A series of chemically converted graphenes (CCGs) covalently functionalized with multiple zincporphyrins (ZnPs) through tuned lengths of linear oligo-p-phenylene bridges (ZnP-ph n -CCG, n = 1−5) were prepared to address the bridge length effect on their photodynamics. Irrespective of the bridge length, photoexcitation of ZnP-ph n -CCG led to exclusive formation of an exciplex state, which rapidly decayed to the ground state without yielding the completely charge-separated state. The notable dependence of the exciplex lifetime as a function of separation distance between the porphyrin and CCG has been observed for the first time, supporting the hypothesis that the decay to the ground state is dominated by the through-space interaction rather than the through-bond one. The basic information on the interaction between ZnP and CCG in the excited state will provide us with deeper insight on the intrinsic nature of the exciplex state as a function of donor− acceptor interaction.

Exclusive photoinduced energy transfer and switching of its direction by rectangular π-extension of nanographene were achieved in porphyrin–nanographene linked systems.