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Control of the hierarchical self-assembly of polyoxometalate-based metallomacrocycles by redox trigger and solvent composition

机译:通过氧化还原触发和溶剂组成控制基于多金属氧酸盐的金属大环化合物的分层自组装

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摘要

Discrete metallomacrocycles are attractive scaffolds for the formation of complex supramolecular architectures with emergent properties. We herein describe the formation of hierarchical nanostructures using preformed metallomacrocycles by coordination-driven self-assembly of a covalent organic–inorganic polyoxometalate (POM)-based hybrid. In this system, we take advantage of the presence of charged subunits (POM, metal linker, and counterions) within the metallomacrocycles, which drive their aggregation through intermolecular electrostatic interactions. We show that the solvent composition and the charge of the metal linker are key parameters that steer the supramolecular organization. Different types of hierarchical self-assemblies, zero-dimensional (0D) dense nanoparticles, and 1D worm-like nanoobjects, can be selectively formed owing to different aggregation modes of the metallomacrocycles. Finally, we report that the worm-like structures drastically enhance the solubility in water of a pyrene derivative and can act as molecular carriers.
机译:离散的金属大环化合物是形成具有新兴特性的复杂超分子结构的诱人支架。我们在此描述了通过共价基于有机-无机多金属氧酸盐(POM)的杂合体的协调驱动自组装,使用预先形成的金属大环化合物形成的分层纳米结构。在该系统中,我们利用了金属大环内带电亚基(POM,金属连接基和抗衡离子)的存在,这些亚基通过分子间静电相互作用驱动其聚集。我们表明,溶剂组成和金属接头的电荷是控制超分子组织的关键参数。由于金属大环化合物的不同聚集模式,可以选择性地形成不同类型的分层自组装体,零维(0D)密集纳米颗粒和一维蠕虫状纳米物体。最后,我们报道蠕虫状结构极大地提高了derivative衍生物在水中的溶解度,并且可以充当分子载体。

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