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6 results on '"Maryam Mirza-Aghayan"'

1. [Review] Graphene loaded with metal nanoparticles/complexes catalyzed cross-coupling reactions: A review

Author

Maryam Mirza-Aghayan, Amir Sepehr Moieni, Rabah Boukherroub, chemistry and chemical engineeting research center of Iran (CCERCI), CHEMISTRY AND CHEMICAL ENGINEERING, Islamic Azad University, 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), and NONE FOUND

Subjects
Inorganic Chemistry, [PHYS]Physics [physics], Heterogeneous catalysis, Cross-coupling reactions, [SPI]Engineering Sciences [physics], Graphene-based nanocatalysts, Organic Chemistry, Materials Chemistry, Physical and Theoretical Chemistry, Carbon-carbon bond formation, Biochemistry
Abstract

International audience; AbstractVarious catalytic reactions under suitable conditions were used for the carbon-carbon (C-C) bond formation, such as the Kumada, Mizoroki-Heck, Sonogashira, Negishi, Stille, Suzuki-Miyaura, Hiyama, andFukuyama cross-coupling reactions. Supporting metal nanoparticles or complexes on functionalizedgraphene oxide (GO) or reduced graphene oxide (rGO) compounds provides new heterogeneous catalysts with enhanced aptitude for the formation of C-C bonds. This review highlights the applications ofmetal decorated on modified GO and rGO derivatives to form C-C bonds. We discuss briefly the generalmechanistic cycle of each reaction and the recent applications of the graphene-based nanocatalysts forthe coupling reactions, along the advantages of each catalyst.

Published
2023

2. An efficient CuO/rGO/TiO2 photocatalyst for the synthesis of benzopyranopyrimidine compounds under visible light irradiation

Author

Maryam Mirza-Aghayan, Mandana Saeedi, Rabah Boukherroub, chemistry and chemical engineeting research center of Iran (CCERCI), CHEMISTRY AND CHEMICAL ENGINEERING, 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), and no information

Subjects
[SPI]Engineering Sciences [physics], Materials Chemistry, General Chemistry, Catalysis
Abstract

This study reports the synthesis of CuO/rGO/TiO2 in coupling reaction under visible light irradiation. Its photocatalytic performance was explored in a pseudo 4-component and a domino reaction for the synthesis of benzopyranopyrimidine compounds. It can be recovered and recycled for 5 runs.

Published
2022

3. 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

Author

Maryam Mirza-Aghayan, Rabah Boukherroub, Marzieh Mohammadi, 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), and 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)

Subjects
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
Abstract

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.

Published
2022

4. Cu2O/reduced graphene oxide/TiO2 nanomaterial: An effective photocatalyst for azide‐alkyne cycloaddition with benzyl halides or epoxide derivatives under visible light irradiation

Author

Maryam Mirza-Aghayan, Rabah Boukherroub, Mandana Saeedi, Institut d’Électronique, de Microélectronique et de Nanotechnologie - UMR 8520 (IEMN), Centrale Lille-Institut supérieur de l'électronique et du numérique (ISEN)-Université de Valenciennes et du Hainaut-Cambrésis (UVHC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS)-Université Polytechnique Hauts-de-France (UPHF), NanoBioInterfaces - IEMN (NBI - IEMN), and Centrale Lille-Institut supérieur de l'électronique et du numérique (ISEN)-Université de Valenciennes et du Hainaut-Cambrésis (UVHC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS)-Université Polytechnique Hauts-de-France (UPHF)-Centrale Lille-Institut supérieur de l'électronique et du numérique (ISEN)-Université de Valenciennes et du Hainaut-Cambrésis (UVHC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS)-Université Polytechnique Hauts-de-France (UPHF)

Subjects
chemistry.chemical_classification, 010405 organic chemistry, Graphene, Epoxide, Alkyne, General Chemistry, [CHIM.CATA]Chemical Sciences/Catalysis, 010402 general chemistry, Photochemistry, 01 natural sciences, Cycloaddition, 0104 chemical sciences, Nanomaterials, law.invention, Inorganic Chemistry, chemistry.chemical_compound, chemistry, law, Click chemistry, Photocatalysis, Azide, ComputingMilieux_MISCELLANEOUS
Abstract

International audience

Published
2020

5. Efficient and Regioselective Ring-opening of Epoxides with Carboxylic Acid Catalyzed by Graphite Oxide

Author

Mahdieh Molaee Tavana, Elaheh Golam Alipour Niazi, Rabah Boukherroub, Maryam Mirza-Aghayan, Institut d’Électronique, de Microélectronique et de Nanotechnologie - UMR 8520 (IEMN), Centrale Lille-Institut supérieur de l'électronique et du numérique (ISEN)-Université de Valenciennes et du Hainaut-Cambrésis (UVHC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS)-Université Polytechnique Hauts-de-France (UPHF), NanoBioInterfaces - IEMN (NBI - IEMN), and Centrale Lille-Institut supérieur de l'électronique et du numérique (ISEN)-Université de Valenciennes et du Hainaut-Cambrésis (UVHC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS)-Université Polytechnique Hauts-de-France (UPHF)-Centrale Lille-Institut supérieur de l'électronique et du numérique (ISEN)-Université de Valenciennes et du Hainaut-Cambrésis (UVHC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS)-Université Polytechnique Hauts-de-France (UPHF)

Subjects
chemistry.chemical_classification, 010405 organic chemistry, Chemistry, Carboxylic acid, Organic Chemistry, Regioselectivity, Graphite oxide, [CHIM.CATA]Chemical Sciences/Catalysis, 010402 general chemistry, Ring (chemistry), 01 natural sciences, 7. Clean energy, Biochemistry, 0104 chemical sciences, Catalysis, chemistry.chemical_compound, Polymer chemistry, ComputingMilieux_MISCELLANEOUS
Abstract

An efficient, simple and regioselective ring-opening reaction of epoxides with various carboxylic acids under metal-free conditions is reported. The ring-opening of epoxides takes place in the presence of graphite oxide as an efficient and available catalyst to produce the corresponding 2-hydroxy monoester and 1,2-diester derivatives in good yields. Regioselective attack of the nucleophile, short reaction times, metal-free conditions and reusability of catalyst are among the advantages of the present protocol.

Published
2020

6. Pd nanoparticles supported on reduced graphene oxide as an effective and reusable heterogeneous catalyst for the Mizoroki–Heck coupling reaction

Author

Maryam Mirza-Aghayan, Rabah Boukherroub, Ahmed Addad, Marzieh Mohammadi, Institut d’Électronique, de Microélectronique et de Nanotechnologie - UMR 8520 (IEMN), Centrale Lille-Institut supérieur de l'électronique et du numérique (ISEN)-Université de Valenciennes et du Hainaut-Cambrésis (UVHC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS)-Université Polytechnique Hauts-de-France (UPHF), NanoBioInterfaces - IEMN (NBI - IEMN), and Centrale Lille-Institut supérieur de l'électronique et du numérique (ISEN)-Université de Valenciennes et du Hainaut-Cambrésis (UVHC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS)-Université Polytechnique Hauts-de-France (UPHF)-Centrale Lille-Institut supérieur de l'électronique et du numérique (ISEN)-Université de Valenciennes et du Hainaut-Cambrésis (UVHC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS)-Université Polytechnique Hauts-de-France (UPHF)

Subjects
010405 organic chemistry, Graphene, Oxide, Palladium nanoparticles, General Chemistry, [CHIM.CATA]Chemical Sciences/Catalysis, 010402 general chemistry, Heterogeneous catalysis, 01 natural sciences, 0104 chemical sciences, law.invention, Inorganic Chemistry, chemistry.chemical_compound, chemistry, Chemical engineering, law, Heck reaction, Pd nanoparticles, Diethylenetriamine, ComputingMilieux_MISCELLANEOUS
Abstract

International audience

Published
2020

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