PEPPSI-type N-heterocyclic carbene palladium(II) complexes as catalysts in the direct C5 arylation of furan and thiophene
Yükleniyor...
Tarih
2025
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Elsevier b.v.
Erişim Hakkı
info:eu-repo/semantics/closedAccess
Özet
In this study, a series of amine-functionalized benzimidazolium salts and their PEPPSI-type N-heterocyclic carbene (NHC) palladium(II) complexes 3a-e were synthesized and characterized by FT-IR, 1H NMR and 13C NMR spectroscopy, elemental analysis, and mass spectrometry. The molecular and crystal structure of 3c and 3d was confirmed by the single-crystal X-ray diffraction (SC-XRD) method. Structural analysis reveals that the geometries of the PdII centers of the complexes adopt slightly distorted square planar environment. The new palladium complexes were tested as catalysts in the direct C5 arylation of 2-acetylfuran and 2-acetylthiophene with aryl bromides at 120 degrees C in N,N-dimethylacetamide. The arylation reactions proceeded selectively at the C5 position of the heteroaromatic compounds, and the corresponding coupling products were obtained in moderate to good yields by using 1 mol% of the palladium complex. Also, solid computational validation of the experimental results was achieved by geometric optimizations, frontier molecular orbital and molecular electrostatic potential studies, as well as natural bonding orbital analysis utilizing density functional theory.
Açıklama
Anahtar Kelimeler
Arylation, DFT, Furan and Thiophene, N-Heterocyclic Carbene, Palladium, PEPPSI Complexes
Kaynak
Inorganica chimica acta
WoS Q Değeri
Q2
Scopus Q Değeri
Q2
Cilt
580
Sayı
Künye
Atakol, A., Yiğit, B., Akdan, H., Evren, E., Celepci, D. B., Yiğit, M., ... & Özdemir, İ. (2025). PEPPSI-type N-heterocyclic carbene palladium (II) complexes as catalysts in the direct C5 arylation of furan and thiophene. Inorganica Chimica Acta, 122612.
