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New Coordination Polymers of Lanthanide(iii) with Tetrazole-1-acetic Acid: Synthesis, Crystal Structures, and Magnetic Properties

机译:镧系元素(iii)与四唑-1-乙酸的新型配位聚合物:合成,晶体结构和磁性

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摘要

New coordination polymers {[Ln(tza)3(H2O)2]·mH2O}n (Ln = LaIII 1 and PrIII 2, m = 2; Ln = NdIII 3, m = 1.5) and {[Sm2(tza)6(H2O)5]·H2O}n 4 (Htza = tetrazole-1-acetic acid) have been synthesized and characterized by IR spectroscopy, elemental analysis, X-ray crystallography, and magnetic measurements. The Htza ligand coordinates to the lanthanide cations through the carboxylate group in a monodentate, bridging bidentate coordination mode or bridging tridentate to two metal centres. Complexes 1 and 2 are isostructural. Complex 3 has a similar structure to 1 and 2, but the arrangement of ligands has changed. Complex 4 consists of two types of metallic molecules. Magnetic measurements show weak antiferromagnetic coupling between the metal centres in complexes 2 and 3.
机译:新的配位聚合物{[Ln(tza)3(H2O)2]·mH2O} n(Ln = LaIII 1和PrIII 2,m = 2; Ln = NdIII 3,m = 1.5)和{[Sm2(tza)6(已经合成并通过红外光谱,元素分析,X射线晶体学和磁测量对H2O)5]·H2O} n 4(Htza =四唑-1-乙酸)进行了表征。 Htza配体以单齿,桥联二齿配位方式或三齿桥联到两个金属中心的方式通过羧酸根与镧系元素阳离子配位。配合物1和2是同构的。配合物3具有与1和2类似的结构,但是配体的排列已改变。配合物4由两种类型的金属分子组成。磁性测量表明,配合物2和3中金属中心之间的反铁磁耦合弱。

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