2015
DOI: 10.1016/j.molcata.2015.04.002
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Magnetically separable γ-Fe2O3 nanoparticles: An efficient catalyst for acylation of alcohols, phenols, and amines using sonication energy under solvent free condition

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Cited by 57 publications
(22 citation statements)
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“…To address these issues, magnetic separation using an external magnetic field is a useful recovery method since it is faster and more efficient as compared to filtration and decantation (Pang et al, 2014;Cao et al, 2015). Besides, magnetic separable catalysts were reported to have good dispersion in reaction suspension, high mechanical stability, and desirable paramagnetic nature for easy separation and reuse (Bhosale et al, 2015). Recently, iron-containing catalysts have attracted wide interest since it is less toxic to the environment as compared to the late-transition metals (Patra et al, 2012).…”
Section: Introductionmentioning
confidence: 99%
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“…To address these issues, magnetic separation using an external magnetic field is a useful recovery method since it is faster and more efficient as compared to filtration and decantation (Pang et al, 2014;Cao et al, 2015). Besides, magnetic separable catalysts were reported to have good dispersion in reaction suspension, high mechanical stability, and desirable paramagnetic nature for easy separation and reuse (Bhosale et al, 2015). Recently, iron-containing catalysts have attracted wide interest since it is less toxic to the environment as compared to the late-transition metals (Patra et al, 2012).…”
Section: Introductionmentioning
confidence: 99%
“…The current study adopted mechanochemical process/mechanical milling as a prospective Fe 2 O 3 -TiO 2 synthesis route. This synthesis method omits the use of volatile organic solvents, toxic reagents, and harsh reaction conditions (Bhosale et al, 2015).…”
Section: Introductionmentioning
confidence: 99%
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“…Binding energies of Fe 2p 3/2 and Fe 2p 1/2 330 were 710.7 and 724.5 eV respectively, verifying the presence of Fe 3+ . An absence of peaks 331 around 707 and 719 eV ruled out the presence of Fe 2+ , firmly supporting the addition of γ-Fe 2 O 3 332 phase into TiO 2 [42]. Peaks corresponding to Ti 4+ were centered at 458.6 and 464.4 eV, which 333 were analogous to Ti 2p 3/2 and Ti 2p 1/2 , respectively.…”
Section: Effect Of Milling Speedmentioning
confidence: 68%
“…Interestingly, other catalysts, such as γ‐Fe 2 O 3 (Table , entry 25), CeCl 3 (Table , entry 28), and Cu/Cu 2 O (Table , entry 29), didn′t promote the hydrogenation of compound 1 a at all. Therefore, we concluded that cerium(IV) was active for the hydrogenation of deactivated α‐keto amides into α‐hydroxy amides, whereas cerium(III) was ineffective.…”
Section: Resultsmentioning
confidence: 99%