Pd@Py2PZ@MSN as a Novel and Efficient Catalyst for C–C Bond Formation Reactions
In this study, a novel catalyst is introduced based on the immobilization of palladium onto dipyrido (3,2-a:2′,3′-c) phenazine–modified mesoporous silica nanoparticles. The dipyrido (3,2-a:2′,3′-c) phenazine (Py2PZ) ligand is synthesized in a simple method from the reaction of 1,10-phenanthroline-5,...
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Frontiers Media S.A.
2022-03-01
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Online Access: | https://www.frontiersin.org/articles/10.3389/fchem.2022.838294/full |
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author | Mohammad Hosein Sayahi Mansoureh Toosibashi Mehdi Bahmaei Hosein Lijan Leila Ma'Mani Mohammad Mahdavi Saeed Bahadorikhalili |
author_facet | Mohammad Hosein Sayahi Mansoureh Toosibashi Mehdi Bahmaei Hosein Lijan Leila Ma'Mani Mohammad Mahdavi Saeed Bahadorikhalili |
author_sort | Mohammad Hosein Sayahi |
collection | DOAJ |
description | In this study, a novel catalyst is introduced based on the immobilization of palladium onto dipyrido (3,2-a:2′,3′-c) phenazine–modified mesoporous silica nanoparticles. The dipyrido (3,2-a:2′,3′-c) phenazine (Py2PZ) ligand is synthesized in a simple method from the reaction of 1,10-phenanthroline-5,6-dione and 3,4-diaminobenzoic acid as starting materials. The ligand is used to functionalize mesoporous silica nanoparticles (MSNs) and modify their surface chemistry for the immobilization of palladium. The palladium-immobilized dipyrido (3,2-a:2′,3′-c) phenazine–modified mesoporous silica nanoparticles (Pd@Py2PZ@MSNs) are synthesized and characterized by several characterization techniques, including TEM, SEM, FT-IR, TGA, ICP, XRD, and EDS analyses. After the careful characterization of Pd@Py2PZ@MSNs, the activity and efficiency of this catalyst is examined in carbon–carbon bond formation reactions. The results are advantageous in water and the products are obtained in high isolated yields. In addition, the catalyst showed very good reusability and did not show significant loss in activity after 10 sequential runs. |
first_indexed | 2024-12-14T05:49:03Z |
format | Article |
id | doaj.art-35e453851e844c2dad0a2a872e1329c2 |
institution | Directory Open Access Journal |
issn | 2296-2646 |
language | English |
last_indexed | 2024-12-14T05:49:03Z |
publishDate | 2022-03-01 |
publisher | Frontiers Media S.A. |
record_format | Article |
series | Frontiers in Chemistry |
spelling | doaj.art-35e453851e844c2dad0a2a872e1329c22022-12-21T23:14:46ZengFrontiers Media S.A.Frontiers in Chemistry2296-26462022-03-011010.3389/fchem.2022.838294838294Pd@Py2PZ@MSN as a Novel and Efficient Catalyst for C–C Bond Formation ReactionsMohammad Hosein Sayahi0Mansoureh Toosibashi1Mehdi Bahmaei2Hosein Lijan3Leila Ma'Mani4Mohammad Mahdavi5Saeed Bahadorikhalili6Department of Chemistry, Payame Noor University (PNU), Tehran, IranSchool of Chemistry, College of Science, University of Tehran, Tehran, IranDepartment of Chemistry, Payame Noor University (PNU), Tehran, IranSchool of Chemistry, College of Science, University of Tehran, Tehran, IranDepartment of Nanotechnology, Agricultural Biotechnology Research Institute of Iran (ABRII), Agricultural Research Education and Extension Organization (AREEO), Karaj, IranEndocrinology and Metabolism Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran University of Medical Sciences, Tehran, IranDepartment of Electronic Engineering, Universitat Rovira i Virgili, Tarragona, SpainIn this study, a novel catalyst is introduced based on the immobilization of palladium onto dipyrido (3,2-a:2′,3′-c) phenazine–modified mesoporous silica nanoparticles. The dipyrido (3,2-a:2′,3′-c) phenazine (Py2PZ) ligand is synthesized in a simple method from the reaction of 1,10-phenanthroline-5,6-dione and 3,4-diaminobenzoic acid as starting materials. The ligand is used to functionalize mesoporous silica nanoparticles (MSNs) and modify their surface chemistry for the immobilization of palladium. The palladium-immobilized dipyrido (3,2-a:2′,3′-c) phenazine–modified mesoporous silica nanoparticles (Pd@Py2PZ@MSNs) are synthesized and characterized by several characterization techniques, including TEM, SEM, FT-IR, TGA, ICP, XRD, and EDS analyses. After the careful characterization of Pd@Py2PZ@MSNs, the activity and efficiency of this catalyst is examined in carbon–carbon bond formation reactions. The results are advantageous in water and the products are obtained in high isolated yields. In addition, the catalyst showed very good reusability and did not show significant loss in activity after 10 sequential runs.https://www.frontiersin.org/articles/10.3389/fchem.2022.838294/fullpalladium catalystimmobilized catalystmesoporous silica nanoparticlesHeck reactionSuziki reaction |
spellingShingle | Mohammad Hosein Sayahi Mansoureh Toosibashi Mehdi Bahmaei Hosein Lijan Leila Ma'Mani Mohammad Mahdavi Saeed Bahadorikhalili Pd@Py2PZ@MSN as a Novel and Efficient Catalyst for C–C Bond Formation Reactions Frontiers in Chemistry palladium catalyst immobilized catalyst mesoporous silica nanoparticles Heck reaction Suziki reaction |
title | Pd@Py2PZ@MSN as a Novel and Efficient Catalyst for C–C Bond Formation Reactions |
title_full | Pd@Py2PZ@MSN as a Novel and Efficient Catalyst for C–C Bond Formation Reactions |
title_fullStr | Pd@Py2PZ@MSN as a Novel and Efficient Catalyst for C–C Bond Formation Reactions |
title_full_unstemmed | Pd@Py2PZ@MSN as a Novel and Efficient Catalyst for C–C Bond Formation Reactions |
title_short | Pd@Py2PZ@MSN as a Novel and Efficient Catalyst for C–C Bond Formation Reactions |
title_sort | pd py2pz msn as a novel and efficient catalyst for c c bond formation reactions |
topic | palladium catalyst immobilized catalyst mesoporous silica nanoparticles Heck reaction Suziki reaction |
url | https://www.frontiersin.org/articles/10.3389/fchem.2022.838294/full |
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