Oxo‐vanadium(IV) unsymmetrical Schiff base complex immobilized on γ‐Fe 2 O 3 nanoparticles: A novel and magnetically recoverable nanocatalyst for selective oxidation of sulfides and oxidative coupling of thiols

In this research, an unsymmetrical salen‐type oxo‐vanadium(IV) complex, [VO(salenac‐OH)] (salenac‐OH = [9‐(2′,4′‐dihydroxyphenyl)‐5,8‐diaza‐4‐methylnona‐2,4,8‐trienato](‐2)), was synthesized and covalently immobilized on the surface of magnetic γ‐Fe 2 O 3 nanoparticles. The resulting γ‐Fe 2 O 3 @[VO...

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Veröffentlicht in:Applied organometallic chemistry 2021-04, Vol.35 (4)
Hauptverfasser: Mahdian, Abolfazl, Ardakani, Mehdi Hatefi, Heydari‐Bafrooei, Esmaeil, Saeednia, Samira
Format: Artikel
Sprache:eng
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Zusammenfassung:In this research, an unsymmetrical salen‐type oxo‐vanadium(IV) complex, [VO(salenac‐OH)] (salenac‐OH = [9‐(2′,4′‐dihydroxyphenyl)‐5,8‐diaza‐4‐methylnona‐2,4,8‐trienato](‐2)), was synthesized and covalently immobilized on the surface of magnetic γ‐Fe 2 O 3 nanoparticles. The resulting γ‐Fe 2 O 3 @[VO(salenac‐OH)] nanoparticles were characterized by several techniques including Fourier transform infrared (FT‐IR) spectroscopy, X‐ray diffraction (XRD), scanning and transmission electron microscopies (SEM and TEM), energy‐dispersive X‐ray (EDX) spectroscopy, vibrating sample magnetometry (VSM), thermal gravimetric analysis (TGA), inductively coupled plasma (ICP), and elemental analysis. The prepared γ‐Fe 2 O 3 @[VO(salenac‐OH)] nanoparticle was utilized as an efficient catalyst for selective oxidation of sulfides to sulfoxides using 30% H 2 O 2 as oxidant and oxidative coupling of thiols into disulfides with urea/H 2 O 2 (UHP) as an oxidizing reagent. The products were achieved with good to excellent yields at room temperature with no over‐oxidation of sulfoxides and disulfides to unexpected by‐products. This catalyst can be magnetically recovered by applying an external magnet and reused for five continuous cycles in both oxidation reactions without a significant loss in its catalytic activity. Furthermore, the FT‐IR spectrum and XRD pattern of the recovered catalyst showed no critical change to those of the fresh one.
ISSN:0268-2605
1099-0739
DOI:10.1002/aoc.6170