An article Transfer hydrogenolysis of aromatic ethers promoted by the bimetallic Pd/Co catalyst WOS:000579549200051 published article about HIGHLY-ACTIVE CATALYST; BENZYL PHENYL ETHER; PARTIAL OXIDATION; BOND-CLEAVAGE; LIGNIN; BIOMASS; LINKAGES; NANOPARTICLES; CONVERSION; REDUCTION in [Mauriello, F.; Paone, E.; Pietropaolo, R.] Univ Mediterranea Reggio Calabria, Dipartimento DICEAM, I-89124 Reggio Di Calabria, Italy; [Ariga-Miwa, H.; Takakusagi, S.; Asakura, K.] Hokkaido Univ, Inst Catalysis, Kita Ku, N21W10, Sapporo, Hokkaido 0010021, Japan in 2020.0, Cited 50.0. The Name is Diphenyl oxide. Through research, I have a further understanding and discovery of 101-84-8. Recommanded Product: 101-84-8
The transfer hydrogenolysis of lignin derived aromatic ethers (benzyl phenyl ether, phenethyl phenyl ether and diphenyl ethers) have been investigated by using the coprecipitated Pd/Co as heterogeneous catalyst and 2propanol as H-donor/solvent. A quantitative conversion of benzyl phenyl ether into toluene and cyclohexanol was obtained after 180 min at 240 degrees C. The bimetallic Pd/Co catalyst is, by far, more efficient if compared to commercial Pd/C and Co-based catalytic systems showing, at the same time, a good reusability. The enhanced ability in the CeO bond cleavage in aromatic ethers is related to the formation of bimetallic Pd-Co ensembles, arisen from the preparation procedure adopted, as confirmed by a complete physico-chemical characterization that includes XRD, SEM, TEM, H-2-TPR, XPS and EXAFS analysis.
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