咪唑基四唑FeII、CoII配合物的2+3原位合成、结构及性质研究

Synthesis, structures and properties of FeII, CoII - imidazolyl tetrazole compounds formed through in situ 2+3 synthesis

  • 摘要: 采用咪唑基配体MID(1-甲基-1H-咪唑-4,5-二甲腈)和NaN3为2+3环加成反应原料,分别在FeSO47H2O和CoSO47H2O作为路易斯酸催化剂条件下进行水热反应,原位合成了2个结构新颖的单核咪唑基四唑配合物 Fe(MTIC)(H2O) (1)和Co(MTIC)(H2O) (2)及1个配体结构(MTIC)(H2O) (3).结果表明:在化合物1-3中,只有1个氰基发生了生成四唑的Sharpless反应,而另一个氰基未发生变化. X-射线单晶衍射分析表明配合物1-3均结晶于P-1空间群.此外,还对上述配合物进行了元素分析、红外光谱、差热分析和粉末衍射等表征.研究结果对开发新型有机金属超分子结构材料具有一定的指导和借鉴意义.

     

    Abstract: Hydrothermal reaction of 1-methyl-1H-imidazole-4,5-dicarbonitrile (MID) and NaN3 in the presence of Lewis acid transition metals sulfate (M = Fe, Co) afforded two coordination compounds Fe(MTIC)(H2O) (1) Co(MTIC)(H2O) (2) and a ligand structure (MTIC)(H2O) (3). The research indicated that only one of the cyano groups changed into tetrazolyl group through the Sharpless reaction while the other didn’t. X-ray diffraction analysis reveals that compounds 1-3 are mononuclear structure and crystallize in the same P-1 space group. In additional, all the complexes have been characterized by elemental analysis, thermal analysis, infrared spectra,and X-ray powder diffractometer. The research will provide a guidance and reference for exploiting new organic metal super-molecules materials.

     

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