Nanoscale Fe <sub>2</sub> O <sub>3</sub> -Based Catalysts for Selective Hydrogenation of Nitroarenes to Anilines

Rajenahally V. Jagadeesh(Leibniz Institute for Catalysis), Annette‐Enrica Surkus(Leibniz Institute for Catalysis), Henrik Junge(Leibniz Institute for Catalysis), Marga‐Martina Pohl(Leibniz Institute for Catalysis), Jörg Radnik(Leibniz Institute for Catalysis), Jabor Rabeah(Leibniz Institute for Catalysis), Heming Huan(University of Kaiserslautern), Volker Schünemann(University of Kaiserslautern), Angelika Brückner(Leibniz Institute for Catalysis), Matthias Beller(Leibniz Institute for Catalysis)
Science
November 28, 2013
Cited by 1,008

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.


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