碳酰肼配体七配位Mn(II)和Co(II)配合物的合成、光谱研究和x射线衍射

T. Seck, A. Sy, Djiby Lo, Papa Aly Gaye, M. L. Sall, O. Diouf, M. Diaw, M. Gaye
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引用次数: 5

摘要

配体1-(1-(吡啶-2-基)亚乙基)碳酰肼(H4L1)和1-(吡啶2-基亚甲基)碳酰亚胺(H4L2)是通过碳酰肼分别与2-乙酰基吡啶或吡啶甲醛在回流甲醇溶液中反应制备的。配合物是通过配体与合适的金属盐反应制备的。通过元素分析、红外光谱和紫外光谱对这些配合物进行了表征,并用单X射线衍射技术测定了它们的结构。在双核配合物[Mn2(H4L1)2(H2O)4]·Cl4的晶体中,1)每个Mn(II)中心由一个配体的两个氮原子和一个羰基原子以及另一个配体分子的一个氮原子与一个羰基氧原子七配位。配位球是由两个水分子组成的。每个羰基氧原子充当两个Mn(II)中心之间的桥梁。单核配合物[Co(H4L2)(NO3)(H2O)2]·(NO3;2) Co(II)中心是七配位的。配体通过两个氮原子和一个羰基氧原子以三齿形式起作用。两个水分子位于顶端位置。一个硝酸盐基团以双齿方式起作用,而另一个硝酸酯基团保持不协调。在这两种配合物中,配位多面体最好用五边形双锥来描述。在每种情况下,分子通过多个氢键相互作用连接在一起,形成三维网络。晶体学数据已存放在剑桥晶体学数据中心[CCCDC编号1944387(复合体1)和1944386(复合体2)]。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis, Spectroscopic Studies and X-Ray Diffraction of Heptacoordinated Mn(II) and Co(II) Complexes with Ligands Derived from Carbonohydrazide
The ligand 1-(1-(pyridin-2-yl)ethylidene)carbonohydrazide (H4L1) and 1-(pyridin-2-ylmethylene)carbonohydrazide (H4L2) were prepared by reaction of carbonohydrazide with 2-acetylpyridine or pyridine carbaldehyde respectively in a reflux methanol solution. The complexes are prepared by reaction of the ligand with the appropriate metal salt. These complexes are well characterized by elemental analysis, IR and UV spectroscopies and their structure were determined by single X-ray diffraction technic. In the crystal of the dinuclear complex [Mn2(H4L1)2(H2O)4]·Cl4, 1) each Mn(II) center is seven coordinated by two nitrogen atom and one carbonyl atom of the one ligand and one nitrogen atom and one carbonyl oxygen atom of another ligand molecule. The coordination sphere is completed by two water molecules. Each of the carbonyl oxygen atom acts as bridge between the two Mn(II) centers. In the mononuclear complex [Co(H4L2)(NO3)(H2O)2]·(NO3); 2) the Co(II) center is heptacoordinated. The ligand acts in tridentate fashion through two nitrogen atoms and one carbonyl oxygen atom. Two water molecules lie in the apical positions. One nitrate group acts in bidentate manner while the other nitrate group remains uncoordinated. In both complexes the coordination polyhedral are best described as a pentagonal bipyramid. The molecules are linked together in each case by multiple hydrogen bond interaction resulting in a three-dimensional network. The crystallographic data has been deposited in Cambridge Crystallographic Data Centre [CCDC No. 1944387 (complex 1) and 1944386 (complex 2)].
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