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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Crystallinity after decarboxylation of a metal-carboxylate framework: indestructible porosity for catalysis
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Crystallinity after decarboxylation of a metal-carboxylate framework: indestructible porosity for catalysis

机译:金属 - 羧酸酯框架脱羧后的结晶度:催化孔隙率

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We report a curious case study of a Zr(IV)-carboxylate framework, which retains significant crystalline order after cascade thermocyclization of its linker components, and - more notably - after the crucial carboxylate links were severed by heat. Vigorous heat treatment (e.g., 450 degrees C and above) benzannulates the multiple alkyne groups on the linker to generate linked nanographene blocks and to afford real stability. The resultant Zr oxide/nanographene hybrid solid is stable in saturated NaOH and concentrated H3PO4, allowing a convenient anchoring of H3PO4 into its porous matrix to enable size-selective heterogeneous acid catalysis. The Zr oxide components can also be removed by strong hydrofluoric acid to further enhance the surface area (up to 650 m(2) g(-1)), without collapsing the nanographene scaffold. The crystallinity order and the extensive thermal transformations were characterized by X-ray diffraction, scanning transmission electron microscopy (STEM), IR, solid state NMR and other instrumental methods.
机译:我们报告了对Zr(iv) - 羧酸羧酸酯框架的一系列奇怪的案例研究,其在其接头组分的级联热循环后保持显着的结晶顺序,更值得注意的是 - 在通过热量切断关键的羧酸盐链路之后。剧烈的热处理(例如,450℃和以上)将链接器上的多个炔基团苯并生成连接的纳米表块,并提供真正的稳定性。所得Zr氧化物/纳米杂交固体在饱和NaOH中稳定并浓缩H3PO4,允许方便的H3PO4锚固到其多孔基质中以使尺寸选择性的异构酸催化。 Zr氧化物组分也可以通过强氢氟酸除去,以进一步增强表面积(高达650μm(2 )g(-1)),而不会坍塌纳米卡烯支架。通过X射线衍射,扫描透射电子显微镜(茎),IR,固态NMR等仪器方法,表征结晶度顺序和广泛的热转化。

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