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Acceptorless, Reversible Dehydrogenation and Hydrogenation of <i>N</i>-Heterocycles with a Cobalt Pincer Catalyst
261
Citations
38
References
2015
Year
Materials ScienceInorganic ChemistryHydrogenation ReactionsEngineeringCatalytic SynthesisHeterogeneous CatalysisReversible DehydrogenationOrganometallic CatalysisCatalysisHomogeneous CatalysisHydrogenChemistryCobalt Pincer CatalystMolecular CatalysisNonbifunctional Hydrogenation MechanismBiomolecular Engineering
Acceptorless, reversible dehydrogenation and hydrogenation reactions involving N-heterocycles are reported with a well-defined cobalt complex supported by an aminobis(phosphine) [PN(H)P] pincer ligand. Several N-heterocycle substrates have been evaluated under dehydrogenation and hydrogenation conditions. The cobalt-catalyzed amine dehydrogenation step, a key step in the dehydrogenation process, has been independently verified. Control studies with related cycloalkanes suggest that a direct acceptorless alkane dehydrogenation pathway is unlikely. The metal–ligand cooperativity is probed with the related [PN(Me)P] derivative of the cobalt catalyst. These results suggest a bifunctional dehydrogenation pathway and a nonbifunctional hydrogenation mechanism.
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