Nanoporous Au/Ag Catalyzed Benzylic sp3C−H Oxidation of 9H‐Fluorene Derivatives and Similar Molecules with TBHP

Author:

Thayssen Jan12ORCID,Riedel Wiebke3ORCID,Risse Thomas3ORCID,Staubitz Anne124ORCID,Wittstock Arne125ORCID

Affiliation:

1. Institute for Organic and Analytical Chemistry University of Bremen Leobener Straße 7 28359 Bremen

2. MAPEX Center for Material and Processes University of Bremen 28359 Bremen

3. Institute for Chemistry and Biology Physical and Theoretical Chemistry Freie Universität Berlin Arminallee 22 14195 Berlin

4. Otto-Diels-Institute for Organic Chemistry University of Kiel Otto-Hahn-Platz 4 24118 Kiel

5. Institute of Applied and Physical Chemistry and Center for Environmental Research and Sustainable Technology Universität Bremen Leobener Straße 6 28359 Bremen

Abstract

AbstractNanoporous gold (npAu) was tested as a catalyst for oxidations of various benzylic sp3‐carbon positions in 9H‐fluorene derivatives and similar hydrocarbons using tertbutyl hydroperoxide (TBHP) as an oxidant. The silver content in the npAu catalyst had a major influence on the overall conversion: Lower silver amounts (0.53 mol%) led to higher conversions, whereas higher amounts of silver increasingly resulted in the disproportionation of TBHP as a competing reaction. Because residual silver from the bulk alloy was oxidized by TBHP and leached into the solution during the reaction, the Ag content diminished over time. Therefore, the recycling of the catalyst had a positive effect on the conversion after each use. Using electron paramagnetic resonance (EPR) spectroscopy, the formation of radicals from TBHP by npAu was evidenced indicating a radical‐based reaction mechanism which was further elucidated by NMR spectroscopic and GC‐MS (trace) product analysis. Subsequent oxidations of benzylic sp3‐carbon positions gave good to excellent conversions and chemoselectivities featuring npAu as a suitable catalyst for such reactions.

Publisher

Wiley

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