首页> 外文期刊>Crystal growth & design >Porous Cadmium(II) Anionic Metal-Organic Frameworks Based on Aromatic Tricarboxylate Ligands: Encapsulation of Protonated Flexible Bis(2-methylimidazolyl) Ligands and Proton Conductivity
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Porous Cadmium(II) Anionic Metal-Organic Frameworks Based on Aromatic Tricarboxylate Ligands: Encapsulation of Protonated Flexible Bis(2-methylimidazolyl) Ligands and Proton Conductivity

机译:基于芳族三羧酸盐配体的多孔镉(II)阴离子金属有机骨架:质子化柔性双(2-甲基咪唑基)配体的包封和质子电导率

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摘要

Two porous 3-D anionic metal-organic frameworks (MOFs) containing protonated bmib, [Cd-2(btc)(2)(H2O)(2)](n)center dot n(H(2)bmib)center dot 6n(H2O) (1) and [Cd-4(cpip)(2)(Hcpip)(2)](n)center dot n(H(2)bmib)center dot n(H2O) (2), have been prepared by hydrothermal reactions of Cd(NO3)(2)center dot 4H(2)O, 1,4-bis(2-methylimidazol-1'-yl)butane (bmib) with 1,3,5-benzenetricarboxylic acid (H(3)btc) and 5-(4-carboxyphenoxy)isophthalic acid (H(3)cpip), respectively. Complexes 1 and 2 are 3-D anionic frameworks containing 1-D channels and consisting of tetranudear Cd(II)-carboxylate units, respectively. H2bmib and lattice water molecules are located in their void spaces and form extensive hydrogen bonds and C-H center dot center dot center dot pi interaction with the anionic frameworks. TGA studies and XRD patterns show the anionic frameworks of 1 and 2 are intact after the removal of lattice water molecules. The luminescent emission of 1 and 2 shows an obvious red shift in comparison with free H(3)btc and H(3)cpip, respectively. Complexes 1 and 2 possess proton conduction owing to the presence of the extensive hydrogen bonds and protonation of bmib; their proton conductivity at 333 K and 95% relative humidity are 5.4 x 10(-5) and 2.2 x 10(-5) S cm(-1), respectively.
机译:包含质子化bmib的两个多孔3-D阴离子金属有机骨架(MOF),[Cd-2(btc)(2)(H2O)(2)](n)中心点n(H(2)bmib)中心点6n制备了(H2O)(1)和[Cd-4(cpip)(2)(Hcpip)(2)](n)中心点n(H(2)bmib)中心点n(H2O)(2) Cd(NO3)(2)中心点4H(2)O,1,4-双(2-甲基咪唑-1'-基)丁烷(bmib)与1,3,5-苯三甲酸(H( 3)btc)和5-(4-羧苯氧基)间苯二甲酸(H(3)cpip)。配合物1和2是3-D阴离子骨架,其包含1-D通道并分别由四核Cd(II)-羧酸酯单元组成。 H2bmib和晶格水分子位于其空隙中,并形成广泛的氢键,并与阴离子骨架形成C-H中心点中心点中心点pi相互作用。 TGA研究和XRD图谱显示,除去晶格水分子后,1和2的阴离子骨架完好无损。 1和2的发光发射分别与游离H(3)btc和H(3)cpip相比显示出明显的红移。配合物1和2由于存在广泛的氢键和bmib的质子化而具有质子传导;它们在333 K和95%相对湿度下的质子传导率分别为5.4 x 10(-5)和2.2 x 10(-5)S cm(-1)。

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