Highly active cationic cobalt(II) hydroformylation catalysts

Author:

Hood Drew M.1ORCID,Johnson Ryan A.1ORCID,Carpenter Alex E.2ORCID,Younker Jarod M.2ORCID,Vinyard David J.3ORCID,Stanley George G.1ORCID

Affiliation:

1. Department of Chemistry, Louisiana State University, Baton Rouge, LA 70803, USA.

2. ExxonMobil Chemical Company, Baytown, TX 77520, USA.

3. Department of Biological Sciences, Louisiana State University, Baton Rouge, LA 70803, USA.

Abstract

Charging up cobalt for hydroformylation Hydroformylation reactions are applied at massive scale in the chemical industry to transform olefins into aldehydes. The original catalysts were neutral cobalt complexes. Hood et al. now report that positively charged cobalt complexes, stabilized by chelating phosphine ligands, show higher activities at lower pressures than their neutral counterparts, approaching the activities of precious rhodium catalysts. These charged catalysts are particularly adept at accelerating the reactions of internal olefins while avoiding decomposition. Spectroscopic studies implicate the involvement of 19-electron intermediates in the catalytic cycle. Science , this issue p. 542

Funder

National Science Foundation

Dow Chemical Company

Exxon Mobil Corporation

Louisiana Board of Regents

LSU LIFT2

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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