Papers by Keyword: Photochromism

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Authors: Pei Jian Yan, Shou Zhi Pu, Shi Qiang Cui
Abstract: A new photochromic diarylethene, 1-(2-ethylbenzo[b]thiophen-3-yl)-2-(2-cyanophenyl) perfluorocyclopentene (1o), was synthesized, and its photochromic and fluorescent properties were investigated. This compound exhibited reversible photochromism and fluorescence photoswitches both in solution and in PMMA films. Using diarylethene 1c/PMMA film as recording medium, optical recording was performed successfully.
1133
Authors: Shang Hua He, Gang Liu, Ren Jie Wang
Abstract: A new unsymmetrical photochromic diarylethene bearing a pyrrole and a thiophene aryl unit 1-(5-cyan-1,2-dimethylpyrrole)-2-(5-aldehyde-2-butylthiophene) perfluorocyclopentene(1a) has been synthesized. Its properties, including photochromism and kinetics were investigated in detail. It underwent reversible cyclization and cycloreversion reactions upon alternating with UV and visible light both in solution and in PMMA film. The results showed that this compound exhibited reversible photochromism, changing from colorless to blue upon irradiation with UV light, in which absorption maximum were observed at 649 nm and 583 nm in solution and PMMA amorphous film, respectively. This new photochromic system also exhibited remarkable reaction kinetics in hexane solution.
2239
Authors: Pei Jian Yan, Zhi Peng Tong, Shou Zhi Pu, Wei Jun Liu
Abstract: A novel photochromic diarylethene, 1-(2-ethyl-benzothiophen-3-yl)-2-(2-methyl-5-(2-cyanophenyl)thien-3-yl)perfluorocyclopentene(1o) was synthesized, and its photochromic and fluorescent properties were investigated. This compound exhibited reversible photochromism, changing from colorless to purle after irradiation with UV light both in solution and in poly-methyl methacrylate (PMMA) amorphous film. Also, it exhibited remarkable fluorescence switching in the solid state. When we used diarylethene 1c/PMMA film as recording medium, rewritable holographic optical storage was performed successfully. The results demonstrated that the diarylethene compound had attractive properties for polarization holographic optical recording, such as high photosensitivity, high spatial resolution, excellent fatigue-resistance.
655
Authors: Hong Liang Liu, Shou Zhi Pu, Shi Qiang Cui, Wei Jun Liu
Abstract: A novel photochromic diarylethene based on pyrazole moiety was synthesized and its photochromic and fluorescent properties were also investigated. The compound exhibited remarkable photochromism, changing from colorless to purple after irradiation with UV light both in solution and in PMMA film. In hexane solution and in PMMA film, the open-ring isomer of the diarylethene 1 exhibited relatively remarkable fluorescence. The results indicated that the pyrazole moiety played a very important role during the process of photochromic reaction for the diarylethene derivative. Using this dithienylethene 1c as optical storage was performed successfully.
53
Authors: Hong Liang Liu, Shou Zhi Pu, Wei Jun Liu, Shi Qiang Cui
Abstract: A novel photochromic diarylethene based on isoxazole moiety was synthesized and its photochromic and fluorescent properties were also investigated. It underwent reversible cyclization and cycloreversion reactions upon alternating irradiation with UV and visible light in hexane and in PMMA film. The compound exhibited remarkable photochromism, changing from colorless to purple after irradiation with UV light. When irradiation with UV light, the fluorescence intensity declined remarkably. The results showed that the diarylethene exhibited a relatively strong fluorescence switch along with the photochromism from open-ring isomer to closed-ring isomer. Using this dithienylethene 1c as optical storage was performed successfully.
3290
Authors: Shu Hong Jing, Cong Bin Fan, Shou Zhi Pu
Abstract: A new photochromic diarylethene compound, 1-[2-methyl-5-(3-thienyl)-3-thieny-2-[2-methyl-5-(3-benzaldehyde)-3-thieny perfluorocyclopentene (1a) was synthesized. Its properties, including photochromism and fluorescence were investigated in detail both in solution and PMMA amorphous film. It underwent reversible cyclization and cycloreversion reactions upon alternating irradiation with UV and visible light in hexane. The compound showed good phtochromism both in solution and in solid states. Diarylethene 1a changed the color from colorless to navy upon irradiation with 297 nm UV light, in which absorption maxima were observed at 577 nm in hexane and at 592 nm in PMMA film, respectively. Using diarylethene 1b/PMMA film as recording medium, optical recording was performed successfully.
65
Authors: Wei Jun Liu, Yan Lu, Shou Zhi Pu
Abstract: A novel unsymmetrical diarylethene derivative bearing both phenyl and thiophene moieties, in which a chlorine group was substituted at the para-positions of the terminal phenyl ring, was synthesized. At the same time, its photochromic properties and fluorescence switch were investigated in detail. The results showed that this compound exhibited reversible photochromism, undergoing reversible cyclization and cycloreversion reactions upon alternating irradiation with UV and visible light both in solution and in PMMA film, and its absorption maxima were observed at 541 nm in hexane and at 550 nm in PMMA amorphous film, respectively, upon irradiation with 297 nm UV light. The fluorescence intensity of diarylethene decreased dramatically along with the photochromism from open-ring isomer to closed-ring isomer upon irradiation with 297 nm UV light in PMMA. In hexane solution, the open-ring isomer of the diarylethene 1 exhibited relatively strong fluorescence at 462 nm when excited at 316 nm.
1519
Authors: Hong Yan Xu, Ren Jie Wang, Shou Zhi Pu
Abstract: A new unsymmetrical photochromic diarylethene compound 1a was synthesized and its photochromism were investigated, such as photochromism and kinetics in solution. The compound exhibited good photochromism in solution with alternating irradiation by UV/Vis light, and the maxima absorption of its closed-ring isomer 1b are 515nm. The open-ring isomer of the diarylethene 1a exhibited relatively strong fluorescence at 424 nm when excited at 280 nm. Its fluorescence intensity decreased along with the photochromism from open-ring isomers to closed-ring isomers upon irradiation with 297 nm UV light.
93
Authors: Zhi Peng Tong, Shou Zhi Pu, Shi Qiang Cui
Abstract: A photochromic diarylethene bearing a six-membered aryl unit 1-[(2,5-dimethyl-3-thienyl)]-2-[2-methy-4-(3,5-difluorophenyl)-phenyl]perfluoroyclopentene (1a) was synthesized and its photochromic and fluorescent properties were also investigated in detail. The results showed that this compound exhibited reversible photochromism, changing from colorless to red after irradiation with UV light, in which absorption maxima were observed at 521 and 536nm in hexane and PMMA film, respectively. The fluorescence intensity decreased along with the photochromism upon irradiation with 297 nm light in hexane.
37
Authors: Martina Vikova, Michal Vik
Abstract: Photochromism is a chemical process in which a compound undergoes a reversible change between two states having separate absorption spectra, i.e. different colors. The change of color in one direction occurs under influence of electromagnetic radiation, usually UV light, and in the other direction by altering or removing the light source or alternatively by using thermal means. Based on photochromic pigment we developed simple textile sensor sensitive to UV light, which is usable for visual indication of intensity UV-A radiation. Main attention was given to colorimetric properties of photochromic textiles during decay phase of photochromic color change, such as saturation change and fatigue resistance.
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