Birkelbach Keanu V A, Vossen Jeroen T, Rösler Thorsten, Kappel Isabella, Meise Ansgar, Heggen Marc, Vorholt Andreas J, Palkovits Regina
Institute for Technical and Macromolecular Chemistry, RWTH Aachen University, Worringerweg 2, 52074, Aachen, Germany.
Institute for a Sustainable Hydrogen Economy, Forschungszentrum Jülich, Marie-Curie-Str. 5, 52428, Jülich, Germany.
Angew Chem Int Ed Engl. 2025 Aug 11;64(33):e202424144. doi: 10.1002/anie.202424144. Epub 2025 Jun 4.
The reductive hydroformylation of olefins is an important process in the chemical industry to produce alcohols directly without isolating the aldehydes as intermediates. As the hydroformylation is a homogeneously catalyzed reaction, the catalyst recycling and down-stream processing is often complex and energy intensive. A heterogeneous reductive hydroformylation catalyst was developed in this work by immobilizing Rh on polymeric amine macroligands to form solid molecular catalysts (SMCs). An iterative macroligand improvement was carried out by increasing the basicity and number of amine groups at the immobilization sites. With the best performing SMC, olefins were fully converted to >99% alcohols without a hydrogenation of the substrate in a solvent free environment, thus requiring only a separation of the heterogeneous catalyst to yield the pure product. The catalyst was successfully recycled over 12 runs with a perpetual Rh leaching as low as 1.2%, and the metal to macroligand ratio was identified as most important parameter in reducing metal loss.
烯烃的还原氢甲酰化反应是化学工业中直接生产醇类的重要过程,无需将醛作为中间体分离出来。由于氢甲酰化反应是均相催化反应,催化剂的回收和下游处理通常很复杂且能耗高。在这项工作中,通过将铑固定在聚合胺大环配体上以形成固体分子催化剂(SMC),开发了一种多相还原氢甲酰化催化剂。通过增加固定位点上胺基的碱性和数量进行了迭代大环配体改进。使用性能最佳的SMC,在无溶剂环境中烯烃完全转化为>99%的醇,且底物不发生氢化反应,因此只需分离多相催化剂即可得到纯产物。该催化剂成功循环使用了12次,铑的持续浸出率低至1.2%,并且确定金属与大环配体的比例是减少金属损失的最重要参数。