Photochromism and Optical Storage of a Novel Unsymmetrical Diarylethene Based on Pyrazole and Benzofuran

2011 ◽  
Vol 295-297 ◽  
pp. 220-223
Author(s):  
Tao Feng Wang ◽  
Gang Liu ◽  
Shi Qiang Cui
Keyword(s):  
Fluorescence Intensity ◽  
Uv Light ◽  
Optical Storage ◽  
Order Reaction ◽  
First Order Reaction ◽  
Pmma Film ◽  
First Order

A new unsymmetrical photochromic diarylethene of bis (1,3,5-trimethyl-4-pyrazole)ethane and bis(2-methyl-3-benzofuran)ethane was synthesized, its photochromic, fluorescent and optical strorage properties were examined, the result indicated that the diarylethene 1a changed the color from colorless to violet upon irradiation with 297 nm UV light, in which new absorption maxima were observed at 539nm and 556nm in hexane and PMMA film, respectively. This new photochromic system exhibited remarkable fluorescence intensity and clear fluorescent switches by photoirradiation in hexane. The results showed that the cyclization/cycloreversion process of the compound was determined to be the zeroth/first order reaction. This new photochromic system also exhibited remarkable optical storage character.

Synthesis, Photochromism and Optical Storage of a Novel Unsymmetrical Diarylethene Compound

2010 ◽  
Vol 156-157 ◽  
pp. 665-669
Author(s):  
Tao Feng Wang ◽  
Zhi Gang Liu ◽  
Shou Zhi Pu ◽  
Gang Liu
Keyword(s):  
Fluorescence Intensity ◽  
Uv Light ◽  
Optical Storage ◽  
Order Reaction ◽  
First Order Reaction ◽  
Pmma Film ◽  
First Order

A new unsymmetrical photochromic diarylethene 1-[2,5-dimethyl-3-thienyl]-2-[3,5-difluorophenyl]perfluoroyclopentene (1a) was synthesized, its photochromic, fluorescent and optical strorage properties were examined, the result indicated that the diarylethene 1a changed the color from colorless to purple upon irradiation with 313 nm UV light, in which absorption maxima were observed at 542nm and 556nm in hexane and PMMA film, respectively. This new photochromic system exhibited remarkable fluorescence intensity and clear fluorescent switches by photoirradiation in PMMA film. The results showed that the cyclization/cycloreversion process of the compound was determined to be the zeroth/first order reaction. This new photochromic system also exhibited remarkable optical storage character.

Synthesis and Property of a Novel Diarylethene Based on Benzofuran and Thienyl Units for Polarization Optical Recording

2011 ◽  
Vol 474-476 ◽  
pp. 1561-1564
Author(s):  
Tao Feng Wang ◽  
Shou Zhi Pu ◽  
Shi Qiang Cui
Keyword(s):  
Fluorescence Intensity ◽  
Optical Storage ◽  
Order Reaction ◽  
Optical Recording ◽  
First Order Reaction ◽  
Pmma Film ◽  
First Order ◽  
Open Ring

A new photochromic diarylethene of bis(3-methyl-2-thienyl)ethene and bis(2-methyl-3- benzofuran)ethene was synthesized. Its photochromic, fluorescent and optical strorage properties were investigated. The compounds exhibited remarkable photochromism both in solution and in PMMA film. In hexane, the open-ring isomer of the diarylethene 1 exhibited relatively strong and clear fluorescent switches when excited at 270 nm. The fluorescence intensity declined along with the photochromism upon irradiation with 297 nm light. The results showed that the cyclization/cycloreversion process of the compound was determined to be the zeroth/first order reaction. This new photochromic system also exhibited remarkable optical storage character.

Synthesis of a Novel Photochromic Diarylethene for Polarization Optical Recording

2011 ◽  
Vol 396-398 ◽  
pp. 2357-2360
Author(s):  
Tao Feng Wang ◽  
Gang Liu ◽  
Wei Jun Liu ◽  
Shi Qiang Cui
Keyword(s):  
Fluorescence Intensity ◽  
Optical Storage ◽  
Order Reaction ◽  
Optical Recording ◽  
First Order Reaction ◽  
Pmma Film ◽  
First Order

A novel unsymmetrical photochromic diarylethene compound bearing a benzofuran unit, 1-[2-methyl-5-formyl-3-thienyl]-2-[2-methyl-3-benzofuran-yl]perfluoroyclopentene(1a) have been synthesized, its photochromic, fluorescence and optical strorage properties were investigated. The compound exhibited obviously photochromism both in hexane and in PMMA film. In hexane, the fluorescence intensity of 1a declined along with the photochromism upon irradiation with 297 nm light. The results showed that the cyclization and cycloreversion process of the compound was determined to be the zeroth/first order reaction. This new photochromic system also exhibited remarkable optical storage character.

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.

Synthesizes and Properties Research of a Photochromic Diarylethene Bearing a Hexatomic Ring

2013 ◽  
Vol 830 ◽  
pp. 278-281
Author(s):  
Zhi Yuan Sun ◽  
Wei Wei Geng ◽  
Shou Zhi Pu
Keyword(s):  
Reaction Kinetics ◽  
Fluorescence Intensity ◽  
Uv Light ◽  
Order Reaction ◽  
First Order Reaction ◽  
First Order ◽  
Solid Films ◽  
Kinetics Of

A new photochromic diarylethene compound 1-(2-cyan-3-phenyl)-2-[5-(4-cyanobenzene) -2-methyl-3-thienyl] perfluorocyclopentene was synthesized. And their properties inculding photochromis, fluorescence in both hexane and solid films, reaction kinetics of cyclization and cycloreversion were studied. And its absorption maxima were observed at 539 nm in hexane and at 552 nm in PMMA films, respectively, upon irradiation with 313 nm UV light. The fluorescence intensity of diarylethene decreased upon irradiation with 313 nm UV light. Besides, the cyclization and cycloreversion processes of the compound were determined to be the zeroth and first order reaction by UV-Vis spectra, respectively.

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.

Synethesis and Properties of 1-(2-trifluoromethylphenyl)-2-[2-methyl-5-(3-N,N-dimethylphenyl)-3-thienyperfluorocyclopentene

2013 ◽  
Vol 473 ◽  
pp. 77-80
Author(s):  
Zhi Yuan Sun ◽  
Dan Dan Xue ◽  
Shou Zhi Pu
Keyword(s):  
Reaction Kinetics ◽  
Fluorescence Intensity ◽  
Uv Light ◽  
Order Reaction ◽  
First Order Reaction ◽  
Fluorescent Properties ◽  
First Order ◽  
Kinetics Of

An unsymmetrical photochromic diarylethene 1-(2-trifluoromethylphenyl)-2-[2-methyl-5-(3-N,N-dimethylphenyl)-3-thienyperfluorocyclopentene (1a) was synthesized and its photochromism, fluorescent properties and reaction kinetics of cyclization and cycloreversion were studied in detail. The compound exhibited remarkable photochromism and its absorption maxima were observed at 552 nm in hexane and at 569 nm in PMMA films upon irradiation with 297 nm UV light. The fluorescence intensity of diarylethene decreased upon irradiation with 297 nm UV light. In addiation, reaction kinetics of the cyclization and cycloreversion processes of the compound were determined to be the zeroth and first order reaction by UV-Vis spectra, respectively.

Synthesis of a New Diarylethene Based on Isoxazole and Benzofuran Units for Polarization Optical Recording

2011 ◽  
Vol 233-235 ◽  
pp. 2476-2479
Author(s):  
Tao Feng Wang ◽  
Shou Zhi Pu ◽  
Shi Qiang Cui
Keyword(s):  
Optical Storage ◽  
Order Reaction ◽  
Optical Recording ◽  
First Order Reaction ◽  
Pmma Film ◽  
First Order

A new photochromic diarylethene1-(3,5-dimethyl-4-isoxazolyl)-2-(2-methyl-3- benzofuran) perfluorocyclopentene (1a) has been synthesized. Its photochromic, fluorescent and optical strorage properties were investigated. The compound exhibited remarkable photochromism and clear fluorescent switches both in solution and in PMMA film. The results showed that the cyclization/cycloreversion process of the compound was determined to be the zeroth/first order reaction. This new photochromic system also exhibited remarkable optical storage character.

Synthesis of a New Photochromic Compound for Optical Storage

2010 ◽  
Vol 156-157 ◽  
pp. 462-466
Author(s):  
Shi Qiang Cui ◽  
Shou Zhi Pu ◽  
Gang Liu ◽  
Wei Jun Liu
Keyword(s):  
Reaction Kinetics ◽  
Uv Light ◽  
Optical Storage ◽  
Order Reaction ◽  
Pmma Film ◽  
Zeroth Order ◽  
Photochromic Compound ◽  
Photochromic Properties ◽  
First Order ◽  
Photochromic Reaction

A new photochromic compound 1-[2,5-dimethyl-3-thienyl]-2-[2-methyl-5-pyridine-3-yl-3-thieyl] perfluoroyclopentene(1a) was synthesized, its photochromic properties were examined, the result indicated that the color of the compound 1a changed from colorless to a purple one upon irradiation with 297 nm UV light, a new absorption maxima were observed at 549 and 553 nm in hexane and PMMA film, respectively. The the photochromic reaction kinetics indicated that the cyclization processes of 1 belong to the zeroth order reaction and the cycloreversion process belong to the first order reaction.This new photochromic system also exhibited remarkable optical storage character.

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.

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