Dichlorido(3-chloropyridine-N)[1,3-dialkylbenzimidazol-2-ylidene] palladium(II) complexes: Synthesis, characterization and catalytic activity in the arylation reaction
Küçük Resim Yok
Tarih
2015
Yazarlar
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Elsevier Science Sa
Erişim Hakkı
info:eu-repo/semantics/closedAccess
Özet
Six novel Pyridine Enhanced Precatalyst Preparation, Stabilization and Initiation (PEPPSI) themed palladium N-heterocyclic carbene (Pd-NHC) complexes (2a-f) were synthesized in good yields from the reaction of 1,3-dialkylbenzimidazolium salts with PdCl2 in the presence of K2CO3 as base in 3-chloropyridine. These synthesized complexes were characterized by means of elemental analysis, FT-IR, H-1 and C-13 NMR spectroscopic methods. The fully characterized novel complexes (2a-f) were tested as catalysts in the direct arylation of 2-n-propylthiazole, 2-n-butylthiophene and 2-n-butylfuran with different aryl bromides at 130 degrees C for 1 h. The complexes exhibited fairly high catalytic activities under the given conditions. The highest conversions were achieved when complexes 2a, 2e and 2f were used as catalysts in direct arylation. (C) 2015 Elsevier B.V. All rights reserved.
Açıklama
Anahtar Kelimeler
PEPPSI palladium complexes, N-Heterocyclic carbene, Benzimidazole, Catalyst, Direct arylation
Kaynak
Inorganica Chimica Acta
WoS Q Değeri
Q2
Scopus Q Değeri
Q2
Cilt
429
