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- W2767873119 abstract "Recent interest in the valorization of lignin has led to reactions involving the cleavage of strong aromatic C-O bonds. However, few experimental mechanistic studies of these reactions have been published. We report detailed mechanistic analysis of the hydrogenolysis of diaryl ethers catalyzed by the combination of Ni(COD)2 (COD = 1,5-cyclooctadiene) and an N-heterocyclic carbene (NHC). Experiments on the catalytic reaction indicated that NaOt-Bu was necessary for catalysis, but kinetic analysis showed that the base is not involved in the rate-limiting C-O bond cleavage. The resting state of the catalyst is an NHC-Ni(η6-arene) complex. Substitution of the coordinated solvent with diaryl ether allowed isolation of a diaryl ether-bound Ni complex. Rate-limiting C-O bond cleavage occurs to generate a three-coordinate product of oxidative addition, a metallacyclic version of which has been prepared independently. Stoichiometric studies show that arene and phenol products are released following reaction with H2. NaOt-Bu was found to deprotonate the phenol product and to prevent formation of inactive NiI dimers." @default.
- W2767873119 created "2017-11-17" @default.
- W2767873119 creator A5026910964 @default.
- W2767873119 creator A5088865204 @default.
- W2767873119 date "2017-11-21" @default.
- W2767873119 modified "2023-10-18" @default.
- W2767873119 title "Mechanistic Investigations of the Hydrogenolysis of Diaryl Ethers Catalyzed by Nickel Complexes of <i>N</i>-Heterocyclic Carbene Ligands" @default.
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- W2767873119 doi "https://doi.org/10.1021/jacs.7b10537" @default.
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