Chinese Journal of Catalysis ›› 2015, Vol. 36 ›› Issue (11): 1825-1836.DOI: 10.1016/S1872-2067(15)60964-0

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

H. N. Hareesha, K. U. Minchithaa, N. Nagarajub, N. Kathyayinia   

  1. a Department of Nanobiosciences, Centre for Emerging Technologies, Jain Global Campus, Jain University, Jakkasandra Post, Kanakapura Taluk, Ramanagara District-562112, Karnataka, India;
    b Catalysis Research Laboratory, Department of Chemistry, St. Joseph's College and Research Centre, 46 Langford Road, Shanthinagar Bengaluru-560027, Karnataka, India
  • Received:2015-06-23 Revised:2015-08-12 Online:2015-11-02 Published:2015-11-02

Abstract:

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.

Key words: Cuprous oxide, Cuprous iodide, Multiwalled carbon nanotube, 2-Aminopyridine, Oxidative amidation