Synthesis, characterization and catalytic activity of copper (II) complex immobilized on magnetic nanoparticles (Fe3O4@SiO2-(Imine-Thiazole)-Cu(OAc)2 nanomaterial) for synthesis of diaryl sulfides and benzothiophenes. Issue 22 (17th November 2022)

• Record Type: Journal Article
• Authors: Feng, Meili; Yao, Wenjun; An, Jingjing; Yao, Yuze
• Is Part Of: Synthetic communications. Volume 52:Issue 22(2022)
• Page Start: 2122
• Page End: 2137
• Publication Date: 2022-11-17
• Subjects: Benzothiophenes -- diaryl sulfides -- Fe3O4@SiO2-(Imine-Thiazole)-Cu(OAc)2 nanomaterial -- nanomagnetic copper catalyst -- organic synthesis; Organic compounds -- Synthesis -- Periodicals; Chemistry, Organic; Synthesis; 547.205
• DOI: 10.1080/00397911.2022.2127365
• Languages: English
• ISSNs: 0039-7911

Abstract

Abstract: Research on the synthesis of organosulfur compounds is an attractive research fields among synthetic chemists. Diaryl sulfides and benzothiophenes are important organosulfur compounds with a diverse range of biological activities which are privileged in the structure of numerous biological molecules and natural products. In this paper, we successfully fabricated copper complex supported on the surface of magnetic nanoparticles modified with imine-thiazole ligand and studied its catalytic activity in the synthesis of diaryl sulfides and benzothiophenes. The structure of Fe3 O4 @SiO2 -(Imine-Thiazole)-Cu(OAc)2 nanomaterial was well characterized by Fourier transform infrared, scanning electron microscope, energy-dispersive X-ray spectrum, transmission electron microscopy, thermal gravimetric analysis, vibrating sample magnetometer, X-ray powder diffraction (XRD), Atomic absorption spectroscopy (AAS) and Inductively coupled plasma-optical emission spectroscopy (ICP-OES) techniques. The Fe3 O4 @SiO2 -(Imine-Thiazole)-Cu(OAc)2 catalyst could be recovered via magnetic attraction and (upon washing with an organic phase and water) could be reused at least seven runs without a noticeable decrease in its performance. Graphical Abstract: UF0001