In the present research, using ethylenediamine and hydrazine
hydrate
as the capping and reducing agents in this investigation, respectively,
Ag–Cu–Ni NPs were immobilized on the functionalized
g–C3N4 surface. This nanocatalyst was
studied in terms of its catalytic activities for the A3-coupling reaction to synthesize propargylamine derivatives. According
to the results, in the presence of 1 mL of toluene as the solvent
and 20 mg of the g–C3N4–TCT–2AEDSEA–Ag–Cu–Ni
nanocatalyst, the maximum efficiency of the nanocatalyst occurred
at a temperature of 80 °C. Products were purified using thin-layer
chromatography plates (silica gel) by employing n-hexane/ethyl acetate with a 90:10 ratio. In addition, the prominent
benefits of the synthesized nanocatalyst include its high yields of
the product, cost-effectiveness, recyclability, and easy separation.
The novelty of the catalyst is due to the presence of Ag–Cu–Ni
nanoparticles at the same time in the structure of the functionalized
g–C3N4 substrate. So, Ag–Cu–Ni
can be strongly connected to the substrate. The structure of the synthesized
nanocatalyst was characterized using Fourier transformed infrared
spectroscopy, X-ray powder diffraction, field emission scanning electron
microscopy, energy-dispersive X-ray spectroscopy, vibrating-sample
magnetometry, and transmission electron microscopy.