Dinickel(II) and dicopper(II) porphyrin dimers have been constructed in which two metalloporphyrin units are widely separated by a long unconjugated dipyrrole bridge. Two macrocycles are aligned somewhat orthogonally to each other, while oxidation of the bridge generates a fully π-conjugated butterfly-like structure, which, in turn, upon stepwise oxidations by stronger oxidants result in the formation of the corresponding one- and two-electron-oxidized species exhibiting unusual long-range charge/radical delocalization to produce intense absorptions in the near-infrared (NIR) region and electron paramagnetic resonance (EPR) signals of a triplet state due to interaction between the unpaired spins on the Cu(II) ions. Although the two metal centers have a large physical separation through the bridge (more than 16 Å), they share electrons efficiently between them, behaving as a single unit rather than two independent centers. Detailed UV-vis-NIR, electrospray ionization mass spectrometry, IR, variable-temperature magnetic study, and EPR spectroscopic investigations along with X-ray structure determination of unconjugated, conjugated, and one electron-oxidized complexes have been exploited to demonstrate the long-range electronic communication through the bridge. The experimental observations are also supported by density functional theory (DFT) and time-dependent DFT calculations. The present study highlights the crucial roles played by a redox-active bridge and metal in controlling the long-range electronic communication.