Temperature-dependent 3D structures of lanthanide coordination polymers based on dicarboxylate mixed ligands

被引:22
作者
Chainok, Kittipong [1 ]
Ponjan, Nutcha [1 ]
Theppitak, Chatphorn [1 ]
Khemthong, Phailyn [2 ]
Kielar, Filip [2 ]
Dungkaew, Winya [3 ]
Zhou, Yan [4 ]
Batten, Stuart R. [5 ]
机构
[1] Thammasat Univ, Fac Sci & Technol, Mat & Text Technol, Khlong Luang 12121, Pathum Thani, Thailand
[2] Naresuan Univ, Fac Sci, Dept Chem, Muang 65000, Phitsanulok, Thailand
[3] Mahasarakham Univ, Fac Sci, Dept Chem, Kantharawichai 44150, Maha Sarakham, Thailand
[4] Hong Kong Univ Sci & Technol, Dept Chem, Kowloon, Clear Water Bay, Hong Kong, Peoples R China
[5] Monash Univ, Sch Chem, Clayton, Vic 3800, Australia
关键词
METAL-ORGANIC FRAMEWORKS; CRYSTAL-STRUCTURES; HYDROTHERMAL SYNTHESIS; LUMINESCENT PROPERTIES; GAS-ADSORPTION; REVERSIBLE DEHYDRATION; SERIES; COMPLEXES; ACID; LN;
D O I
10.1039/c8ce01430b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Fourteen three-dimensional (3D) lanthanide coordination polymers (CPs) with dicarboxylate mixed ligands, [Ln(fum)(1.5)(H2O)(2)]center dot 0.5(H(2)bdc)center dot H2O (Ln = Sm(1), Tb (2)), [Ln(2)(fum)(2)(bdc)(H2O)(4)]center dot 2H(2)O (Ln = Sm(3), Eu (4), Tb (5), Er (6)), [Ln(fum)(0.5)(bdc)] (Ln = Sm (7), Eu (8), Tb (9), Er (10)), and [Ln(2)(bdc)(2)(ox)(H2O)(4)]center dot 0.7H(2)O (Ln = Sm (11), Gd (12), Tb (13), Dy (14)), have been synthesized hydrothermally from the self-assembly of lanthanide.III) ions (Ln(3+)), fumaric acid (H(2)fum), and terephthalic acid (H(2)bdc) in the presence of potassium hydroxide at different temperatures. The compounds fall into four classes. Compounds 1 and 2 were isolated from hydrothermal reactions performed at a relatively low temperature of 100 degrees C and found to crystallize in the triclinic space group P (1) over bar. The 3D framework is assembled from 2D layers of [Ln(fum)center dot H2O)(2)] units pillared by the chelating fum ligands and has 1D rhombic channels templated by H(2)bdc and lattice H2O molecules. The framework presents a binodal (4,5)-connected tcs topology with the point symbol (4(4)center dot 6(2)) (4(4)center dot 6(6)). Raising the reaction temperature to 140 degrees C resulted in the formation of compounds 3-6. These materials crystallize in the monoclinic system with the polar space group P2(1) and feature a 3D network constructed from dinuclear {Ln(2)(OCO)(6)(H2O)(4)} units interlinked by fum and bdc ligands, showing a uninodal 6-connected two-fold interpenetrated pcu topology. The small channels of the framework are occupied by lattice H2O molecules. Further increase of the reaction temperature to 160 degrees C gave rise to the formation of compounds 7-10, crystallizing in the orthorhombic space group Pbca. The 3D framework is generated from 2D corrugated sheets of [Ln(fum)](2+) bound by bdc ligands and contains no intercalated H2O molecules in the lattice. The framework possesses a trinodal (4,6,7)-connected net with the point symbol (4(2)center dot 6(4))(2)(4(6)center dot 6(8)center dot 8)(4(12)center dot 6(9))(2). Finally, compounds 11-14 contained an in situ generated oxalate (ox) ligand formed under hydrothermal conditions conducted at a high reaction temperature of 180 degrees C. These compounds crystallize in the monoclinic space group P2(1)/c and possess a 3D open framework consisting of a dinuclear [Ln(2)(ox)(H2O)(4)](2+) unit linked by bridging bdc ligands and has small void channels occupied by lattice H2O molecules. The frameworks were topologically simplified as a binodal (4,5)-connected tcj/hc net with a total point symbol of (4(2)center dot 5(2)center dot 7(2))(4(2)center dot 5(3)center dot 7(5)). In the solid state at room temperature, the Tb (2, 5, 9, and 13) and Eu (4 and 8) compounds emit green and red light, respectively.
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页码:7446 / 7457
页数:12
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