Abstract

Perylenebisimide (PBI)–phenothiazine (PTZ) and PBI–diphenylamine (DPA) dyads were prepared, with the PTZ or DPA as the electron donor and the 6-subsituted PBI unit as the electron acceptor. The dyads were designed in such a way that electronic coupling (magnitude is the matrix elements, VDA and VDA*) between the electron donor and acceptor is controlled by conformation restriction. The effects of the electronic coupling on UV–Vis absorption and emission were studied. More significant charge-transfer (CT) absorption and CT fluorescence emission bands were observed for dyads with smaller dihedral angles between the electron donor and acceptor, thus stronger electronic coupling (VDA = 3290 cm–1 and VDA* = 4317 cm–1) was observed than those with larger dihedral angle, showing weaker coupling effect (VDA = 1210 cm–1 and VDA* = 2770 cm–1). Triplet state production was observed only for PBI–DPA but not for PBI–PTZ dyads. With an intermolecular triplet photosensitizing method, the triplet state of PBI–PTZ dyads w...

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