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

  • Nanostructured 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.

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Metadaten
Document Type:Article
Author:Christof BauerORCiD, Felix Müller, Sercan Keskin, Mirjam ZobelORCiD, Rhett KempeORCiD
URN:urn:nbn:de:bsz:291:415-7135
DOI:https://doi.org/10.1002/chem.202300561
Parent Title (English):Chemistry – A European Journal
Volume:29
Issue:30
First Page:e202300561
Language:English
Year of first Publication:2023
Release Date:2023/06/22
Tag:catalyst synthesis; cobalt; heterocycles; heterogeneous catalysis; hydrogenation
Impact:03.90 (2023)
Funding Information:Deutsche Forschungsgemeinschaft. Grant Numbers: KE 756/34-1, Exellenzcluster 2186
Scientific Units:Innovative Electron Microscopy
DDC classes:500 Naturwissenschaften und Mathematik / 540 Chemie
Open Access:Open Access
Signature:INM 2023/021
Licence (German):License LogoCreative Commons - CC BY - Namensnennung 4.0 International