Ligand-enabled and magnesium-activated hydrogenation with earth-abundant cobalt catalysts.

RSC Adv

Laboratory of New Energy & New Function Materials, Shaanxi Key Laboratory of Chemical Reaction Engineering, College of Chemistry and Chemical Engineering, Yan'an University Yan'an 716000 P. R. China

Published: December 2021

AI Article Synopsis

  • Replacing costly noble metals like platinum and palladium with cheaper, earth-abundant metals like cobalt is gaining popularity in catalysis research.
  • A new hydrogenation method using a magnesium-activated cobalt catalyst shows high activity for selectively hydrogenating polycyclic aromatic hydrocarbons (PAHs) and olefins.
  • This approach allows for the efficient reduction of challenging PAHs under mild conditions, providing a more affordable and environmentally friendly way to create complex hydrocarbon structures.

Article Abstract

Replacing expensive noble metals like Pt, Pd, Ir, Ru, and Rh with inexpensive earth-abundant metals like cobalt (Co) is attracting wider research interest in catalysis. Cobalt catalysts are now undergoing a renaissance in hydrogenation reactions. Herein, we describe a hydrogenation method for polycyclic aromatic hydrocarbons (PAHs) and olefins with a magnesium-activated earth-abundant Co catalyst. When diketimine was used as a ligand, simple and inexpensive metal salts of CoBr in combination with magnesium showed high catalytic activity in the site-selective hydrogenation of challenging PAHs under mild conditions. Co-catalyzed hydrogenation enabled the reduction of two side aromatics of PAHs. A wide range of PAHs can be hydrogenated in a site-selective manner, which provides a cost-effective, clean, and selective strategy to prepare partially reduced polycyclic hydrocarbon motifs that are otherwise difficult to prepare by common methods. The use of well-defined diketimine-ligated Co complexes as precatalysts for selective hydrogenation of PAHs and olefins is also demonstrated.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9044643PMC
http://dx.doi.org/10.1039/d1ra07266hDOI Listing

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