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Homogeneous CO Hydrogenation: Ligand Effects on the Lewis Acid-Assisted Reductive Coupling of Carbon Monoxide

Miller, Alexander J. M. and Labinger, Jay A. and Bercaw, John E. (2010) Homogeneous CO Hydrogenation: Ligand Effects on the Lewis Acid-Assisted Reductive Coupling of Carbon Monoxide. Organometallics, 29 (20). pp. 4499-4516. ISSN 0276-7333. https://resolver.caltech.edu/CaltechAUTHORS:20101103-110627454

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Abstract

Structure-function studies on the role of pendent Lewis acids in the reductive coupling of CO are reported. Cationic rhenium carbonyl complexes containing zero, one, or two phosphinoborane ligands (Ph_2P(CH_2)_nB(C_8H_(14)), n=1-3) react with the nucleophilic hydride [HPt(dmpe)_2]^+ to reduce [M-CO]^+ to M-CHO; this step is relatively insensitive to the Lewis acid, as both pendent (internal) and external boranes of appropriate acid strength can be used. In contrast, whether a second hydride transfer and C-C bond forming steps occur depends strongly on the number of carbon atoms between P and B in the phosphinoborane ligands, as well as the number of pendent acids in the complex: shorter linker chain lengths favor such reductive coupling, whereas longer chains and external boranes are ineffective. A number of different species containing partially reduced CO groups, whose exact structures vary considerably with the nature and number of phosphinoborane ligands, have been crystallographically characterized. The reaction of [(Ph -2P(CH_2)_2B(C_8H_(14)))_2Re(CO)4]^+ with [HPt(dmpe)_2]^+ takes place via a “hydride shuttle” mechanism, in which hydride is transferred from Pt to a pendent borane and thence to CO, rather than by direct hydride attack at CO. Addition of a second hydride in C_6D_5Cl at -40 ºC affords an unusual anionic bis(carbene) complex, which converts to a C-C bonded product on warming. These results support a working model for Lewis acid-assisted reductive coupling of CO, in which B (pendent or external) shuttles hydride from Pt to coordinated CO, followed by formation of an intramolecular B-O bond, which facilitates reductive coupling.


Item Type:Article
Related URLs:
URLURL TypeDescription
http://dx.doi.org/10.1021/om100638dDOIArticle
http://pubs.acs.org/doi/full/10.1021/om100638dPublisherArticle
ORCID:
AuthorORCID
Labinger, Jay A.0000-0002-1942-9232
Additional Information:© 2010 American Chemical Society. Received July 1, 2010. Published In Issue October 25, 2010. Article ASAP September 29, 2010. Larry Henling and Mike Day assisted with crystallography. The Bruker KAPPA APEXII X-ray diffractometer was purchased via an NSF CRIF:MU award to the California Institute of Technology (CHE-0639094). David VanderVelde assisted with 2D and PGSE NMR spectroscopy. Dr. Daniel L. DuBois and Dr. Nathan M. West contributed enlightening discussions. This work was funded by BP (MC2 Program) and the Moore Foundation.
Funders:
Funding AgencyGrant Number
BP MC2 programUNSPECIFIED
Gordon and Betty Moore FoundationUNSPECIFIED
Issue or Number:20
Record Number:CaltechAUTHORS:20101103-110627454
Persistent URL:https://resolver.caltech.edu/CaltechAUTHORS:20101103-110627454
Official Citation:Homogeneous CO Hydrogenation: Ligand Effects on the Lewis Acid-Assisted Reductive Coupling of Carbon Monoxide Alexander J. M. Miller, Jay A. Labinger, John E. Bercaw Organometallics 2010 29 (20), 4499-4516
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:20649
Collection:CaltechAUTHORS
Deposited By: Ruth Sustaita
Deposited On:03 Nov 2010 20:07
Last Modified:03 Oct 2019 02:13

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