由托吡司他原位生成的含N, o供体配体的锌(II)配合物的合成、表征、发光和催化性能

Chenwanli Qin, Zhong‐Hua Sun, Xin Rong, Sheng-Chun Chen, Mingyang He, Qun Chen
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摘要

摘要利用著名的选择性黄嘌呤氧化酶抑制剂托吡司他,水热合成了一种新的锌(II)配合物Zn(L)2(H2O)2 (1) [HL = 4-(3-(吡啶-4-基)- 1h -1,2,4-三唑-5-基)吡啶酸],托吡司他水解后形成原位配体。通过元素分析、红外光谱、热重分析、粉末x射线衍射和单晶x射线衍射对配合物进行了结构表征。x射线结构分析表明配合物1是一个N, o螯合的单核Zn(II)配合物。配合物1表现出良好的热稳定性,在室温下表现出固态光致发光。此外,配合物1在无溶剂开环聚合ε-己内酯时也被证明是有效的,无需任何助催化剂或引发剂。
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Synthesis, characterization, luminescence, and catalytic properties of a zinc(II) complex with a N,O-donor ligand generated in situ from topiroxostat
Abstract By utilizing the well-known selective xanthine oxidase inhibitor topiroxostat, a new zinc(II) complex Zn(L)2(H2O)2 (1) [HL = 4-(3-(pyridine-4-yl)-1H-1,2,4-triazol-5-yl)picolinic acid] has been hydrothermally synthesized, involving in-situ ligand formation upon hydrolysis of topiroxostat. The complex has been structurally characterized by elemental analysis, IR spectroscopy, thermogravimetric analysis, powder X-ray diffraction, and single-crystal X-ray diffraction. X-ray structural analysis revealed that complex 1 is a N,O-chelating mononuclear Zn(II) complex. Complex 1 shows good thermal stability and exhibits photoluminescence in the solid state at room temperature. Moreover, complex 1 has been shown to be effective in the solvent-free ring-opening polymerization of ε-caprolactone without any co-catalyst or initiator.
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