Synthesis and characterization of palladium nanoparticles immobilized on graphene oxide functionalized with triethylenetetramine or 2,6-diaminopyridine and application for the Suzuki cross-coupling reaction
Autor: | Maryam Mirza-Aghayan, Rabah Boukherroub, Marzieh Mohammadi |
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Přispěvatelé: | Chemistry and Chemical Engineering Research Center of Iran, Tehran, Institut d’Électronique, de Microélectronique et de Nanotechnologie - UMR 8520 (IEMN), Centrale Lille-Université de Lille-Centre National de la Recherche Scientifique (CNRS)-Université Polytechnique Hauts-de-France (UPHF)-JUNIA (JUNIA), Université catholique de Lille (UCL)-Université catholique de Lille (UCL), NanoBioInterfaces - IEMN (NBI - IEMN), Université catholique de Lille (UCL)-Université catholique de Lille (UCL)-Centrale Lille-Université de Lille-Centre National de la Recherche Scientifique (CNRS)-Université Polytechnique Hauts-de-France (UPHF)-JUNIA (JUNIA) |
Jazyk: | angličtina |
Rok vydání: | 2022 |
Předmět: |
Nanocomposite
Suzuki cross-coupling reaction Graphene Aryl Organic Chemistry Graphene oxide derivatives Biochemistry Palladium nanoparticles Coupling reaction Catalysis law.invention Inorganic Chemistry Solvent chemistry.chemical_compound [SPI]Engineering Sciences [physics] Suzuki reaction chemistry Triethylenetetramine law Polymer chemistry Materials Chemistry Triethylenetetramine2 6-Diaminopyridine [CHIM]Chemical Sciences Physical and Theoretical Chemistry |
Zdroj: | Journal of Organometallic Chemistry Journal of Organometallic Chemistry, 2022, 957, pp.122160. ⟨10.1016/j.jorganchem.2021.122160⟩ |
ISSN: | 0022-328X |
Popis: | International audience; Graphene oxide (GO) was functionalized with two organic ligands, triethylenetetramine (TETA) or 2,6-diaminopyridine (DAP), followed by palladium nanoparticles (Pd NPs) for the synthesis of Pd NPs/GO-TETA and Pd NPs/GO-DAP nanocomposites, respectively. The two heterogeneous nanocomposites were fully characterized and their efficiency was investigated for C-C bond formation for the synthesis of biaryl compounds via the Suzuki cross-coupling reaction of aryl halides with arylboronic acid derivatives. The obtained results indicated that the Pd NPs/GO-TETA nanocomposite was more effective in the Suzuki coupling reaction as compared to Pd NPs/GO-DAP. Thus, the Suzuki cross-coupling reaction of different aryl halides with arylboronic acid derivatives using Pd NPs/GO-TETA nanocomposite catalyst in the presence of Na2CO3 as base in DMF/H2O (1 /1) as solvent at 90 degrees C was carried out to afford the desired biaryl compounds in high to excellent yields (81-100%) and short reaction times (10-90 min). Additionally, Pd NPs/GO-TETA nanocomposite can be recovered and reused for 8 consecutive runs without any apparent loss of its catalytic activity, proving its high stability and potential use in organic transformations. (C) 2021 Elsevier B.V. All rights reserved. |
Databáze: | OpenAIRE |
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