
Journal of Organometallic Chemistry p. 253 - 264 (1987)
Update date:2022-08-17
Topics:
Ozawa, Fumiyuki
Hidaka, Takahiro
Yamamoto, Takakazu
Yamamoto, Akio
The mechanism of reaction of trans-PdAr2L2 (Ar = m-tolyl or phenyl, L = PEt2Ph) with aryl iodides affording biaryls has been studied.The rate of reaction is independent of the concentration of aryl iodide but is significantly accelerated by the presence of trans-PdAr(I)L2.Cross-over experiments on the reaction of diarylpalladium complexes with monoarylpalladium iodides reveals the occurrence of two types of intermolecular processes between the diaryl and monoaryl complexes.The first process results in a scrambling of aryl groups between the diaryl and monoaryl complexes without formation of biaryls, while the second yields the reductive elimination products, biaryls.
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