4.8 Article

Surface-Bound Ligands Modulate Chemoselectivity and Activity of a Bimetallic Nanoparticle Catalyst

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ACS CATALYSIS
卷 5, 期 4, 页码 2529-2533

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acscatal.5b00262

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cinnamaldehyde; selective hydrogenation; ligand effects; bimetallic nanoparticles; fluorous chemistry

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  1. King Abdullah University of Science and Technology

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Naked metal nanoparticles (NPs) are thermodynamically and kinetically unstable in solution. Ligands, surfactants, or polymers, which adsorb at a particle's surface, can be used to stabilize NPs; however, such a mode of stabilization is undesirable for catalytic catalytic activity and the stability of NPs are usually inversely correlated. applications because the adsorbates block the surface active sites. The Here, we describe an example of a bimetallic (PtFe) NP catalyst stabilized by carboxylate surface ligands that bind preferentially to one of the metals (Fe). NPs stabilized by fluorous ligands were found to be remarkably competent in catalyzing the hydrogenation of cinnamaldehyde; NPs stabilized by hydrocarbon ligands were significantly less active. The chain length of the fluorous ligands played a key role in determining the chemoselectivity of the FePt NP catalysts.

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