Co-Catalyzed P–H Activation and Related Cp*Co(III) Phosphine Complexes

This study reports that the well-known Co(III) precursor Co(η<sup>5</sup>-Cp*)I<sub>2</sub>(CO) (<b>1</b>) is an effective precatalyst for dehydrocoupling reactions of phosphines. Reaction monitoring by NMR, complemented by ESI-MS and EPR, suggests that Co(III) complexes containing secondary and primary phosphine ligands play an important role in this catalysis but that redox chemistry is also facile for these complexes, resulting in paramagnetic species. Representative examples of the mono(phosphine) complexes Co(η<sup>5</sup>-Cp*)I<sub>2</sub>(PR<sub>2</sub>H) (<b>2</b>) and Co(η<sup>5</sup>-Cp*)I<sub>2</sub>(PRH<sub>2</sub>) (<b>4</b>) and bis(phosphine) complexes [Co(η<sup>5</sup>-Cp*)I(PR<sub>2</sub>H)<sub>2</sub>] I (<b>3</b>) have been prepared. The characterization of these complexes through structural, computational, spectroscopic, and electrochemical analysis is reported and serves as a foundation for considering their mechanistic significance in the observed catalytic dehydrocoupling chemistry.

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Publication Details

Journal
Inorganic Chemistry
Published
2024-11-11
DOI
https://doi.org/10.1021/acs.inorgchem.4c03207
Citations
4
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
0.63

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article

Co-Catalyzed P–H Activation and Related Cp*Co(III) Phosphine Complexes

Dimitrios A. Pantazis, Jin Yang, Lisa Rosenberg, Cameron H. M. Zheng et al.
4 citations
Inorganic Chemistry
Asymmetric Hydrogenation and Catalysis
0.63
article

Co-Catalyzed P–H Activation and Related Cp*Co(III) Phosphine Complexes

Dimitrios A. Pantazis, Jin Yang, Lisa Rosenberg, Cameron H. M. Zheng, Robert McDonald, Michael J. Ferguson, Mursaleem Ansari
article en
4 citations

Abstract

This study reports that the well-known Co(III) precursor Co(η<sup>5</sup>-Cp*)I<sub>2</sub>(CO) (<b>1</b>) is an effective precatalyst for dehydrocoupling reactions of phosphines. Reaction monitoring by NMR, complemented by ESI-MS and EPR, suggests that Co(III) complexes containing secondary and primary phosphine ligands play an important role in this catalysis but that redox chemistry is also facile for these complexes, resulting in paramagnetic species. Representative examples of the mono(phosphine) complexes Co(η<sup>5</sup>-Cp*)I<sub>2</sub>(PR<sub>2</sub>H) (<b>2</b>) and Co(η<sup>5</sup>-Cp*)I<sub>2</sub>(PRH<sub>2</sub>) (<b>4</b>) and bis(phosphine) complexes [Co(η<sup>5</sup>-Cp*)I(PR<sub>2</sub>H)<sub>2</sub>] I (<b>3</b>) have been prepared. The characterization of these complexes through structural, computational, spectroscopic, and electrochemical analysis is reported and serves as a foundation for considering their mechanistic significance in the observed catalytic dehydrocoupling chemistry.

Inorganic ChemistryVol. 63(47)
University of Alberta (CA), University of Victoria (CA), Max-Planck-Institut für Kohlenforschung (DE)
Max-Planck-Gesellschaft, Natural Sciences and Engineering Research Council of Canada
Openalex Percentile: Top 36%
Asymmetric Hydrogenation and Catalysis
0.63
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Co-Catalyzed P–H Activation and Related Cp*Co(III) Phosphine Complexes — Dimitrios A. Pantazis, Jin Yang, et al. · Inorganic Chemistry (2024) | TGRS Research Map | TGRS