Nanoscale Fe 2 O 3 -Based Catalysts for Selective Hydrogenation of Nitroarenes to Anilines

Author:

Jagadeesh Rajenahally V.1,Surkus Annette-Enrica1,Junge Henrik1,Pohl Marga-Martina1,Radnik Jörg1,Rabeah Jabor1,Huan Heming2,Schünemann Volker2,Brückner Angelika1,Beller Matthias1

Affiliation:

1. Leibniz-Institut für Katalyse e.V. an der Universität Rostock, Albert-Einstein Strasse 29a, D-18059 Rostock, Germany

2. Technische Universität Kaiserslautern, Fachbereich Physik, Erwin-Schrödinger-Strasse 46, D-67663 Kaiserslautern, Germany.

Abstract

Lighter Hydrogenation Catalysts Enzymes have evolved to use abundant metals such as iron, cobalt, and nickel for redox catalysis. However, synthetic catalysis has generally relied on the rarer, heavier relatives of these elements: ruthenium, rhodium, iridium, palladium, and platinum (see the Perspective by Bullock ). Friedfeld et al. (p. 1076 ) used high-throughput screening to show that the right cobalt precursor can be activated for asymmetric hydrogenation catalysis by using the traditional ligands developed for the precious metals. Zuo et al. (p. 1080 ) focused on iron, demonstrating a highly effective asymmetric transfer hydrogenation catalyst that uses a ligand rationally designed after careful mechanistic study. Jagadeesh et al. (p. 1073 ) prepared supported iron catalysts that selectively reduce nitro substituents on aromatic rings to amines, thereby facilitating the preparation of a wide range of aniline derivatives.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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