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note
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Moreover, the transient absorptions of a solution containing LMWG 1 (1.0 mM) and compound 2 (1.0 mM) in toluene were measured. Fig. S3 displays the differential absorption spectra after excitation at 440 nm with femtosecond laser, and the decay of the absorption at 683 nm with time. The absorption centered at 620 nm appears instantaneously after photoexcitation, but it decays rather quickly. At time delay of 16.4 ps, a new absorption around 683 nm emerges, and it can be still detected even with time delay of 60 ps. According to previous reports (ref. 47c), the absorptions around 620 nm and 683 nm can be ascribed to the excited state of exTTF unit and the radical cation of exTTF unit, respectively. Therefore, the detection of the absorption at 683 nm (albeit weak) may indicate the generation of the radical cation of exTTF unit in the solution of LMWG 1 and compound 2 after photoexcitation, which should be due to the intermolecular photoinduced electron transfer between LMWG 1 and compound 2.
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