In this study, CuO/TiO nanocomposites were biologically synthesized using cell-free supernatant (CFS) of Alcaligenes aquatilis growth culture by two-step synthesis method, one-pot method with sequential addition of precursors, and one-pot method with simultaneous addition of precursors. The one-pot method with simultaneous addition of precursors was found to be the best method for the synthesis in terms of degradation of reactive blue-220 (RB-220) and acid yellow-17 (AY-17) dyes under visible light irradiation. CuO/TiO nanocomposite was found to have the crystallite size of 14.7nm and the bandgap energy of 2.5 eV. The effect of synthesis parameters such as synthesis time, pH of CFS, and the ratio of Cu to Ti in the synthesis mixture on the photocatalytic degradation efficacy of these nanocomposite structures under visible light irradiation was studied. The optimum conditions for the synthesis of CuO/TiO nanocomposite particles by one-pot method with simultaneous addition of precursors were found to be pH 12 of CFS, synthesis duration of 24 h, and molar ratio of Cu to Ti in the synthesis mixture as 1:22 for RB-220 dye and 1:25 for AY-17 degradation. CuO/TiO nanocomposite particles synthesized under the optimum conditions and without any calcination could degrade RB-220 and AY-17 dyes completely in 120 min and 150 min, respectively. The kinetics of degradation of RB-220 and AY-17 by CuO@TiO nanocomposite particles followed first-order kinetic model with rate constant of 0.028 min and 0.018 min, respectively.
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http://dx.doi.org/10.1007/s11356-023-28489-7 | DOI Listing |
Org Biomol Chem
January 2025
Department of Chemistry and Biochemistry, The University of Tulsa 800 South Tucker Drive, Tulsa, OK 74104, USA.
A variety of dearomatized compounds have been prepared in moderate to excellent yields from planar scaffolds using trichloroisocyanuric acid (TCCA) as an atom-economical chlorinating agent. The method tolerates a broad range of functionalities and can take place in several green and/or sustainable solvents. Twenty-one examples of 1,1-dichlorinated products of dearomatized 2-naphthols and analogous heteroarenes (quinolinols, isoquinolinols, and quinazolinol) are reported along with five examples of monochlorinated dearomatized products.
View Article and Find Full Text PDFFront Plant Sci
December 2024
College of Life Science, Zhejiang Chinese Medical University, Hangzhou, Zhejiang, China.
Introduction: f. sp. (Fol) is one of the most devastating plant pathogenic fungi, the causal agent of root rot for tractylides macrocephala Koidz (AMK).
View Article and Find Full Text PDFRSC Adv
January 2025
Department of Fundamental Chemistry, Institute of Chemistry, University of São Paulo 05508-000 São Paulo SP Brazil
New tetrakis Eu and Gd β-diketonate complexes containing benzimidazolium (Bzim) as the counterion were synthesized by the one-pot method. The Bzim[Eu(tta)]·HO complex was further incorporated into a poly(methyl methacrylate) matrix (PMMA) at 1, 5, and 10% (w/w), which revealed highly desirable photonic features. The Eu and Gd complexes were characterized by elemental and thermal analyses, in addition to ESI-MS spectrometry, FTIR, and Raman spectroscopy.
View Article and Find Full Text PDFACS Omega
December 2024
SupraSelen Laboratory, Department of Chemistry, Universidade Federal Fluminense, Institute of Chemistry, Campus do Valonguinho, 24020-141 Niterói-RJ, Brazil.
Our research presents selective direct selenylation at the C-4 pyrazole ring using KSO as an oxidant under simple and mild conditions. This elegant synthesis involves the one-pot method under acidic conditions, thus minimizing reaction steps and waste generation. This innovative method allowed us to create a library of 4-selanylpyrazoles in good to excellent yields.
View Article and Find Full Text PDFCurr Pharm Des
January 2025
Institute of Materials Research, Tsinghua Shenzhen International Graduate School (SIGS), Tsinghua University, Shenzhen 518055, China.
Introduction: An efficient and four-component one-pot facile synthesis of tetra-substituted imidazole is achieved by cyclo-condensation reaction of benzil with subsequent successive substitution of aromatic aldehydes, ester substituted amine and ammonium acetate via refluxing the mixture for almost two hours at 140°C.
Method: The ending point of the understudy reaction was examined by TLC after regular intervals. Synthesized 1,2,4-tetrasubstituted imidazoles were characterized by physical data and the structural features were analyzed using spectroscopic techniques such as FTIR, NMR and elemental analysis.
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