Palladium nanoparticles immobilized on EDTA‐modified Fe3O4@SiO2 nanospheres as an efficient and magnetically separable catalyst for Suzuki and Sonogashira cross‐coupling reactions
In this study, a novel heterogeneous palladium catalyst was synthesized by anchoring palladium onto ethylenediaminetetraacetic acid (EDTA)‐coated Fe3O4@SiO2 magnetic nanocomposite and used for the Suzuki and Sonogashira cross‐coupling reactions. The properties of the magnetic catalyst were character...
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Veröffentlicht in: | Applied organometallic chemistry 2018-04, Vol.32 (4), p.n/a |
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Sprache: | eng |
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Zusammenfassung: | In this study, a novel heterogeneous palladium catalyst was synthesized by anchoring palladium onto ethylenediaminetetraacetic acid (EDTA)‐coated Fe3O4@SiO2 magnetic nanocomposite and used for the Suzuki and Sonogashira cross‐coupling reactions. The properties of the magnetic catalyst were characterized by FT‐IR, XRD, TEM, FE‐SEM, DLS EDX, XPS, N2 adsorption‐desorption isotherm analysis, TGA, VSM, elemental analysis and the loading level of Pd in catalyst was measured to be 0.51 mmol/g by ICP. The catalyst was used in Suzuki cross‐coupling reactions of various aryl halides, including less reactive chlorobenzenes with phenylboronic acid without any additive or ligand under green conditions. Furthermore, we have reported this recyclable catalytic system for Sonogashira cross‐coupling reactions of various aryl halides (I, Br, Cl) under copper and ligand‐free conditions in the presence of DMF/H2O (1:2/v:v) as a solvent. The magnetic catalyst could also be separated by an external magnet and reused six times without any significant loss of activity.
Palladium nanoparticles supported on EDTA‐modified Fe3O4@SiO2 nanospheres was used in Suzuki cross‐coupling reactions of various aryl halides under green conditions. Furthermore, we have reported this recyclable catalytic system for Sonogashira cross‐coupling reactions under copper and ligand‐free conditions in the presence of DMF/H2O (1:2/v:v) as a solvent. |
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ISSN: | 0268-2605 1099-0739 |
DOI: | 10.1002/aoc.4302 |