Pd-PEPPSI-type expanded ring N-heterocyclic carbene complexes: synthesis, characterization, and catalytic activity in Suzuki-Miyaura cross coupling
dc.authorid | Touj, Nedra/0000-0001-6071-4361 | |
dc.authorwosid | Touj, Nedra/G-6828-2019 | |
dc.contributor.author | Alnasser, Sarah | |
dc.contributor.author | Touj, Nedra | |
dc.contributor.author | Alomar, Suliman | |
dc.contributor.author | Mansour, Lamjed | |
dc.contributor.author | Sauthier, Mathieu | |
dc.contributor.author | Gurbuz, Nevin | |
dc.contributor.author | Ozdemir, Ismail | |
dc.date.accessioned | 2024-08-04T20:56:12Z | |
dc.date.available | 2024-08-04T20:56:12Z | |
dc.date.issued | 2024 | |
dc.department | İnönü Üniversitesi | en_US |
dc.description.abstract | In this work, we synthesized a series of six unsymmetrical benzimidazolium salts 2 and their pyridine-enhanced precatalyst preparation stabilization and initiation (PEPPSI)-themed palladium N-heterocyclic carbene complexes [PdCl2(NHC)(Py)]. All the products were isolated in satisfactory yields (75-85%). The synthesis of these novel palladium PEPPSI complexes involved in reacting NHC precursors with PdCl2 in pyridine at 60 degrees C in the presence of excess K2CO3. The structures of all compounds have been characterized by H-1 NMR, C-13 NMR, HRMS and IR spectroscopy, as well as elemental analysis techniques, which support the proposed structures. The catalytic activity of the six complexes was assessed in the Suzuki-Miyaura cross-coupling of phenylboronic acid and aryl halides. The reactions required only a low catalyst loading (0.1 mol%) and were carried out under mild aerobic conditions in a green, water-based solvent mixture. | en_US |
dc.description.sponsorship | King Saud University, Riyadh, Saudi Arabia [RSP2024R75] | en_US |
dc.description.sponsorship | The authors extended their appreciation to the Researchers Supporting Project number (RSP2024R75), King Saud University, Riyadh, Saudi Arabia. | en_US |
dc.identifier.doi | 10.1080/17518253.2024.2370268 | |
dc.identifier.issn | 1751-8253 | |
dc.identifier.issn | 1751-7192 | |
dc.identifier.issue | 1 | en_US |
dc.identifier.scopus | 2-s2.0-85197716855 | en_US |
dc.identifier.scopusquality | Q1 | en_US |
dc.identifier.uri | https://doi.org/10.1080/17518253.2024.2370268 | |
dc.identifier.uri | https://hdl.handle.net/11616/102100 | |
dc.identifier.volume | 17 | en_US |
dc.identifier.wos | WOS:001263270600001 | en_US |
dc.identifier.wosquality | N/A | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.language.iso | en | en_US |
dc.publisher | Taylor & Francis Ltd | en_US |
dc.relation.ispartof | Green Chemistry Letters and Reviews | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Palladium N-heterocyclic carben complex | en_US |
dc.subject | benzimidazole | en_US |
dc.subject | Suzuki-Miyaura cross coupling | en_US |
dc.subject | C-C bond formation | en_US |
dc.subject | water | en_US |
dc.title | Pd-PEPPSI-type expanded ring N-heterocyclic carbene complexes: synthesis, characterization, and catalytic activity in Suzuki-Miyaura cross coupling | en_US |
dc.type | Article | en_US |