Three new 3D metal-organic frameworks based on the tetrakis(imidazol-1-ylmethyl)methane and 1,4-benzenedicarboxylic acid ligands with transition metal (Zn/Cd/Co) and properties research

被引:6
|
作者
Du, Lin [1 ]
Yan, Tong [1 ]
Zhao, Yi-Dan [1 ]
Wang, Xiao [1 ]
Qian, Xing-Can [1 ]
Wang, Quan [1 ]
Zhao, Qi-Hua [1 ]
机构
[1] Yunnan Univ, Sch Chem Sci & Technol & Pharm, Key Lab Med Chem Nat Resource, Educ Minist, Kunming, Peoples R China
基金
美国国家科学基金会;
关键词
MOFs; Crystal structure; Fluorescent property; Magnetic property; COORDINATION POLYMERS; TETRAKIS(IMIDAZOLE) LIGAND; LUMINESCENT PROPERTIES; CRYSTAL-STRUCTURES; DICARBOXYLATES; 4,4'-BIPYRIDINE; ADSORPTION; SEPARATION; DESIGN;
D O I
10.1016/j.ica.2016.08.030
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Three novel 3D metal-organic frameworks, {[Zn-2(L)(BDC)(2)]center dot H2O}(n) (1), {[Cd-2(L)(2)(BDC)]center dot(BDC)center dot 7.7(H2O)}(n) (2), and {[Co(L)(H2O)(2)]center dot(BDC)center dot 5(H2O)) (3) (L = tetrakis(imidazol-1-ylmethyl)methane, H2BDC = 1,4-benzenedicarboxylic acid), have been successfully synthesized by self-assembly of transition-metal salts with a flexible N-containing ligand and 1,4-dicarboxybenzene ligand. Complexes 1-3 have 3D structures with various topologies. In complex 1, the L connects Zn(II) atoms to form 2D layers, which are linked by two kinds of 1D [Zn(BDC)](n) chains to generate a 4-connected three-dimensional structure with (6.8(5)) (6(4).8(2))(8(6)) topology. In complex 2, Cd(II) atoms are coordinated by L to furnish a 2D layer, and the adjacent layers are linked by BDC ligands as bridging ligands to general a new (4,5)-connected three-dimensional network with a point symbol of (4(4).6(2))(4(4).6(6)). In Complex 3, the L ligands act as 4-connected linkers connecting Co(II) ions to display a 4-connected three-dimensional structure with 4.6(5) topological net directly. In addition, the solid-state fluorescence, infrared spectra, magnetic property and thermal stability of these complexes have also been investigated. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:292 / 297
页数:6
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