Cargando…

Facile route to synthesize Fe(3)O(4)@acacia–SO(3)H nanocomposite as a heterogeneous magnetic system for catalytic applications

In this work, a novel catalytic system for facilitating the organic multicomponent synthesis of 9-phenyl hexahydroacridine pharmaceutical derivatives is reported. Concisely, this catalyst was constructed from acacia gum (gum arabic) as a natural polymeric base, iron oxide magnetic nanoparticles (Fe(...

Descripción completa

Detalles Bibliográficos
Autores principales: Taheri-Ledari, Reza, Esmaeili, Mir Saeed, Varzi, Zahra, Eivazzadeh-Keihan, Reza, Maleki, Ali, Shalan, Ahmed Esmail
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9057486/
https://www.ncbi.nlm.nih.gov/pubmed/35520839
http://dx.doi.org/10.1039/d0ra07986c
Descripción
Sumario:In this work, a novel catalytic system for facilitating the organic multicomponent synthesis of 9-phenyl hexahydroacridine pharmaceutical derivatives is reported. Concisely, this catalyst was constructed from acacia gum (gum arabic) as a natural polymeric base, iron oxide magnetic nanoparticles (Fe(3)O(4) NPs), and sulfone functional groups on the surface as the main active catalytic sites. Herein, a convenient preparation method for this nanoscale composite is introduced. Then, essential characterization methods such as various spectroscopic analyses and electron microscopy (EM) were performed on the fabricated nano-powder. The thermal stability and magnetic properties were also precisely monitored via thermogravimetric analysis (TGA) and vibrating-sample magnetometry (VSM) methods. Then, the performance of the presented catalytic system (Fe(3)O(4)@acacia–SO(3)H) was further investigated in the referred organic reaction by using various derivatives of the components involved in the reaction. Optimization, mechanistic studies, and reusability screening were carried out for this efficient catalyst as well. Overall, remarkable reaction yields (94%) were obtained for the various produced derivatives of 9-phenyl hexahydroacridine in the indicated optimal conditions.