Metal-free solid base catalysis: Boron-doped graphitic carbon nitride for the efficient synthesis of ethyl coumarin-3-carboxylate
In this work, boron doped graphitic carbon nitride materials (BgCN-x) were successfully prepared by thermal copolymerization of melamine and boric acid. The comprehensive characterization using various techniques, including powder X-ray diffraction (PXRD), Fourier transform infrared spectroscopy (FT...
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Veröffentlicht in: | Applied catalysis. A, General General, 2024-08, Vol.683, p.119827, Article 119827 |
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Zusammenfassung: | In this work, boron doped graphitic carbon nitride materials (BgCN-x) were successfully prepared by thermal copolymerization of melamine and boric acid. The comprehensive characterization using various techniques, including powder X-ray diffraction (PXRD), Fourier transform infrared spectroscopy (FT-IR), UV-Visible spectroscopy (UV-Vis), Field emission scanning electron microscopy (FESEM), Energy-Dispersive X-ray spectroscopy (EDS), Field emission transmission electron microscopy (FETEM), and X-ray photoelectron spectroscopy (XPS) revealed the uniform doping of boron in the tri-s-triazine rings of g-C3N4 by substituting the carbon or nitrogen atoms. Furthermore, the basic site concentrations of the catalysts were evaluated using CO2-TPD technique. The BgCN catalysts exhibited significantly enhanced catalytic activity in the base-catalyzed Knoevenagel condensation between salicylaldehyde and diethyl malonate for coumarin synthesis. This work underscores the potential of boron-doped or two-dimensional boron-dominant materials as promising candidates for metal-free heterogeneous base catalysis, paving the way for further advancements in the field.
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•Successfully B is doped into graphitic carbon nitride (BgCN)•BgCN exhibited base-catalyzed Knoevenagel reaction for coumarin synthesis•High basicity consisted with BgCN catalyst (0.8) as determined by CO2-TPD technique•Introduced a new heterogeneous catalyst in organic synthesis |
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ISSN: | 0926-860X 1873-3875 |
DOI: | 10.1016/j.apcata.2024.119827 |