Dinuclear, divalent acetylacetonato (acac) complexes of the type [M( acac) {mu- C6H2(chemical anion NR)(4)} M( acac)] ( M = Ni, Pd) have been prepared by the reaction of the corresponding bis( acac) metal precursor with 2,5-diamino-1,4-benzoquinonediimines C6H2(NHR)(2)(=NR)(2) (4a, R = CH2-t-Bu; 4b, R = CH2Ph; 4c, R = Ph), which are metalated and become bridging ligands, also like in the complex [(C8H11) Pt {mu- C6H2(chemical anionNCH(2)-t-Bu)(4)} Pt(C8H11)] ( 6) obtained by the reaction of 4a with [PtCl2(COD)]. The complexes were fully characterized, including by X-ray diffraction for [Ni(acac) {mu-C6H2(chemical anion NCH2Ph)(4)} Ni( acac)] (9b) and [Pd(acac) {mu-C6H2(chemical anion NCH2- t- Bu)(4)} Pd(acac)] (10a). The coordination geometry around the metal ions is square-planar, and a complete electronic delocalization of the quinonoid pi system occurs between the metal centers over the two N chemical anion C chemical anion C chemical anion C chemical anion N halves of the ligand. The nature of the N substituent explains the differences between the supramolecular stacking arrangements found for [Ni( acac) {mu-C6H2(chemical anion NR)(4)} Ni(acac)] (9a; R = CH2-t-Bu; 9b, R = CH2Ph). The Ni complexes were evaluated as catalyst precursors for ethylene oligomerization in the presence of AlEtCl2 or MAO as the cocatalyst, in particular in order to study possible cooperative effects resulting from electronic communication between the metal centers and to examine the influence of the N substituent on the activity and selectivity. These catalysts afforded mostly ethylene dimers and trimers.