RU2004131492A - Фотоуправляемые фотохромные электролюминесцирующие и электропроводящие полимеры для фотоники - Google Patents
Фотоуправляемые фотохромные электролюминесцирующие и электропроводящие полимеры для фотоники Download PDFInfo
- Publication number
- RU2004131492A RU2004131492A RU2004131492/04A RU2004131492A RU2004131492A RU 2004131492 A RU2004131492 A RU 2004131492A RU 2004131492/04 A RU2004131492/04 A RU 2004131492/04A RU 2004131492 A RU2004131492 A RU 2004131492A RU 2004131492 A RU2004131492 A RU 2004131492A
- Authority
- RU
- Russia
- Prior art keywords
- photochromic
- polyazomethines
- monomers
- producing
- photonics
- Prior art date
Links
- 239000002322 conducting polymer Substances 0.000 title 1
- 229920001940 conductive polymer Polymers 0.000 title 1
- 239000000178 monomer Substances 0.000 claims 6
- 229920000343 polyazomethine Polymers 0.000 claims 6
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 claims 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims 3
- FCEHBMOGCRZNNI-UHFFFAOYSA-N 1-benzothiophene Chemical compound C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 claims 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 2
- 150000004984 aromatic diamines Chemical class 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 claims 2
- 238000006068 polycondensation reaction Methods 0.000 claims 2
- 230000010933 acylation Effects 0.000 claims 1
- 238000005917 acylation reaction Methods 0.000 claims 1
- 150000001299 aldehydes Chemical class 0.000 claims 1
- 230000015572 biosynthetic process Effects 0.000 claims 1
- 150000001720 carbohydrates Chemical class 0.000 claims 1
- 230000000747 cardiac effect Effects 0.000 claims 1
- 239000007795 chemical reaction product Substances 0.000 claims 1
- HKYGSMOFSFOEIP-UHFFFAOYSA-N dichloro(dichloromethoxy)methane Chemical compound ClC(Cl)OC(Cl)Cl HKYGSMOFSFOEIP-UHFFFAOYSA-N 0.000 claims 1
- 125000005594 diketone group Chemical group 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 230000003287 optical effect Effects 0.000 claims 1
- YVOFTMXWTWHRBH-UHFFFAOYSA-N pentanedioyl dichloride Chemical compound ClC(=O)CCCC(Cl)=O YVOFTMXWTWHRBH-UHFFFAOYSA-N 0.000 claims 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims 1
- 230000005855 radiation Effects 0.000 claims 1
- 238000007363 ring formation reaction Methods 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- 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
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K9/00—Tenebrescent materials, i.e. materials for which the range of wavelengths for energy absorption is changed as a result of excitation by some form of energy
- C09K9/02—Organic tenebrescent materials
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/46—Polymerisation initiated by wave energy or particle radiation
- C08F2/48—Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/14—Macromolecular compounds
- C09K2211/1408—Carbocyclic compounds
- C09K2211/1425—Non-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/14—Macromolecular compounds
- C09K2211/1441—Heterocyclic
- C09K2211/1458—Heterocyclic containing sulfur as the only heteroatom
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
Claims (8)
2. Способ получения фотохромных мономеров по п.1, включающий ацилирование бензотиофена дихлорангидридом глутаровой кислоты в хлористом метилене в присутствии хлористого алюминия и последующую восстановительную циклизацию полученных дикетонов под действием TiCL4, Zn в ТГФ в присутствии пиридина с дальнейшим формилированием продуктов реакции дихлорметиловым эфиром в нитробензоле в присутствии хлористого алюминия.
4. Способ получения фотохромных полиазометинов по п.3, включающий поликонденсацию в растворе фотохромного мономера по п.1 с ароматическими диаминами или диальдегидами при температуре примерно от 20 до 200°С.
6. Способ получения кардовых фотохромных полиазометинов по п.5, включающий поликонденсацию в растворе фотохромных мономеров по п.1 с кардовыми ароматическими диаминами или альдегидами при температуре примерно 20-200°С.
7. Применение фотохромных полиазометинов по п.3 в устройствах фотоники.
8. Применение фотохромных кардовых полиазометинов по п.5 в устройствах фотоники, особенно в фотоуправляемых дисплеях, а также трехмерной оперативной оптической памяти, линейных и нелинейно-оптических фотопереключателях излучения.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
RU2004131492/04A RU2345998C2 (ru) | 2004-10-28 | 2004-10-28 | Фотоуправляемые фотохромные электролюминесцирующие и электропроводящие полимеры для фотоники |
KR1020050073123A KR101222146B1 (ko) | 2004-10-28 | 2005-08-10 | 광제어 광색성 전계발광 및 광기술용 도전성 폴리머 |
US11/259,281 US7297751B2 (en) | 2004-10-28 | 2005-10-27 | Photocontrolled photochromic electroluminescent and electroconductive polymers for photonics |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
RU2004131492/04A RU2345998C2 (ru) | 2004-10-28 | 2004-10-28 | Фотоуправляемые фотохромные электролюминесцирующие и электропроводящие полимеры для фотоники |
Publications (2)
Publication Number | Publication Date |
---|---|
RU2004131492A true RU2004131492A (ru) | 2006-04-10 |
RU2345998C2 RU2345998C2 (ru) | 2009-02-10 |
Family
ID=36260759
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU2004131492/04A RU2345998C2 (ru) | 2004-10-28 | 2004-10-28 | Фотоуправляемые фотохромные электролюминесцирующие и электропроводящие полимеры для фотоники |
Country Status (3)
Country | Link |
---|---|
US (1) | US7297751B2 (ru) |
KR (1) | KR101222146B1 (ru) |
RU (1) | RU2345998C2 (ru) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2609887C (en) * | 2005-05-25 | 2015-12-29 | Switch Materials Inc. | Photochromic and electrochromic compounds and synthesis and use thereof |
PL2449051T3 (pl) * | 2009-07-02 | 2016-10-31 | Rozpuszczalne, naprzemienne, skoniugowane polimery elektrochromowe typu donor-akceptor | |
US10451195B2 (en) | 2016-10-25 | 2019-10-22 | International Business Machines Corporation | Hose with tunable flexibility using cyclizable, photochromic molecules |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20030025622A (ko) | 2001-09-21 | 2003-03-29 | 한국화학연구원 | 비닐기 함유 디아릴에텐 단량체 및 이를 이용하여 제조한광활성 고분자 |
RU2345997C2 (ru) * | 2004-09-24 | 2009-02-10 | Самсунг Электроникс Ко., Лтд. | Фотохромные полимеры для трехмерной оперативной оптической памяти |
-
2004
- 2004-10-28 RU RU2004131492/04A patent/RU2345998C2/ru active
-
2005
- 2005-08-10 KR KR1020050073123A patent/KR101222146B1/ko active IP Right Grant
- 2005-10-27 US US11/259,281 patent/US7297751B2/en active Active
Also Published As
Publication number | Publication date |
---|---|
KR101222146B1 (ko) | 2013-01-14 |
US20060091364A1 (en) | 2006-05-04 |
US7297751B2 (en) | 2007-11-20 |
RU2345998C2 (ru) | 2009-02-10 |
KR20060050357A (ko) | 2006-05-19 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Sartor et al. | Exploiting charge-transfer states for maximizing intersystem crossing yields in organic photoredox catalysts | |
Nazir et al. | π-expanded ketocoumarins as efficient, biocompatible initiators for two-photon-induced polymerization | |
Abbotto et al. | Novel heterocycle-based two-photon absorbing dyes | |
Wang et al. | Polymer-based tris (2-phenylpyridine) iridium complexes | |
Goetz et al. | Versatile applications of metallopolymers | |
Nagai et al. | BODIPY-based chain transfer agent: reversibly thermoswitchable luminescent gold nanoparticle stabilized by BODIPY-terminated water-soluble polymer | |
US9920147B2 (en) | Polymeric materials having active cross-linkers, methods for making them, and use thereof | |
Zhang et al. | Irreversible humidity-responsive phosphorescence materials from cellulose for advanced anti-counterfeiting and environmental monitoring | |
Johnson et al. | Metalloinitiation routes to biocompatible poly (lactic acid) and poly (acrylic acid) stars with luminescent ruthenium tris (bipyridine) cores | |
Shelton et al. | High efficiency platinum acetylide nonlinear absorption chromophores covalently linked to poly (methyl methacrylate) | |
Shen et al. | Toward a highly sensitive fluorescence sensing system of an amphiphilic molecular rod: facile synthesis and significant solvent-assisted photophysical tunability | |
US20210355261A1 (en) | Multi-coat polymer photonic crystal films | |
RU2004131492A (ru) | Фотоуправляемые фотохромные электролюминесцирующие и электропроводящие полимеры для фотоники | |
Chung et al. | Dual stimuli-responsive block copolymers for controlled release triggered by upconversion luminescence or temperature variation | |
Chang et al. | Excited-state intramolecular proton transfer via a preexisting hydrogen bond in semirigid polyquinoline | |
Gandini et al. | Furan derivatives and furan chemistry at the service of macromolecular materials | |
Li et al. | Synthesis and characterization of nylons based on hexadecane diacid | |
Kohsaka et al. | Polymer chemistry of α-substituted acrylates designed for functional-group synergy | |
Shikinaka et al. | Stiff and hierarchical chain nature of atactic and stereoregular poly (substituted methylene) s | |
Ouchi et al. | Synthesis of a Stimuli‐Responsive P‐Chiral Polymer with Chiral Phosphorus Atoms and Azobenzene Moieties in the Main Chain | |
Kasprzyk et al. | Fluorescent citric acid-modified silicone materials | |
Yang et al. | Control of molecular structures and photophysical properties of zinc (II) porphyrin dendrimers using bidentate guests: Utilization of flexible dendrimer structures as a controllable mold | |
US9024037B1 (en) | Two-photon absorbing polymers based on triarylamine-benzobisthiazole-triarylamine quadrupolar-structure motif | |
Vacareanu et al. | New symmetrical conjugated thiophene-azomethines containing triphenylamine or carbazole units: Synthesis, thermal and optoelectrochemical properties | |
Yang et al. | Synthesis, chemosensory properties, and self-assembly of terpyridine-containing conjugated polycarbazole through RAFT polymerization and Heck coupling reaction |