Solvent-induced generation of two cadmium-based metal-organic frameworks from 1, 3, 5-benzenetricarboxylic acid ligand

被引:6
|
作者
Liu, Wanyi [1 ]
He, Hongming [1 ]
Song, Yang [1 ]
Du, Jianshi [2 ]
Sun, Fuxing [1 ]
机构
[1] Jilin Univ, State Key Lab Inorgan Synth & Preparat Chem, Changchun 130012, Peoples R China
[2] Jilin Univ, China Japan Union Hosp, Changchun 130031, Peoples R China
关键词
Metal-organic framework; Cadmium; 1; 3; 5-benzenetricarboxylic acid; Luminescent; Topological structure; COORDINATION POLYMERS; LUMINESCENCE PROPERTIES; PHOTOLUMINESCENCE; ADSORPTION; CATALYSIS; EMISSION; SORPTION; CLUSTER; UNITS; BI;
D O I
10.1016/j.inoche.2015.04.012
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Two cadmium-based metal-organic frameworks (MOFs), namely [Cd-5(BTC)(4)(DMAc)(2)(H2O)(2)DMF]center dot 2[H2N(CH3)(2)]center dot 4DMAc (JUC-133) and [Cd-3(BTC)(2)(DMSO)(4)] (JUC-134) (JUC = Jilin University, China), based on 1, 3, 5-benzenetricarboxylic acid ligand (H3BTC) were synthesized by solvent-induced strategy under solvothermal conditions and characterized by single crystal X-ray diffraction, elemental analysis, FT-IR spectroscopy, luminescent spectroscopy, TGA analysis, and powder X-ray diffraction. The ligand is connected to cadmium metals to form different cores with distinctive coordination modes to generate different structures. JUC-133 displays a new three-dimensional (3D) topology with the point symbol (4 center dot 6(2))(4)(4 center dot 8(2))(4)(4(2)center dot 6(5)center dot 8(3))(4)(8(6)) based on Cd-2(COO)(5) and Cd-2(COO)(4) as secondary building units (SBUs), which is unknown in previously reported MOFs. JUC-134 can be symbolized as a rutile (rtl) topology with the point symbol (4 center dot 6(2))(2)(4(2)center dot 6(10)center dot 8(3)) based on Cd-3(COO)(6) as SBUs. Furthermore, the luminescent of the ligand H3BTC and compounds were measured at room temperature. It is worth noting that the solvent could play an important role in the structural assembly process. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:11 / 14
页数:4
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