Catalytic activities in the direct C5 arylation of novel palladium N-heterocyclic carbene complexes containing benzimidazol-2-ylidene nucleus

AKKOÇ S., GÖK Y., AKKURT M., Tahir M. N.

INORGANICA CHIMICA ACTA, vol.413, pp.221-230, 2014 (SCI-Expanded) identifier identifier

  • Publication Type: Article / Article
  • Volume: 413
  • Publication Date: 2014
  • Doi Number: 10.1016/j.ica.2014.01.015
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.221-230
  • Erciyes University Affiliated: Yes


New palladium N-heterocyclic carbene (NHC) complexes (1a-e) were synthesized in very good yields by the reaction of 1-phenyl-3-alkylbenzimidazolium salts with Pd(OAc)(2) in dimethyl sulfoxide. These synthesized complexes were fully characterized using elemental analyses, FT-IR, H-1 NMR, C-13 NMR and LC-MS (for 1a, 1c and 1e) spectroscopy data. Also, the molecular structure of the bis[1-phenyl-3-(2methyl-1,4-benzodioxane)benzimidazol-2-ylidene] dibromopalladium(II) complex (1d) was structurally characterized by single crystal X-ray diffraction study. The new Pd-II complexes (1a-e) were tested as catalysts in the direct C5 arylation of 2-n-butylfuran, 2-n-butylthiophene and 2-n-propylthiazole with various aryl bromides at 130 degrees C for 1 h. Also, some experiments were carried out by using aryl chlorides in order to be used for comparison. The results are reported herein. These complexes exhibited quite high catalytic activities under the given conditions. (C) 2014 Elsevier B.V. All rights reserved.