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A Convenient and Stable Heterogeneous Nickel Catalyst for Hydrodehalogenation of Aryl Halides Using Molecular Hydrogen

Hydrodehalogenation is an effective strategy for transforming persistent and potentially toxic organohalides into their more benign congeners. Common methods utilize Pd/C or Raney‐nickel as catalysts, which are either expensive or have safety concerns. In this study, a nickel‐based catalyst supporte...

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Detalles Bibliográficos
Autores principales: Leonard, David K., Ryabchuk, Pavel, Anwar, Muhammad, Dastgir, Sarim, Junge, Kathrin, Beller, Matthias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9306955/
https://www.ncbi.nlm.nih.gov/pubmed/34978382
http://dx.doi.org/10.1002/cssc.202102315
Descripción
Sumario:Hydrodehalogenation is an effective strategy for transforming persistent and potentially toxic organohalides into their more benign congeners. Common methods utilize Pd/C or Raney‐nickel as catalysts, which are either expensive or have safety concerns. In this study, a nickel‐based catalyst supported on titania (Ni‐phen@TiO(2)‐800) is used as a safe alternative to pyrophoric Raney‐nickel. The catalyst is prepared in a straightforward fashion by deposition of nickel(II)/1,10‐phenanthroline on titania, followed by pyrolysis. The catalytic material, which was characterized by SEM, TEM, XRD, and XPS, consists of nickel nanoparticles covered with N‐doped carbon layers. By using design of experiments (DoE), this nanostructured catalyst is found to be proficient for the facile and selective hydrodehalogenation of a diverse range of substrates bearing C−I, C−Br, or C−Cl bonds (>30 examples). The practicality of this catalyst system is demonstrated by the dehalogenation of environmentally hazardous and polyhalogenated substrates atrazine, tetrabromobisphenol A, tetrachlorobenzene, and a polybrominated diphenyl ether (PBDE).