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  Ruthenium Phenoxo Complexes: An Isolobal Ligand to Cp with Improved Properties

Schulte, T., Wang, Z., Li, C.-C., Hamad, A., Waldbach, F., Pampel, J., et al. (2024). Ruthenium Phenoxo Complexes: An Isolobal Ligand to Cp with Improved Properties. Journal of the American Chemical Society, 146(23), 15825-15832. doi:10.1021/jacs.4c02088.

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 Creators:
Schulte, Tim1, 2, Author           
Wang, Zikuan3, Author           
Li, Chen-Chen1, Author           
Hamad, Aboubakr1, 2, Author           
Waldbach, Felix1, Author           
Pampel, Julius1, Author           
Petzold, Roland1, Author           
Leutzsch, Markus4, Author           
Bahns, Fritz1, 2, Author
Ritter, Tobias1, Author           
Affiliations:
1Research Department Ritter, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_2040308              
2Institute of Organic Chemistry, RWTH Aachen University, Landoltweg 1, 52074 Aachen, Germany, ou_persistent22              
3Research Group Manganas, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_2541709              
4Service Department Farès (NMR), Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_1445623              

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 Abstract: Catalytic π-arene activation is based on catalysts that allow for arene exchange. To date, cyclopentadiene (Cp)-derived catalysts are the most commonly used in π-arene activation despite their low arene exchange rates. Herein, we report the synthesis, analysis, and catalytic application of Ru(II) complexes supported by phenoxo ligands, which are isolobal alternatives to Cp. The phenoxo complexes exhibit arene exchange rates significantly faster than those of the corresponding Cp complexes. The rate can be further increased through the choice of appropriate counterions. The mechanism of the arene exchange process is elucidated by kinetic and computational analyses. We demonstrate the utility of the new catalysts through an SNAr reaction between fluorobenzene and alcohols, including secondary alcohols that could not be used previously in related reactions. Moreover, the catalytic thermal decarboxylation of phenylacetic acids is presented.

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Language(s): eng - English
 Dates: 2024-02-092024-05-312024-06-12
 Publication Status: Issued
 Pages: 8
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1021/jacs.4c02088
 Degree: -

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Title: Journal of the American Chemical Society
  Other : JACS
  Abbreviation : J. Am. Chem. Soc.
Source Genre: Journal
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Publ. Info: Washington, DC : American Chemical Society
Pages: - Volume / Issue: 146 (23) Sequence Number: - Start / End Page: 15825 - 15832 Identifier: ISSN: 0002-7863
CoNE: https://pure.mpg.de/cone/journals/resource/954925376870