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  A Cooperative Rhodium/Secondary Phosphine Oxide [Rh/P(O)nBu2] Template for Catalytic Hydrodefluorination of Perfluoroarenes

Chang, W.-C., Randel, H., Weyhermüller, T., Auer, A. A., Farès, C., & Werlé, C. (2023). A Cooperative Rhodium/Secondary Phosphine Oxide [Rh/P(O)nBu2] Template for Catalytic Hydrodefluorination of Perfluoroarenes. Angewandte Chemie International Edition, 62(23): e202219127. doi:10.1002/anie.202219127.

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 Creators:
Chang, Wei-Chieh1, 2, Author
Randel, Helena1, 2, Author
Weyhermüller, Thomas1, Author
Auer, Alexander A.3, Author           
Farès, Christophe4, Author           
Werlé, Christophe1, 2, Author
Affiliations:
1Max Planck Institute for Chemical Energy Conversion, Stiftstr. 34–36, 45470 Mülheim an der Ruhr, Germany, ou_persistent22              
2Ruhr University Bochum, Universitätsstr. 150, 44801 Bochum, Germany, ou_persistent22              
3Research Group Auer, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_2541705              
4Service Department Farès (NMR), Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_1445623              

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Free keywords: Cooperative Template; Homogeneous Catalysis; Hydrodefluorination; Rhodium; Secondary Phosphine Oxide
 Abstract: The selective activation of C-F bonds under mild reaction conditions remains an ongoing challenge of bond activation. Here, we present a cooperative [Rh/P(O)nBu2] template for catalytic hydrodefluorination (HDF) of perfluoroarenes. In addition to substrates presenting electron-withdrawing functional groups, the system showed a high tolerance for exceedingly rare electron-donating functionalities and heterocycles. The high chemoselectivity of the catalyst and its readiness to be deployed at a preparative scale illustrate its practicality. Empirical mechanistic studies and a density functional theory (DFT) study have identified a rhodium(I) dihydride complex as a catalytically relevant species and the determining role of phosphine oxide as a cooperative fragment. Altogether, we demonstrate that molecular templates based on these design elements can be assembled to create catalysts with increased reactivity for challenging bond activations.

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Language(s): eng - English
 Dates: 2022-12-262023-03-012023-06-05
 Publication Status: Issued
 Pages: 10
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1002/anie.202219127
 Degree: -

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Title: Angewandte Chemie International Edition
  Abbreviation : Angew. Chem., Int. Ed.
Source Genre: Journal
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Publ. Info: Weinheim : Wiley-VCH
Pages: - Volume / Issue: 62 (23) Sequence Number: e202219127 Start / End Page: - Identifier: ISSN: 1433-7851
CoNE: https://pure.mpg.de/cone/journals/resource/1433-7851