• Macromolecular Research
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• v.13 no.4
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• pp.321-326
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• 2005

Photochromic diarylethene polymers (DPs) in which 1,2-bis(2-methylbenzo[b ]thiophene-3-yl)hexafluorocyclopentene (BTF6) were covalently grafted onto the polymer main chain as pendant photochromic units were newly synthesized and their photochromic properties were investigated using steady-state and picosecond timeresolved spectroscopies. Polysiloxanes substituted with BTF6 molecules were prepared by sol-gel process using a mixture of tetraethoxysilane (TEOS), a silylated BTF6, and an organically modified silane precursor in the presence of HCl. The polysiloxane film (DP1) prepared from $\omega-methoxy$ poly(ethylene glycol) 3-(triethoxysilyl) propylcarbainate (MPGSC) as the silane precursor showed a much lower glass transition temperature than that (DP2) from heptadecafluorodecyltrimethoxysilane (HDFTMS). The ring-closure quantum yields of DP1 and DP2 were determined to be 0.20 and 0.02, respectively. Such a large difference in the quantum yield was attributed to the polymer matrix environment of the free inner volume.

• Bulletin of the Korean Chemical Society
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• v.29 no.4
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• pp.827-832
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• 2008

A new diarylethene compound with donor and acceptor substituent was synthesized from 2,3-bis(2-methylbenzo[b]thiophene-3-yl)hexafluorocyclopentene (BTF) over 5 steps. The donor-acceptor structured BTF compound (TBTFE) showed spectral change to a longer wavelength through photochromism with a high cyclization quantum yield (0.56). The 3,4-ethylenedioxythiophene (T) and carboethoxy (E) groups directly connected to BTF unit promoted electrical change accompanied with the photoisomerization of the BTF unit. Photo-induced electrical switching was achieved from a photocell containing TBTFE doped polymer film, which showed reversible and stable current change over repeated cycles by the alternative UV/Vis irradiation, as estimated by the I-V plot.

• ETRI Journal
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• v.25 no.4
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• pp.253-257
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• 2003

This study investigated the photochromic properties and characterization of acetyl-substituted diarylethene (DAMBTF6)-doped fluoroacrylates media for holographic storage. For the rewritable holographic recording media, we prepared photochromic polymer films using an acrylate matrix by simple photocuring methods. Switching light sources from a visible (532 nm) to an ultraviolet (365 nm) produced transparent films that changed from pale yellow to red. Holographic recording was performed on the photochromic films by two interfering collimated plane wave beams. Excitation with a visible or ultraviolet light completely erased the records, and the film was rewritable either by 532 nm laser or by 325 nm laser within 2 seconds. Images were recorded onto a pixelated spatial light modulator with rectangular pixel apertures and reconstructed on the photochromic films to show recovery of the original images with high resolution.

• Korean Journal of Optics and Photonics
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• v.15 no.2
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• pp.109-113
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• 2004

We have manufactured and characterized the fiber-to-Planar Waveguide Coupler for analysis of the photo-induced refractive index change of DM-BTE .(l,2-bis[2,5-dimethylthio-phen-3-yl]-hexafluorocyclopentene) When irradiated with ultraviolet light, the colorless diarylethene(DM-BTE)-crystal turned red while keeping the crystal shape. The red color was bleached by irradiation with visible light(λ＞450 nm). The resonant wavelength was shifted and recovered owing to the refractive index variation of the planar waveguide because of its photo-functional properties on exposure to UV and visible light. The wavelength responses of this switch by UV exposure were measured as 0.057 nm/sec with saturation time of 60 seconds. and when illuminated by visible light, resonance wavelength variations were measured as 0.028 nm/sec, with recovery time of 140 seconds.