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Uncovering the Structural Diversity of Y(III) Naphthalene-2,6-Dicarboxylate MOFs Through Coordination Modulation

机译:通过配位调制揭示Y(III)萘-2,6-二羧酸甲酯MOF的结构多样性

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摘要

Metal-organic frameworks (MOFs)—network structures built from metal ions or clusters and connecting organic ligands—are typically synthesized by solvothermal self-assembly. For transition metal based MOFs, structural predictability is facilitated by control over coordination geometries and linker connectivity under the principles of isoreticular synthesis. For rare earth (RE) MOFs, coordination behavior is dominated by steric and electronic factors, leading to unpredictable structures, and poor control over self-assembly. Herein we show that coordination modulation—the addition of competing ligands into MOF syntheses—offers programmable access to six different Y(III) MOFs all connected by the same naphthalene-2,6-dicarboxylate ligand, despite controlled synthesis of multiple phases from the same metal-ligand combination often being challenging for rare earth MOFs. Four of the materials are isolable in bulk phase purity, three are amenable to rapid microwave synthesis, and the fluorescence sensing ability of one example toward metal cations is reported. The results show that a huge variety of structurally versatile MOFs can potentially be prepared from simple systems, and that coordination modulation is a powerful tool for systematic control of phase behavior in rare earth MOFs.
机译:从金属离子或簇和连接的有机配体,通常是通过溶剂热自组装合成的内置金属 - 有机骨架(MOF) - 网络结构。对于基于过渡金属的MOF,结构预测由下isoreticular合成的原理在协调的几何形状控制和连接器的连接变得容易。对于稀土(RE)的MOF,协调行为受到空间和电子因素占主导地位,导致不可预知的结构和控制不良战胜自我组装。本文我们显示,协调调制加入竞争性配体为MOF合成-提供到六个不同的Y(III)的MOF所有由相同的萘-2,6-二羧酸酯的配体连接,可编程存取尽管从相同的多相位的控制合成的金属 - 配体组合常常是用于稀土类的MOF挑战。材料中的四个是在本体相纯度可分离,三是适合于快速微波合成,并朝向金属阳离子一个实例的荧光感测能力被报道。结果表明,多功能MOFs材料种类繁多的结构有可能从简单的系统准备,并协调调制是稀土MOFs材料的相行为的系统控制的有力工具。

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