Anorganische Chemie II-Katalysatordesign, Universität Bayreuth, 95440 Bayreuth (Germany).
Angew Chem Int Ed Engl. 2015 Dec 7;54(50):15046-50. doi: 10.1002/anie.201507955. Epub 2015 Oct 16.
The implementation of inexpensive, Earth-abundant metals in typical noble-metal-mediated chemistry is a major goal in homogeneous catalysis. A sustainable or green reaction that has received a lot of attention in recent years and is preferentially catalyzed by Ir or Ru complexes is the alkylation of amines by alcohols. It is based on the borrowing hydrogen or hydrogen autotransfer concept. Herein, we report on the Co-catalyzed alkylation of aromatic amines by alcohols. The reaction proceeds under mild conditions, and selectively generates monoalkylated amines. The observed selectivity allows the synthesis of unsymmetrically substituted diamines. A novel Co complex stabilized by a PN5 P ligand catalyzes the reactions most efficiently.
将廉价、丰富的地球金属应用于典型的贵金属介导的化学中是均相催化的主要目标。近年来,一种可持续或绿色的反应受到了广泛关注,并且优先被 Ir 或 Ru 配合物催化,这种反应是醇对胺的烷基化反应。它基于氢 borrowing 或氢自动转移概念。在此,我们报告了 Co 催化的醇对芳胺的烷基化反应。该反应在温和的条件下进行,并且选择性地生成单烷基化的胺。观察到的选择性允许合成不对称取代的二胺。一种由 PN5 P 配体稳定的新型 Co 配合物最有效地催化反应。