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二-μ-氯代-双-(氯代-{N'-[苯基(吡啶-2-基-κN)亚甲基]吡啶-2-碳酰肼-κ(2) N',O})镉

Di-μ-chlorido-bis-(chlorido-{N'-[phen-yl(pyridin-2-yl-κN)methyl-idene]pyridine-2-carbohydrazide-κ(2) N',O}cadmium).

作者信息

Akkurt Mehmet, Khandar Ali Akbar, Tahir Muhammad Nawaz, Afkhami Farhad Akbari, Yazdi Seyed Abolfazl Hosseini

机构信息

Department of Physics, Faculty of Sciences, Erciyes University, 38039 Kayseri, Turkey.

Department of Inorganic Chemistry, Faculty of Chemistry, University of Tabriz, Tabriz, Iran.

出版信息

Acta Crystallogr Sect E Struct Rep Online. 2014 May 17;70(Pt 6):m213-4. doi: 10.1107/S1600536814010630. eCollection 2014 Jun 1.

Abstract

The title compound, [Cd2Cl4(C18H14N4O)2], was obtained from the reaction of Cd(NO3)2·4H2O with 2-phenyl-pyridine-keton picolinoyl hydrazone and sodium chloride. Each Cd(2+) cation is coordinated by two N atoms and one O atom of the tridentate ligand and three chloride anions, forming a distorted CdNOCl3 octahedron. Each pair of adjacent metal cations is linked by two bridging chloride ligands, resulting in a dinuclear complex unit. The mol-ecular conformation is stabilized by intra-molecular N-H⋯N and C-H⋯O hydrogen bonds. In the crystal, mol-ecules are linked by nonclassical C-H⋯O and C-H⋯Cl hydrogen bonds into a three-dimensional network. In addition, π-π stacking inter-actions [centroid-centroid distances = 3.777 (2) and 3.631 (2) Å] contribute to the stabilization of the crystal packing.

摘要

标题化合物[Cd₂Cl₄(C₁₈H₁₄N₄O)₂]是由Cd(NO₃)₂·4H₂O与2-苯基吡啶酮吡啶甲酰腙和氯化钠反应制得的。每个Cd(2+)阳离子由三齿配体的两个N原子和一个O原子以及三个氯离子配位,形成一个扭曲的CdNOCl₃八面体。每对相邻的金属阳离子通过两个桥联氯配体相连,形成一个双核配合物单元。分子构象通过分子内的N-H⋯N和C-H⋯O氢键得以稳定。在晶体中,分子通过非经典的C-H⋯O和C-H⋯Cl氢键连接成三维网络。此外,π-π堆积相互作用[质心-质心距离 = 3.777 (2) 和3.631 (2) Å]有助于晶体堆积的稳定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a45/4051065/c4e1735acf06/e-70-0m213-fig1.jpg

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