scholarly journals Switching Between Bicyclic and Linear Peptides — The Sulfhydryl-Specific Linker TPSMB Enables Reversible Cyclization of Peptides

2018 ◽  
Vol 6 ◽  
Author(s):  
Christoph Ernst ◽  
Johannes Heidrich ◽  
Catharina Sessler ◽  
Julia Sindlinger ◽  
Dirk Schwarzer ◽  
...  
Keyword(s):  
Reversible Cyclization

Synthesis and Characterization of Unsymmetrical Diarylethene Based on Phenylpentane

2014 ◽  
Vol 707 ◽  
pp. 60-63
Author(s):  
Xiao Dong Zhang ◽  
Sha Sha Wei ◽  
Shou Zhi Pu
Keyword(s):  
Visible Light ◽  
Synthesis And Characterization ◽  
Reversible Cyclization

An unsymmetrical photochromic diarylethene, 1-[2-methyl-3-benzothiophene]-2-[2-methyl-5-(4-pentylphenyl)-3-thienyl] perfluorocyclopentene (1a), has been synthesized, and its properties including photochromism and fluorescence have been investigated. The results showed that this compound undergo reversible cyclization and cycloreversion reactions upon alternating irradiation with UV and visible light in solution.

Photochromism and Fluorescence of a Novel Unsymmetrical Diarylethene Material Bearing Benzene and Thiophene Ring

2012 ◽  
Vol 164 ◽  
pp. 251-254 ◽  
Author(s):  
Shu Hong Jing ◽  
Shou Zhi Pu ◽  
Hui Li
Keyword(s):  
Visible Light ◽  
Uv Light ◽  
Thiophene Ring ◽  
Amorphous Film ◽  
Optical Storage ◽  
Optical Recording ◽  
Pmma Film ◽  
Recording Medium ◽  
Solid States ◽  
Reversible Cyclization

A new photochromic diarylethene compound, 1-[2-methyl-(5-(4- dioxolane) phenyl)-3-thienyl]-2-(2-methyl-3-benzothiophene)perfluorocyclopentene (1o)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 1o changed the color from colorless to purple upon irradiation with 297 nm UV light, in which absorption maxima were observed at 539 nm in hexane and at 547nm in PMMA film, respectively. Using diarylethene 1c/PMMA film as recording medium, optical recording was performed successfully. This new photochromic system also exhibited remarkable optical storage character

Synthesis, Photochromism Properties of a Hybrid Diarylethene Based on Hydroxyl Group

2011 ◽  
Vol 393-395 ◽  
pp. 385-388
Author(s):  
Duo Hua Jiang ◽  
Wei Jun Liu ◽  
Shi Qiang Cui ◽  
Gang Liu
Keyword(s):  
Visible Light ◽  
Uv Light ◽  
Amorphous Film ◽  
Methanol Solution ◽  
Fluorescence Properties ◽  
Hydroxyl Group ◽  
Pmma Film ◽  
Open Ring ◽  
Reversible Cyclization

A novel unsymmetrical diarylethene derivative 1-[2-methyl-5-(3-trifluoromethylphenyl)-3-thienyl]-2-[2-methyl-5-(4-hydroxylphenyl)-3-thienyl]hexafluorocyclopentene (1a) was successfully synthesized. The properties of the compound, including photochromic and fluorescence properties of the diarylethene were also investigated systematically. 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 593 nm in methanol and at 598 nm in PMMA amorphous film, respectively, upon irradiation with 297 nm UV light. In methanol solution, the open-ring isomer of the diarylethene 1 exhibited relatively fluorescence at 569 nm when excited at 360 nm.

An α-diketone from the condensation product of glucose and ethyl acetoacetate

1964 ◽  
Vol 17 (10) ◽  
pp. 1174 ◽  
Author(s):  
LK Dalton
Keyword(s):  
Hydrogen Peroxide ◽  
Solid State ◽  
Hydrogen Chloride ◽  
Ethyl Acetoacetate ◽  
Condensation Product ◽  
Side Chain ◽  
Furoic Acid ◽  
Aliphatic Side Chain ◽  
Benzilic Acid ◽  
Reversible Cyclization

When the product from the condensation of glucose and ethyl acetoacetate, ethyl 2-D-arabino-tetrahydroxybutyl-5-methyl-4-furoate (Ia), is heated in ethanolic hydrogen chloride, an a-diketone (IVa) is produced. It exists as a mono-enol in solution and in the solid state. Although this diketone is formed with an aliphatic side chain, there is at first a predominant, but reversible, cyclization to the "difuran" (II). With hydrogen peroxide the diketone yields 2-carboxymethy1-5- methyl-4-furoic acid (VII), and with alkali it undergoes a benzilic acid rearrangement.

Study on Composite Photochromic Properties of New Diarylethenes Bearing Naphthyl Rings

2012 ◽  
Vol 583 ◽  
pp. 134-137
Author(s):  
Pan Pan Ren ◽  
Shou Zhi Pu
Keyword(s):  
Visible Light ◽  
Uv Light ◽  
Amorphous Film ◽  
Optoelectronic Properties ◽  
Pmma Film ◽  
Amorphous Films ◽  
Photochromic Properties ◽  
Reversible Cyclization

A novel photochromic diarylethene, 1-[(2-methyl-5-(4-fluorophenyl)-3-thienyl)]-2-(2-methyl-1-naphthyl) perfluorocyclopentene (1o), was synthesized. Its optoelectronic properties, such as photochromism in solution as well as in poly-methylmethacrylate (PMMA) amorphous films, fluorescences 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 511 nm in hexane and at 522 nm in PMMA amorphous film, respectively, upon irradiation with 297 nm UV light.

Synthesis and Application of 1-[2-Methyl-5-Phenyl-3-Thiophene]-2-[2-Methyl-5-Phenyl-(4-Vinyl)-3-Thiophene]Perfluorocyclopentene

2014 ◽  
Vol 662 ◽  
pp. 87-90
Author(s):  
Ying Long Fu ◽  
Xue Li ◽  
Gang Liu
Keyword(s):  
Visible Light ◽  
Uv Light ◽  
Reversible Cyclization

A new unsymmetrical photochromic diarylethene 1-(2-methyl-5-phenyl-3-thiophene)-2-[2-methyl-5-phenyl-(4-vinyl)-3-thiophene] perfluorocyclopentene (1o) has been synthesized, and its photochromic reactivity, fluorescent were also investigated. The results showed this compound exhibited reversible photochromism, undergoing reversible cyclization and cycloreversion reactions upon alternating irradiation with UV and visible light in solution,Diarylethene 1 changed the color from colorless to blue upon irradiation with 297 nm UV light, in which absorption maxima were observed at 596 nm in acetonitrile.

Synthesis and Properties of a New Unsymmetrical Diarylethene Bearing Two Thiophene Rings

2012 ◽  
Vol 490-495 ◽  
pp. 3672-3675
Author(s):  
Hui Li ◽  
Yuan Ming Tu ◽  
Gang Liu
Keyword(s):  
Visible Light ◽  
Fluorescence Intensity ◽  
Fluorescence Property ◽  
Pmma Film ◽  
Isomeric Compound ◽  
Fluorescence Switch ◽  
Reversible Cyclization

A new unsymmetrical photochromic diarylethene has been synthesized, namely {1-(2,5-dimethyl-3-thienyl),2-[2-methyl-5-(4-trifluoromethylphenyl)-3-thienyl]}perfluorocyclopentene. Its properties, including photochromic reactivity in solution and fluorescence property both in solution and in PMMA film were investigated. It underwent reversible cyclization and cycloreversion reactions upon alternating irradiation with UV and visible light. The isomeric compound functioned as a fluorescence switch by photoirradiation both in solution and in PMMA film. The fluorescence intensity also showed regular changes along with the change of concentration.

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