Leibniz-Institut für Katalyse e.V. an der Universität Rostock, Albert-Einstein Straße 29a, Rostock 18059, Germany.
Nat Chem. 2013 Jun;5(6):537-43. doi: 10.1038/nchem.1645. Epub 2013 May 12.
Molecularly well-defined homogeneous catalysts are known for a wide variety of chemical transformations. The effect of small changes in molecular structure can be studied in detail and used to optimize many processes. However, many industrial processes require heterogeneous catalysts because of their stability, ease of separation and recyclability, but these are more difficult to control on a molecular level. Here, we describe the conversion of homogeneous cobalt complexes into heterogeneous cobalt oxide catalysts via immobilization and pyrolysis on activated carbon. The catalysts thus produced are useful for the industrially important reduction of nitroarenes to anilines. The ligand indirectly controls the selectivity and activity of the recyclable catalyst and catalyst optimization can be performed at the level of the solution-phase precursor before conversion into the active heterogeneous catalyst.
分子结构明确的均相催化剂在各种化学转化中得到了广泛的应用。可以详细研究分子结构的微小变化,并将其用于优化许多过程。然而,由于稳定性、易于分离和可回收性,许多工业过程需要使用多相催化剂,但这些催化剂在分子水平上更难控制。在这里,我们通过在活性炭上的固载和热解,将均相钴配合物转化为多相钴氧化物催化剂。所制备的催化剂可用于工业上重要的硝基芳烃还原为苯胺。配体间接控制了可回收催化剂的选择性和活性,并且可以在转化为活性多相催化剂之前,在溶液相前体的水平上进行催化剂优化。