Tetra(β-phenothiazinyl) zinc phthalocyanine: An easily prepared D 4–A system for efficient photoinduced electron transfer

Abstract

Four identical electron donor (D) moieties, phenothiazines (PTZs), were covalently attached onto the same acceptor (A), zinc phthalocyanine (ZnPc), to form ZnPc(β-PTZ) 4, i.e. D 4–A. The symmetrical D 4–A was synthesized by the condensation method to examine intra-molecular photoinduced electron transfer (PET). The common electron donor-spacer–acceptor (D–A) photosynthetic models, which involve the asymmetrical synthesis of a mono-substituted porphyrin or its analogs, suffer from a low yield and arduous isolation, since D–A is only one of several products (D n –A or A n –D, n = 0, 2–4). The D 4–A preparation, however, can be carried out without the problem. The steady state and time-resolved fluorescence of the D 4–A were measured and compared with that of ZnPc(β-R) 4 (R = H, OPh). The result showed that the excited singlet state of phthalocyanine moiety in the D 4–A molecule was efficiently quenched by phenothiazine units owing to intra-molecular PET. The rate constant of PET ( k et) was calculated and the value is much higher than the rate constant of fluorescence emission, intersystem crossing and internal conversion of ZnPc moiety. The laser flash photolysis study revealed the presence of a long-lived charge-separated state due to PET. The results suggest that a D 4–A system can be a more efficient artificial photosynthetic model than D–A towards the practical commercial use.