Oxidative dinuclear addition of a PdI-PdI moiety to arenes: generation of μ-η3:η3-arene-Pd(II)2 species.

J Am Chem Soc

Department of Applied Chemistry, Graduate School of Engineering, Osaka University, Suita, Osaka, Japan.

Published: September 2011

We report the oxidative dinuclear addition of a Pd(I)-Pd(I) bond to arenes. The oxidative dinuclear addition products, which have a bi-π-allyl-type arene dipalladium(II) structure, were obtained from [2.2]paracyclophane, anthracene, tetracene, and pentacene. A systematic study of the reaction of [Pd(2)(CH(3)CN)(6)][BF(4)](2) with benzene and polyacenes showed that the larger polyacenes, tetracene and pentacene, afforded the oxidative dinuclear addition products, while benzene, naphthalene, and anthracene gave the π-sandwich Pd(I)-Pd(I) complexes.

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http://dx.doi.org/10.1021/ja206076uDOI Listing

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