scholarly journals Nickel-Fe3O4 Magnetic Nanoparticles Supported on Multiwalled Carbon Nanotubes: Effective Catalyst in Suzuki Cross Coupling Reactions

Catalysts ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 495
Author(s):  
Sojeong K. Folsom ◽  
Destiny J. Ivey ◽  
Frank S. McNair ◽  
Ali R. Siamaki

Nickel-Fe3O4 nanoparticles supported on multi-walled carbon nanotubes (Ni-Fe3O4/MWCNTs) were synthesized by mechanical grinding of a sample of nickel salt, Fe3O4 and MWCNTs using a ball-mill mixer. The preparation method allows for bulk production of Ni-Fe3O4 nanoparticles at room temperature without the necessity of any solvent or chemical reagent. The nanoparticles prepared by this method exhibit small particles size of 5–8 nm with uniform dispersion of nickel nanoparticles on the surface of multi-walled carbon nanotubes. The Ni-Fe3O4/MWCNTs demonstrated remarkable catalytic activity for Suzuki cross coupling reactions of functionalized aryl halides and phenylboronic acids with excellent turnover number and turnover frequency (e.g., 76,000 h−1) using Monowave 50 conventional heating reactor at 120 °C within a very short reaction time of 15 min. The catalyst is air-stable and exhibits easy removal from the reaction mixture due to its magnetic properties, recyclability with no loss of activity, and significantly better performance than the other well-known commercial nickel catalyst. The Ni-Fe3O4/MWCNTs nanoparticles were fully characterized by a variety of spectroscopic techniques including X-ray Diffraction (XRD), Transmission Electron Microscopy (TEM) and X-ray Photoelectron Spectroscopy (XPS). Since nickel offers similar properties to other more expensive transition metals including the most widely used palladium counterpart in cross coupling catalysis, this work demonstrates a promising lower-cost, air-moisture stable and efficient alternative catalyst based on nickel nanoparticles for cross coupling reactions.

2019 ◽  
Vol 72 (9) ◽  
pp. 674 ◽  
Author(s):  
Maryam Sadat Ghasemzadeh ◽  
Batool Akhlaghinia

The new ferromagnetic nanostructured FMMWCNTs@CPA@SMTU@PdII NPs (IV) as an eco-friendly heterogeneous nanocatalyst with a particle size of ~20–30nm reported earlier by our group has been found to be very effective for Suzuki–Miyaura and Mizoroki–Heck cross-coupling reactions at ambient temperature. The procedure has been applied for a wide range of aryl halides, arylboronic acids, and alkenes. The magnetic separation by an external magnetic field, mild reaction conditions, and catalyst reusability up to four times without significant decrease in catalytic activity (reduced catalytic activity from 11 to 18% in the fifth, sixth, and seventh cycles) made the present method sustainable and economically viable for C–C cross-coupling reactions.


Author(s):  
Tilman Lechel ◽  
Irene Brüdgam ◽  
Hans-Ulrich Reissig

A series of trifluoromethyl-substituted 3-alkoxypyridinol derivatives has been deprotected to furnish pyridine-3,4-diol derivatives in good yields. The X-ray crystal structure analysis proved that a 1:1 mixture of pyridine-3,4-diols and their pyridin-4-one tautomers exist in the solid state. Subsequent conversion into bis(perfluoroalkanesulfonate)s were smoothly achieved. The obtained compounds were used as substrates for palladium-catalyzed coupling reactions. Fluorescence measurements of the biscoupled products showed a maximum of emission in the violet region of the spectrum.


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