Irie et al., 2018 - Google Patents
Photoswitchable turn-on mode fluorescent diarylethenes: strategies for controlling the switching responseIrie et al., 2018
- Document ID
- 12620603331397818590
- Author
- Irie M
- Morimoto M
- Publication year
- Publication venue
- Bulletin of the Chemical Society of Japan
External Links
Snippet
A new type of photoswitchable fluorescent diarylethenes, which have no fluorophore unit but emit strong fluorescence (Φf∼ 0.9) in the closed-ring isomers, has been developed. They are sulfone derivatives of 1, 2-bis (2-alkyl-4-methyl-5-phenyl-3-thienyl) …
- 150000001988 diarylethenes 0 title abstract description 42
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using infra-red, visible or ultra-violet light
- G01N21/62—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
- G01N21/63—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
- G01N21/64—Fluorescence; Phosphorescence
- G01N21/6428—Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes"
- G01N2021/6432—Quenching
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using infra-red, visible or ultra-violet light
- G01N21/62—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
- G01N21/63—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
- G01N21/64—Fluorescence; Phosphorescence
- G01N21/645—Specially adapted constructive features of fluorimeters
- G01N21/6456—Spatial resolved fluorescence measurements; Imaging
- G01N21/6458—Fluorescence microscopy
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1003—Carbocyclic compounds
- C09K2211/1007—Non-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K9/00—Tenebrescent materials, i.e. materials for which the range of wavelength for energy absorption is changed as result of excitation by some form of energy
- C09K9/02—Organic tenebrescent materials
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1018—Heterocyclic compounds
- C09K2211/1025—Heterocyclic compounds characterised by ligands
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1003—Carbocyclic compounds
- C09K2211/1011—Condensed systems
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Irie et al. | Photoswitchable turn-on mode fluorescent diarylethenes: strategies for controlling the switching response | |
| Uno et al. | In situ preparation of highly fluorescent dyes upon photoirradiation | |
| Fukaminato et al. | Single-molecule fluorescence photoswitching of a diarylethene− perylenebisimide dyad: non-destructive fluorescence readout | |
| Kim et al. | Multicolor Fluorescence Photoswitching: Color‐Correlated versus Color‐Specific Switching | |
| Mutoh et al. | Turn-on mode fluorescence switch by using negative photochromic imidazole dimer | |
| Cheng et al. | Dual-stimulus luminescent lanthanide molecular switch based on an unsymmetrical diarylperfluorocyclopentene | |
| Roubinet et al. | Fluorescent photoswitchable diarylethenes for biolabeling and single-molecule localization microscopies with optical superresolution | |
| Uno et al. | Turn-on mode diarylethenes for bioconjugation and fluorescence microscopy of cellular structures | |
| Tian et al. | Photoswitching-enabled novel optical imaging: innovative solutions for real-world challenges in fluorescence detections | |
| Bossi et al. | Multicolor far-field fluorescence nanoscopy through isolated detection of distinct molecular species | |
| Matsuda et al. | Diarylethene as a photoswitching unit | |
| Xiong et al. | Photoswitchable spiropyran dyads for biological imaging | |
| Sumi et al. | Fluorescent photochromic diarylethene that turns on with visible light | |
| Chen et al. | Design and synthesis of FRET-mediated multicolor and photoswitchable fluorescent polymer nanoparticles with tunable emission properties | |
| Kacenauskaite et al. | Rational design of bright long fluorescence lifetime dyad fluorophores for single molecule imaging and detection | |
| Mutoh et al. | Rapid fluorescence switching by using a fast photochromic [2.2] paracyclophane-bridged imidazole dimer | |
| Cheng et al. | Photocontrolled reversible luminescent lanthanide molecular switch based on a diarylethene–europium dyad | |
| Fukaminato et al. | Photocyclization Reaction of Diarylethene− Perylenebisimide Dyads upon Irradiation with Visible (> 500 nm) Light | |
| Lonshakov et al. | New fluorescent switches based on photochromic 2, 3-diarylcyclopent-2-en-1-ones and 6-ethoxy-3-methyl-1H-phenalen-1-one | |
| Wan et al. | Antiphase dual-color correlation in a reactant–product pair imparts ultrasensitivity in reaction-linked double-photoswitching fluorescence imaging | |
| Li et al. | Photo-induced fluorochromism of a star-shaped photochromic dye with 2, 4-dimethylthiazole attaching to triangle terthiophene | |
| Ji et al. | Investigating the properties of double triangle terthiophene configured dumbbell-like photochromic dye with ethyne and 1, 3-butadiene bridge | |
| Zhao et al. | High-contrast fluorescence switching using a photoresponsive dithienylethene coordination compound | |
| US12312456B1 (en) | Acrylate/chalcone polystyrene composite and uses thereof | |
| Nakabayashi et al. | Electric-field-induced changes in absorption and fluorescence of the green fluorescent protein chromophore in a PMMA film |