Silver cluster-promoted heterogeneous copper catalyst for N-alkylation of amines with alcohols

A series of metal(M)-loaded Al2O3 catalysts (M/Al2O3) and bimetallic catalysts, CuxAg1-x/Al2O3 with different compositions, Cu0.95Ag0.05/MOx with different supports (MOx), and Cu0.95M[prime or minute]0.05/Al2O3 with different promoter (M[prime or minute]), were prepared by an impregnation method, fo...

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Veröffentlicht in:RSC advances 2011-01, Vol.1 (7), p.1310-1317
Hauptverfasser: Shimizu, Ken-ichi, Shimura, Katsuya, Nishimura, Masanari, Satsuma, Atsushi
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Sprache:eng
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Zusammenfassung:A series of metal(M)-loaded Al2O3 catalysts (M/Al2O3) and bimetallic catalysts, CuxAg1-x/Al2O3 with different compositions, Cu0.95Ag0.05/MOx with different supports (MOx), and Cu0.95M[prime or minute]0.05/Al2O3 with different promoter (M[prime or minute]), were prepared by an impregnation method, followed by H2-reduction at 600 [degree]C. For the N-alkylation of amines with alcohols, Al2O3-supported copper-silver bimetallic catalysts with a Cu/Ag molar ratio of 95/5 (Cu0.95Ag0.05/Al2O3) was found to be the most effective heterogeneous catalyst. The alkylation of anilines and aliphatic amines with various alcohols (benzyl and aliphatic alcohols) was achieved with a small amount of the catalyst (1 mol%). Mechanistic studies show that the reaction proceeds through a hydrogen-borrowing mechanism initiated by alcohol dehydrogenation as the rate-limiting step. Structural studies indicate that small Ag nanoclusters are supported on Cu nanoparticles possibly through Ag-O-Cu bonds at the silver-copper boundary. This bimetallic structure can be crucial to an effective promotion of the alcohol dehydrogenation and hydride transfer to the imines.
ISSN:2046-2069
2046-2069
DOI:10.1039/c1ra00560j