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Palladium Complexes of C2-, C3-, and C4-Bridged Bis(phospholyl) Ligands:  Remarkably Active Catalysts for the Copolymerization of Ethylene and Carbon Monoxide

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posted on 06.08.1999 by Simon Doherty, Graham R. Eastham, Robert P. Tooze, Tom H. Scanlan, Dilys Williams, Mark R. J. Elsegood, William Clegg
The C2-, C3-, and C4-bridged bis(2,3,4,5-tetramethylphospholes) (1a, X = C2H4; 1b, X = C3H6; 1c, X = (CH2)2C6H4) and their corresponding palladium complexes [(P-P)PdCl2] (2ac) have been prepared and characterized. A single-crystal X-ray analysis of [{bis(2,3,4,5-tetramethylphospholyl)-o-xylene}PdCl2] (2c) reveals that 1c forms a seven-membered chelate; the phosphole rings are oriented perpendicular to the PdP2Cl2 plane. Methanol solutions of [(P-P)Pd(OAc)2] (3a, P-P = 1b; 3b, P-P = 1c) and methanesulfonic acid are active for the copolymerization of ethylene and carbon monoxide, generating high-molecular-weight polymers with narrow molecular weight distributions. Under our conditions, the activity of catalyst systems containing 1c is comparable to that based on bis(diphenylphosphino)propane (dppp).

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