Functionalised β-lactones and β-lactams were prepared starting from propargyl alcohols and propargyl tosyl amides by means of efficient silylcarbocyclisation reactions catalysed by rhodium nanoparticles derived from mesitylene-solvated Rh atoms (Metal Vapour Synthesis technique, MVS) and deposited on inorganic (C, γ-Al2O3 Fe2O3) and organic matrices (PBI). All the MVS supported nanoclusters resulted more active than the analogous commercial Rh/C and Rh/γ-Al2O3, as well as homogeneous Rh4(CO)12 used as reference catalyst. In particular, metal vapour derived Rh/C afforded the β-lactones and β-lactams in high yields and chemoselectivity. Preliminary investigations on the nature of the real active metal species involved in the catalytic process showed that rhodium(0) naked nanoparticles are leached by the support. The high catalytic activity encountered with Rh/C could be ascribed to the easy leaching of metal nanoparticles from carbon into solution. Indeed, the presence of a more polar matrix determined a minor catalytic efficiency probably due to a stronger interaction between the metal and the support. Therefore MVS Rh/C species represents a source, stable with ageing at room temperature, of highly active metal nanoparticles.

Metal vapour derived supported rhodium nanoparticles in the synthesis of β-lactams and β-lactones derivatives

ARONICA, LAURA ANTONELLA;
2012-01-01

Abstract

Functionalised β-lactones and β-lactams were prepared starting from propargyl alcohols and propargyl tosyl amides by means of efficient silylcarbocyclisation reactions catalysed by rhodium nanoparticles derived from mesitylene-solvated Rh atoms (Metal Vapour Synthesis technique, MVS) and deposited on inorganic (C, γ-Al2O3 Fe2O3) and organic matrices (PBI). All the MVS supported nanoclusters resulted more active than the analogous commercial Rh/C and Rh/γ-Al2O3, as well as homogeneous Rh4(CO)12 used as reference catalyst. In particular, metal vapour derived Rh/C afforded the β-lactones and β-lactams in high yields and chemoselectivity. Preliminary investigations on the nature of the real active metal species involved in the catalytic process showed that rhodium(0) naked nanoparticles are leached by the support. The high catalytic activity encountered with Rh/C could be ascribed to the easy leaching of metal nanoparticles from carbon into solution. Indeed, the presence of a more polar matrix determined a minor catalytic efficiency probably due to a stronger interaction between the metal and the support. Therefore MVS Rh/C species represents a source, stable with ageing at room temperature, of highly active metal nanoparticles.
2012
Aronica, LAURA ANTONELLA; Caporusso, A. M.; Evangelisti, C.; Botavina, M.; Alberto, G.; Martra, G.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11568/173427
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