The reaction of the palladium chloroallyl dimer [Pd(mu-Cl)(eta(3)-C3H5)](2)
, 1, with 2 equiv of the sodium salt of 2,6-di-tert-butyl-4-methylphenol (N
aOAr) gives a thermally unstable, aryloxide-bridged binuclear allyl complex
[Pd(mu-OAr)(eta(3)-C3H5)](2). In contrast, 2, the nickel analogue of 1, fu
rnishes an unusual mononuclear allyl derivative, 4, which contains a pi,eta
(5)-aryloxide ligand. Larger amounts of the sodium aryloxide react with 1 o
r 2, affording binuclear "ate" complexes containing both sigma,mu- and pi,e
ta(5)-aryloxide ligands.