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Nanostructures in Uranium Oxocompounds

机译:铀氧化合物中的纳米结构

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摘要

Examples of uranium-oxide-based nanostructures are considered, including 2D organic-inorganic nanocomposites and nanotubules. In nanocomposites, interfacial interactions between organic and inorganic substructures can be studied by charge-density matching principle. Application of this principle to uranyl compounds requires special attention since surface area of uranyl-based 2D units is higher than that of other inorganic oxysalts units (i.e. metal phosphates). The charge-density matching principle is, however, observed either through tail interdigitation (for long-chain monoamines) or incorporation of acid-water interlayers into organic substructure (for long-chain diamines). In some compounds, protonated amine molecules form cylindrical micelles that involves self-assembly governed by competing hydrophobic/hydrophillic interactions. The flexible inorganic complexes present in the reaction mixture could then form around cylindrical micelles to produce highly undulated 2D sheets or nanotubules.
机译:考虑了基于铀氧化物的纳米结构的示例,包括2D有机-无机纳米复合材料和纳米管。在纳米复合材料中,可以通过电荷密度匹配原理研究有机和无机亚结构之间的界面相互作用。由于基于铀酰的2D单元的表面积要比其他无机含氧盐单元(即金属磷酸盐)的表​​面积大,因此需要特别注意将此原则应用于铀酰化合物。然而,电荷密度匹配原理是通过尾叉指叉(对于长链单胺)或将酸水中间层掺入有机亚结构(对于长链二胺)来观察的。在某些化合物中,质子化的胺分子形成圆柱形胶束,该胶束涉及通过竞争性疏水/亲水相互作用控制的自组装。然后,可以在圆柱形胶束周围形成反应混合物中存在的柔性无机络合物,以产生高度起伏的2D薄片或纳米管。

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