Oxidative reactions that are catalysed by bulk gold consisting of ∼50 000 nm gold powder particles or gold (∼50 nm) supported on Al2O3 are reviewed. Using O2 as the oxidizing agent, bulk gold catalyzes the following types of reactions in organic solvents at 45–90 °C: (1) the conversion of amines to imines [(RCH2)2NH → RCH2NCHR], (2) the oxidation of benzyl alcohol to benzaldehyde, (3) the reaction of isocyanides with primary amines to give carbodiimides [CN–R + H2N–R′ → R′–NCN–R] and with secondary amines to give ureas , (4) the reactions of CO with primary amines to give ureas [CO + H2N–R → OC(NHR)2], and (5) the reactions of diazoalkanes with amines to give enamines . In some of these reactions, amine oxides (e.g., Me3N–O) may be used in place of O2. Mechanisms of these and related reactions are examined. These studies show that bulk, non-nanogold is capable of catalysing a variety of different reactions.
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Robert J. Angelici (2012) studied this question.
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