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Synthesis of Highly Porous Mn2O3-Doped Fe3O4 NPs with a Dual Catalytic Function Using Asymmetric Water Soluble Mn-Salen Complex as a Reducing Agent and Template: Catalytic Activity over One-Pot Strecker Synthesis from Alcohols in Recyclable TAIm[CN] Ionic Liquid

Authors :
Khalaf, Eman
Alameri, Ameer A.
Malviya, Jitendra
Kumar, T. CH. Anil
Altalbawy, Farag M. A.
Alfilh, Raed H. C.
Kazemnejadi, Milad
Source :
Catalysis Letters. Oct2023, Vol. 153 Issue 10, p3053-3073. 21p.
Publication Year :
2023

Abstract

An asymmetric Mn/TEMPO-Salen complex was utilized as a reducing agent and template for the synthesis of Mn/TEMPO-doped Fe3O4 NPs in situ. The subsequent thermal decomposition of Mn/TEMPO-doped Fe3O4 NPs, as a precursor, provides the highly porous (641 m2 g–1) Mn2O3-doped Fe3O4 NPs. The highly porous NPs was characterized by FTIR, BET, TGA, VSM, ICP, TEM, XRD, UV–Vis, and XPS analyses. High stability and catalytic activity was found for the NPs in the synthesis of α-aminonitriles via the Strecker synthesis from primary and secondary alcohols under mild conditions. TAIm[CN] ionic liquid (IL) was used as an efficient solvent and nitrile-required reagent to synthesis of α-aminonitriles. TAIm[CN] IL could be recycled for several times by a simple recovery and subsequent treatment. Also, the catalytic activity of the NPs was evaluated toward the selective alcohol oxidation to carbonyl compounds and the direct transformation of imines from alcohols and aryl amines. Mn2O3-doped Fe3O4 NPs could be recovered and reused for several consecutive cycles without any considerable reactivity loss. Highly porous MnO-doped Fe3O4 NPs were synthesized via thermal decomposition of Mn/TEMPO-doped Fe3O4 NPs as a precursor, and used as an efficient recyclable catalyst for the Strecker synthesis from alcohols in TAIm[CN] ionic liquid [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
1011372X
Volume :
153
Issue :
10
Database :
Academic Search Index
Journal :
Catalysis Letters
Publication Type :
Academic Journal
Accession number :
171951808
Full Text :
https://doi.org/10.1007/s10562-022-04210-0