Near-infrared phosphorescence emission of three-fold interpenetrated MOF based on 1,4-bis(imidazole-1-ylmethyl)benzene: Syntheses, structure and photoelectron performance

被引:11
|
作者
Chang, Xin-Hong [1 ]
Ling, Xun-Li [1 ]
Lu, Xiao-Min [1 ,2 ]
Yang, Xiao-Gang [1 ]
Li, Fei-Fei [3 ]
Guo, Yu-Ming [2 ]
机构
[1] Luoyang Normal Univ, Coll Chem & Chem Engn, Henan Prov Funct Oriented Porous Mat Key Lab, Luoyang 471934, Peoples R China
[2] Henan Normal Univ, Coll Chem & Chem Engn, Xinxiang 453007, Henan, Peoples R China
[3] Henan Polytech Univ, Coll Chem & Chem Engn, Jiaozuo 454000, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
Metal-organic framework; Interpenetrated network; Phosphorescence; METAL-ORGANIC FRAMEWORKS;
D O I
10.1016/j.jssc.2020.121694
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
One new Zn(II) based 3D metal-organic framework (MOF) [Zn(IPA) (TBMIM)] (1) (IPA = isophthalic acid, TBMIM = 1,4-bis(imidazole-1-ylmethyl)benzene) has been synthesized under hydrothermal conditions. X-ray single-crystal diffraction analysis indicates that the title MOF exhibits a 3-fold interpenetrated diamond network with new type of molecular braid. Time-resolved measurements reveal that 1 emissions rare example of near-infrared phosphorescence at room temperature. The density functional theoretical (DFT) calculations indicate complete separation of molecular orbits between IPA and TBMIM ligands, which is in favor of the generation of triplet state excitons. This MOF also shows well photoelectron responds performance owing to the abundant pi center dot center dot center dot pi stacking in the entanglement molecular braids, which afford long-range pi electrons delocalization for efficient electron transport.
引用
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页数:6
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