AI Article Synopsis

  • AlCl-loaded ZnO nanoparticles were developed as an effective catalyst for synthesizing 1,4-dihydropyridines under mild, solvent-free conditions.
  • The catalyst was created by loading 20% aluminum chloride onto ZnO nanoparticles, which were characterized through various advanced techniques and confirmed to have an average particle size of 70-80 nm.
  • This AlCl@ZnO catalyst achieved a high yield of 92% for the target reaction and is considered an environmentally friendly alternative to traditional catalytic methods.

Article Abstract

AlCl-loaded ZnO nanoparticles have been explored as an efficient catalyst for 1,4-dihydropyridine synthesis under ambient temperature and solvent-free conditions. For this purpose, ZnO nanoparticles were synthesized by a simple solution-based precipitation technique using a stoichiometric amount of zinc sulfate and oxalic acid. The AlCl@ZnO nanocrystalline catalyst was prepared by loading 20% AlCl on ZnO nanoparticles by a simple wet-impregnation technique. This catalyst efficiently performed Hantzsch pyridine reactions with various aromatic aldehydes, ethyl acetoacetate and ammonium acetate. The nanostructured AlCl-loaded ZnO catalyst was characterized by UV-DRS, XRD, FESEM, EDS, FETEM-STEM-EDS and XPS techniques. The comprehensive characterization reveals the formation of AlCl-loaded ZnO catalysts with an average particle size of 70-80 nm. The loading of AlCl on the ZnO surface was confirmed by minor shifts in the XPS and XRD peaks. FETEM-STEM-EDS also indicates reasonable AlCl loading on ZnO nanoparticles. The 20% AlCl-loaded ZnO nanocatalyst (AlCl@ZnO) confers 92% yield for the synthesis of 1,4-dihydropyridine under solvent-free and ambient temperature conditions. The synthesized 1,4-dihydropyridines were characterized by H-NMR, C-NMR, HRMS and FT-IR spectroscopic techniques. The reported catalyst is highly efficient, environmentally friendly and could become an alternative to homogenous and heterogenous catalytic reactions.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10437094PMC
http://dx.doi.org/10.1039/d3ra04277dDOI Listing

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