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  • 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
ZUSAMMENFASSUNG

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.

MATERIALIEN
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Produktbeschreibung

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