Abstract

A new Ag (Ⅰ) complex (C) containing phosphoric triamide ligand (L) with a formula of [Ag ((C5H4NC (O) NHP (O) (NC6H12)2)2NO3] 2 was synthesized by the reaction of AgNO3 with N-nicotinyl –N′, N″-bis (hexamethylenyl) phosphoric triamide. The complex (C) was characterized by Fourier transform infrared spectroscopy (FT-IR), molar conductivity, thermal gravimetric analysis (TGA), and X-ray crystallography techniques. Results showed that complexation occurred via the nitrogen atom of the pyridine ring. The molecular structure of C, refined from single-crystal X-ray diffraction, is triclinic with a P-1 space group. The complex was immobilized on SBA-15 and the produced compound (C@SBA-15) was identified by BET, AAS, FT-IR, XRD, and TGA methods. Successful loading of the complex on SBA-15 was determined by the BET method. According to AAS findings, the amount of silver in the C@SBA-15 composition was 18%. FT-IR and XRD results showed that the complex was absorbed on the support physically and the hexagonal structure of the support was retained after immobilization. Thermal stability of C@SBA-15 was confirmed by TGA analysis. The homogeneous complex (C) and heterogeneous C@SBA-15 were used as catalysts in the oxidation reaction of aromatic aldehydes and sulfides and their catalytic properties compared. H2O2 was used as a green oxidant, some effective parameters (reaction temperature, substrate to oxidant molar ratio, catalyst amount, and solvent type) were optimized, and the conversion percentages of 70% (for C catalyst) and 50% (for C@SBA-15 catalyst) obtained. The reusability of C@SBA-15 and the generality of both catalysts were evaluated and confirmed. The results showed that when the complex was immobilized on SBA-15, its catalytic efficiency decreased, and its recoverability increased. A comparison with other published reports showed that the catalytic efficiency of the catalysts in the oxidation reaction of aldehydes and sulfides was within acceptable limits.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.