Two new isomeric zinc(II) metal–organic frameworks based on 1,5‐bis(2‐methyl‐1H‐imidazol‐1‐yl)pentane and 5‐methylisophthalate ligands

Many factors, such as temperature, solvent, the central metal atom and the type of coligands, may affect the nature of metal–organic frameworks (MOFs) and the framework formation in the self‐assembly process, which results in the complexity of these compounds and the uncertainty of their structures....

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Veröffentlicht in:Acta crystallographica. Section C, Crystal structure communications Crystal structure communications, 2017-02, Vol.73 (2), p.78-83
Hauptverfasser: Tan, Xiong-Wen, Li, Heng-Feng, Li, Chang-Hong
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Sprache:eng
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Zusammenfassung:Many factors, such as temperature, solvent, the central metal atom and the type of coligands, may affect the nature of metal–organic frameworks (MOFs) and the framework formation in the self‐assembly process, which results in the complexity of these compounds and the uncertainty of their structures. Two new isomeric ZnII metal–organic frameworks (MOFs) based on mixed ligands, namely, poly[[μ‐1,5‐bis(2‐methyl‐1H‐imidazol‐1‐yl)pentane‐κ2N3:N3′](μ‐5‐methylisophthalato‐κ2O1:O3)zinc(II)], [Zn(C9H6O4)(C13H20N4)]n, (I), and poly[[μ‐1,5‐bis(2‐methyl‐1H‐imidazol‐1‐yl)pentane‐κ2N3:N3′](μ3‐5‐methylisophthalato‐κ3O1:O1′:O3)(μ3‐5‐methylisophthalato‐κ4O1:O1′:O3,O3′)dizinc(II)], [Zn2(C9H6O4)2(C13H20N4)]n, (II), have been synthesized under hydrothermal conditions and characterized by single‐crystal X‐ray diffraction, IR spectroscopy, elemental analysis and thermogravimetric analysis. Complex (I) displays a two‐dimensional layer net, while complex (II) exhibits a twofold interpenetrating three‐dimensional framework. Both complexes show high stability and good fluorescence in the solid state at room temperature. Two‐ and three‐dimensional zinc metal–organic frameworks (MOFs) constructed from 1,5‐bis(2‐methyl‐1H‐imidazol‐1‐yl)pentane and 5‐methylisophthalic acid are reported. Both complexes show high stability and good fluorescence in the solid state at room temperature.
ISSN:2053-2296
0108-2701
2053-2296
1600-5759
DOI:10.1107/S2053229616020520