Abstract:The facile two-step preparation procedure of a novel magnetic nano-solid acid catalyst is described, which includes grafting an ionic liquid onto Fe 3 O 4 nanoparticles, followed by the sulfonation of phenyl groups in the ionic liquid. The catalytic performance of this novel material has been systematically studied in the acetal formation of benzaldehyde and ethylene glycol. The experimental results testify this catalyst possesses high catalytic activity with a yield of 97% under mild reaction conditions. Furt… Show more
“…6,7 Recently, functionalized magnetite nanoparticles were used as efficient catalytic systems in many chemical transformations including synthesis of α-amino nitriles, 8 1,1-diacetates from aldehydes, 9 diazepine derivatives, 10 indazolo[2,1-b]phthalazine-triones and pyrazolo [1,2-b]phthalazine-diones, 11 3,4-dihydropyrimidin-2(1H)-ones, 12 2-amino-4H-chromen-4-yl phosphonates, 13 1,4-dihydropyridines 14 and pyrrole synthesis. 15 In addition, a series of organic reactions such as Knoevenagel condensation/Michael addition, 16 Suzuki/Heck cross-coupling, 17 asymmetric aldol reaction, 18 Suzuki coupling, 19 asymmetric hydrogenation of aromatic ketones, 20 acetalization reaction, 21 Ritter reaction, 22 23 Henry reaction, 24 enantioselective directaddition of terminal alkynes to imines 25 have been done using functionalized nanostructures.…”
In this research, the significant application of Fe 3 O 4 @SiO 2 core-shell nanoparticles as efficient, green, robust, cost-effective and recoverable nanocatalyst for the multi-component reaction of aldehydes, 2-naphthol and dimedone has been developed in aqueous ethanol media under reflux conditions. In the presented procedure we had avoided to use of hazardous reagents and solvents and therefore this method can be considered as a green alternative pathway in comparison with the previous method. Simple procedure, environmentally benign, excellent yields, short reaction times, simple purification and facile catalyst separation are advantages of this protocol. Characterization and structural elucidation of the prepared products have been done on the basis of chemical, analytical and spectral analysis. In addition, the heterogeneous nanoparticles were fully characterized by FT-IR, XRD, EDX, VSM and SEM analysis.
“…6,7 Recently, functionalized magnetite nanoparticles were used as efficient catalytic systems in many chemical transformations including synthesis of α-amino nitriles, 8 1,1-diacetates from aldehydes, 9 diazepine derivatives, 10 indazolo[2,1-b]phthalazine-triones and pyrazolo [1,2-b]phthalazine-diones, 11 3,4-dihydropyrimidin-2(1H)-ones, 12 2-amino-4H-chromen-4-yl phosphonates, 13 1,4-dihydropyridines 14 and pyrrole synthesis. 15 In addition, a series of organic reactions such as Knoevenagel condensation/Michael addition, 16 Suzuki/Heck cross-coupling, 17 asymmetric aldol reaction, 18 Suzuki coupling, 19 asymmetric hydrogenation of aromatic ketones, 20 acetalization reaction, 21 Ritter reaction, 22 23 Henry reaction, 24 enantioselective directaddition of terminal alkynes to imines 25 have been done using functionalized nanostructures.…”
In this research, the significant application of Fe 3 O 4 @SiO 2 core-shell nanoparticles as efficient, green, robust, cost-effective and recoverable nanocatalyst for the multi-component reaction of aldehydes, 2-naphthol and dimedone has been developed in aqueous ethanol media under reflux conditions. In the presented procedure we had avoided to use of hazardous reagents and solvents and therefore this method can be considered as a green alternative pathway in comparison with the previous method. Simple procedure, environmentally benign, excellent yields, short reaction times, simple purification and facile catalyst separation are advantages of this protocol. Characterization and structural elucidation of the prepared products have been done on the basis of chemical, analytical and spectral analysis. In addition, the heterogeneous nanoparticles were fully characterized by FT-IR, XRD, EDX, VSM and SEM analysis.
Tetrabutylammonium valinate ionic liquid [NBu 4 ][Val] supported on 3-chloropropyltriethoxysilane graftedsuperparamagnetic Fe 3 O 4 NPs (VSF) was synthesized and characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), transmission electronic microscopy (TEM), scanning electronic microscopy (SEM), thermal gravimetric analysis (TGA), and vibrating sample magnetometer (VSM). The VSF catalyst was used as an efficient "quasi-homogeneous" catalyst for the multi-component synthesis of 1,4-dihydropyridines and 2-amino-4-(indol-3-yl)-4H-chromenes at room temperature. The VSF catalyst was recovered using an external magnet and recycled six times without a significant loss in the catalytic activity. Moreover, VSF as a "quasi-homogeneous" catalyst can bridge the gap between homogeneous and heterogeneous catalyses.
“…Recently functionalized magnetic nano particle have been used as efficient catalytic system in many chemical transformation including synthesis of α-amino nitriles [10], 1-1 diacetates form aldehyde [11], diazepiene derivatives [12], indazalo [2,1-b] phthalazine triones, pyrazoles [1,2-b] phthalazine-diones [13], 3,4 dihydro pyrimidines-2(1H)ones [14], 1,4 dihydropyrimidines [15], and pyrrole synthesis [16]. Also a series of organic reaction such as Michael addition [17], Suzuki/Heck cross-coupling [18], asymmetric aldol reaction [19], Suzuki coupling [20], acetalization reaction [21], Ritter reaction [22], cyanosilylation of carbonyl compounds [23], Henry reaction [24], enantioselective direct addition of terminal alkynes to imines [25] have been done using functionalized nanostructure.…”
MgFe 2 O 4 nanoparticle ferrites were synthesized by combustion technique using pure ferric nitrate and magnesium carbonate. The magnetically separable MgFe 2 O 4 MNP's were found to be hyper active catalyst for the synthesis of a wide range of biologically active five and six-membered heterocyclic moieties at refluxing conditions. Reaction times are lowest in comparison to all reported in literature with excellent yields. Strong electron pull of Fe 3+ is responsible for its hyper activity, which has been substantiated by substitution of Fe 3+ by other trivalent metal ions. Mg 2+ has a unique role because replacement of Mg 2+ has poor catalytic activity. The developed protocol has been efficiently utilized for the synthesis of a series of substituted mono/bis pyrimidines, pyrimidin-2-ol, pyrimidin-2-thiol, pyrazoles and isoxazoles by condensing monochalcones/1,4-bischalcones with various bis-nucleophiles in the presence of catalytic amount of heterogenous magnetic MgFe 2 O 4 nanoparticles. The structure of these synthesized compounds was determined by FTIR, 1 H, 13 C and mass spectra. The catalyst can be removed easily from reaction mixture by using a simple external magnet. Nanoparticles of ferrite were recovered and reused with no appreciable change in the activity even after the five runs. Nanoparticles are characterized by XRD, TEM and IR spectroscopy.
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