Background: Diarylethenes are well-known photochromic compounds, which undergo cyclization and cycloreversion reactions between open- and closed-ring isomers. Recently, diarylethene derivatives with photoswitchable fluorescent properties were prepared. They are applicable for imaging and bio-imaging. On the other hand, new system called “excited state intramolecular proton transfer (ESIPT)” is reported. In the system, absorption and emission bands are divided due to the proton transfer, hence it showed strong fluorescence even in the crystalline state. We aimed to construct the photochromic system incorporating the ESIPT mechanism.
Results: A diarylethene incorporating a fluorescent moiety that exhibit excited state intramolecular proton transfer (ESIPT) behavior was prepared. The ESIPT is one of the examples which express the mechanisms of aggregation-induced emission (AIE). This compound emits orange fluorescence with a large Stokes shift derived from ESIPT in aprotic solvents such as THF or hexane, while it exhibits only photochromic reaction in protic solvents such as methanol. In addition, it shows turn-off type fluorescence switching in an aprotic solvent and in crystals. The fluorescence is quenched as content of closed-ring isomers increases upon UV light irradiation.
Conclusions: A diarylethene containing ESIPT functional group was prepared. It showed fluorescent turn-off behavior during photochromism in aprotic solvents as well as crystalline state upon UV light irradiation. Furthermore, it showed AIE in THF/water mixtures with blue-shift of the emission.
Keywords: diarylethene; fluorescent switching; turn-off fluorescence; AIE; ESIPT
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When a peer-reviewed version of this preprint is available in the Beilstein Journals, this information will be updated in the information box above. If no peer-reviewed version is available, please cite this preprint using the following information:
Kono, L.; Nakagawa, Y.; Fujimoto, A.; Nishimura, R.; Hattori, Y.; Mutai, T.; Yasuda, N.; Koizumi, K.; Yokojima, S.; Nakamura, S.; Uchida, K. Beilstein Arch. 2019, 201966. doi:10.3762/bxiv.2019.66.v1
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