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用于铑催化氢化反应的倒置超临界二氧化碳/水双相介质

Inverted supercritical carbon dioxide/aqueous biphasic media for rhodium-catalyzed hydrogenation reactions.

作者信息

Burgemeister Katja, Franciò Giancarlo, Gego Volker H, Greiner Lasse, Hugl Herbert, Leitner Walter

机构信息

Institut für Technische und Makromolekulare Chemie, RWTH Aachen, Worringerweg 1, D-52074 Aachen, Germany.

出版信息

Chemistry. 2007;13(10):2798-804. doi: 10.1002/chem.200601717.

Abstract

An inverted supercritical carbon dioxide (scCO(2))/aqueous biphasic system has been used as reaction media for Rh-catalysed hydrogenation of polar substrates. Chiral and achiral CO(2)-philic catalysts were efficiently immobilised in scCO(2) as the stationary phase, while the polar substrates and products were contained in water as the mobile phase. Notably, product separation and catalyst recycling were conducted without depressurisation of the autoclave. The catalyst phase was reused several times with high conversion and product recovery of more than 85 %. Loss of rhodium and phosphorus by leaching were found to be below the detection limit after the first two cycles in the majority of repetitive experiments. The reaction conditions were optimised with a minimum of experiments by using a simplex algorithm in a sequential optimisation. Total turnover numbers (TTNs) of up to 1600, turnover frequencies (TOFs) of up to 340 h(-1) and ee's up to 99 % were obtained in repetitive batch operations. The scope of the devised catalytic system has been investigated and a semicontinuous reaction setup has been implemented. The chiral ligand (R,S)-3-H(2)F(6)-BINAPHOS allowed highly enantioselective hydrogenation of itaconic acid and methyl-2-acetamidoacrylate combined with a considerable catalyst stability in these reaction media.

摘要

倒置超临界二氧化碳(scCO₂)/水双相体系已被用作铑催化极性底物氢化反应的介质。手性和非手性亲二氧化碳催化剂作为固定相有效地固定在scCO₂中,而极性底物和产物则作为流动相包含在水中。值得注意的是,产物分离和催化剂循环利用无需对高压釜进行减压操作。催化剂相可重复使用多次,转化率高,产物回收率超过85%。在大多数重复实验中,在前两个循环后,铑和磷的浸出损失低于检测限。通过在顺序优化中使用单纯形算法,以最少的实验次数优化了反应条件。在重复间歇操作中,总周转数(TTNs)高达1600,周转频率(TOFs)高达340 h⁻¹,对映体过量值(ee's)高达99%。已研究了所设计催化体系的适用范围,并实施了半连续反应装置。手性配体(R,S)-3-H₂F₆-BINAPHOS能够实现衣康酸和甲基-2-乙酰氨基丙烯酸酯的高度对映选择性氢化,并且在这些反应介质中具有相当高的催化剂稳定性。

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