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 in | Catalysis letters Vol. 154; no. 4; pp. 1440 - 1450 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
New York
Springer US
01.04.2024
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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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.
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 1011-372X 1572-879X |
DOI: | 10.1007/s10562-023-04430-y |