Autocatalytic Activation of a Ruthenium-PNN-Pincer Hydrogenation Catalyst

In this article, we describe a detailed experimental and computational study of the activation mechanism for a highly active pincer ruthenium(0) precatalyst for the hydrogenation of polar organic compounds. The precatalyst activates by reaction with 2 equiv of hydrogen, resulting in a net oxidative addition to ruthenium and hydrogenation of an imine functional group on the supporting ligand. The kinetics of precatalyst hydrogenation were measured by UV-visible spectroscopy under catalytically relevant conditions (10-39 bar hydrogen, 298 K). The kinetic data, in combination with density functional theory calculations, support an intriguing autocatalytic mechanism, where the product ruthenium(II) complex catalyzes the hydrogenation of the ruthenium(0) precatalyst.

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Publication Details

Journal
ACS Catalysis
Published
2024-10-23
DOI
https://doi.org/10.1021/acscatal.4c04475
Citations
7
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
1.11

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article

Autocatalytic Activation of a Ruthenium-PNN-Pincer Hydrogenation Catalyst

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7 citations
ACS Catalysis
Asymmetric Hydrogenation and Catalysis
1.11
article

Autocatalytic Activation of a Ruthenium-PNN-Pincer Hydrogenation Catalyst

Cole Jarczyk, Eamon F. Reynolds, Benjamin T. Joseph, Fallyn Kirlin, Jason M. Keith, A. Chianese, Jose Fernando Carbajal Perez
article en
7 citations

Abstract

In this article, we describe a detailed experimental and computational study of the activation mechanism for a highly active pincer ruthenium(0) precatalyst for the hydrogenation of polar organic compounds. The precatalyst activates by reaction with 2 equiv of hydrogen, resulting in a net oxidative addition to ruthenium and hydrogenation of an imine functional group on the supporting ligand. The kinetics of precatalyst hydrogenation were measured by UV-visible spectroscopy under catalytically relevant conditions (10-39 bar hydrogen, 298 K). The kinetic data, in combination with density functional theory calculations, support an intriguing autocatalytic mechanism, where the product ruthenium(II) complex catalyzes the hydrogenation of the ruthenium(0) precatalyst.

ACS CatalysisVol. 14(21)
Colgate University (US)
National Science Foundation, Colgate University, Division of Chemistry
Openalex Percentile: Top 25%
Asymmetric Hydrogenation and Catalysis
1.11
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