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首页> 外文期刊>Central European Journal of Chemistry >The effect of substituents of immobilized Rh complexes on the asymmetric hydrogenation of acetophenone derivatives
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The effect of substituents of immobilized Rh complexes on the asymmetric hydrogenation of acetophenone derivatives

机译:固定化Rh配合物的取代基对苯乙酮衍生物不对称氢化的影响

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摘要

Using a modified Augustine's method variously substituted Rh complexes were anchored on Al2O3 support. The prepared catalysts were characterized by spectroscopic methods and were applied in the hydrogenation of several acetophenone derivatives (p-CF3- acetophenone, acetophenone, p-NH2-acetophenone). Enantioselective C=O hydrogenations were observed with reasonable activity and selectivity on all heterogenized complexes, e.e. up to 80%. At the same time the immobilized samples showed the advantages of the heterogeneous systems: easy handling and recyclability.
机译:使用改良的奥古斯丁方法,将各种取代的Rh络合物固定在Al2O3载体上。制备的催化剂用光谱法表征,并用于几种苯乙酮衍生物(对-CF3-苯乙酮,苯乙酮,对-NH2-苯乙酮)的加氢反应。观察到对所有杂化的配合物,例如对映体,具有合理的活性和选择性的对映选择性C = O氢化。高达80%。同时,固定化样品显示出异质系统的优势:易于处理和可回收利用。

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