Cationic palladacycles as catalyst precursors for phenyl acetylene polymerization
Artikel i vetenskaplig tidskrift, 2011
Novel cationic palladacycles based on benzylidene-2,6-diisopropylphenylimines were prepared via C-H activation using Pd(CH(3)CN)(2)Cl(2) as metal precursor. The complexes were fully characterized by IR and NMR spectroscopy, mass spectrometry and elemental analysis. The cationic palladacycles were found to be active catalysts for the polymerization of phenylacetylene producing largely trans-cisoidal PPA.
Phenyl acetylene polymerization
metalation reactions
cyclopalladated compounds
Benzylidene-amines complexes
Cationic palladacycles
phenylacetylene
palladium(ii)
zwitterionic rhodium(i) complex
x-ray
living
Polyphenylacetylene
n-benzylideneamines
molecular-structure
polymerization
ray crystal-structure
Författare
N. Mungwe
University of the Western Cape
A. J. Swarts
Universiteit Stellenbosch
S. F. Mapolie
Universiteit Stellenbosch
Gunnar Westman
Chalmers, Kemi- och bioteknik, Organisk kemi
Journal of Organometallic Chemistry
0022-328X (ISSN)
Vol. 696 22 3527-3535Ämneskategorier
Kemi
DOI
10.1016/j.jorganchem.2011.07.044