A Highly Active Cobalt Catalyst for the General and Selective Hydrogenation of Aromatic Heterocycles

Author:

Bauer Christof1,Müller Felix2,Keskin Sercan3,Zobel Mirijam2,Kempe Rhett1ORCID

Affiliation:

1. Inorganic Chemistry II – Catalyst Design Sustainable Chemistry Centre University of Bayreuth 95440 Bayreuth Germany

2. Institute of Crystallography RWTH Aachen University 52066 Aachen Germany

3. INM - Leibniz Institute for New Materials Campus D2 2 66123 Saarbrücken Germany

Abstract

AbstractNanostructured earth abundant metal catalysts that mediate important chemical reactions with high efficiency and selectivity are of great interest. This study introduces a synthesis protocol for nanostructured earth abundant metal catalysts. Three components, an inexpensive metal precursor, an easy to synthesize N/C precursor, and a porous support material undergo pyrolysis to give the catalyst material in a simple, single synthesis step. By applying this catalyst synthesis, a highly active cobalt catalyst for the general and selective hydrogenation of aromatic heterocycles could be generated. The reaction is important with regard to organic synthesis and hydrogen storage. The mild reaction conditions observed for quinolines permit the selective hydrogenation of numerous classes of N‐, O‐ and S‐heterocyclic compounds such as: quinoxalines, pyridines, pyrroles, indoles, isoquinoline, aciridine amine, phenanthroline, benzofuranes, and benzothiophenes.

Funder

Deutsche Forschungsgemeinschaft

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

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