Structural and Electronic Properties of Polyoxovanadoborates Containing the [V12B18O60] Core in Different Mixed Valence States

P. Hermosilla‐Ibáñez, K. Muñoz-Becerra, V. Paredes-García, E. L. Fur, E. Spodine, D. Venegas‐Yazigi
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引用次数: 6

Abstract

This review summarizes all published data until April 2015 related to crystalline lattices formed by the [V12B18O60] core, which generates polyanionic clusters with different degrees of protonation and mixed-valence ratios. The negative charge of this cluster is counterbalanced by different cations such as protonated amines, hydronium, and alkaline, and transition metal ions. The cluster is shown to form extended 1D, 2D, or 3D frameworks by forming covalent bonds or presenting hydrogen bond interactions with the present secondary cations. These cations have little influence on the solid state reflectance UV-visible spectra of the polyanionic cluster, but are shown to modify the FT-IR spectra and the magnetic behavior of the different reported species.
含[V12B18O60]核不同混合价态多钒酸盐的结构和电子性质
本文综述了截至2015年4月的所有已发表的与[V12B18O60]核形成的晶格相关的数据,这些晶格产生了不同程度的质子化和混合价比的聚阴离子团簇。该簇的负电荷由不同的阳离子如质子化胺、水合氢离子、碱性离子和过渡金属离子来平衡。通过形成共价键或与当前的仲阳离子呈现氢键相互作用,该簇可以形成扩展的1D、2D或3D框架。这些阳离子对聚阴离子簇的固态反射率紫外可见光谱影响不大,但对FT-IR光谱和不同种类的磁性行为有影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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