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Construction of two Zn(II) complexes based on the oxime-containing Schiff base ligand with NO and N2O donor sets

机译:基于含肟的席夫碱配体与NO和N2O供体组的两种Zn(II)配合物的构建

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摘要

Two zinc(II) complexes with NO-and N2O-set oxime-containing Schiff base ligand of 2-hydroxyimino-N'-[l-(2-pyridyl)ethylidene]propanohydrazone (Hpop), namely [Zn3(pop)2-(CH3OH)2Cl4] (1) and (Zn(pop) Cl]4-(H2O)2 (2), have been successfully synthesized from the reaction of Hpop with ZnCl2 in CH3OH under different temperatures and fully characterized by X-ray single-crystal diffraction, EA and 1R as well as TG. At the low temperature, the linear M3L2-type trinuclear Zn(II) compound 1 was obtained, however, the grid-like Zn4L4-type tetranuclear Zn(II) compound 2 was given at the high temperature from the same reactants. Interestingly, compound 1 may be irreversibly transformed into 2 via ring-closed coordination reaction under the high temperature, accompanied by the corresponding changes in fluorescent property.
机译:具有2-羟基亚氨基-N'-[1-(2-吡啶基)亚乙基]丙hydr(Hpop)的含NO和N2O的含肟席夫碱配体的两个锌(II)配合物,即[Zn3(pop)2- (CH3OH)2Cl4](1)和(Zn(pop)Cl] 4-(H2O)2(2)是由Hpop与ZnCl2在不同温度下在CH3OH中的反应成功合成的,并通过X射线单次表征晶体衍射,EA和1R以及TG。在低温下获得了线性M3L2型三核Zn(II)化合物1,但给出了网格状Zn4L4型四核Zn(II)化合物2有趣的是,化合物1可能在高温下通过闭环配位反应不可逆地转化为2,同时伴随着荧光性质的相应变化。

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