首页> 外文期刊>Polyhedron: The International Journal for Inorganic and Organometallic Chemistry >H-bonded supramolecular synthon induced magnetic superexchange phenomenon results weak ferromagnetic and strong antiferromagnetic interactions in two new copper-orotate coordination network
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H-bonded supramolecular synthon induced magnetic superexchange phenomenon results weak ferromagnetic and strong antiferromagnetic interactions in two new copper-orotate coordination network

机译:H键合超分子合成诱导磁性超高速现象结果导致两种新的铜室内协调网络中的铁磁性和强磁磁相互作用弱

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摘要

Hydrothermal self-assembly of orotic acid (C5H4N2O4=OrH(3)) with metal salt Cu(Ac)(2)center dot H2O yielded a new OrH based hydrogen bonded coordination network of formula [Cu(OrH)(2NH(3))(H2O)]center dot H2O (1) and [Cu (OrH) (2NH(3))](2) (2). Single crystal X-ray study on 1 confirms that +2 charges on the metal ions (Cu2+) are balanced by OrH anion. N-H center dot center dot center dot O and O-H center dot center dot center dot O hydrogen bonding synthons are the only artifact for the resulting hydrogen bonded copper-OrH architecture. Temperature dependent measurements of magnetic susceptibility reveals the occurrence of competitive exchange interactions with a net ferromagnetic character in 1 (J = +0.48 cm(-1)) and strong antiferromagnetic interaction in 2 (J = -4.93 cm(-1)). Magnetic superexchange interaction transmitted through equatorial-axial hydrogen bridge system promotes weak ferromagnetic interactions in 1 while in 2 it is in basal-basal position, in which two d(x2-y2)orbitals is involved in exchange mechanism reveals the coexistence of two antiferromagnetic exchange pathways, intramolecular much stronger than intermolecular. The natural bond orbital (NBO) analysis applied separately to alpha and beta spin density matrices clearly shows two important magnetic superexchange pathway with shorter Cu center dot center dot center dot Cu contact 5.542(4) angstrom and 4.845(4) angstrom or 5.755(1) angstrom in (1) and inter dimer 6.665(1) angstrom and 4.6744(9) angstrom for (2). (C) 2017 Elsevier Ltd. All rights reserved.
机译:用金属盐Cu(AC)(2)中心点H2O的单次酸性酸(C5H4N2O4 = ORH(3))的水热包装(C5H4N2O4 = ORH(3))产生了一种基于ORH的式[Cu(ORH)的新的氢键配位网络(2NH(3)) (H2O)]中心点H 2 O(1)和[Cu(OrH)(2NH(3))](2)(2)。单晶X射线研究1表示金属离子(Cu2 +)上的+2电荷由Orh阴离子平衡。 N-H中心点中心点中心点O和O-H中心点中心点COT CEDOT O氢键合成器是所得氢粘结铜扫描结构的唯一工件。磁化率的温度依赖性测量揭示了在1(J = + 0.48cm(-1))中与净铁磁特性的竞争交换相互作用的发生,并且在2(J = -4.93cm(-1))中强的反铁磁性相互作用。通过赤道轴向氢气桥系统传输的磁性超高速相互作用促进1的弱铁磁性相互作用,而在2中是基部基础位置,其中涉及交换机制的两个D(X2-Y2)轨道揭示了两种反铁磁交换的共存途径,分子内比分区强。自然键轨道(NBO)分析分别适用于α和β自旋密度矩阵清楚地示出了具有更短的铜中心点中心的点中心的点的Cu接触的两个重要磁性超交换途径5.542(4)埃和4.845(4)埃或5.755(1 )(1)和24.665(1)埃和4.6744(9)埃的埃赫斯特朗姆(2)。 (c)2017 Elsevier Ltd.保留所有权利。

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