以5-(4-吡啶基)四氮酸盐为配体的大环二镍配合物的合成与结构

S. Voitekhovich, B. Kersting, O. Ivashkevich
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引用次数: 0

摘要

双核镍(II)配合物[Ni2LmClO4] +与5-(4-吡啶基)四唑(PyrCN4H)反应生成双核配合物[Ni2Lm(PyrCN4)]+,其中Lm代表一个24元的大环六氮杂二硫代苯酚配体。新的配合物分离得到高氯酸盐或四苯基硼酸盐,并通过元素分析和红外光谱进行了表征。通过单晶x射线衍射测定了[Ni2Lm(PyrCN4)]BPh4⋅MeCN的结构,结果表明,四氮化盐单元呈N2, n3桥接模式,生成了二八面体N3Ni(µ-S)2(µ-N4CPyr)NiN3核。
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Synthesis and structure of macrocyclic dinickel(II) complex with 5-(4-pyridyl)tetrazolate as coligand
The dinuclear nickel(II) complex [Ni2LmClO4] + , where Lm represents a 24-membered macrocyclic hexaaza-dithiophenolate ligand, reacts with 5-(4-pyridyl)tetrazole (PyrCN4H) to give the dinuclear complex [Ni2Lm(PyrCN4)]+ . The new complex was both isolated as perchlorate or tetraphenylborate salts and characterised by elemental analysis and IR spectroscopy. The structure of [Ni2Lm(PyrCN4)]BPh4 ⋅ MeCN was determined by single crystal X-ray diffraction, showing that tetrazolate units are in a N2,N3-bridging mode to generate dioctahedral N3Ni(µ-S)2(µ-N4CPyr)NiN3 core.
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