Ni/Al2O3: Catalyzed Carbonylative Homocoupling of Aryl Iodides for the Synthesis of Symmetrical Diaryl Ketone Using Co2(CO)8 as CO Surrogate

This work reports the carbonylative homo-coupling reactions for the synthesis of diaryl ketones using nickel supported on Al 2 O 3 . A heterogeneous Ni/Al 2 O 3 catalyst was prepared from the reaction of nickel acetate and aluminum oxide in the presence of sodium borohydride. The catalyst was employ...

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Published inCatalysis letters Vol. 154; no. 4; pp. 1440 - 1450
Main Authors Mahajan, Vijay P., Kolekar, Yuvraj A., Bhanage, Bhalchandra M.
Format Journal Article
LanguageEnglish
Published New York Springer US 01.04.2024
Springer Nature B.V
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Summary:This work reports the carbonylative homo-coupling reactions for the synthesis of diaryl ketones using nickel supported on Al 2 O 3 . A heterogeneous Ni/Al 2 O 3 catalyst was prepared from the reaction of nickel acetate and aluminum oxide in the presence of sodium borohydride. The catalyst was employed as a heterogeneous catalyst for carbonylative homo-coupling of aryl iodides under carbon monoxide gas-free conditions. Co 2 (CO) 8 was used as the carbon monoxide source and the desired symmetrical diaryl ketones were achieved in good to excellent yields. Moreover, the catalyst was reused for up to five consecutive cycles without significant loss of activity. The Ni/Al 2 O 3 catalyst was characterized by inductively coupled plasma optical emission spectroscopy, energy dispersive X-ray spectroscopy, X-ray diffraction, scanning electron microscopy, transmission electron microscopy, and thermogravimetric analysis. The use of Co 2 (CO) 8 as a cheap, less toxic, and solid surrogate is an additional advantage over the current protocol. Graphical Abstract
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ISSN:1011-372X
1572-879X
DOI:10.1007/s10562-023-04430-y