Palladium PEPPSI complexes: Synthesis and catalytic activity on the Suzuki-Miyaura coupling reactions for aryl bromides at room temperature in aqueous media

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dc.authoridÖzdemir, İsmail/0000-0001-6325-0216
dc.authoridTouj, Nedra/0000-0001-6071-4361
dc.authoridTouj, Nedra/0000-0001-6071-4361
dc.authoridYaşar, Sedat/0000-0001-7285-2761
dc.authoridGurbuz, Nevin/0000-0003-3201-3597
dc.authorwosidÖzdemir, İsmail/ABI-5192-2020
dc.authorwosidTouj, Nedra/AAM-2982-2021
dc.authorwosidTouj, Nedra/G-6828-2019
dc.authorwosidYaşar, Sedat/ABG-8356-2020
dc.authorwosidGurbuz, Nevin/A-3069-2016
dc.contributor.authorTouj, Nedra
dc.contributor.authorGurbuz, Nevin
dc.contributor.authorHamdi, Naceur
dc.contributor.authorYasar, Sedat
dc.contributor.authorOzdemir, Ismail
dc.date.accessioned2024-08-04T20:44:26Z
dc.date.available2024-08-04T20:44:26Z
dc.date.issued2018
dc.departmentİnönü Üniversitesien_US
dc.description.abstractA new series of palladium N-heterocyclic carbene complexes having methoxyethyl on the side chain (3a-d, 4a-e) have been synthesized and fully characterized by NMR, HRMS and IR. Next, the palladium-NHC-PEPPSI complexes 3a-e and 4a-e were used as catalyst in Suzuki-Miyaura coupling reactions were investigated for aryl bromides at room temperature in aqueous media. 3a-d and 4a-e complexes showed good catalytic activity for electron-donating or electron-drawing aryl bromides with arylboronic acid. Complex 4b exhibited higher activity compared to other analogues due to bearing more electronically donating NHC ligands. (C) 2018 Elsevier B.V. All rights reserved.en_US
dc.description.sponsorshipInonu University Research Fund [BAP:2016-195]; Technological and Scientific Research Council of Turkey TUBITAK-MHESRS (Tunisia)en_US
dc.description.sponsorshipThis project was supported by Inonu University Research Fund (BAP:2016-195). We are also grateful to the Technological and Scientific Research Council of Turkey TUBITAK-MHESRS (Tunisia) for the financial support to NedraTouj.en_US
dc.identifier.doi10.1016/j.ica.2018.04.018
dc.identifier.endpage194en_US
dc.identifier.issn0020-1693
dc.identifier.issn1873-3255
dc.identifier.scopus2-s2.0-85045445771en_US
dc.identifier.scopusqualityQ2en_US
dc.identifier.startpage187en_US
dc.identifier.urihttps://doi.org/10.1016/j.ica.2018.04.018
dc.identifier.urihttps://hdl.handle.net/11616/98243
dc.identifier.volume478en_US
dc.identifier.wosWOS:000430989200023en_US
dc.identifier.wosqualityQ2en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.publisherElsevier Science Saen_US
dc.relation.ispartofInorganica Chimica Actaen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectPalladium N-heterocyclic carbene complexen_US
dc.subjectBenzimidazoleen_US
dc.subjectSuzuki-Miyaura cross couplingen_US
dc.subjectC-C bond formationen_US
dc.subjectAqueous mediaen_US
dc.titlePalladium PEPPSI complexes: Synthesis and catalytic activity on the Suzuki-Miyaura coupling reactions for aryl bromides at room temperature in aqueous mediaen_US
dc.typeArticleen_US

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