Phototunable Polychromatic Luster in Microcrystalline Film Using Photocyclization-Cycloreversion and Photochemical Side Reactions of Diarylethene

We report a phototunable polychromatic luster material based on photocyclization-cycloreversion and photochemical side reactions of diarylethene. Through recrystallization, the open-ring isomers formed plate-like microcrystals, which were then laminated to form a film. The silver-colored textured film was produced through a combination of the absence of absorption in the visible light region of diarylethene and specular reflection from the surface of the stacked microcrystals. This film showed a change in color to navy blue due to the generation of closed-ring isomers by the photocyclization of diarylethene upon UV light irradiation. The film reverted to its original color upon visible light irradiation due to the photocycloreversion reaction of the diarylethene. Further UV light irradiation of the navy blue film produced reddish-purple photounresponsive fused-ring isomers by a photochemical side reaction. Accordingly, a phototunable polychromatic luster film was achieved by light manipulation of open-, closed-, and fused-ring isomers of diarylethene.

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Publication Details

Journal
Crystal Growth & Design
Published
2025-04-05
DOI
https://doi.org/10.1021/acs.cgd.4c01546
Primary Topic
Photochromic and Fluorescence Chemistry
Type
article
Field-Weighted Citation Impact
0.00

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article

Phototunable Polychromatic Luster in Microcrystalline Film Using Photocyclization-Cycloreversion and Photochemical Side Reactions of Diarylethene

Satoshi Yokojima, Ryo Nishimura, Kingo Uchida, Shinichiro Nakamura et al.
Crystal Growth & Design
Photochromic and Fluorescence Chemistry
article

Phototunable Polychromatic Luster in Microcrystalline Film Using Photocyclization-Cycloreversion and Photochemical Side Reactions of Diarylethene

Satoshi Yokojima, Ryo Nishimura, Kingo Uchida, Shinichiro Nakamura, Masakazu Morimoto, Yuma Nakagawa, Ryotaro Shiromae
article en

Abstract

We report a phototunable polychromatic luster material based on photocyclization-cycloreversion and photochemical side reactions of diarylethene. Through recrystallization, the open-ring isomers formed plate-like microcrystals, which were then laminated to form a film. The silver-colored textured film was produced through a combination of the absence of absorption in the visible light region of diarylethene and specular reflection from the surface of the stacked microcrystals. This film showed a change in color to navy blue due to the generation of closed-ring isomers by the photocyclization of diarylethene upon UV light irradiation. The film reverted to its original color upon visible light irradiation due to the photocycloreversion reaction of the diarylethene. Further UV light irradiation of the navy blue film produced reddish-purple photounresponsive fused-ring isomers by a photochemical side reaction. Accordingly, a phototunable polychromatic luster film was achieved by light manipulation of open-, closed-, and fused-ring isomers of diarylethene.

Crystal Growth & DesignVol. 25(12)
Ryukoku University (JP), Rikkyo University (JP), Tokyo University of Pharmacy and Life Sciences (JP), Shiga University of Medical Science (JP), Kumamoto University (JP)
Japan Society for the Promotion of Science
Openalex Percentile: Top 95%
Photochromic and Fluorescence Chemistry
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Phototunable Polychromatic Luster in Microcrystalline Film Using Photocyclization-Cycloreversion and Photochemical Side Reactions of Diarylethene — Satoshi Yokojima, Ryo Nishimura, et al. · Crystal Growth & Design (2025) | TGRS Research Map | TGRS