JP2007533773A5 - - Google Patents
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- JP2007533773A5 JP2007533773A5 JP2006523220A JP2006523220A JP2007533773A5 JP 2007533773 A5 JP2007533773 A5 JP 2007533773A5 JP 2006523220 A JP2006523220 A JP 2006523220A JP 2006523220 A JP2006523220 A JP 2006523220A JP 2007533773 A5 JP2007533773 A5 JP 2007533773A5
- Authority
- JP
- Japan
- Prior art keywords
- fluorinated
- alkyl
- heteroalkyl
- aryl
- heteroaryl
- 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.)
- Pending
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- 125000000217 alkyl group Chemical group 0.000 claims description 147
- 125000003118 aryl group Chemical group 0.000 claims description 122
- 125000004404 heteroalkyl group Chemical group 0.000 claims description 122
- 125000001072 heteroaryl group Chemical group 0.000 claims description 122
- 239000000975 dye Substances 0.000 claims description 110
- 239000003086 colorant Substances 0.000 claims description 109
- 229910052739 hydrogen Inorganic materials 0.000 claims description 66
- 239000001257 hydrogen Substances 0.000 claims description 66
- 125000002947 alkylene group Chemical group 0.000 claims description 56
- 150000002431 hydrogen Chemical class 0.000 claims description 54
- 125000000732 arylene group Chemical group 0.000 claims description 34
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims description 26
- 229910052731 fluorine Inorganic materials 0.000 claims description 26
- 239000011737 fluorine Substances 0.000 claims description 26
- 229910052736 halogen Inorganic materials 0.000 claims description 22
- 150000002367 halogens Chemical class 0.000 claims description 22
- 229920002313 fluoropolymer Polymers 0.000 claims description 14
- 229910052760 oxygen Inorganic materials 0.000 claims description 14
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 12
- 125000005647 linker group Chemical group 0.000 claims description 11
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 8
- 239000002184 metal Substances 0.000 claims description 8
- 229910052751 metal Inorganic materials 0.000 claims description 8
- LKKPNUDVOYAOBB-UHFFFAOYSA-N naphthalocyanine Chemical compound N1C(N=C2C3=CC4=CC=CC=C4C=C3C(N=C3C4=CC5=CC=CC=C5C=C4C(=N4)N3)=N2)=C(C=C2C(C=CC=C2)=C2)C2=C1N=C1C2=CC3=CC=CC=C3C=C2C4=N1 LKKPNUDVOYAOBB-UHFFFAOYSA-N 0.000 claims description 8
- 239000001301 oxygen Substances 0.000 claims description 8
- FYNROBRQIVCIQF-UHFFFAOYSA-N pyrrolo[3,2-b]pyrrole-5,6-dione Chemical compound C1=CN=C2C(=O)C(=O)N=C21 FYNROBRQIVCIQF-UHFFFAOYSA-N 0.000 claims description 8
- 238000006467 substitution reaction Methods 0.000 claims description 8
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 claims description 6
- 229910052717 sulfur Inorganic materials 0.000 claims description 6
- 125000001624 naphthyl 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 5
- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 claims description 4
- XJHABGPPCLHLLV-UHFFFAOYSA-N benzo[de]isoquinoline-1,3-dione Chemical compound C1=CC(C(=O)NC2=O)=C3C2=CC=CC3=C1 XJHABGPPCLHLLV-UHFFFAOYSA-N 0.000 claims description 4
- 125000003709 fluoroalkyl group Chemical group 0.000 claims description 4
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims description 4
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 claims description 4
- 150000004032 porphyrins Chemical class 0.000 claims description 4
- 239000002904 solvent Substances 0.000 claims description 4
- 239000000984 vat dye Substances 0.000 claims description 4
- 229910052802 copper Inorganic materials 0.000 claims description 3
- 229910052725 zinc Inorganic materials 0.000 claims description 3
- 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 claims description 2
- 239000001000 anthraquinone dye Substances 0.000 claims description 2
- 150000004056 anthraquinones Chemical class 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- 239000000460 chlorine Substances 0.000 claims description 2
- 229910052749 magnesium Inorganic materials 0.000 claims description 2
- CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 claims description 2
- 239000001007 phthalocyanine dye Substances 0.000 claims description 2
- 229910052710 silicon Inorganic materials 0.000 claims description 2
- 229910052719 titanium Inorganic materials 0.000 claims description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- 0 CCC(*C*)*1C=Cc(cc(c(C2=*3*4(*56)*(C(c7cc8ccccc8cc77)=*8)C7=*2)c2)C3=*C5=C(C=C(C=CC=C3)C3=C3)C3=C6*=C3*4=C8C4=Cc5ccccc5CC34)c2C=C1 Chemical compound CCC(*C*)*1C=Cc(cc(c(C2=*3*4(*56)*(C(c7cc8ccccc8cc77)=*8)C7=*2)c2)C3=*C5=C(C=C(C=CC=C3)C3=C3)C3=C6*=C3*4=C8C4=Cc5ccccc5CC34)c2C=C1 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US49370303P | 2003-08-08 | 2003-08-08 | |
| US50192103P | 2003-09-10 | 2003-09-10 | |
| US10/903,923 US7390901B2 (en) | 2003-08-08 | 2004-07-29 | Fluorinated dyes or colorants and their uses |
| PCT/US2004/024932 WO2005017046A2 (en) | 2003-08-08 | 2004-07-30 | Fluorinated dyes or colorants and their uses |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2007533773A JP2007533773A (ja) | 2007-11-22 |
| JP2007533773A5 true JP2007533773A5 (cg-RX-API-DMAC7.html) | 2008-01-10 |
Family
ID=34198962
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006523220A Pending JP2007533773A (ja) | 2003-08-08 | 2004-07-30 | フッ素化染料又は着色剤及びそれらの使用 |
Country Status (5)
| Country | Link |
|---|---|
| US (3) | US7390901B2 (cg-RX-API-DMAC7.html) |
| EP (1) | EP1664202A4 (cg-RX-API-DMAC7.html) |
| JP (1) | JP2007533773A (cg-RX-API-DMAC7.html) |
| TW (1) | TWI291981B (cg-RX-API-DMAC7.html) |
| WO (1) | WO2005017046A2 (cg-RX-API-DMAC7.html) |
Families Citing this family (91)
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| TWI293715B (en) * | 2002-10-10 | 2008-02-21 | Sipix Imaging Inc | A method for inducing or enhancing the threshold of an electrophoretic display, an electrophoretic fluid and an electrophoretic display |
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| US7572394B2 (en) * | 2003-11-04 | 2009-08-11 | Sipix Imaging, Inc. | Electrophoretic dispersions |
| US7374634B2 (en) * | 2004-05-12 | 2008-05-20 | Sipix Imaging, Inc. | Process for the manufacture of electrophoretic displays |
| US8625188B2 (en) * | 2004-05-12 | 2014-01-07 | Sipix Imaging, Inc. | Process for the manufacture of electrophoretic displays |
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2004
- 2004-07-29 US US10/903,923 patent/US7390901B2/en not_active Expired - Fee Related
- 2004-07-30 WO PCT/US2004/024932 patent/WO2005017046A2/en not_active Ceased
- 2004-07-30 JP JP2006523220A patent/JP2007533773A/ja active Pending
- 2004-07-30 EP EP04779863A patent/EP1664202A4/en not_active Withdrawn
- 2004-08-03 TW TW093123192A patent/TWI291981B/zh not_active IP Right Cessation
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2006
- 2006-05-31 US US11/444,969 patent/US7473782B2/en not_active Expired - Fee Related
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2008
- 2008-03-21 US US12/053,492 patent/US7951938B2/en not_active Expired - Fee Related