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Diarylethene Molecular Photoswitches. Masahiro IrieЧитать онлайн книгу.

Diarylethene Molecular Photoswitches - Masahiro Irie


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and six‐membered rings [30]. The 1,2‐bis(2‐methyl‐1‐benzothiophen‐3‐yl)perfluorocycloalkenes underwent reversible photoinduced cyclization/cycloreversion reactions in polar methanol and acetonitrile. Among the three derivatives having four‐, five‐, and six‐membered rings, five‐membered 1,2‐bis(2‐methyl‐1‐benzothiophen‐3‐yl)perfluorocyclopentene was found to offer the highest resistance to photofatigue. Since then, perfluorocyclopentene derivatives have been mainly studied.

Chemical reaction depicts the development of diarylethene molecular photoswitches.

      Although diarylethene photoswitches exhibit brilliant color changes upon photoirradiation, most of them are nonfluorescent or very weakly fluorescent in both isomer forms. It was a long‐standing ambition to prepare photoswitchable fluorescent diarylethenes without attaching fluorescent chromophores to the diarylethenes. In 2011, sulfone derivatives of 1,2‐bis(2‐ethyl‐6‐aryl‐1‐benzothiophen‐3‐yl)perfluorocyclopentene were found to exhibit very strong fluorescence (fluorescence quantum yield ∼ 0.9) in the closed‐ring isomers [31]. The turn‐on mode fluorescent diarylethenes are now extensively applied to super‐resolution fluorescence microscopy in materials science and biological systems. Diarylethenes are able to switch both absorption (color) and fluorescence emission upon photoirradiation.

Color changes of diarylethene derivatives 1-7 in toluene upon irradiation with UV and visible light. Chemical structures and absorption spectra of open- and closed-ring isomers of (a) 3 and (b) 1 in n-hexane.

      Figures 1.7 shows the chemical structures of the open‐ and the closed‐ring isomers and their absorption spectra. In both derivatives 3 and 1, upon irradiation with appropriate wavelength of light (λ1 or λ3) a single bond is formed between the central reactive carbon atoms and the double bonds change the position. Upon irradiation with another wavelength of light (λ2 or λ4) the single bond is broken and the molecule returns to the initial structure. The color is controlled by the length of π‐conjugation. In the open‐ring isomers, two thiophene rings have no particular interaction and the spectra are comparable to substituted thiophenes. In the closed‐ring isomers, the π‐conjugation length depends on the attached position of thiophene rings to the ethene bridge. When the thiophene rings are attached to the ethene bridge at 3‐position, such as derivative 3, π‐conjugation is delocalized throughout the molecule in the closed‐ring isomer and the delocalization results in red color. The π‐conjugation is further extended when phenyl groups are substituted at 5‐ and 5′‐positions of the thiophene rings, such as 5. The long π‐conjugation shifts the absorption band to longer wavelengths, resulting in blue color. On the other hand, when the thiophene rings are attached to the ethene bridge at 2‐position, such as derivative 1, π‐conjugation is localized in the central part. The short π‐conjugation results in yellow color in the closed‐ring isomer.

      Digital on/off photoswitching between two discrete states was confirmed by measuring the switching response at a single‐molecule level. Figure 1.8c shows the fluorescence photoswitching of a single molecule of derivative 8 upon alternate irradiation with UV and visible light. Upon irradiation with UV light, the fluorescence abruptly switches from the off‐state to the on‐state, while upon irradiation with visible light the on‐state abruptly returns to the off‐state. The digital photoswitching response definitely indicates that diarylethene photoswitch 8 has bistable states. The photoisomerization between two discrete isomer states expressed by the


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