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Self-organized three dimensional architectures based on non-covalent interactions in square planar Cu(II) thiosemicarbazone: Solvent mediated crystallization and EPR based correlation study

机译:基于非共价相互作用的方形平面铜(II)硫代吡吩的非共价相互作用的自组织三维架构:溶剂介导的结晶和基于EPR的相关研究

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摘要

A series of copper complexes of 2-acetylpyridine-N-4-methylthiosemicarbazone (HL4M) were synthesized and characterized by elemental analyses, UV-Vis, FT-IR, conductivity and EPR studies. The molecular structures of [Cu(L4M)Cl] (1), [Cu(L4M)I] (2), [Cu(L4M)OAc].H2O (3) and [Cu(mu-S-L4M)(NCS)](2).DMSO (4) were confirmed by single crystal X-ray crystallography. Complexes 1, 2 and 3 have square planar geometry constituted by NNS donor sites from deprotonated thiosemicarbazone ligand and the fourth site is occupied by anionic group/atom. Complex 4 is a centrosymmetric dimer. The XRD results revealed that the solvents play a decisive role in the crystallization of products. These four complexes exhibit strong hydrogen bonding interactions in the solid state and are self-assembled into infinite 3D supramolecular structure via pi center dot center dot center dot pi stacking interactions. The g vertical bar vertical bar and A vertical bar vertical bar of complexes were analyzed by Peisach-Blumberg plot which proves an inverse correlation among NNS and ONS thiosemicarbazone complexes. (C) 2018 Elsevier B.V. All rights reserved.
机译:通过元素分析,UV-Vis,FT-IR,电导率和EPR研究,合成了一系列2-乙酰吡啶-N-4-甲基硫代哌王(HL4M)的铜络合物。 [Cu(L4M)Cl](1),[Cu(L4M)I](2),[Cu(L4M)OAC] .H2O(3)和[Cu(MU-S-L4M)(NCS)的分子结构(NCS )](2)。通过单晶X射线晶体学证实了.DMSO(4)。复合物1,2和3具有由去质子化硫代吡嗪酮配体的NNS供体部位构成的方形平面几何形状,第四位点被阴离子组/原子占据。复合物4是柠檬色二聚体。 XRD结果表明,溶剂在产品的结晶中发挥着决定性作用。这四个复合物在固态中表现出强烈的氢键相互作用,通过PI中心点中心点中心点PI堆叠相互作用自组装成无限3D超分子结构。通过Peisach-Blumberg Plot分析G垂直条垂直条和垂直条垂直条,证明NNS和硫代蓟虫毒酶复合物之间的反比相关性。 (c)2018年elestvier b.v.保留所有权利。

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