A series of binuclear homo- and heterobimetallic complexes of the general type (PNP)M-[linker]-M(PNP) have been prepared (M = Ni, Pd, Pt; PNP = a diarylamido/ bis(phosphine) pincer ligand; -[linker]- = -C C-, -C CC C-, -C CC6H4C C-). Each (PNP)M site can be oxidized by one electron, and this work reports the investigation of the mixed-valence behavior in terms of the communication between the two redox sites and the degree of the delocalization in the monooxidized cation. The compounds were evaluated using cyclic voltammetry, UV-vis-NIR and EPR spectroscopy, X-ray crystallography, and DFT calculations. The complex with the longest examined linker, (PNP)Ni-C CC6H4C C-Ni(PNP) (9Ni), exhibited no discernible communication between the redox sites. The homobimetallic complexes (PNP)M-C CC C-M(PNP) (6M) displayed a lower degree of communication in comparison to the -C C- linker analogues (PNP)M-C C-M(PNP) (3M). Within each of these two subsets, the relative degree of communication and delocalization was determined to be Pd < Ni <= Pt. On the Robin-Day scale, compounds 6M can be assigned class I for M = Pd and class II for M = Ni, Pt. Complex 3Pd also falls into class II, while 3Ni and 3Pt may be viewed as borderline class II/III cases. It is likely that the communication in the Ni systems has the advantage of the smaller size of Ni, resulting in a greater physical proximity of the redox sites, while the Sd metal Pt possesses the greatest ability for orbital interaction with the -C C- linker.