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A MIL-100(Fe) supported Pd–Ni BMNP catalyst has been fabricated, and the catalyst exhibits superior catalytic performance toward the intramolecular transfer hydrogenolysis of lignin model compounds and organosolv lignin. Alcoholic groups (CαH-OH) of lignin were exploited as the hydrogen source, and selective cleavage of β-O-4 linkages in lignin was realized without an extra hydrogen donor. This protocol was suitable for organosolv lignin as well as model compounds; several phenols and functionalized acetophenones were detected when extracted lignin was treated in our system. The catalyst exhibits outstanding catalytic stability during the reaction process, which can be ascribed to the porous structure and the strong water stability of MIL-100(Fe). The excellent catalytic performance of Pd1Ni4/MIL-100(Fe) highlights the “synergistic effect” between the BMNPs and the functional synergy between MNPs and MOFs, and our work shows the bright future of BMNPs and MOFs in the development of catalysts for sustainable chemistry. [ABSTRACT FROM AUTHOR]

β-O-4 and α-O-4 linkages can be selectively cleaved by Pd–Ni bimetallic nanoparticles in ionic liquids using hydrogen gas as the hydrogen donor under ambient pressure and neutral conditions. No hydrogenation of the benzene ring takes place in the catalytic system. An obvious improvement in activity is found compared with single nickel and palladium catalysts based on the results of experiments and characterization. After the reaction, the catalytic system still remains in the reactor by simple extraction, which can be reused without further treatment. [ABSTRACT FROM AUTHOR]

An efficient, recyclable Pd–Cu bimetallic nanoparticle catalyst has been prepared, which exhibits superior activity and selectivity toward the hydrosilylation of internal and terminal alkynes under mild reaction conditions with a low catalyst loading. Distinct enhancement in catalytic performance is observed when compared with traditional monometallic catalysts, and the composition of BMNPs is found to be crucial in both selectivity and yield. This kind of elevation in catalytic performance can be ascribed to the enrichment of active sites (Pd) on the catalyst surface and a phenomenon collectively referred to as “synergistic effects”. The successful application of BMNPs as catalysts in the alkyne hydrosilylation opens up new possibilities for the excavation of the value of bimetallic nanoparticles in catalysts’ development for sustainable chemistry. [ABSTRACT FROM AUTHOR]

The β-O-4 linkage in lignin can be selectively cleaved by Pd–Ni bimetallic nanoparticles supported on ZrO2 using hydrogen gas as the hydrogen donor under ambient pressure and neutral conditions. Conspicuous enhancement in activity is observed compared with single nickel and palladium catalysts based on the results of experiments and characterization. Moreover, hydrogenation of the produced phenols is tuned by adjusting the amount of NaBH4. The catalyst can be reused over ten times in the model reaction and over five times in the hydrogenolysis of lignin without an obvious change in activity and selectivity. [ABSTRACT FROM AUTHOR]

The β-O-4 linkage in lignin can be selectively cleaved by Pd–Ni bimetallic nanoparticles supported on ZrO2 using hydrogen gas as the hydrogen donor under ambient pressure and neutral conditions. Conspicuous enhancement in activity is observed compared with single nickel and palladium catalysts based on the results of experiments and characterization. Moreover, hydrogenation of the produced phenols is tuned by adjusting the amount of NaBH4. The catalyst can be reused over ten times in the model reaction and over five times in the hydrogenolysis of lignin without an obvious change in activity and selectivity. [ABSTRACT FROM AUTHOR]

β-O-4 and α-O-4 linkages can be selectively cleaved by Pd-Ni bimetallic nanoparticles in ionic liquids using hydrogen gas as the hydrogen donor under ambient pressure and neutral conditions. No hydrogenation of the benzene ring takes place in the catalytic system. An obvious improvement in activity is found compared with single nickel and palladium catalysts based on the results of experiments and characterization. After the reaction, the catalytic system still remains in the reactor by simple extraction, which can be reused without further treatment.