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氮杂大环和叔胺可用于形成尺寸可调的中空结构或单分散的氧化物纳米颗粒,这取决于“M”源。

Azamacrocycles and tertiary amines can be used to form size tuneable hollow structures or monodisperse oxide nanoparticles depending on the 'M' source.

机构信息

Biomolecular and Materials Interface Research Group, Interdisciplinary Biomedical Research Centre, Nottingham Trent University, Clifton Lane, Nottingham NG11 8NS, UK.

出版信息

Dalton Trans. 2019 Oct 22;48(41):15470-15479. doi: 10.1039/c9dt02080b.

Abstract

We show that the azamacrocycle 'cyclam' (1,4,8,11-tetraazacyclodecane) in conjunction with a silicon catecholate ion generates novel hollow tetragonal tube-like crystalline materials [(C6H4O2)3Si][C10H26N4]·H2O, whose dimensions can be tuned according to the pH of the reaction medium. The synthesis approach was successful for both silicon and germanium and we hypothesise that a range of other catecholate precursors of elements such as iron could be used to generate a large array of inorganic materials with interesting morphologies. The synthesis approach can be extended to tertiary diamines with functional group spacing playing an important role in the efficacy of complexation. Of the molecules explored to date, a C2 spacing (N,N,N',N'-tetramethylethylenediamine (4MEDAE)), leads to the most efficient structure control with hollow hexagonal tube-like structures being formed. In addition, we show that azamacrocycles, in the presence of unbuffered tetramethoxysilane (TMOS) solutions can be used to manipulate silica formation and provide a fast (ca. 10 minutes) synthesis route to particles whose diameter can be tuned from ca. 20 nm to several hundreds of nm under reaction conditions (no extremes of pH) that make the sols suitable for direct use in biotechnological applications.

摘要

我们表明,偕氮大环“环三亚甲基胺”(1,4,8,11-四氮杂环十二烷)与硅邻苯二酚离子结合,生成新型的中空四方管状结晶材料[(C6H4O2)3Si][C10H26N4]·H2O,其尺寸可根据反应介质的 pH 值进行调节。该合成方法对硅和锗均有效,我们假设可以使用一系列其他邻苯二酚前体元素,如铁,来生成具有有趣形态的大量无机材料。该合成方法可以扩展到具有官能团间隔的叔二胺,其在络合效率中起着重要作用。在迄今为止探索的分子中,C2 间隔(N,N,N',N'-四甲基乙二胺(4MEDAE))导致最有效的结构控制,形成中空六方管状结构。此外,我们表明,偕氮大环在未缓冲的四甲氧基硅烷(TMOS)溶液的存在下,可以用于操纵二氧化硅的形成,并提供一种快速(约 10 分钟)的合成途径,得到的颗粒直径可以在反应条件下(无极端 pH 值)从约 20nm 调至数百纳米,使溶胶适用于直接在生物技术应用中使用。

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