JP2002268097A5 - - Google Patents
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- JP2002268097A5 JP2002268097A5 JP2001070371A JP2001070371A JP2002268097A5 JP 2002268097 A5 JP2002268097 A5 JP 2002268097A5 JP 2001070371 A JP2001070371 A JP 2001070371A JP 2001070371 A JP2001070371 A JP 2001070371A JP 2002268097 A5 JP2002268097 A5 JP 2002268097A5
- Authority
- JP
- Japan
- Prior art keywords
- ring
- group
- display device
- organic compound
- electrophoretic 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
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- 238000001962 electrophoresis Methods 0.000 claims 5
- 150000002894 organic compounds Chemical class 0.000 claims 3
- ZYGHJZDHTFUPRJ-UHFFFAOYSA-N Coumarin Chemical compound C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 claims 2
- 239000002612 dispersion media Substances 0.000 claims 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims 2
- 239000002245 particle Substances 0.000 claims 2
- -1 pyrerazine ring Chemical group 0.000 claims 2
- DYHJTAONEPZTCO-UHFFFAOYSA-N 1,2-dihydrophenanthrene Chemical compound C1=CC=CC2=C(C=CCC3)C3=CC=C21 DYHJTAONEPZTCO-UHFFFAOYSA-N 0.000 claims 1
- CUFNKYGDVFVPHO-UHFFFAOYSA-N Azulene Chemical compound C1=CC=CC2=CC=CC2=C1 CUFNKYGDVFVPHO-UHFFFAOYSA-N 0.000 claims 1
- NNBZCPXTIHJBJL-UHFFFAOYSA-N Decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 claims 1
- CXWGKAYMVASWDQ-UHFFFAOYSA-N Dithiane Chemical group C1CCSSC1 CXWGKAYMVASWDQ-UHFFFAOYSA-N 0.000 claims 1
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N Fluorene Chemical compound C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 claims 1
- YBYIRNPNPLQARY-UHFFFAOYSA-N Indene Chemical compound C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 claims 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N Tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 claims 1
- 125000004423 acyloxy group Chemical group 0.000 claims 1
- 125000003342 alkenyl group Chemical group 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 125000000304 alkynyl group Chemical group 0.000 claims 1
- 125000003277 amino group Chemical group 0.000 claims 1
- 125000006367 bivalent amino carbonyl group Chemical group [H]N([*:1])C([*:2])=O 0.000 claims 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 1
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 239000000460 chlorine Substances 0.000 claims 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- 229960000956 coumarin Drugs 0.000 claims 1
- 235000001671 coumarin Nutrition 0.000 claims 1
- 125000004093 cyano group Chemical group *C#N 0.000 claims 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 1
- 125000000596 cyclohexenyl group Chemical group C1(=CCCCC1)* 0.000 claims 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 1
- 125000004663 dialkyl amino group Chemical group 0.000 claims 1
- 125000000532 dioxanyl group Chemical group 0.000 claims 1
- 229910052731 fluorine Inorganic materials 0.000 claims 1
- 239000011737 fluorine Substances 0.000 claims 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N furane Chemical group C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 125000004435 hydrogen atoms Chemical class [H]* 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 229910052740 iodine Inorganic materials 0.000 claims 1
- 239000011630 iodine Substances 0.000 claims 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- YNAVUWVOSKDBBP-UHFFFAOYSA-N morpholine Chemical group C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 125000003386 piperidinyl group Chemical group 0.000 claims 1
- JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 1
- 125000000714 pyrimidinyl group Chemical group 0.000 claims 1
- 125000000168 pyrrolyl group Chemical group 0.000 claims 1
- SMWDFEZZVXVKRB-UHFFFAOYSA-N quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- 125000001424 substituent group Chemical group 0.000 claims 1
- 125000000542 sulfonic acid group Chemical group 0.000 claims 1
- WYURNTSHIVDZCO-UHFFFAOYSA-N tetrahydrofuran Chemical group C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims 1
- 125000004001 thioalkyl group Chemical group 0.000 claims 1
- YTPLMLYBLZKORZ-UHFFFAOYSA-N thiophene Chemical group C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims 1
- 125000004954 trialkylamino group Chemical group 0.000 claims 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
Claims (3)
前記有機化合物の分散媒中の含有率は３０体積％以上であることを特徴とする請求項１記載の電気泳動表示装置。
【化１】
式中、Ａ１〜Ａ６は、ベンゼン環、シクロヘキサン環、ジオキサン環、ピリミジン環、フラン環、テトラヒドロフラン環、ジチアン環、ピペリジン環、ピレラジン環、モーホリン環、シクロペンタン環、シクロブタン環、ピリジン環、チオフェン環、ピロール環、またはシクロヘキセン環であり、
Ｘ１〜Ｘ４，Ｙ１〜Ｙ３，Ｚは、１個または複数個の置換基（水素、フッ素、塩素、臭素、ヨウ素、シアノ基、ニトロ基、アミノ基、ヒドロキシル基、アルカノイルオキシ基、アルコキシカルボニル基、カルボキシ基、トリフルオロメチル基、トリフルオロメトキシ基、アルコキシメチレン基、アルキル基、アルコキシ基、アルケニル基、アルキニル基、スルホン酸基、チオアルキル基、モノ、ジ、またはトリアルキルアミノ基）を示し、
Ｂ１〜Ｂ４は、なし（環同士の単結合）か、ＣＯＯ、ＯＣＯ、ＣＨ＝Ｎ、Ｎ＝ＣＨ、ＣＨ＝ＣＨ、（ＣＨ2)n Ｏ、Ｏ（ＣＨ2)n 、（ＣＨ2)n 、Ｏ（ＣＨ2)n Ｏ、ＣＨ＝ＣＨ−ＣＯＯ、ＯＣＯ−ＣＨ＝ＣＨ、Ｏ、ＣＯ、ＮＨＣＯ、ＣＯＮＨ、Ｎ＝Ｎ、Ｎ2 Ｏ、Ｃ≡Ｃ、ＳＯ、ＳＯ2 、またはＮＨを示し（ｎは１〜１０の整数）、
Ｃ１，Ｃ２は、ナフタレン、テトラヒドロナフタレン、デカヒドロナフタレン、インデン、キノリン、クマリン、アズレン、フルオレン、ジヒドロフェナントレンを示す。The organic compound is one or a mixture of two or more represented by any one of the following structural formulas (1) to (4):
The electrophoretic display device according to claim 1, wherein the content of the organic compound in the dispersion medium is 30% by volume or more.
[Chemical 1]
In the formula, A1 to A6 are benzene ring, cyclohexane ring, dioxane ring, pyrimidine ring, furan ring, tetrahydrofuran ring, dithiane ring, piperidine ring, pyrerazine ring, morpholine ring, cyclopentane ring, cyclobutane ring, pyridine ring, thiophene ring. , A pyrrole ring, or a cyclohexene ring,
X1-X4, Y1-Y3, Z are one or more substituents (hydrogen, fluorine, chlorine, bromine, iodine, cyano group, nitro group, amino group, hydroxyl group, alkanoyloxy group, alkoxycarbonyl group, Carboxy group, trifluoromethyl group, trifluoromethoxy group, alkoxymethylene group, alkyl group, alkoxy group, alkenyl group, alkynyl group, sulfonic acid group, thioalkyl group, mono, di, or trialkylamino group)
B1~B4 either without (single bond rings), COO, OCO, CH = N, N = CH, CH = CH, (CH 2) n O, O (CH 2) n, (CH 2) n , O (CH 2 ) n O, CH═CH—COO, OCO—CH═CH, O, CO, NHCO, CONH, N═N, N 2 O, C≡C, SO, SO 2 , or NH (N is an integer from 1 to 10),
C1, C2 represents naphthalene, tetrahydronaphthalene, decahydronaphthalene, indene, quinoline, coumarin, azulene, fluorene, dihydrophenanthrene.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2001070371A JP4048721B2 (en) | 2001-03-13 | 2001-03-13 | Dispersion medium |
| US10/097,361 US6650463B2 (en) | 2001-03-13 | 2002-03-12 | Electrophoretic display device |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2001070371A JP4048721B2 (en) | 2001-03-13 | 2001-03-13 | Dispersion medium |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2002268097A JP2002268097A (en) | 2002-09-18 |
| JP2002268097A5 true JP2002268097A5 (en) | 2005-03-03 |
| JP4048721B2 JP4048721B2 (en) | 2008-02-20 |
Family
ID=18928256
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001070371A Expired - Fee Related JP4048721B2 (en) | 2001-03-13 | 2001-03-13 | Dispersion medium |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP4048721B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2637884A1 (en) * | 2006-02-13 | 2007-08-23 | Wellstat Therapeutics Corporation | Compounds for the treatment of metabolic disorders |
-
2001
- 2001-03-13 JP JP2001070371A patent/JP4048721B2/en not_active Expired - Fee Related
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