| نویسندگان | حنانه حسن پور,حسین نعیمی |
| نشریه | RSC Advances |
| شماره صفحات | 17296 |
| شماره مجلد | 14 |
| ضریب تاثیر (IF) | 3.9 |
| نوع مقاله | Full Paper |
| تاریخ انتشار | 2024-05-29 |
| رتبه نشریه | علمی - پژوهشی |
| نوع نشریه | الکترونیکی |
| کشور محل چاپ | ایران |
| نمایه نشریه | JCR ,SCOPUS |
چکیده مقاله
This study presents a description of the catalytic synthesis of indeno[1,2-b]indolone derivatives. In this
method, initially, a Schiff base compound was synthesized from the reaction of acetylacetone with 2-
hydroxyaniline. Then, the prepared Schiff base was immobilized on chelated magnetic copper ferrite
nanoparticles with a chitosan surface to design and prepare the CuFe2O4@CS-SB nanocomposite.
Further, the one-pot multi-component cyclization reaction of aniline, dimedone and ninhydrin was
conducted using the synthesized nanocomposite as a heterogeneous acid catalyst in water solvent
under thermal conditions. In this reaction, the products were obtained in excellent yields and short
reaction times, and the catalyst could be recycled and reused six times without any loss in product
yields. By conducting FT-IR spectroscopy, 1H NMR spectroscopy, XRD, FE-SEM, TGA, elemental mapping
scanning, EDX and BET analyses, the structure of the nanocatalyst was characterized. In addition, for the
identification of organic compounds, FT-IR, 1H NMR, and 13C NMR spectroscopies and melting point
analysis were used, which confirmed the synthesis of this class of derivatives.