Research on Photochromic Materials with Synthesis and Properties of 1-(3,5-Dimethyl-4-isoxazolyl)-2-[2-methyl-5-(p-ethoxyphenyl)-3-thienyl]perfluorocyclopentene

2014 ◽  
Vol 1003 ◽  
pp. 27-30
Author(s):  
Guan Ming Liao ◽  
Dan Dan Xue ◽  
Chun Hong Zheng ◽  
Shou Zhi Pu
Keyword(s):  
Uv Light ◽  
Order Reaction ◽  
First Order Reaction ◽  
Photochromic Properties ◽  
First Order ◽  
Photochromic Materials ◽  
Hexane Solution

An asymmetrical photochromic diarylethene 1-(3,5-Dimethyl-4-isoxazolyl)-2-[2-methyl-5-(p-ethoxyphenyl)-3-thienyl] perfluorocyclopentene (1o) was synthesized and its photochromic properties were investigated. Upon irradiation with 297 nm UV light, 1o exhibited photochromism in hexane solution. The kinetic experiments showed that the cyclization and cycloreversion processes were zeroth and first order reaction, respectively. Moreover, diarylethene 1o also exhibited obviously fluorescence switches along with the photochromism.

Study on Photochromic Materials with Synthesizes and Properties of a Novel Unsymmetrical Photochromic Diarylethene

2013 ◽  
Vol 327 ◽  
pp. 78-82
Author(s):  
Zhi Yuan Sun ◽  
Xiao Dan Zhang ◽  
Shi Qiang Cui ◽  
Shou Zhi Pu
Keyword(s):  
Methyl Methacrylate ◽  
Absorption Maximum ◽  
Uv Light ◽  
Order Reaction ◽  
First Order Reaction ◽  
Pmma Film ◽  
First Order ◽  
Open Ring ◽  
Photochromic Materials ◽  
Hexane Solution

A novel unsymmetrical photochromic diarylethene 1-(2-methyl-3-benzofuran)-2-[5-(2-methylbenzene)-2-methyl-3-thieny perfluorocyclopentene1owas synthesized, then its photochromic, Kinetics and fluorescence properties were investigated. The results showed that the diarylethene compound had good photochromism upon irradiation with 297 nm UV light, in which the absorption maximum were observed at 510 nm in hexane solution and 524 nm in poly methyl methacrylate (PMMA) film. Besides, the cyclization and cycloreversion process of the compound were determined to be the zeroth and first order reaction by UV-Vis spectra, respectively. And, the open-ring isomer of the diarylethene exhibited relatively stronger fluorescence at 427 nm when excited at 273 nm in hexane solution.

Synthesis a New Function Materials and Photochromic Properties of Diarylethene Bearing a Naphthalene and Isoxazole Moiety

2012 ◽  
Vol 164 ◽  
pp. 243-246
Author(s):  
Ren Jie Wang ◽  
Shi Qiang Cui ◽  
Shou Zhi Pu
Keyword(s):  
Fluorescence Intensity ◽  
Uv Light ◽  
Order Reaction ◽  
First Order Reaction ◽  
Fluorescent Properties ◽  
Photochromic Properties ◽  
First Order ◽  
Closed Ring ◽  
Hexane Solution

A new photochromic diarylethene compound 1-(2-methylnaphthyl)-2-(3, 5-dimethyl-4-isoxazolyl)perfluorocyclopentene (1o), was synthesized and its photochromic and fluorescent properties were investigated. Diarylethene 1o changed the color from colorless to yellow upon irraditation with 297 nm UV light, which the absorption maxima were observed at 446 nm in hexane solution. The kinetic experiments indicated that the cyclization/cycloreversion process of the compound was determined to be the zeroth/first order reaction in hexane solution. The fluorescence intensity decreased along with the photochromism upon irradiation with 297 nm light and its closed-ring isomer showed weak fluorescence

Efficient Synthesis and Photochromic Properties of a New Diarylethene Bearing a Condensed Aromatics Moiety

2012 ◽  
Vol 455-456 ◽  
pp. 33-36
Author(s):  
Ren Jie Wang ◽  
Hong Ying Xia ◽  
Gang Liu ◽  
Shi Qiang Cui
Keyword(s):  
Uv Light ◽  
Optical Storage ◽  
Hybrid Structure ◽  
Order Reaction ◽  
Pmma Film ◽  
Efficient Synthesis ◽  
Photochromic Properties ◽  
First Order ◽  
New Class ◽  
Hexane Solution

A new class of diarylethenes based on a hybrid structure of thiophene and naphthalene has been developed and its properties including photochromism, kinetics and fluorescence were investigated in detail. The results showed that the compound exhibited obvious photochromism, changing from colorless to red after irradiation with 297 nm UV light both in solution and in PMMA film. The kinetic experiments indicated that the cyclization/cycloreversion process of the compound was determined to be the zeroth/first order reaction in hexane solution. At last, the results demonstrated that the diarylethene compound had attractive properties for potential application in optical storage.

Synthesis and Photochromism Studies of 1-(2-methyl-3-benzothiophene)-2-[2-methyl-5-(4-aminomethanephenyl)-3-thienyl]perfluorocyclopentene

2014 ◽  
Vol 886 ◽  
pp. 143-146
Author(s):  
Xiao Rong Dong ◽  
Sha Sha Wei ◽  
Gang Liu ◽  
Shou Zhi Pu
Keyword(s):  
Reaction Kinetics ◽  
Uv Light ◽  
Order Reaction ◽  
First Order Reaction ◽  
Acetonitrile Solution ◽  
Zeroth Order ◽  
Photochromic Properties ◽  
First Order ◽  
Fluorescence Switching ◽  
Photochromic Reaction

A new unsymmetrical photochromic diarylethene compound, 1-(2-methyl-3-benzothiophene)-2-[2-methyl-5-(4-aminomethanephenyl)-3-thienyperfluorocyclopentene (1a) was synthesized, its photochromic properties were examined, the result indicated that the Diarylethene 1a changed the color from colorless to purple upon irradiation with 297 nm UV light, in which absorption maxima were observed at 564 in acetonitrile. The photochromic reaction kinetics indicated that the cyclization processes of 1a belong to the zeroth order reaction and the cycloreversion process belong to the first order reaction. This new photochromic system also exhibited fluorescence switching in acetonitrile solution.

Research on Photochromic Compounds with Synthesis and Photochromism of 1-(2-methyl-3-benzofuryl)-2-{2-methyl-5-[4-formyloxyethyl (Rhodamine-B)] phenyl-3-thienyl} Perfluoroyclopentene

2014 ◽  
Vol 1003 ◽  
pp. 55-58
Author(s):  
Dan Dan Xue ◽  
Guan Ming Liao ◽  
Chun Hong Zheng ◽  
Shou Zhi Pu
Keyword(s):  
Visible Light ◽  
Rhodamine B ◽  
Uv Light ◽  
Amorphous Film ◽  
Order Reaction ◽  
First Order Reaction ◽  
Pmma Film ◽  
Photochromic Properties ◽  
Photochromic Compounds ◽  
First Order

A new photochromic diarylethene compound bearing a rhodamine B unit, 1-(2-methyl-3-benzofuryl)-2-{2-methyl-5-[4-formyloxyethyl (rhodamine-B)] phenyl-3-thienyl} perfluorocyclopentene (1o) was synthesized, and its photochromic properties such as photochromism in solution as well as in a polymethylmethacrylate (PMMA) amorphous film were investigated specfically. 1o exhibits good photochromism upon alternating irradiation with UV light and visible light (> 510 nm) in hexane and a PMMA film. The kinetic experiments showed that the cyclization and cycloreversion processes were zeroth and first order reaction, respectively.

Synthesis and Properties of 1-(2-Cyano-1,5-Dimethyl-4-Pyrryl)-2-{2-Methyl-[5-(4-Methylene-Hydroxyl)Phenyl]-3-Thienyl}Perfluorocyclopentene

2014 ◽  
Vol 662 ◽  
pp. 83-86
Author(s):  
Fang Duan ◽  
Gang Liu
Keyword(s):  
Uv Light ◽  
Amorphous Film ◽  
Order Reaction ◽  
First Order Reaction ◽  
Acetonitrile Solution ◽  
Photochromic Properties ◽  
First Order

A new asymmetrical photochromic diarylethene 1-(2-cyano-1,5-dimethyl-4-pyrryl)-2-{2-methyl-[5-(4-methylene-hydroxyl) phenyl]-3-thienyl} perflu-orocyclopentene (1o) was synthesized and its photochromic properties were investigated systematically. Upon irradiation with 297 nm UV light, 1o exhibited photochromism in acetonitrile solution and in a PMMA amorphous film. The kinetic experiments showed that the cyclization and cycloreversion processes were zeroth and first order reaction, respectively. In addition, diarylethene 1o also exhibited obvious fluorescence switches along with the photochromism.

Synthesis and Properties of 1-(3,5-dimethyl-4-isoxazole)-2-(2-methyl-(5-ethynyl)-3-thienyl)perfluorocyclopentene

2014 ◽  
Vol 1078 ◽  
pp. 82-85
Author(s):  
Mei Li Cai ◽  
Zhao Yan Tian ◽  
Shi Qiang Cui ◽  
Shou Zhi Pu
Keyword(s):  
Response Time ◽  
Ring Opening ◽  
Color Change ◽  
Uv Light ◽  
Order Reaction ◽  
First Order Reaction ◽  
Fluorescence Properties ◽  
First Order ◽  
Ring Opening Reaction ◽  
Hexane Solution

A new photochromic diarylethene of 1-(3,5-dimethyl-4-isoxazole)-2- (2-methyl-(5-ethynyl)-3-thienyl) perfluorocyclopentene (1o) was synthesized. Its photochromic and fluorescence properties were investigated systematically. Upon irradiation with UV light with the extended response time, the diarylethene underwent a ring opening reaction to produce closed forms and color change in solution. The results showed the compound exhibited good photochromism in hexane solution. The kinetic experiments showed that the cyclization and cycloreversion processes were zeroth and first order reaction, respectively. Moreover, diarylethene1oalso exhibited obviously fluorescence switches along with the photochromism.

Synthesis and Photochromism Studies of 1-(2,5-Dimethyl-3-Thienyl)-2-[2-Methyl-5- Pyrenyl-3-Thienyl]Perfluorocyclopentene

2014 ◽  
Vol 662 ◽  
pp. 79-82
Author(s):  
Xiao Rong Dong ◽  
Ren Jie Wang ◽  
Shou Zhi Pu
Keyword(s):  
Uv Light ◽  
Order Reaction ◽  
First Order Reaction ◽  
Acetonitrile Solution ◽  
Pmma Film ◽  
First Order ◽  
Fluorescence Switching ◽  
Condensed Nucleus ◽  
Hexane Solution

A new unsymmetrical photochromic diarylethene1o, which contains condensed nucleus was synthesized. Its photochromic both in hexane solution and in PMMA film and kinetics experiment were investigated in detail. The result indicated that this diarylethene had reversible photochromism, changing the color from colorless to purple in hexane solution upon appropriate irradiation with 297 nm UV light, respectively. What’s more, The kinetic experiments showed that the cyclization and cycloreversion processes were zeroth and first order reaction, respectively. This new photochromic system also exhibited fluorescence switching in acetonitrile solution.

Synthesis and Properties of 1-(2-methyl-3-benzothienyl)-2-[2-methyl-5-(3-trifluoromethyl)-3-thienyl]perfluorocyclopentene

2014 ◽  
Vol 1078 ◽  
pp. 106-109
Author(s):  
Jing Jing Liu ◽  
Hong Jing Jia ◽  
Shou Zhi Pu
Keyword(s):  
Uv Light ◽  
Order Reaction ◽  
First Order Reaction ◽  
Fluorescent Properties ◽  
First Order ◽  
Open Ring ◽  
Hexane Solution

A novel asymmetrical photochromic diarylethene 1-(2-methyl-3-benzothienyl)-2-[2-methyl-5-(3-trifluoromethyl)-3-thienyl] perfluorocyclopentene was synthesized and its photochromic and fluorescent properties were also investigated. The compound exhibited remarkable photochromism, changing from colorless to red after irradiation with UV light and the open-ring isomer of the diarylethene 1 exhibited relatively remarkable fluorescence in hexane solution. The cyclization/cycloreversion process of the compound was determined to be the zeroth/first order reaction.

Synthesis and Properties of 1-(2,4-Dimethyl-5-thiazolyl)-2-(2-methyl-5-(2-methyl)-3-thienyl)perfluorocyclopentene

2014 ◽  
Vol 952 ◽  
pp. 71-74
Author(s):  
Guan Ming Liao ◽  
Chun Hong Zheng ◽  
Shou Zhi Pu
Keyword(s):  
Uv Light ◽  
Order Reaction ◽  
First Order Reaction ◽  
Pmma Film ◽  
Photochromic Properties ◽  
First Order

An asymmetrical photochromic diarylethene 1-(2,4-dimethyl-5-thiazolyl)-2-(2-methyl-5-(2-methyl)-3-thienyl) perfluorocyclopentene (1o) was synthesized and its photochromic properties were investigated. Upon irradiation with 297 nm UV light, 1o exhibited photochromism in solution and in PMMA film. The kinetic experiments showed that the cyclization and cycloreversion processes were zeroth and first order reaction, respectively. Moreover, diarylethene 1o also exhibited obviously fluorescence switches along with the photochromism.

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