催化作用
铑
钴
铱
化学
钌
钯
组合化学
配体(生物化学)
镍
铂金
转移加氢
过渡金属
苯胺
有机化学
受体
生物化学
作者
Rajenahally V. Jagadeesh,Annette‐Enrica Surkus,Henrik Junge,Marga‐Martina Pohl,Jörg Radnik,Jabor Rabeah,Heming Huan,Volker Schünemann,Angelika Brückner,Matthias Beller
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2013-11-28
卷期号:342 (6162): 1073-1076
被引量:930
标识
DOI:10.1126/science.1242005
摘要
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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