基于三足四齿配体的镍(II)配合物的合成及Сrystal结构

IF 1.1 3区 化学 Q4 CHEMISTRY, INORGANIC & NUCLEAR
C. Q. Shen, J. N. Wang, Jin Liu, J. R. Liu, L. Y. Liu, Q. X. Ma
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引用次数: 0

摘要

以三脚四齿配体(三(1-甲基- 1h -苯并[d]咪唑-2-基)甲基)胺,L)合成了两个新型镍基配合物[Ni(H2O)LCl]Cl (Ι)]和[(Ni2L2Cl2)](NO3)2 (ΙΙ)]。这两个配合物具有不同的核性和镍原子的配位环境:配合物Ι由两个单核t型构建单元组装而成,通过分子间π -π相互作用形成双核配合物;复合体ΙΙ的构造单元类似于复合体Ι,但由于两个桥接氯原子,它导致了不同的中心对称双核复合体。通过单晶x射线衍射(CCDC号:2363616 (Ι)和2363615 (ΙΙ))测定了这两种配合物的晶体结构。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Synthesis and Сrystal Structures of Nickel(II) Complexes Based on Tripodal Tetradentate Ligand

Synthesis and Сrystal Structures of Nickel(II) Complexes Based on Tripodal Tetradentate Ligand

Two novel nickel-based complexes [Ni(H2O)LCl]Cl (Ι) and [(Ni2L2Cl2)](NO3)2 (ΙΙ) were synthesized with the tripodal tetradentate ligand (tris((1-methyl-1H-benzo[d]imidazol-2-yl)methyl)amine, L). Two complexes show different nuclearity and coordination environment of nickel atoms: complex Ι is assembled from two mononuclear T-shaped building units, forming a binuclear complex through intermolecular π–π interactions; the building unit of complex ΙΙ resembles complex Ι, but it leads to a diverse centrosymmetric binuclear complex due to the two bridging chlorine atoms. The crystal structures of the two complexes were determined by single-crystal X-ray diffraction (CCDC nos. 2363616 (Ι) and 2363615 (ΙΙ)).

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来源期刊
Russian Journal of Coordination Chemistry
Russian Journal of Coordination Chemistry 化学-无机化学与核化学
CiteScore
2.40
自引率
15.80%
发文量
85
审稿时长
7.2 months
期刊介绍: Russian Journal of Coordination Chemistry is a journal that publishes reviews, original papers, and short communications on all aspects of theoretical and experimental coordination chemistry. Modern coordination chemistry is an interdisciplinary science that makes a bridge between inorganic, organic, physical, analytical, and biological chemistry.
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