Metal-Organic Framework Fe3O(BPDC)3 as an efficient catalyst for the oxidative couling reaction of benzaldehyde and (E)-1-phenylethan-1-one O-acetyl oxime
DOI:
https://doi.org/10.51316/jca.2020.005Keywords:
acetyl oxime, benzaldehyde, di-tert-butyl peroxide, Arylpyridines, Fe3O(BPDC)3Abstract
A porous crytalline metal-organic framework Fe3O(BPDC)3 was synthesized, and its properties were characterized by various techniques, including X-ray powder diffraction (PXRD), Fourier transform infrared (FT-IR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and nitrogen physisorption measurements. The Fe3O(BPDC)3 was used as an efficient catalyst for the oxidative coupling reaction of benzaldehyde and (E)-1-phenylethan-1-one O-acetyl oxime to form 2,4,6-triphenylpyridine as desired product. The reaction could proceed readily, with more than 83 % reaction yield being achieved after 360 min at 140 oC in the presence of 10 mol% Fe3O(BPDC)3) catalyst and Di-tert-butyl peroxide as an oxidant. This Fe-MOF exhibited higher activity than other MOFs and traditional homogeneous catalysts in the oxidative coupling reaction. The transformation could only proceed to obtain main product in the presence of Fe3O(BPDC)3.
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