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Citation: H. N. Hareesh, K. U. Minchitha, N. Nagaraju, N. Kathyayini. Catalytic role of Cu(I) species in Cu2O/CuI supported on MWCNTs in the oxidative amidation of aryl aldehydes with 2-aminopyridines[J]. Chinese Journal of Catalysis, ;2015, 36(11): 1825-1836. doi: 10.1016/S1872-2067(15)60964-0 shu

Catalytic role of Cu(I) species in Cu2O/CuI supported on MWCNTs in the oxidative amidation of aryl aldehydes with 2-aminopyridines

  • 1.

    a Department of Nanobiosciences, Centre for Emerging Technologies, Jain Global Campus, Jain University, Jakkasandra Post, Kanakapura Taluk, Ramanagara District-562112, Karnataka, India;

  • Corresponding author: N. Kathyayini, 
  • Received Date: 23 June 2015
    Available Online: 12 August 2015

  • Cu2O and CuI were supported on multiwalled carbon nanotubes (MWCNTs) using a wet impregnation method, and the resulting materials were fully characterized by powder X-ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy with energy dispersive X-ray spectroscopy, transmission electron microscopy, and temperature-programmed desorption with ammonia analysis. The results of these experiments revealed that Cu2O and CuI were deposited on the MWCNTs in the cubic and γ phases, respectively. These results also showed that the Cu-containing MWCNTs exhibited weak to strong electron-accepting (Lewis acidic) properties. The catalytic activities of these materials were studied for the synthesis of biologically significant N-(pyridin-2-yl)benzamides via the oxidative amidation of aryl aldehydes with 2-aminopyridines. The yields of the products were in the range 50%-95% with 100% selectivity. Notably, the CuI/MWCNT catalyst was much more effective than the Cu2O/MWCNT catalyst with respect to the isolated yield of the product, although the latter of these two catalysts exhibited much better recyclability. A preferential interaction was observed between the polar nature of the acid-activated MWCNTs and the ionic Cu2O compared with covalent CuI. The differences in these interactions had a significant impact on the rate of the nucleophilic attack of the amino group of 2-aminopyridine substrate on the carbonyl group of the aryl aldehyde.
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