Wood ash biocatalyst as a novel green catalyst and its application for the synthesis of benzochromene derivatives

Wood ash is a naturally alkaline derived substance containing organic and inorganic constituents. This study investigates the catalytic activity of wood ash as a heterogeneous catalyst for the synthesis of benzochromene derivatives. Several wood ash catalysts, comprising calcium- and potassium-rich...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Scientific reports 2022-01, Vol.12 (1), p.1145-11, Article 1145
Hauptverfasser: Rostamian, Rezvaneh, Khalilzadeh, Mohammad A., Zareyee, Daryoush
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Wood ash is a naturally alkaline derived substance containing organic and inorganic constituents. This study investigates the catalytic activity of wood ash as a heterogeneous catalyst for the synthesis of benzochromene derivatives. Several wood ash catalysts, comprising calcium- and potassium-rich carbonates, were prepared from different natural resources under various combustion temperatures. The prepared catalysts were characterized by Fourier transform infrared, scanning electron microscopy, energy dispersive X-ray analysis, transmission electron microscopy, and X-ray diffraction techniques. Catalytic efficiency of the resultant catalysts was tested in the synthesis of benzochromene derivatives. The experimental studies clarified that the catalyst prepared at 850 °C could efficiently expedite the formation of three-component synthesis of benzochromene derivatives in water at 80 °C with high yields. Indeed, alkali, alkaline metal, and metal oxides such as Al 2 O 3 , SiO 2 , MgO, CaO, and Fe 2 O 3 , are widely utilized as both catalyst and catalyst support in the heterogeneous catalytic processes. The prepared wood ash catalysts (possessing metal oxides, e.g., CuO, Al 2 O 3 , SiO 2 , and CaO) could effectively prompt the electrophilic activity of the carbonyl groups during the nucleophilic attack intermediate, enhancing the efficiency of the reactions.
ISSN:2045-2322
2045-2322
DOI:10.1038/s41598-022-05133-x