A tris(triazolate) ligand for a highly active and magnetically recoverable palladium catalyst of selective alcohol
Dong Wang1, Christophe Deraedt, Lionel Salmon
1ISM, Université de Bordeaux, 351 Cours de la Libération, 33405 Talence Cedex (France).
Abstract:
High efficiency and selectivity, easy magnetic recovery and recycling, and use of air as the oxidant at atmospheric pressure are major objectives for oxidation catalysis in terms of sustainable and green processes. A tris(triazolyl) ligand, so far only used in copper-catalyzed alkyne azide cycloadditions, was found to be extremely efficient in SiO2 /γ-Fe2 O3 -immobilized palladium complexes. It was characterized by inductively coupled plasma (ICP) analysis, transmission electron microscopy (TEM), scanning transmission electron microscopy (STEM), energy-dispersive X-ray spectroscopy (EDX), and X-ray photoelectron spectra (XPS) and found to fulfill the combined conditions for the selective oxidation of alcohols to aldehydes and ketones.
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