韦尔型多氧阴离子和过渡金属-双吡嗪-双酰胺配位配合物的金属有机配合物的首例。本文报道了标题配合物的荧光性质。此外,标题配合物作为苄醇氧化的多相路易斯酸催化剂,并且还可以回收再利用而活性没有任何显著损失。值得注意的是,具有三维金属有机骨架的化合物1在10小时时对苯甲酸的转化率为99.4%,选择性为98.8%,比具有三维超分子网络的化合物2表现出更高的催化性能。