Synthesis, Properties and Application in Optical Memory of a Photochromic Diarylethene Bearing Pyridine Unit

2012 ◽  
Vol 455-456 ◽  
pp. 41-44
Author(s):  
Ming Liu ◽  
Gang Liu ◽  
Shi Qiang Cui
Keyword(s):  
Optical Memory ◽  
Amorphous Film ◽  
Fluorescence Properties ◽  
Fluorescent Properties ◽  
Synthesis Properties

A new photochromic diarylethene compound, 1-(2-methyl-3-benzothiophene)-2- [2-methyl-5-(2-pyridine)-3-thienyl] perfluorocyclopentene (1a) was synthesized. its photochromic and fluorescent properties have been investigated in detail. It showed good photochromism both in solution and PMMA amorphous film upon photoirradiation. Its fluorescence properties in the solution also were reaearched.

Synthesis, Photochromic Properties and Application in Optical Memory of a Diarylethene Based on Pyrrole Ring

2011 ◽  
Vol 399-401 ◽  
pp. 1107-1110
Author(s):  
Ren Jie Wang ◽  
Gang Liu ◽  
Shi Qiang Cui ◽  
Hong Ying Xia
Keyword(s):  
Pyrrole Ring ◽  
Uv Light ◽  
Optical Memory ◽  
Amorphous Film ◽  
Optical Recording ◽  
Fluorescence Properties ◽  
Recording Medium ◽  
Photochromic Properties

A new unsymmetrical photochromic diarylethene compound, 1-[(2-methyl-5-(4-dioxolane-phenyl)-3-thienyl)]-2-(5-cyano-1,5-dimethyl-4-pyrryl)perfluorocyclopentene (1o), was synthesized and its photochemical, fluorescence properties were investigated in detail both in solution and PMMA amorphous film. The results showed that the compound exhibited remarkable photochromism, changing from colorless to violet after irradiation with 297 nm UV light. Finally, using this diarylethene as recording medium, polarization optical recording was carried out successfully.

Synthesis, Properties and Application in Optical Memory of a Photochromic Diarylethene Bearing Chlorine Atoms

2011 ◽  
Vol 239-242 ◽  
pp. 1674-1677 ◽  
Author(s):  
Ming Liu ◽  
Shou Zhi Pu ◽  
Gang Liu
Keyword(s):  
Uv Light ◽  
Optical Memory ◽  
Amorphous Film ◽  
Optical Storage ◽  
Induced Anisotropy ◽  
Strong Fluorescence ◽  
Chlorine Atoms ◽  
Open Ring ◽  
Synthesis Properties

A new unsymmetrical photochromic diarylethene compound, 1-(2,4-dimethyl-5-thiazolyl)-2-[5-(2-chlorobenzene)-2-methyl-3-thienyl]perfluorocyclopentene(1a), was synthesized and its photochromism and photo-induced anisotropy was investigated. Diarylethene 1a changed the color from colorless to Orange-red upon irradiation with 297 nm UV light, in which absorption maxima were observed at 479 nm in hexane and at 485 nm in PMMA amorphous film, respectively. It also showed good photochromism and functioned as an effective fluorescent photoswitch in solution. In hexane, the open-ring isomer of the diarylethene 1a exhibited relatively strong fluorescence at 428 nm when excited at 315 nm. This new photochromic system also exhibited remarkable optical storage character.

Synthesis, Properties and Application in Optical Memory of a New Type Diarylethene with Benzene Ring

2011 ◽  
Vol 239-242 ◽  
pp. 833-836
Author(s):  
Pei Jian Yan ◽  
Shi Qiang Cui ◽  
Shou Zhi Pu
Keyword(s):  
Benzene Ring ◽  
Fluorescence Spectra ◽  
Optical Memory ◽  
Optical Recording ◽  
Pmma Film ◽  
Recording Medium ◽  
Fluorescent Properties ◽  
Synthesis Properties ◽  
New Type

A new type photochromic diarylethene, 1-(2-ethylbenzo[b]thiophen-3-yl)-2- (2-methylphenyl)perfluorocyclopentene (1o), was synthesized, and its photochromic and fluorescent properties were investigated. This compound exhibited reversible photochromism and notable fluorescence photoswitches both in solution and in PMMA films. In addition, the fluorescence spectra of diarylethene 1o evidently depended on the concentration in hexane. Using diarylethene 1c/PMMA film as recording medium, optical recording was carried out successfully.

Synthesis, Properties and Application in Optical Memory of a Photochromic Diarylethene Based on Benzene Ring

2011 ◽  
Vol 295-297 ◽  
pp. 224-227
Author(s):  
Ming Liu ◽  
Ren Jie Wang ◽  
Gang Liu
Keyword(s):  
Benzene Ring ◽  
Fluorescence Intensity ◽  
Uv Light ◽  
Optical Memory ◽  
Amorphous Film ◽  
Induced Anisotropy ◽  
Strong Fluorescence ◽  
Closed Ring ◽  
Open Ring ◽  
Synthesis Properties

A new photochromic diarylethene compound, 1-(2-methyl-5-(2,4-difluorophenyl)-3-thienyl)-2-(2-cyanophenyl)perfluorocyclopentene (1a), was synthesized and its photochromism and photo-induced anisotropy was investigated. The results showed that this compound exhibited reversible photochromism, changing from colorless to purple after irradiation with UV light both in solution and in PMMA amorphous film. In hexane, the open-ring isomer of the diarylethene 1a exhibited relatively strong fluorescence at 459 nm when excited at 316 nm. The fluorescence intensity decreased along with the photochromism upon irradiation with 297 nm light and its closed-ring isomer showed weak fluorescence.

Synthesis, Properties and Application in Optical Memory of a New Photochromic Diarylethene Based on a Chlorine Atom

2012 ◽  
Vol 455-456 ◽  
pp. 25-28 ◽  
Author(s):  
Zhi Peng Tong ◽  
Gang Liu ◽  
Shi Qiang Cui
Keyword(s):  
Chlorine Atom ◽  
Uv Light ◽  
Optical Memory ◽  
Optical Recording ◽  
Pmma Film ◽  
Recording Medium ◽  
Photochromic Properties ◽  
Synthesis Properties

A new unsymmetrical photochromic diarylethene 1-(2,4-dimethyl-3-isoxazol)-2-[2-methyl-5-(2-chlorophenyl) -3-thienyl] perfluorocyclopentene (1a) has been synthesized. Its photochromic properties in solution and PMMA film were investigated. Diarylethene 1a changed the color from colorless to red upon irradiation with 297 nm UV light, in which absorption maxima were observed at 515 nm in hexane and at 526 nm in PMMA film, The results demonstrated that it can be potentially used as polarization holographic optical recording medium.

Investigating structure-fluorescence properties of imidazole fused tetraphenylethylene AIEgens: Reversible mechanofluorochromism and polymer matrix controlled fluorescence tuning

CrystEngComm ◽  
2021 ◽  
Author(s):  
Palaniyappan Nagarasu ◽  
Anu Kundu ◽  
Vijay Thiruvenkatam ◽  
Raghavaiah Pallepogu ◽  
Philip Philip Anthony ◽  
...  
Keyword(s):  
Solid State ◽  
Polymer Matrix ◽  
Fluorescence Properties ◽  
Stimuli Responsive ◽  
Fluorescent Properties ◽  
Imidazole Derivatives

A series of stimuli-responsive AIEgens of tetraphenylethyelene (TPE) fused Imidazole derivatives (1-7) were synthesized and explored their substituents controlled fluorescent properties in the solid state. The structure of the synthesized...

Study on Photochromic Materials with a Novel Photochromic Diarylethene use for Polarization Holographic Recording

2013 ◽  
Vol 763 ◽  
pp. 61-64 ◽  
Author(s):  
Shang Hua He ◽  
Gang Liu ◽  
Shi Qiang Cui
Keyword(s):  
Fluorescence Spectra ◽  
Uv Light ◽  
Amorphous Film ◽  
Quantum Yields ◽  
Holographic Recording ◽  
Pmma Film ◽  
Recording Medium ◽  
Fluorescent Properties ◽  
Image Recording ◽  
Photochromic Materials

A novel unsymmetrical photochromic diarylethene 1-(2, 5-dimethyl-3-thienyl)-2-[2-methyl-5-(2,2-dibutylfluorene)-3-thienyperfluorocyclo-pentene (1o) was synthesized and its photochromic and fluorescent properties were investigated. Diarylethene 1 changed the color from colorless to hyacinthine upon irradiation with 297 nm UV light, in which absorption maxima were observed at 554 nm in hexane and at 565 nm in PMMA amorphous film, respectively. This new photochromic system also exhibited remarkable fluorescence intensity both in solution and in PMMA film. The fluorescence spectra showed a systematic red-shift with the emission intensity of diarylethene 1 in a photo-stationary state was quenched to ca. 64%. The cyclization and cycloreversion quantum yields of 1 in hexane were determined to be 0.56 and 0.002. Polarization multiplexed image recording can be carried out in this diarylethene 1c/PMMA film as recording medium film.

scholarly journals Characterization of steady-state fluorescence properties of polystyrene latex spheres using off- and online spectroscopic methods

2018 ◽  
Vol 11 (7) ◽  
pp. 3987-4003 ◽  
Author(s):  
Tobias Könemann ◽  
Nicole J. Savage ◽  
J. Alex Huffman ◽  
Christopher Pöhlker
Keyword(s):  
Steady State ◽  
Polystyrene Latex ◽  
Fluorescence Properties ◽  
Minor Role ◽  
Spectroscopic Techniques ◽  
Fluorescent Properties ◽  
Qualitative Comparison ◽  
Steady State Fluorescence ◽  
Research Communities ◽  
Latex Spheres

Abstract. Fluorescent dyed polystyrene latex spheres (PSLs) are commonly used for characterization and calibration of instruments detecting fluorescence signals from particles suspended in the air and other fluids. Instruments like the Ultraviolet Aerodynamic Particle Sizer (UV-APS) and the Waveband Integrated Bioaerosol Sensor (WIBS) are widely used for bioaerosol research, but these instruments present significant technical and physical challenges requiring careful characterization with standard particles. Many other research communities use flow cytometry and other instruments that interrogate fluorescence from individual particles, and these also frequently rely on fluorescent PSLs as standards. Nevertheless, information about physical properties of commercially available PSLs provided by each manufacturer is generally proprietary and rarely available, making their use in fluorescence validation and calibration very difficult. This technical note presents an overview of steady-state fluorescence properties of fluorescent and non-fluorescent PSLs, as well as of polystyrene-divinylbenzene (PS-DVB) particles, by using on- and offline spectroscopic techniques. We show that the “fluorescence landscape” of PSLs is more complex than the information typically provided by manufacturers may imply, especially revealing multimodal emission patterns. Furthermore, non-fluorescent PSLs also exhibit defined patterns of fluorescent emission originating from a mixture of polystyrene and detergents, which becomes a crucial point for fluorescence threshold calibrations and qualitative comparison between instruments. By comparing PSLs of different sizes, but doped with the same dye, changes in emission spectra from bulk solutions are not immediately obvious. On a single-particle scale, however, fluorescence intensity values increase with increasing particle size. No significant effect in the fluorescence signatures was detectable by comparing PSLs in dry vs. wet states, indicating that solvent water may only play a minor role as a fluorescence quencher. Because information provided by manufacturers of commercially available PSLs is generally very limited, we provide the steady-state excitation–emission matrices (EEMs) of PSLs as open-access data within the Supplement. Detergent and solvent effects are also discussed in order to provide information not available elsewhere to researchers in the bioaerosol and other research communities. These data are not meant to serve as a fundamental library of PSL properties because of the variability of fluorescent properties between batches and as a function of particle aging and agglomeration. The data presented, however, provide a summary of spectral features which are consistent across these widely used fluorescent standards. Using these concepts, further checks will likely be required by individual researchers using specific lots of standards.

Synthesis, Properties and Application in Optical Memory of a Novel Photochromic Diarylethene Bearing an Anthracene Ring

2011 ◽  
Vol 399-401 ◽  
pp. 1055-1058
Author(s):  
Shang Hua He ◽  
Gang Liu ◽  
Shi Qiang Cui
Keyword(s):  
Optical Memory ◽  
Order Reaction ◽  
Photochromic Properties ◽  
Strong Fluorescence ◽  
First Order ◽  
Cyclization Process ◽  
Open Ring ◽  
Synthesis Properties ◽  
Photochromic Reaction ◽  
Hexane Solution

In the present study, we designed a novel unsymmetrical isomeric diarylethene derivative bearing both thiophene and anthracene moieties. Its photochromic properties and fluorescence were investigated in detail. In hexane solution, the open-ring isomer of the diarylethene 1 exhibited relatively strong fluorescence. The photochromic reaction kinetics indicated that the cyclization process of 1o belongs to the zeroth order reaction and the cycloreversion process belongs to the first order reaction. This new photochromic system also exhibited remarkable optical storage character.

Sign in / Sign up

Export Citation Format

Share Document