A Series of Lanthanide−Organic Frameworks Based on 2-Propyl-1H-imidazole-4,5-dicarboxylate and Oxalate: Syntheses, Structures, Luminescence, and Magnetic Properties

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• 作者：Xun Feng ; Jianshe Zhao ; Bin Liu ; Liya Wang ; Seikweng Ng ; Gai Zhang ; Jiange Wang ; Xinge Shi ; Yongyong Liu
• 刊名：Crystal Growth & Design
• 出版年：2010
• 出版时间：March 3, 2010
• 年：2010
• 卷：10
• 期：3
• 页码：1399-1408
• 全文大小：985K
• 年卷期：v.10,no.3(March 3, 2010)
• ISSN：1528-7505

文摘

A family of self-assembly lanthanide−organic coordination polymers with both rigid and flexible ligands formulated as {[Ln₂(Hpimda)₂(μ₄-C₂O₄)·2H₂O]·4H₂O}_n (Ln = Sm (1), Eu (2), Tb (3), Dy (4), Ho (5), Er (6), H₃pimda = 2-propyl-1H-imidazole-4,5-dicarboxylic acid) has been synthesized from the reactions of H₃pimda with trivalent lanthanide salts in the presence of oxalate as coligand. X-ray diffraction analysis reveals that these complexes are isomorphous and isostructural, and each forms a novel three-dimensional (3D) frameworks structure, in which the metalloligands' two-dimensional (2D) networks were constructed from the lanthanide ion, 2-propyl-imidazole-dicarboxylate as well as oxalate ligands, and the oxalate further acts as a pillar to link the [Ln(Pimda)(oxo)] 2D grids to generate the 3D open frameworks, leaving one-dimensional channels, which are occupied by water clusters displaying an intricate array. The luminescence emission spectra of the complexes vary depending on which lanthanide ion is present. In addition, compounds 3, 4, and 5 exhibited weak but significant ferromagnetic couplings within the two adjacent magnetic centers bridged through oxalato, whereas dominant antiferromagnetic interaction was observed in the erbium compound of 6, respectively.