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首页> 外文期刊>Journal of Organometallic Chemistry >Rational design and syntheses of 0-D, 1-D, and 2-D metal-organic frameworks (MOFs) from ferrocenedicarboxylate tetrametallic macrocyclic building units and subsidiary ligands
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Rational design and syntheses of 0-D, 1-D, and 2-D metal-organic frameworks (MOFs) from ferrocenedicarboxylate tetrametallic macrocyclic building units and subsidiary ligands

机译:从二茂铁羧酸二金属四环大环结构单元和辅助配体中合理设计和合成0-D,1-D和2-D金属有机骨架(MOF)

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摘要

We have designed and synthesized three new metal-1,1'-ferrocenedicarboxylate complexes containing tetrametallic macrocyclic building units, namely, [Cd-2(eta(2)-O(2)CFcCO(2)-eta(2))(2)(phen)(2)(H2O)(2)] center dot 4CH(3)OH (1) (Fc = (eta(5)-C5H4)Fe(C5H4-eta(5)), phen = 1,10-phenanthroline), {[Cd(eta(2)-O(2)CFcCO(2))(pebbm)(H2O)] center dot 2H(2)O}(n) (2) (pebbm=1,1'-(1,5-pentanediyl)bis-1H-benzimidazole) and {[Cd(eta(2)-O(2)CFcCO(2)-eta(2))(prbbm)(H2O)] center dot 3H(2)O}(n) (3) (prbbm = 1,1'-(1,3-propanediyl)bis-1H-benzimidazole). Compound 1 is a 0-D discrete tetrametallic macrocyclic framework. Compound 2 features an infinite 1-D ribbon of rings structure constructed by the subsidiary ligands pebbm connecting tetrametallic macrocyclic building units. For 3, its tetrametallic macrocyclic building units are linked by the subsidiary ligands prbbm to form a 2-D network structure. The structural features of these complexes indicate that the ferrocenedicarboxylate tetrametallic macrocycle can be used as a successful molecular building unit and the shapes and conformational flexibility of subsidiary ligands play a crucial role in the manipulation of the configuration of the resultant MOFs. Their fluorescence spectra in solid state at room temperature suggest that the fluorescence emissions of 1-3 are ruled by 1,1'-ferrocenedicarboxylate ligand. (c) 2007 Published by Elsevier B.V.
机译:我们设计和合成了三个新的金属,1,1'-二茂铁羧酸二盐配合物,它们包含四金属大环结构单元,即[Cd-2(eta(2)-O(2)CFcCO(2)-eta(2))(2 )(phen)(2)(H2O)(2)]中心点4CH(3)OH(1)(Fc =(eta(5)-C5H4)Fe(C5H4-eta(5)),phen = 1,10 -菲咯啉),{[Cd(eta(2)-O(2)CFcCO(2))(pebbm)(H2O)]中心点2H(2)O}(n)(2)(pebbm = 1,1' -(1,5-戊二基)双-1H-苯并咪唑)和{[Cd(eta(2)-O(2)CFcCO(2)-eta(2))(prbbm)(H2O)]中心点3H(2 } O}(n)(3)(prbbm = 1,1'-(1,3-丙二基)双-1H-苯并咪唑)。化合物1是0-D离散的四金属大环骨架。化合物2具有无限的一维带状环结构,该结构由连接四金属大环结构单元的辅助配体pebbm构成。对于3,其四金属大环结构单元通过辅助配体prbbm连接以形成2-D网络结构。这些配合物的结构特征表明,二茂铁羧酸二金属盐大环化合物可以用作成功的分子构建单元,辅助配体的形状和构象柔韧性在操纵所得MOF的构型中起关键作用。它们在室温下处于固态的荧光光谱表明1-3的荧光发射受1,1'-二茂铁二羧酸酯配体支配。 (c)2007年由Elsevier B.V.

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