2017
DOI: 10.1002/aoc.3720
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A highly reactive and magnetic recyclable catalyst based on silver nanoparticles supported on ferrite for N‐monoalkylation of amines with alcohols

Abstract: Fe 3 O 4 @SiO 2 -Ag catalyst was found to be highly active and selective in the N-alkylation of amines with a variety of aromatic and linear alcohols. The heterogeneous nature of the Fe 3 O 4 @SiO 2 -Ag catalyst allows easy recovery and regeneration by applying an external magnet for six subsequent reaction cycles. The prepared catalyst was characterized using electron microscopy techniques, X-ray diffraction, vibrating sample magnetometry and atomic absorption spectroscopy.

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Cited by 12 publications
(6 citation statements)
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“…Noble metals-based catalysts are well-imminent with their outstanding electrocatalytic activity and sensitivity towards enzymtic-free H 2 O 2 detection [20]. Among these noble metals, silver nanoparticles (Ag NPs) have unique optical, catalytic, and anti-bacterial properties [21,22,23,24]. Furthermore, the great abundance in the nature of Ag makes it more feasible for large-scale applications.…”
Section: Introductionmentioning
confidence: 99%
“…Noble metals-based catalysts are well-imminent with their outstanding electrocatalytic activity and sensitivity towards enzymtic-free H 2 O 2 detection [20]. Among these noble metals, silver nanoparticles (Ag NPs) have unique optical, catalytic, and anti-bacterial properties [21,22,23,24]. Furthermore, the great abundance in the nature of Ag makes it more feasible for large-scale applications.…”
Section: Introductionmentioning
confidence: 99%
“…When aniline was reacted with Ph−Me and Ph−MeO substituted benzyl alcohols (Table , entry 2 and entry 3) good yields, of ∼97 % and ∼98 %, respectively, are achieved. On other hand, secondary alcohols are challenging alkylating agents compared with primary alcohols because of the dehydrogenation of secondary alcohols to the corresponding ketones is more difficult than that of primary alcohols (Table entry 4) . When benzyl alcohol substituted electron‐withdrawing ‐Cl group reacts with aniline the alkylation results more slowly than with primary alcohols (Table entry 5).…”
Section: Resultsmentioning
confidence: 99%
“…A full comparison of such catalysts is provided in tabular form in the SI (Table S6). Catalysts of this type are described in refs ,, .…”
Section: Borrowing Hydrogen Amination Of Benzyl Alcohol By Anilinementioning
confidence: 99%
“…A tabular comparison of the reaction conditions for different reaction types (Figure ) of the target process is provided in SI (Table S10). The literature cited included refs , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , ,,, , , , , , , , , , , , , , , , , , , , …”
Section: Borrowing Hydrogen Amination Of Alcohols Using Different N-n...mentioning
confidence: 99%