Syntheses and Structures of Bulky Monophosphine-Ligated Methylpalladium Complexes:  Application to Homo- and Copolymerization of Norbornene and/or Methoxycarbonylnorbornene

• Published in: Organometallics 2006-09, Vol.25 (19), p.4588-4595
• Main Authors: Yamashita, Makoto, Takamiya, Ikuko, Jin, Koichiro, Nozaki, Kyoko
• Format: Article
• Language: English
• ISSN: 0276-7333; 1520-6041
• DOI: 10.1021/om060347w

Several new bulky monophosphine-ligated methylpalladium complexes were synthesized. Treatment of Pd(cod)MeCl (cod = cyclooctadiene) with bulky phosphines, P t Bu3, or P(o-tol)3 afforded monophosphine-ligated methylpalladium chloride complexes 1a and 1b, which were isolated as crystalline solids in excellent yields. The structures depended on the shape of the ligand:  a mononuclear three-coordinate structure for 1a and a chloride-bridged dinuclear structure for 1b. Absorption of chloride from methylpalladium chloride complexes 1a and 1b afforded the corresponding methylpalladium triflate complexes 2a and 2b, which were structurally characterized by NMR spectroscopy and X-ray crystallography. In the presence of NaB[3,5-(CF3)2C6H3]4, 1a and 1b catalyzed the addition homopolymerization of norbornene or methoxycarbonylnorbornene. The activity of the catalyst was found to be dependent on the structure of the complexes and the counteranions. The catalyst system 1a-NaB[3,5-(CF3)2C6H3]4 was also active for the copolymerization of norbornene and methoxycarbonylnorbornene to form a block-type copolymer. The obtained copolymer has the highest ester content probably due to the two vacant sites on the palladium. The molecular weight distribution reached the narrowest value, indicating the long lifetime of the catalyst.