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含有噻吩 -2- 羧酸盐和 2- 氨基 -4,6- 二甲氧基嘧啶配体的钴(II)和铜(II)配合物中的超分子结构

Supramolecular architectures in Co(II) and Cu(II) complexes with thiophene-2-carboxylate and 2-amino-4,6-dimethoxypyrimidine ligands.

作者信息

Karthikeyan Ammasai, Thomas Muthiah Packianathan, Perdih Franc

机构信息

School of Chemistry, Bharathidasan University, Tiruchirappalli 620 024, Tamilnadu, India.

Faculty of Chemistry and Chemical Technology, University of Ljubljana, Vecna pot 113, PO Box 537, SI-1000 Ljubljana, Slovenia.

出版信息

Acta Crystallogr C Struct Chem. 2016 May 1;72(Pt 5):442-50. doi: 10.1107/S2053229616006148. Epub 2016 Apr 21.

Abstract

The coordination chemistry of mixed-ligand complexes continues to be an active area of research since these compounds have a wide range of applications. Many coordination polymers and metal-organic framworks are emerging as novel functional materials. Aminopyrimidine and its derivatives are flexible ligands with versatile binding and coordination modes which have been proven to be useful in the construction of organic-inorganic hybrid materials and coordination polymers. Thiophenecarboxylic acid, its derivatives and their complexes exhibit pharmacological properties. Cobalt(II) and copper(II) complexes of thiophenecarboxylate have many biological applications, for example, as antifungal and antitumor agents. Two new cobalt(II) and copper(II) complexes incorporating thiophene-2-carboxylate (2-TPC) and 2-amino-4,6-dimethoxypyrimidine (OMP) ligands have been synthesized and characterized by X-ray diffraction studies, namely (2-amino-4,6-dimethoxypyrimidine-κN)aquachlorido(thiophene-2-carboxylato-κO)cobalt(II) monohydrate, [Co(C5H3O2S)Cl(C6H9N3O2)(H2O)]·H2O, (I), and catena-poly[copper(II)-tetrakis(μ-thiophene-2-carboxylato-κ(2)O:O')-copper(II)-(μ-2-amino-4,6-dimethoxypyrimidine-κ(2)N(1):N(3))], [Cu2(C5H3O2S)4(C6H9N3O2)]n, (II). In (I), the Co(II) ion has a distorted tetrahedral coordination environment involving one O atom from a monodentate 2-TPC ligand, one N atom from an OMP ligand, one chloride ligand and one O atom of a water molecule. An additional water molecule is present in the asymmetric unit. The amino group of the coordinated OMP molecule and the coordinated carboxylate O atom of the 2-TPC ligand form an interligand N-H...O hydrogen bond, generating an S(6) ring motif. The pyrimidine molecules also form a base pair [R2(2)(8) motif] via a pair of N-H...N hydrogen bonds. These interactions, together with O-H...O and O-H...Cl hydrogen bonds and π-π stacking interactions, generate a three-dimensional supramolecular architecture. The one-dimensional coordination polymer (II) contains the classical paddle-wheel [Cu2(CH3COO)4(H2O)2] unit, where each carboxylate group of four 2-TPC ligands bridges two square-pyramidally coordinated Cu(II) ions and the apically coordinated OMP ligands bridge the dinuclear copper units. Each dinuclear copper unit has a crystallographic inversion centre, whereas the bridging OMP ligand has crystallographic twofold symmetry. The one-dimensional polymeric chains self-assemble via N-H...O, π-π and C-H...π interactions, generating a three-dimensional supramolecular architecture.

摘要

混合配体配合物的配位化学仍然是一个活跃的研究领域,因为这些化合物有广泛的应用。许多配位聚合物和金属有机框架正作为新型功能材料出现。氨基嘧啶及其衍生物是具有多种键合和配位模式的柔性配体,已被证明可用于构建有机-无机杂化材料和配位聚合物。噻吩羧酸及其衍生物以及它们的配合物具有药理性质。噻吩羧酸钴(II)和铜(II)配合物有许多生物学应用,例如作为抗真菌和抗肿瘤剂。已经合成了两种包含噻吩 - 2 - 羧酸盐(2 - TPC)和2 - 氨基 - 4,6 - 二甲氧基嘧啶(OMP)配体的新型钴(II)和铜(II)配合物,并通过X射线衍射研究对其进行了表征,即一水合(2 - 氨基 - 4,6 - 二甲氧基嘧啶 - κN)水氯(噻吩 - 2 - 羧基 - κO)钴(II),[Co(C5H3O2S)Cl(C6H9N3O2)(H2O)]·H2O,(I),以及链状聚[铜(II) - 四(μ - 噻吩 - 2 - 羧基 - κ(2)O:O') - 铜(II) - (μ - 2 - 氨基 - 4,6 - 二甲氧基嘧啶 - κ(2)N(1):N(3))],[Cu2(C5H3O2S)4(C6H9N3O2)]n,(II)。在(I)中,Co(II)离子具有扭曲的四面体配位环境,涉及来自单齿2 - TPC配体的一个O原子、来自OMP配体的一个N原子、一个氯配体和一个水分子的O原子。不对称单元中存在一个额外的水分子。配位的OMP分子的氨基和2 - TPC配体的配位羧酸根O原子形成配体间N - H...O氢键,产生S(6)环 motif。嘧啶分子还通过一对N - H...N氢键形成碱基对[R2(2)(8) motif]。这些相互作用,连同O - H...O和O - H...Cl氢键以及π - π堆积相互作用,产生三维超分子结构。一维配位聚合物(II)包含经典的桨轮状[Cu2(CH3COO)4(H2O)2]单元,其中四个2 - TPC配体的每个羧酸根基团桥连两个方形金字塔配位的Cu(II)离子,顶端配位的OMP配体桥连双核铜单元。每个双核铜单元具有晶体学反演中心,而桥连的OMP配体具有晶体学二重对称性。一维聚合物链通过N - H...O、π - π和C - H...π相互作用自组装,产生三维超分子结构。

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