4.8 Article

Acceptor less, Reversible Dehydrogenation and Hydrogenation of N-Heterocycles with a Cobalt Pincer Catalyst

Journal

ACS CATALYSIS
Volume 5, Issue 11, Pages 6350-6354

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acscatal.5b02002

Keywords

acceptorless dehydrogenation; hydrogenation; cobalt catalysis; N-heterocycles; pincer ligands; H-2 storage materials

Funding

  1. Center for Electrocatalysis, Transport Phenomena, and Materials (CETM) for Innovative Energy Storage, an EFRC - U.S. DOE [DE-SC0001055]
  2. ESD NYSTAR program
  3. NSF under the CCI Center for Enabling New Technologies through Catalysis (CENTC) [CHE-1205189]
  4. U.S. Department of Energy (DOE) [DE-SC0001055] Funding Source: U.S. Department of Energy (DOE)
  5. Direct For Mathematical & Physical Scien
  6. Division Of Chemistry [1205189] Funding Source: National Science Foundation

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Acceptor less, 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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