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Metal-organic frameworks and self-assembled supramolecular coordination complexes: Comparing and contrasting the design, synthesis, and functionality of metal-organic materials

机译:金属有机骨架和自组装的超分子配位化合物:比较和对比金属有机材料的设计,合成和功能

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摘要

A comparison of synthesis and functionality of metal-organic framework (MOF) and self-assembled supramolecular coordination complexes (SCC) is performed. The former are comprised of infinite networks of metal centers or inorganic clusters bridged by simple organic linkers through metal-ligand coordination bonds. The latter encompass discrete systems in which carefully selected metal centers undergo self-assembly with ligands containing multiple binding sites oriented with specific angularity to generate a finite supramolecular complex. Functionalization of both MOFs and SCCs can occur either by preserving or by disrupting the overall topology of the MOMs. It is also possible to initiate postsynthetic modifications (PSMs) of MOFs by treatment with exogenous ligands rather than metals. Both MOFs and SCCs have shown promise in sensing and other photophysical-based applications, since the binding of an analyte to their internal cavities can oftentimes induce electronic structure changes, which result in emission changes.
机译:进行了金属有机骨架(MOF)和自组装的超分子配位化合物(SCC)的合成和功能比较。前者由金属中心或无机团簇的无限网络组成,这些团簇由简单的有机接头通过金属-配体配位键桥接。后者包括离散的系统,其中精心选择的金属中心与包含多个以特定角度定向的结合位点的配体进行自组装,以生成有限的超分子配合物。 MOF和SCC的功能可以通过保留或破坏MOM的整体拓扑来实现。也可以通过用外源配体而不是金属进行处理来引发MOF的合成后修饰(PSM)。 MOF和SCC在传感和其他基于光物理的应用中都显示出了希望,因为分析物与其内腔的结合经常会引起电子结构变化,从而导致发射变化。

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