Well-defined palladium N-heterocyclic carbene complexes bearing CF3 moiety: Synthesis, characterization, crystal structure, direct C4-arylation of 3,5-dimethylisoxazole and antioxidant activity
| dc.contributor.author | Kalcik, Aysegul | |
| dc.contributor.author | Kaloglu, Nazan | |
| dc.contributor.author | Keser, Serhat | |
| dc.contributor.author | Sahin, Zarife Sibel | |
| dc.contributor.author | Dusunceli, Serpil Demir | |
| dc.date.accessioned | 2026-04-04T13:34:59Z | |
| dc.date.available | 2026-04-04T13:34:59Z | |
| dc.date.issued | 2026 | |
| dc.department | İnönü Üniversitesi | |
| dc.description.abstract | A series of palladium N-heterocyclic carbene (NHC) complexes including trans-[Pd(NHC)Br2L] (L = C5H5N, 3-ClC5H4N, and N-methylimidazole) and [Pd(NHC)2Br2] have been prepared from {1-(benzyl)-3-(3,5-(bis(tri-fluoromethyl)benzyl)benzimidazolium bromide}. The structures of these new compounds were confirmed by NMR, FT-IR, and elemental analyses. The crystal structures of the dibromo-[1-(benzyl)-3-(3,5-(bis(tri-fluoromethyl)benzyl)benzimidazole-2-ylidene]-(pyridine)-palladium(II) and dibromo-[1-(benzyl)-3-(3,5-(bis (trifluoromethyl)benzyl)benzimidazole-2-ylidene]-(N-methylimidazole)-palladium(II) were determined by single-crystal X-ray diffraction. Palladium complexes were developed as efficient pre-catalysts for direct C4-arylation of 3,5-dimethylisoxazole and aryl bromides. Biological efficiency of trans-[Pd(NHC)Br2L]was evaluated by antioxidant activities like ABTS, OH and DPPH radical scavenging activity assays. | |
| dc.description.sponsorship | Inonue University Research Fund (I.UE.B.A.P.) [FYL-2025-3933, Ibull;..B.A.P] | |
| dc.description.sponsorship | The research is financially supported by the Icenter dotnonu University Research Fund (Icenter dot.U.B.A.P. Project No: FYL-2025-3933) . | |
| dc.identifier.doi | 10.1016/j.jorganchem.2025.123975 | |
| dc.identifier.issn | 0022-328X | |
| dc.identifier.issn | 1872-8561 | |
| dc.identifier.scopus | 2-s2.0-105024237072 | |
| dc.identifier.scopusquality | Q2 | |
| dc.identifier.uri | https://doi.org/10.1016/j.jorganchem.2025.123975 | |
| dc.identifier.uri | https://hdl.handle.net/11616/109521 | |
| dc.identifier.volume | 1045 | |
| dc.identifier.wos | WOS:001640819100001 | |
| dc.identifier.wosquality | Q2 | |
| dc.indekslendigikaynak | Web of Science | |
| dc.indekslendigikaynak | Scopus | |
| dc.language.iso | en | |
| dc.publisher | Elsevier Science Sa | |
| dc.relation.ispartof | Journal of Organometallic Chemistry | |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | |
| dc.rights | info:eu-repo/semantics/closedAccess | |
| dc.snmz | KA_WOS_20250329 | |
| dc.subject | Palladium complex | |
| dc.subject | N -Heterocyclic carbene | |
| dc.subject | Direct C4-arylation | |
| dc.subject | Isoxazole | |
| dc.subject | Antioxidant activity | |
| dc.title | Well-defined palladium N-heterocyclic carbene complexes bearing CF3 moiety: Synthesis, characterization, crystal structure, direct C4-arylation of 3,5-dimethylisoxazole and antioxidant activity | |
| dc.type | Article |











