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The synthesis, characterization, and catalytic properties of ($\kappa ^{2}-C,N)$-palladacycles with N-heterocyclic carbene-based ancillary ligands
Author(s) -
M. Emın Günay,
Gülcan GENÇAY ÇOĞAŞLIOĞLU,
Rukiye Fırıncı
Publication year - 2015
Publication title -
turkish journal of chemistry
Language(s) - English
Resource type - Journals
eISSN - 1303-6130
pISSN - 1300-0527
DOI - 10.3906/kim-1507-90
Subject(s) - chemistry , carbene , catalysis , dimer , aryl , medicinal chemistry , nuclear magnetic resonance spectroscopy , elemental analysis , proton nmr , stereochemistry , organic chemistry , alkyl
Novel five-membered ($\kappa ^{2}-C,N)$-palladacyclic complexes were prepared from the reaction of the corresponding acetate-bridged palladacycle dimer with N-heterocyclic carbene (NHC) ligands in high yields. Palladacyclic complexes (\textbf{3}) were fully characterized by elemental analysis and $^{1}$H and $^{13}$C NMR spectroscopy. Palladacyclic complexes were tested as catalyst for the C--C bond forming reaction. These complexes were found to be efficient catalysts for the Suzuki--Miyaura reaction of aryl bromides.

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