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由环三磷腈功能化六羧酸配体构建的二维镧系(III)配位聚合物的合成、结构与性质

Synthesis, Structure, and Properties of 2D Lanthanide(III) Coordination Polymers Constructed from Cyclotriphosphazene-Functionlized Hexacarboxylate Ligand.

作者信息

Jia Qi, Yao Yicheng, Zhu Xiaoming, Wang Juntao, Li Zeyu, Ji Liudi, Hu Peng

机构信息

School of Pharmacy, Hubei University of Science and Technology, Xianning 437100, China.

Hubei Key Laboratory of Radiation Chemistry and Functional Materials, School of Nuclear Technology and Chemistry & Biology, Hubei University of Science and Technology, Xianning 437100, China.

出版信息

Molecules. 2024 Nov 27;29(23):5602. doi: 10.3390/molecules29235602.

Abstract

The design and synthesis of novel lanthanide-based coordination polymers (Ln-CPs) from flexible organic ligands is still attractive and challenging. In this work, two isostructural Ln-CPs with a unique 2D network, namely, [Ln(HL)(DMF)]] (Ln = Dy for , Tb for ) based on a flexible polycarboxylic acid ligand hexakis(4-carboxylato-phenoxy)cyclotriphosphazene (HL), have been solvothermally synthesized and structurally characterized. Significantly, it is the first observation of polycarboxylic acid ligands participating in coordination in the construction of coordination polymers in the form of semi-deprotonation. Magnetic measurements showed the presence of field-induced slow magnetic relaxation in complex . The luminescence property of had been studied in the solid state at room temperature.

摘要

利用柔性有机配体设计和合成新型镧系配位聚合物(Ln-CPs)仍然具有吸引力且颇具挑战性。在本工作中,基于柔性多元羧酸配体六(4-羧基苯氧基)环三磷腈(HL),通过溶剂热法合成并对两种具有独特二维网络结构的同构Ln-CPs,即[Ln(HL)(DMF)]](Ln = Dy时为 ,Tb时为 )进行了结构表征。值得注意的是,这是首次观察到多元羧酸配体以半去质子化形式参与配位聚合物的构建。磁性测量表明配合物 中存在场诱导的慢磁弛豫现象。已在室温下对 的固态发光性质进行了研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f70/11643244/eae0849323a1/molecules-29-05602-sch001.jpg

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