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  Selective hydrodeoxygenation of hydroxyacetophenones to ethyl-substituted phenol derivatives using a FeRu@SILP catalyst

Goclik, L., Offner-Marko, L. R., Bordet, A., & Leitner, W. (2020). Selective hydrodeoxygenation of hydroxyacetophenones to ethyl-substituted phenol derivatives using a FeRu@SILP catalyst. Chemical Communications, 56(66), 9509-9512. doi:10.1039/d0cc03695a.

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Item Permalink: https://hdl.handle.net/21.11116/0000-0007-A70B-1 Version Permalink: https://hdl.handle.net/21.11116/0000-0007-A70C-0
Genre: Journal Article

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 Creators:
Goclik, Lisa1, Author           
Offner-Marko, Lisa Ramona1, Author           
Bordet, Alexis1, Author           
Leitner, Walter1, 2, Author           
Affiliations:
1Research Department Leitner, Max Planck Institute for Chemical Energy Conversion, Max Planck Society, ou_3023872              
2Institut für Technische Chemie und Makromolekulare Chemie, Rheinisch‐Westfälische Technische Hochschule Aachen, Worringer Weg 1, 52074 Aachen, Germany, ou_persistent22              

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 Abstract: The selective hydrodeoxygenation of hydroxyacetophenone derivatives is achieved opening a versatile pathway for the production of valuable substituted ethylphenols from readily available substrates. Bimetallic iron ruthenium nanoparticles immobilized on an imidazolium-based supported ionic liquid phase (Fe25Ru75@SILP) show high activity and stability for a broad range of substrates without acidic co-catalysts.

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Language(s): eng - English
 Dates: 2020
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: ISI: 000560564400017
DOI: 10.1039/d0cc03695a
 Degree: -

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Title: Chemical Communications
  Other : Chem. Commun.
Source Genre: Journal
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Publ. Info: Cambridge, UK : Royal Society of Chemistry
Pages: - Volume / Issue: 56 (66) Sequence Number: - Start / End Page: 9509 - 9512 Identifier: ISSN: 1359-7345
CoNE: https://pure.mpg.de/cone/journals/resource/954928495413