Sonochemically Synthesized Spin-Canted CuFe2O4 Nanoparticles for Heterogeneous Green Catalytic Click Chemistry
Author(s) -
Bibhas Mondal,
Mousumi Kundu,
Siba Prasad Mandal,
Rajat Saha,
Ujjal Kanti Roy,
Anirban Roychowdhury,
D. Das
Publication year - 2019
Publication title -
acs omega
Language(s) - Uncategorized
Resource type - Journals
ISSN - 2470-1343
DOI - 10.1021/acsomega.9b01477
Subject(s) - raman spectroscopy , ferrimagnetism , materials science , superparamagnetism , spinel , catalysis , nanoparticle , rietveld refinement , magnetization , powder diffraction , chemical engineering , nanotechnology , crystallography , chemistry , organic chemistry , magnetic field , crystal structure , physics , engineering , quantum mechanics , optics , metallurgy
Heterogeneous green catalysis by using magnetically separable nanometal-oxide catalysts has become a subject of prime focus recently. PXRD (powder X-ray diffraction), FESEM (field emission scanning electron microscopy), and HRTEM (high-resolution tunneling electron microscopy) with IR and Raman spectroscopy are applied to analyze the structural and microstructural properties of nanosized (∼15.3 nm) CuFe 2 O 4 synthesized by both sonochemical and mechanochemical processes. The sonochemical process provides a better uniformity of sizes of the nanoparticles (NPs). Rietveld refinement with the PXRD pattern reveals the inverse spinel-like architecture of CuFe 2 O 4 NPs. The Raman spectra also indicate the phase purity of the synthesized material. The static magnetic measurements are performed at different magnetic fields and temperature ranges from 300 to 5 K, which confirms the existence of the ferrimagnetic phase mixed with some finer superparamagnetic (SPM) nanophases within the sample. Unsaturated magnetization is observed even at an applied 5 T magnetic field for the presence of spin-canting nature in the partially inverted copper ferrite phases at the surfaces of the nanoparticles. Now, these coupled magnetic CuFe 2 O 4 NPs are used as a heterogeneous catalyst for three-component Huisgen 1,3-dipolar cycloaddition click reaction in aqueous media. By this catalyst system, we were able to couple alkyl halide, epoxide, or boronic acid with alkynes efficiently to furnish 1,4-disubstituted 1,2,3-triazoles in excellent yields within very short reaction time. The test for heterogeneity, reusability, and reproducibility of the catalyst has also been performed successfully without prominent decrease in yield up to the fifth cycle.
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