Synthesis, Supramolecular Insight, Hirshfeld Surface Analyses and Magnetic Properties of Two Lanthanide Complexes of 1,8-naphthalene Dicarboxylate

J.K. Nath, R. Borah
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Abstract

Two isostructural mononuclear complexes of Lanthanides (Ln = La and Pr) constructed from 1,8-naphthalene dicarboxylate (NDC) and 1,10-Phenanthroline (Phen) as auxiliary ligand are reported. Both the complexes were formed through an in situ hydrolytic ring opening reaction of 1,8-naphthalic anhydride with Phen ligands. 3D supramolecular structures are observed which are guided by different weak interactions. The crystal structures of both the complexes were determined by single crystal X-ray diffraction. The room temperature photoluminescence studies, carried out in the powder state displayed three noticeable peaks from excited ( 3 P J ; J = 2, 1, and 0) to ground state ( 3 H 4) at ~464, 497, and 538 nm respectively, under UV excitation. Temperature dependent dc susceptibility (c = M/H) as a function of temperature is investigated where Pr-complex shows antiferromagnetic behavior. The Hirshfeld surface analysis of the two complexes is also described.
两种1,8-萘二羧酸镧系配合物的合成、超分子洞察、Hirshfeld表面分析和磁性能
报道了以1,8-萘二甲酸酯(NDC)和1,10-菲罗啉(Phen)为辅助配体构建的两种镧系元素(Ln = La和Pr)同结构单核配合物。这两种配合物都是通过1,8-萘酸酐与苯配体的原位水解开环反应形成的。观察到不同弱相互作用引导下的三维超分子结构。用单晶x射线衍射测定了两种配合物的晶体结构。在粉末状态下进行的室温光致发光研究显示,从激发(3pj;J = 2、1和0)分别在~464、497和538 nm处达到基态(3h4)。在r-配合物表现出反铁磁行为的情况下,研究了随温度变化的直流磁化率(c = M/H)。本文还描述了这两种配合物的赫希菲尔德表面分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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