A robust magnetically recoverable nickel nanocatalyst for α-olefination of nitriles using primary alcohols

Abstract A novel nickel nanocatalyst with a magnetic core was designed and synthesized through a multi-step procedure. First, an iron oxide core was synthesized (Fe 3 O 4 ), then coated with a silica layer (Fe 3 O 4 @SiO 2 ). The catalyst support was further functionalized using epichlorohydrin (EP) and ortho -phenylenediamine (OPDA) (Fe 3 O 4 @SiO 2 /EP/OPDA), and finally, nickel was loaded onto the structure to obtain the finished catalyst (Fe 3 O 4 @SiO 2 /EP/OPDA@Ni). Its successful fabrication was confirmed by various characterization techniques, including X-ray diffraction, transmission electron microscopy, energy-dispersive X-ray spectroscopy, and vibrating-sample magnetometry. The nanocatalyst was then effectively applied in the α-olefination of nitriles using primary alcohols through the reaction of a benzyl alcohol derivative with a benzyl cyanide derivative in refluxing toluene, using KO t -Bu as the base. The catalyst could be easily separated from the reaction mixture by applying an external magnetic field. It was also reusable, retaining its activity with only a minor loss over at least five consecutive cycles.

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Publication Details

Journal
Transition Metal Chemistry
Published
2026-11-03
DOI
https://doi.org/10.1007/s11243-026-00792-5
Primary Topic
Catalytic Cross-Coupling Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

A robust magnetically recoverable nickel nanocatalyst for α-olefination of nitriles using primary alcohols

Hossein Eshghi, Effat Vatankhah, Ali Shiri
2 links
Transition Metal Chemistry
Catalytic Cross-Coupling Reactions
article

A robust magnetically recoverable nickel nanocatalyst for α-olefination of nitriles using primary alcohols

Hossein Eshghi, Effat Vatankhah, Ali Shiri
article en

Abstract

Abstract A novel nickel nanocatalyst with a magnetic core was designed and synthesized through a multi-step procedure. First, an iron oxide core was synthesized (Fe 3 O 4 ), then coated with a silica layer (Fe 3 O 4 @SiO 2 ). The catalyst support was further functionalized using epichlorohydrin (EP) and ortho -phenylenediamine (OPDA) (Fe 3 O 4 @SiO 2 /EP/OPDA), and finally, nickel was loaded onto the structure to obtain the finished catalyst (Fe 3 O 4 @SiO 2 /EP/OPDA@Ni). Its successful fabrication was confirmed by various characterization techniques, including X-ray diffraction, transmission electron microscopy, energy-dispersive X-ray spectroscopy, and vibrating-sample magnetometry. The nanocatalyst was then effectively applied in the α-olefination of nitriles using primary alcohols through the reaction of a benzyl alcohol derivative with a benzyl cyanide derivative in refluxing toluene, using KO t -Bu as the base. The catalyst could be easily separated from the reaction mixture by applying an external magnetic field. It was also reusable, retaining its activity with only a minor loss over at least five consecutive cycles.

Transition Metal ChemistryVol. 51(6)
Ferdowsi University of Mashhad (IR)
Ferdowsi University of Mashhad
Openalex Percentile: Top 84%
Catalytic Cross-Coupling Reactions
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