Abstract

Light-harvesting subphthalocyanine–ferrocenophane (SubPc–Fc; 1) and subphthalocyanine–naphthalenediimide (SubPc–NDI; 2) dyads have been synthesized, characterized, and probed by femtosecond laser photolysis. In dyads 1 and 2, both the electron-donating ferrocenophane and the electron-accepting naphthalenediimide are axially linked with the functional O–Ph groups (at the para position) in the axial positions of SubPc. Electrochemical data show that the SubPcs can act as both electron donors and electron acceptors. The geometric and electronic structures of dyads 1 and 2 were calculated by ab initio B3LYP/6-311G methods. The optimized structures showed that the Fc and NDI entities are separated from SubPc by 8.32 A (for dyad 1) and 8.85 A (For dyad 2). The distribution of HOMOs and LUMOs suggests the formation of SubPc•––Fc+ and SubPc•+–NDI•– as charge-separated states for dyads 1 and 2, respectively. Upon photoexcitation of the subphthalocyanine unit, these arrays undergo photoinduced electron transfer to ...

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