JPS60200233A - エレクトロクロミツク表示素子 - Google Patents
エレクトロクロミツク表示素子Info
- Publication number
- JPS60200233A JPS60200233A JP59056608A JP5660884A JPS60200233A JP S60200233 A JPS60200233 A JP S60200233A JP 59056608 A JP59056608 A JP 59056608A JP 5660884 A JP5660884 A JP 5660884A JP S60200233 A JPS60200233 A JP S60200233A
- Authority
- JP
- Japan
- Prior art keywords
- group
- electrode
- polymer film
- electrochromic
- display
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000000463 material Substances 0.000 claims abstract description 28
- 229920006254 polymer film Polymers 0.000 claims abstract description 21
- 239000000758 substrate Substances 0.000 claims abstract description 19
- 238000006479 redox reaction Methods 0.000 claims abstract description 10
- PCCVSPMFGIFTHU-UHFFFAOYSA-N tetracyanoquinodimethane Chemical compound N#CC(C#N)=C1C=CC(=C(C#N)C#N)C=C1 PCCVSPMFGIFTHU-UHFFFAOYSA-N 0.000 claims abstract description 4
- 150000003839 salts Chemical class 0.000 claims abstract description 3
- 239000000126 substance Substances 0.000 claims description 13
- -1 heterocyclic aldehyde Chemical class 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 150000003934 aromatic aldehydes Chemical class 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 238000006482 condensation reaction Methods 0.000 claims description 2
- 125000004122 cyclic group Chemical group 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 2
- 125000001424 substituent group Chemical group 0.000 claims description 2
- 125000004434 sulfur atom Chemical group 0.000 claims description 2
- 125000002947 alkylene group Chemical group 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 230000004044 response Effects 0.000 abstract description 6
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 239000004020 conductor Substances 0.000 abstract 1
- 125000005504 styryl group Chemical group 0.000 abstract 1
- 239000000243 solution Substances 0.000 description 10
- 239000010408 film Substances 0.000 description 9
- 238000003411 electrode reaction Methods 0.000 description 8
- 229920000642 polymer Polymers 0.000 description 7
- 229920005597 polymer membrane Polymers 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- 239000000975 dye Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 5
- 239000003792 electrolyte Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000005562 fading Methods 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 239000000565 sealant Substances 0.000 description 3
- 238000007789 sealing Methods 0.000 description 3
- 238000012546 transfer Methods 0.000 description 3
- 239000004793 Polystyrene Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 2
- 150000004056 anthraquinones Chemical class 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 239000011356 non-aqueous organic solvent Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- KBLZDCFTQSIIOH-UHFFFAOYSA-M tetrabutylazanium;perchlorate Chemical compound [O-]Cl(=O)(=O)=O.CCCC[N+](CCCC)(CCCC)CCCC KBLZDCFTQSIIOH-UHFFFAOYSA-M 0.000 description 2
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
- 229910001111 Fine metal Inorganic materials 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000011981 development test Methods 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000007606 doctor blade method Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000004070 electrodeposition Methods 0.000 description 1
- 239000008151 electrolyte solution Substances 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920001290 polyvinyl ester Polymers 0.000 description 1
- DNXIASIHZYFFRO-UHFFFAOYSA-N pyrazoline Chemical compound C1CN=NC1 DNXIASIHZYFFRO-UHFFFAOYSA-N 0.000 description 1
- 238000009790 rate-determining step (RDS) Methods 0.000 description 1
- 230000004043 responsiveness Effects 0.000 description 1
- 239000003566 sealing material Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
Classifications
-
- G—PHYSICS
- G02—OPTICS
- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
- G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour
- G02F1/15—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on an electrochromic effect
- G02F1/153—Constructional details
- G02F1/1533—Constructional details structural features not otherwise provided for
Landscapes
- Physics & Mathematics (AREA)
- Nonlinear Science (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Electrochromic Elements, Electrophoresis, Or Variable Reflection Or Absorption Elements (AREA)
- Devices For Indicating Variable Information By Combining Individual Elements (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59056608A JPS60200233A (ja) | 1984-03-23 | 1984-03-23 | エレクトロクロミツク表示素子 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59056608A JPS60200233A (ja) | 1984-03-23 | 1984-03-23 | エレクトロクロミツク表示素子 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS60200233A true JPS60200233A (ja) | 1985-10-09 |
| JPH0361170B2 JPH0361170B2 (enrdf_load_stackoverflow) | 1991-09-19 |
Family
ID=13031952
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP59056608A Granted JPS60200233A (ja) | 1984-03-23 | 1984-03-23 | エレクトロクロミツク表示素子 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS60200233A (enrdf_load_stackoverflow) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7399319B2 (en) | 2005-07-22 | 2008-07-15 | L'oreal S.A. | Dyeing composition comprising a dye chosen from styryl and imine dyes and methods for dyeing keratin fibers |
| US7527654B2 (en) | 2006-10-13 | 2009-05-05 | L'oreal S.A. | Dyeing process using a dye of styryl or imine type in combination with a weak acid, and device for implementing the process |
| US7585332B2 (en) | 2006-10-13 | 2009-09-08 | L'oreal S.A. | Composition containing a styryl or imine type dye and a thiol compound, hair coloring process and device |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5050892A (enrdf_load_stackoverflow) * | 1973-07-30 | 1975-05-07 | ||
| JPS5848031A (ja) * | 1981-09-17 | 1983-03-19 | Matsushita Electric Ind Co Ltd | エレクトロクロミツク表示素子 |
| JPS58136685A (ja) * | 1982-02-08 | 1983-08-13 | Pilot Pen Co Ltd:The | エレクトロクロミツク表示材料およびその製造法並びにエレクトロクロミツク表示体 |
-
1984
- 1984-03-23 JP JP59056608A patent/JPS60200233A/ja active Granted
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5050892A (enrdf_load_stackoverflow) * | 1973-07-30 | 1975-05-07 | ||
| JPS5848031A (ja) * | 1981-09-17 | 1983-03-19 | Matsushita Electric Ind Co Ltd | エレクトロクロミツク表示素子 |
| JPS58136685A (ja) * | 1982-02-08 | 1983-08-13 | Pilot Pen Co Ltd:The | エレクトロクロミツク表示材料およびその製造法並びにエレクトロクロミツク表示体 |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7399319B2 (en) | 2005-07-22 | 2008-07-15 | L'oreal S.A. | Dyeing composition comprising a dye chosen from styryl and imine dyes and methods for dyeing keratin fibers |
| US7527654B2 (en) | 2006-10-13 | 2009-05-05 | L'oreal S.A. | Dyeing process using a dye of styryl or imine type in combination with a weak acid, and device for implementing the process |
| US7585332B2 (en) | 2006-10-13 | 2009-09-08 | L'oreal S.A. | Composition containing a styryl or imine type dye and a thiol compound, hair coloring process and device |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0361170B2 (enrdf_load_stackoverflow) | 1991-09-19 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |