The subporphyrazine (SubPz) dimer diboron(III) [μ‐1′,4′‐benzenediolato][bis‐(1,2,6,7,11,12‐hexapropylsubporphyrazinato)] (2) and trimer triboron(III)[μ‐1′,3′,5′‐benzenetriolato][tris‐(1,2,6,7,11,12‐hexapropylsubporphyrazinato)] (4), consisting of SubPz units assembled through their axial positions by hydroquinone‐ and phloroglucinol‐linkers, respectively, have been prepared. Selective ruthenium‐π‐coordination to the linking aromatic rings afforded SubPz arrays 8 and 9, respectively. These latter systems displayed different degrees of electronic communication between the macrocycles relative to 2 and 4 as inferred from analyses of the ground‐ and excited‐state features. For instance, as revealed by time‐resolved pump probe transient absorption spectroscopy, the excited singlet states of dimer 2 and trimer 4 undergo rather rapid deactivation. In contrast, the presence of a ruthenoarene linker, as in 8 and 9, serves to increase the SubPz singlet excited state lifetimes; these now reach values similar to those seen in the case of monomeric SubPz compounds that either do or do not contain ruthenoarene subunits (i.e., 7 and 6, respectively). These findings are ascribed to the redox active nature of the hydroquinone and phloroglucinol linkers in 2 and 4 and a change in the electronics that results from organometallic functionalization.