Published October 16, 2013 | Version Supplemental Material
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Boryl-Mediated Reversible H_2 Activation at Cobalt: Catalytic Hydrogenation, Dehydrogenation, and Transfer Hydrogenation

  • 1. ROR icon California Institute of Technology

Abstract

We describe the synthesis of a cobalt(I)–N2 complex (2) supported by a meridional bis-phosphino-boryl (PBP) ligand. Complex 2 undergoes a clean reaction with 2 equiv of dihydrogen to afford a dihydridoboratocobalt dihydride (3). The ability of boron to switch between a boryl and a dihydridoborate conformation makes possible the reversible conversion of 2 and 3. Complex 3 reacts with HMe_2N–BH_3 to give a hydridoborane cobalt tetrahydridoborate complex. We explore this boryl–cobalt system in the context of catalytic olefin hydrogenation as well as amine–borane dehydrogenation/transfer hydrogenation.

Additional Information

© 2013 American Chemical Society. Publication Date (Web): September 30, 2013. Received: August 13, 2013. This material is based upon work performed by the Joint Center for Artificial Photosynthesis, a DOE Energy Innovation Hub, supported through the Office of Science of the U.S. Department of Energy under Award No. DE-SC0004993. The authors declare no competing financial interest.

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Additional details

Identifiers

Eprint ID
42256
DOI
10.1021/ja408397v
Resolver ID
CaltechAUTHORS:20131105-144406165

Funding

Department of Energy (DOE)
DE-SC0004993

Dates

Created
2013-11-06
Created from EPrint's datestamp field
Updated
2021-11-10
Created from EPrint's last_modified field

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