The focus of this work is to use fly ash, a waste generated by thermal power plants, to synthesize an economical and efficient heterogeneous catalyst for the fine chemicals industry. To achieve this goal, fly ash zeolite (FAZ) was prepared from fly ash and Cu(II), Ni(II) and Co(II) complexes of 4-hydroxy-3-methoxybenzaldehyde [M(VAN)-FAZ] were loaded in the channels of zeolite matrix by flexible ligand strategy. The prepared FAZ was characterized by XRD, SEM, FT-IR, TGA, XRF and BET analyses. Encapsulation of metal complexes in zeolite gains the advantage of heterogeneity thereby facilitating easy separation of products and selectivity. The incorporation of metal complexes in the framework of FAZ was further assured by FT-IR, XRD, TGA, AAS and UV-Visible analyses of M(VAN)-FAZ. Thermographs indicated a loading of 6.70-16.09% of the metal complexes in FAZ. The -OH stretching reported at 3184 cm for the free ligand was absent in the FT-IR spectra of the encapsulated metal complexes, indicating the binding of this group with the metal ion. The loading of metal complexes in the pores of FAZ have been further confirmed by AAS reports. The FAZ encapsulated transition metal complexes of vanillin have been established as catalysts for phenol hydroxylation. The extent of phenol conversion increased with time, after 240 min, 90% phenol conversion was observed and the preferential catalytic activity of [M(VAN)-FAZ] was observed as: [Cu(II)(VAN)-FAZ] > [Co(II)(VAN)-FAZ] > [Ni(II)(VAN)-FAZ]. The products were characterized by GC-MS analysis and the recyclability of the prepared catalyst was assessed up to three cycles.
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http://dx.doi.org/10.1016/j.chemosphere.2021.133167 | DOI Listing |
Chem Biodivers
January 2025
St Xavier's College, Kolkata, Department of Chemistry, 30, Mother teresa Sarani, Kol-16, 700016, Kolkata, INDIA.
Amino-quinolines are potential candidates that may provide some insight into the current chemotherapeutic research due to their demonstrated anti-cancer activity. This led us to synthesize and explore a new amino-azo-quinoline ligand H2L 1 and its square planar nickel(II) complexes [Ni(HL)(OAc)], 2 and [Ni(HL)Cl], 3 and the structures were determined by SCXRD. Theoretical investigation of redox orbitals of the complexes discloses that the reduction process is due to ligand reduction whereas both metal and ligand are contributing towards oxidation.
View Article and Find Full Text PDFAppl Biochem Biotechnol
January 2025
Department of Chemistry, College of Sciences for Women, University of Baghdad, Baghdad, Iraq.
Azo dye was used to prepare a new series of complexes with chlorides of rhodium (Rh), ruthenium (Ru), and corona (Au). The prepared materials were subjected to infrared, ultraviolet-visible, and mass spectrometry, as well as thermogravimetric analysis, differential calorimetry, and elemental analysis. Conductivity, magnetic susceptibility, metal content, and chlorine content of the complexes were also measured.
View Article and Find Full Text PDFDalton Trans
January 2025
CLIC, Institut de Chimie de Strasbourg, UMR 7177 CNRS-Unistra, 4 rue Blaise Pascal, 67000 Strasbourg, France.
Iron-copper complexes have been extensively studied in the search for efficient cytochrome oxidase models. Whereas most dinuclear materials usually focus on fine-tuning the coordination of heme-Fe, this work shows that the coordination of copper in cytochrome oxidase models should be carefully taken into consideration. A β-cyclodextrin dimer was built around a bipyridine linker and combined with Fe-tetraphenylsulfonatoporphyrinate (FeTPPS) to generate a self-assembled hydrosoluble cytochrome oxidase model.
View Article and Find Full Text PDFDalton Trans
January 2025
Normandy University, ENSICAEN, UNICAEN, CNRS, LCMT, 6 Bd du Maréchal Juin, 14050 Caen, France.
Light-emitting electrochemical cells (LECs) are an attractive technology in the field of solid state light devices (SSLDs) as their simple architectures allow the preparation of cost-effective lighting devices. Consequently, low-cost and sustainable emitters are highly desirable. Transition metal complexes are attractive in this field as they have been proved to possess compatible optoelectronic properties.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
Department of Chemistry, University of Pennsylvania, 231 S 34th St, Philadelphia, Pennsylvania 19104, United States.
Molecular Zr phosphides are extremely rare, with no examples containing a one-coordinated and terminal triple-bonded phosphorus atom. We report here an isolable and relatively stable Zr phosphide complex, [(PN)Zr≡P{μ-Na(OEt)}] (), stemming from a cyclometalated Zr-hydride, [(PN)(PN')Zr(H)] (), and NaPH. Complex is prepared from two- or one-electron reductions of precursors [(PN)ZrCl] () or metastable Zr[(PN)ZrCl], respectively.
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