Abstract

Reaction of equimolar amounts of μ-1–3-η:6–8-η-octadienatobis(1,1,1,5,5,5-hexafluoroacetylacetonatopalladium) and triisopropylphosphine gives a bimetallic octadienyl-bridged complex, in which one palladium atom is η 1 -bound to the terminal carbon of the octadienyl chain. Insertion of CO 2 into this PdC bond gives a carboxylate complex; acidic decomposition and hydrogenation of the carboxylate complex gives pelargonic acid. The results are discussed in relation to the mechanism of the palladium-catalyzed reaction between butadiene and carbon dioxide.

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