基于紫精配体的新型铀酰配位聚合物的合成、结构和光致变色性能

    Synthesis, Structures, and Photochromic Behaviors of Novel Viologen Based Uranyl Coordination Polymers

    • 摘要: 配体的选择直接影响铀酰配合物的自组装模型,对配合物的结构和功能具有决定性作用。在这项工作中,使用水热法实现了多种配体与铀酰离子的组装,合成了三种基于紫精功能基团的铀酰配位聚合物。三种配位聚合物的主体骨架均是一维链状结构。其中,配合物1和2均表现出明显的荧光性质。此外,配合物2具有显著可逆的光致/热致变色性质。紫外可见光谱和电子顺磁共振(EPR)光谱表明这种可逆的颜色变化是由于紫精配体在光照后产生了紫精自由基所致。这项研究实现了多例基于紫精配体的铀酰配位聚合物的组装合成,为更多贫铀功能性材料的开发提供了思路。

       

      Abstract: The chosen of ligands directly affects the self-assembly behaviors of uranyl compounds, and plays a critical role in the structure and function of the compounds. In this work, several ligands were selected to assembled with uranyl ions by hydrothermal method, and three uranyl coordination polymers(CPs) based on viologen functional groups were synthesized. The main skeleton of the CPs is one-dimensional(1D) chain structure. Among them, compounds 1 and 2 exhibit obvious fluorescence properties. In addition, compound 2 exhibit significantly reversible photochromic/thermochromic properties. Ultraviolet-visible spectrum and electron paramagnetic resonance(EPR) spectrum indicate that the reversible color change is due to the generation of viologen radicals from viologen ligands after irradiation. This research has realized the assembly and synthesis of several uranyl CPs based on viologen ligands, and lead to design and development of more functional materials containing depleted uranium.

       

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