Skip to Content
Merck
  • P-chiral phosphine-sulfonate/palladium-catalyzed asymmetric copolymerization of vinyl acetate with carbon monoxide.

P-chiral phosphine-sulfonate/palladium-catalyzed asymmetric copolymerization of vinyl acetate with carbon monoxide.

Journal of the American Chemical Society (2012-07-25)
Akifumi Nakamura, Takeharu Kageyama, Hiroki Goto, Brad P Carrow, Shingo Ito, Kyoko Nozaki
ABSTRACT

Utilization of palladium catalysts bearing a P-chiral phosphine-sulfonate ligand enabled asymmetric copolymerization of vinyl acetate with carbon monoxide. The obtained γ-polyketones have head-to-tail and isotactic polymer structures. The origin of the regio- and stereoregularities was elucidated by stoichiometric reactions of acylpalladium complexes with vinyl acetate. The present report for the first time demonstrates successful asymmetric coordination-insertion (co)polymerization of vinyl acetate.

MATERIALS
Product Number
Brand
Product Description

Supelco
Vinyl acetate solution, certified reference material, 5000 μg/mL in acetonitrile
Sigma-Aldrich
Vinyl acetate, CP
Supelco
Vinyl acetate, analytical standard
Sigma-Aldrich
Vinyl acetate, contains 3-20 ppm hydroquinone as inhibitor, ≥99%
Vinyl acetate, European Pharmacopoeia (EP) Reference Standard