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首页> 外文期刊>CrystEngComm >Active site engineering in UiO-66 type metal-organic frameworks by intentional creation of defects: a theoretical rationalization
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Active site engineering in UiO-66 type metal-organic frameworks by intentional creation of defects: a theoretical rationalization

机译:通过故意创建缺陷在UiO-66型金属有机框架中进行主动站点工程:理论上的合理化

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The catalytic activity of the Zr-benzenedicarboxylate (Zr-BDC) UiO-66 can be drastically increased if some BDC linkers are missing, as this removes the full coordination of the framework metal ions. As a result, metal centers become more accessible and thus more active for Lewis acid catalysed reactions. Addition of modulators (MDL) to the synthesis mixture can create more linker deficiencies (Vermoortele et al., J. Am. Chem. Soc., 2013, 135, 11465) and leads to a significant increase in the catalytic activity due to the creation of a larger number of open sites. In this paper, we rationalize the function of the modulators under real synthesis conditions by the construction of free energy diagrams. The UiO-66 type materials form a very appropriate test case as the effect of addition of modulators hydrochloric acid (HCl) and trifluoroacetate (TFA) has been intensively investigated experimentally for the synthesis process and post-synthetic thermal activation. Under synthesis conditions, direct removal of BDC linkers requires a high free energy, but replacement of such linker by one or more TFA species might occur especially at high TFA : BDC ratios in the reaction mixture. Post-synthesis activation procedures at higher temperatures lead to substantial removal of the species coordinated to the Zr bricks, creating open metal sites. A mechanistic pathway is presented for the dehydroxylation process of the hexanuclear Zr cluster. For the citronellal cyclization, we show that the presence of some residual TFA in the structure may lead to faster reactions in complete agreement with the experiment. Hirshfeld-e partial charges for the Zr ions have been computed to investigate their sensitivity to substituent effects; a strong correlation with the experimental Hammett parameters and with the rates of the citronellal cyclization is found. The theoretical rationalization may serve as a basis for detailed active site engineering studies.
机译:如果缺少某些BDC连接基,则Zr-苯二甲酸(Zr-BDC)UiO-66的催化活性会大大提高,因为这消除了骨架金属离子的完全配位。结果,金属中心变得更易接近,因此对于路易斯酸催化的反应更具活性。在合成混合物中添加调节剂(MDL)可能会导致更多接头缺陷(Vermoortele等人,J。Am。Chem。Soc。,2013,135,11465),并由于该反应而导致催化活性显着提高大量的开放网站。在本文中,我们通过构建自由能图来合理化调制器在实际合成条件下的功能。 UiO-66型材料形成了非常合适的测试用例,因为已针对合成过程和合成后的热活化进行了实验性的深入研究,研究了添加调制剂盐酸(HCl)和三氟乙酸盐(TFA)的效果。在合成条件下,直接除去BDC接头需要很高的自由能,但是用一种或多种TFA取代此类接头可能会发生,特别是在反应混合物中的TFA:BDC比率高的情况下。较高温度下的合成后活化程序导致大量去除与Zr砖配位的物质,从​​而形成开放的金属位点。提出了六核Zr团簇的脱羟基过程的机械途径。对于香茅醛环化,我们表明结构中一些残留的TFA的存在可能导致更快的反应,这与实验完全一致。计算了Zr离子的Hirshfeld-e部分电荷,以研究其对取代基效应的敏感性。发现与实验哈米特参数和香茅醛环化速率密切相关。理论上的合理化可以作为详细的主动站点工程研究的基础。

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