RU98100245A - Новые прекрасители - Google Patents
Новые прекрасителиInfo
- Publication number
- RU98100245A RU98100245A RU98100245/04A RU98100245A RU98100245A RU 98100245 A RU98100245 A RU 98100245A RU 98100245/04 A RU98100245/04 A RU 98100245/04A RU 98100245 A RU98100245 A RU 98100245A RU 98100245 A RU98100245 A RU 98100245A
- Authority
- RU
- Russia
- Prior art keywords
- dye
- formula
- following formula
- composition
- hydroxyphenyl
- Prior art date
Links
- 231100000489 sensitizer Toxicity 0.000 claims 8
- WQINSVOOIJDOLJ-UHFFFAOYSA-N 2-(1,3-dioxoisoindol-2-yl)acetic acid Chemical group C1=CC=C2C(=O)N(CC(=O)O)C(=O)C2=C1 WQINSVOOIJDOLJ-UHFFFAOYSA-N 0.000 claims 4
- GJKGAPPUXSSCFI-UHFFFAOYSA-N 2-hydroxy-1-[4-(2-hydroxyethoxy)phenyl]-2-methylpropan-1-one Chemical group CC(C)(O)C(=O)C1=CC=C(OCCO)C=C1 GJKGAPPUXSSCFI-UHFFFAOYSA-N 0.000 claims 4
- CMYKNVKCQCJOKO-UHFFFAOYSA-N 2-hydroxy-2-methyl-1-[4-[2-[4-(3-oxobutyl)phenoxy]ethoxy]phenyl]propan-1-one Chemical compound C1=CC(CCC(=O)C)=CC=C1OCCOC1=CC=C(C(=O)C(C)(C)O)C=C1 CMYKNVKCQCJOKO-UHFFFAOYSA-N 0.000 claims 4
- -1 4- (4-hydroxyphenyl) -2-butanone-1- (4- (2-hydroxyethoxy) phenyl) -2-hydroxy-2-methylpropan-1-one Chemical compound 0.000 claims 4
- AODLDBUFTUGNEM-UHFFFAOYSA-N 4-[4-(4-benzoylcyclohexyl)oxyphenyl]butan-2-one Chemical compound C1=CC(CCC(=O)C)=CC=C1OC1CCC(C(=O)C=2C=CC=CC=2)CC1 AODLDBUFTUGNEM-UHFFFAOYSA-N 0.000 claims 4
- 125000004203 4-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 4
- NJGBTKGETPDVIK-UHFFFAOYSA-N Raspberry ketone Chemical compound CC(=O)CCC1=CC=C(O)C=C1 NJGBTKGETPDVIK-UHFFFAOYSA-N 0.000 claims 4
- 150000002148 esters Chemical class 0.000 claims 4
- NYNCZOLNVTXTTP-UHFFFAOYSA-N ethyl 2-(1,3-dioxoisoindol-2-yl)acetate Chemical compound C1=CC=C2C(=O)N(CC(=O)OCC)C(=O)C2=C1 NYNCZOLNVTXTTP-UHFFFAOYSA-N 0.000 claims 4
- 150000002576 ketones Chemical class 0.000 claims 4
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 4
- 229940004296 Formula 21 Drugs 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims 1
- 230000002427 irreversible Effects 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- OZAIFHULBGXAKX-UHFFFAOYSA-N precursor Substances N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 claims 1
Claims (1)
1. Композиция прекрасителя, содержащая молекулу прекрасителя, включающую краситель, ковалентно связанный с трансорбером излучения, приспособленный так, чтобы молекула прекрасителя была бесцветной и образовывала цвет при обработке излучением, причем трансорбер излучения содержит селективный для длины волны сенсибилизатор, ковалентно связанный с фотореактором, генерирующим реакционноспособную разновидность молекулы.
2. Композиция прекрасителя по п.1, отличающаяся тем, что краситель представляет аминотриарилметан или его производное.
3. Композиция прекрасителя по п.1, отличающаяся тем, что фотореактор представляет 1-[4-(2-гидроксиэтокси)фенил] -2-гидрокси-2-метилпропан-1-он, имеющий следующую формулу
или 1-гидроксициклогексанфенилкетон, имеющий следующую формулу
4. Композиция прекрасителя по п.1, отличающаяся тем, что селективный для длины волны сенсибилизатор представляет фталоилглицин, имеющий формулу
или 4-(4-гидроксифенил)бутан-2-он, имеющий следующую формулу
5. Композиция прекрасителя по п. 1, отличающаяся тем, что трансорбер излучения представляет 2-(п-(2-метиллактоил)-фенокси)этил-1,3-диоксо-2-изоиндолинацетат, имеющий формулу
эфир фталоилглицилциклогексилфенилкетона, имеющий формулу
4-(4-оксифенил)-2-бутанон-1-(4-(2-оксиэтокси)фенил)-2-гидрокси-2-метилпропан-1-он (или 2-гидрокси-2-метил-4'-(2-(п-(3-оксобутил)фенокси)этокси)пропиофенон), имеющий формулу
или 4-(4-оксифенил)-2-бутанонциклогексилфенилкетон (или 4-(п-((4-бензоилциклогексил)окси)фенил)-2-бутанон), имеющий формулу
6. Композиция прекрасителя по п. 1, отличающаяся тем, что краситель представляет кристаллический фиолетовый и молекула прекрасителя имеет следующую формулу
где Х представляет трансорбер излучения.
или 1-гидроксициклогексанфенилкетон, имеющий следующую формулу
4. Композиция прекрасителя по п.1, отличающаяся тем, что селективный для длины волны сенсибилизатор представляет фталоилглицин, имеющий формулу
или 4-(4-гидроксифенил)бутан-2-он, имеющий следующую формулу
5. Композиция прекрасителя по п. 1, отличающаяся тем, что трансорбер излучения представляет 2-(п-(2-метиллактоил)-фенокси)этил-1,3-диоксо-2-изоиндолинацетат, имеющий формулу
эфир фталоилглицилциклогексилфенилкетона, имеющий формулу
4-(4-оксифенил)-2-бутанон-1-(4-(2-оксиэтокси)фенил)-2-гидрокси-2-метилпропан-1-он (или 2-гидрокси-2-метил-4'-(2-(п-(3-оксобутил)фенокси)этокси)пропиофенон), имеющий формулу
или 4-(4-оксифенил)-2-бутанонциклогексилфенилкетон (или 4-(п-((4-бензоилциклогексил)окси)фенил)-2-бутанон), имеющий формулу
6. Композиция прекрасителя по п. 1, отличающаяся тем, что краситель представляет кристаллический фиолетовый и молекула прекрасителя имеет следующую формулу
где Х представляет трансорбер излучения.
7. Композиция прекрасителя по п. 6, отличающаяся тем, что молекула прекрасителя имеет формулу
или
8. Композиция прекрасителя по п. 1, отличающаяся тем, что молекула прекрасителя имеет формулу
где Х представляет трансорбер излучения и где R представляет водород, метильную или этильную группу.
или
8. Композиция прекрасителя по п. 1, отличающаяся тем, что молекула прекрасителя имеет формулу
где Х представляет трансорбер излучения и где R представляет водород, метильную или этильную группу.
9. Способ проявления цвета, заключающийся в получении композиции прекрасителя, содержащей молекулу прекрасителя, включающую краситель, ковалентно связанный с трансорбером излучения, приспособленный так, чтобы молекула прекрасителя была бесцветной и образовывала цвет при обработке излучением, причем трансорбер излучения содержит селективный для длины волны сенсибилизатор, ковалентно связанный с фотореактором, генерирующим реакционноспособную разновидность молекулы, и обработке композиции прекрасителя излучением при длине волны и уровне дозировки, достаточных для необратимого изменения молекулы прекрасителя.
10. Способ по п.9, отличающийся тем, что краситель представляет собой аминотриарилметан или его производное.
11. Способ по п.9, отличающийся тем, что фотореактор представляет 1-[4-(2-гидроксиэтокси)фенил]-2-гидрокси-2-метилпропан-1-он, имеющий следующую формулу
или 1-гидроксициклогексанфенилкетон, имеющий следующую формулу
12. Способ по п. 9, отличающийся тем, что селективный для длины волны сенсибилизатор представляет фталоилглицин, имеющий следующую формулу
или 4-(4-гидроксифенил)бутан-2-он, имеющий следующую формулу
13. Способ по п. 9, отличающийся тем, что трансорбер излучения представляет собой 2-(п-(2-метиллактоил)-фенокси)-этил-1,3-диоксо-2-изоиндолинацетат, имеющий формулу
эфир фталоилглицилциклогексилфенилкетона, имеющий формулу
4-(4-оксифенил)-2-бутанон-1-(4-(2-оксиэтокси)фенил)-2-гидрокси-2-метилпропан-1-он (или 2-гидрокси-2-метил-4'-(2-(п-(3-оксобутил)фенокси)этокси)пропиофенон), имеющий формулу
или 4-(4-оксифенил)-2-бутанонциклогексилфенилкетон (или 4-(п-((4-бензоилциклогексил)окси)фенил)-2-бутанон), имеющий формулу
14. Способ по п.9, отличающийся тем, что краситель представляет кристаллический фиолетовый и молекула прекрасителя имеет следующую формулу
где Х представляет трансорбер излучения.
или 1-гидроксициклогексанфенилкетон, имеющий следующую формулу
12. Способ по п. 9, отличающийся тем, что селективный для длины волны сенсибилизатор представляет фталоилглицин, имеющий следующую формулу
или 4-(4-гидроксифенил)бутан-2-он, имеющий следующую формулу
13. Способ по п. 9, отличающийся тем, что трансорбер излучения представляет собой 2-(п-(2-метиллактоил)-фенокси)-этил-1,3-диоксо-2-изоиндолинацетат, имеющий формулу
эфир фталоилглицилциклогексилфенилкетона, имеющий формулу
4-(4-оксифенил)-2-бутанон-1-(4-(2-оксиэтокси)фенил)-2-гидрокси-2-метилпропан-1-он (или 2-гидрокси-2-метил-4'-(2-(п-(3-оксобутил)фенокси)этокси)пропиофенон), имеющий формулу
или 4-(4-оксифенил)-2-бутанонциклогексилфенилкетон (или 4-(п-((4-бензоилциклогексил)окси)фенил)-2-бутанон), имеющий формулу
14. Способ по п.9, отличающийся тем, что краситель представляет кристаллический фиолетовый и молекула прекрасителя имеет следующую формулу
где Х представляет трансорбер излучения.
15. Способ по п.14, отличающийся тем, что молекула прекрасителя имеет формулу
или
16. Композиция изменяемого красителя, содержащая лейкокраситель, смешанный с трансорбером излучения, содержащим селективный для длины волны сенсибилизатор, ковалентно связанный с фотореактором, генерирующим реакционноспособную разновидность молекулы.
или
16. Композиция изменяемого красителя, содержащая лейкокраситель, смешанный с трансорбером излучения, содержащим селективный для длины волны сенсибилизатор, ковалентно связанный с фотореактором, генерирующим реакционноспособную разновидность молекулы.
17. Композиция изменяемого красителя по п.16, отличающаяся тем, что лейкокраситель представляет собой лейкоаминотриарилметан или его производное.
18. Композиция изменяемого красителя по п.16, отличающаяся тем, что фотореактор представляет собой 1-[4-(2-гидроксиэтокси)фенил]-2-гидрокси-2-метилпропан-1-он, имеющий следующую формулу
или 1-гидроксициклогексанфенилкетон, имеющий формулу
19. Композиция изменяемого красителя по п.16, отличающаяся тем, что селективный для длины волны сенсибилизатор представляет фталоилглицин, имеющий следующую формулу
или 4-(4-гидроксифенил)бутан-2-он, имеющий следующую формулу
20. Композиция изменяемого красителя по п.16, отличающаяся тем, что трансорбер излучения представляет собой 2-(п-(2-метиллактоил)-фенокси)-этил-1,3-диоксо-2-изоиндолинацетат, имеющий формулу
эфир фталоилглицилциклогексилфенилкетона, имеющий формулу
4-(4-оксифенил)-2-бутанон-1-(4-(2-оксиэтокси)фенил)-2-гидрокси-2-метилпропан-1-он (или 2-гидрокси-2-метил-4'-(2-(п-(3-оксобутил)фенокси)этокси)пропиофенон), имеющий формулу
или 4-(4-оксифенил)-2-бутанонциклогексилфенилкетон (или 4-(п-((4-бензоилциклогексил)окси)фенил)-2-бутанон), имеющий формулу
21. Способ проявления цвета, заключающийся в получении композиции, содержащей лейкокраситель, смешанный с трансорбером излучения, содержащим селективный для длины волны сенсибилизатор, ковалентно связанный с фотореактором, генерирующим реакционноспособную разновидность молекулы, и обработке композиции излучением при длине волны и уровне дозировки, достаточных для необратимого изменения лейкокрасителя.
или 1-гидроксициклогексанфенилкетон, имеющий формулу
19. Композиция изменяемого красителя по п.16, отличающаяся тем, что селективный для длины волны сенсибилизатор представляет фталоилглицин, имеющий следующую формулу
или 4-(4-гидроксифенил)бутан-2-он, имеющий следующую формулу
20. Композиция изменяемого красителя по п.16, отличающаяся тем, что трансорбер излучения представляет собой 2-(п-(2-метиллактоил)-фенокси)-этил-1,3-диоксо-2-изоиндолинацетат, имеющий формулу
эфир фталоилглицилциклогексилфенилкетона, имеющий формулу
4-(4-оксифенил)-2-бутанон-1-(4-(2-оксиэтокси)фенил)-2-гидрокси-2-метилпропан-1-он (или 2-гидрокси-2-метил-4'-(2-(п-(3-оксобутил)фенокси)этокси)пропиофенон), имеющий формулу
или 4-(4-оксифенил)-2-бутанонциклогексилфенилкетон (или 4-(п-((4-бензоилциклогексил)окси)фенил)-2-бутанон), имеющий формулу
21. Способ проявления цвета, заключающийся в получении композиции, содержащей лейкокраситель, смешанный с трансорбером излучения, содержащим селективный для длины волны сенсибилизатор, ковалентно связанный с фотореактором, генерирующим реакционноспособную разновидность молекулы, и обработке композиции излучением при длине волны и уровне дозировки, достаточных для необратимого изменения лейкокрасителя.
22. Способ по п.21, отличающийся тем, что лейкокраситель представляет собой лейкоаминотриарилметан или его производное.
23. Способ по п.21, отличающийся тем, что фотореактор представляет собой 1-[4-(2-гидроксиэтокси)фенил] -2-гидрокси-2-метилпропан-1-он, имеющий следующую формулу
или 1-гидроксициклогексанфенилкетон, имеющий следующую формулу
24. Способ по п.21, отличающийся тем, что селективный для длины волны сенсибилизатор представляет собой фталоилглицин, имеющий следующую формулу
или 4-(4-гидроксифенил)бутан-2-он, имеющий следующую формулу
25. Способ по п.21, отличающийся тем, что трансорбер излучения представляет собой 2-(п-(2-метиллактоил)-фенокси)-этил-1,3-диоксо-2-изоиндолинацетат, имеющий формулу
эфир фталоилглицилциклогексилфенилкетона, имеющий формулу
4-(4-оксифенил)-2-бутанон-1-(4-(2-оксиэтокси)фенил)-2-гидрокси-2-метилпропан-1-он (или 2-гидрокси-2-метил-4'-(2-(п-(3-оксобутил)фенокси)этокси)пропиофенон), имеющий формулу
или 4-(4-оксифенил)-2-бутанонциклогексилфенилкетон (или 4-(п-((4-бензоилциклогексил)окси)фенил)-2-бутанон), имеющий формулу
или 1-гидроксициклогексанфенилкетон, имеющий следующую формулу
24. Способ по п.21, отличающийся тем, что селективный для длины волны сенсибилизатор представляет собой фталоилглицин, имеющий следующую формулу
или 4-(4-гидроксифенил)бутан-2-он, имеющий следующую формулу
25. Способ по п.21, отличающийся тем, что трансорбер излучения представляет собой 2-(п-(2-метиллактоил)-фенокси)-этил-1,3-диоксо-2-изоиндолинацетат, имеющий формулу
эфир фталоилглицилциклогексилфенилкетона, имеющий формулу
4-(4-оксифенил)-2-бутанон-1-(4-(2-оксиэтокси)фенил)-2-гидрокси-2-метилпропан-1-он (или 2-гидрокси-2-метил-4'-(2-(п-(3-оксобутил)фенокси)этокси)пропиофенон), имеющий формулу
или 4-(4-оксифенил)-2-бутанонциклогексилфенилкетон (или 4-(п-((4-бензоилциклогексил)окси)фенил)-2-бутанон), имеющий формулу
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US46318795A | 1995-06-05 | 1995-06-05 | |
US08/463,187 | 1995-06-05 | ||
US08/649,754 US5786132A (en) | 1995-06-05 | 1996-05-29 | Pre-dyes, mutable dye compositions, and methods of developing a color |
US08/649,754 | 1996-05-29 |
Publications (2)
Publication Number | Publication Date |
---|---|
RU98100245A true RU98100245A (ru) | 2000-02-10 |
RU2170943C2 RU2170943C2 (ru) | 2001-07-20 |
Family
ID=27040572
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU98100245/04A RU2170943C2 (ru) | 1995-06-05 | 1996-06-05 | Новые прекрасители |
Country Status (14)
Country | Link |
---|---|
US (2) | US5837429A (ru) |
EP (1) | EP0830638B1 (ru) |
JP (1) | JP2001515524A (ru) |
AT (1) | ATE195815T1 (ru) |
AU (1) | AU6378696A (ru) |
BR (1) | BR9608367A (ru) |
CA (1) | CA2219450A1 (ru) |
DE (1) | DE69609967T2 (ru) |
ES (1) | ES2148776T3 (ru) |
MX (1) | MX9709250A (ru) |
PL (1) | PL323727A1 (ru) |
RU (1) | RU2170943C2 (ru) |
SK (1) | SK160497A3 (ru) |
WO (1) | WO1996039646A1 (ru) |
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DE69609967T2 (de) | 1995-06-05 | 2001-04-12 | Kimberly-Clark Worldwide, Inc. | Farbstoffvorläufer und diese enthaltende zusammensetzungen |
US5747550A (en) | 1995-06-05 | 1998-05-05 | Kimberly-Clark Worldwide, Inc. | Method of generating a reactive species and polymerizing an unsaturated polymerizable material |
US5786132A (en) | 1995-06-05 | 1998-07-28 | Kimberly-Clark Corporation | Pre-dyes, mutable dye compositions, and methods of developing a color |
GB9515304D0 (en) | 1995-07-26 | 1995-09-20 | Ilford Ag | Azo dyes |
US5531821A (en) | 1995-08-24 | 1996-07-02 | Ecc International Inc. | Surface modified calcium carbonate composition and uses therefor |
US5782963A (en) | 1996-03-29 | 1998-07-21 | Kimberly-Clark Worldwide, Inc. | Colorant stabilizers |
US5855655A (en) | 1996-03-29 | 1999-01-05 | Kimberly-Clark Worldwide, Inc. | Colorant stabilizers |
US5709976A (en) | 1996-06-03 | 1998-01-20 | Xerox Corporation | Coated papers |
-
1996
- 1996-06-05 DE DE69609967T patent/DE69609967T2/de not_active Expired - Fee Related
- 1996-06-05 MX MX9709250A patent/MX9709250A/es not_active IP Right Cessation
- 1996-06-05 SK SK1604-97A patent/SK160497A3/sk unknown
- 1996-06-05 JP JP50135297A patent/JP2001515524A/ja not_active Abandoned
- 1996-06-05 US US08/659,497 patent/US5837429A/en not_active Expired - Fee Related
- 1996-06-05 ES ES96923216T patent/ES2148776T3/es not_active Expired - Lifetime
- 1996-06-05 RU RU98100245/04A patent/RU2170943C2/ru not_active IP Right Cessation
- 1996-06-05 AT AT96923216T patent/ATE195815T1/de not_active IP Right Cessation
- 1996-06-05 EP EP96923216A patent/EP0830638B1/en not_active Expired - Lifetime
- 1996-06-05 WO PCT/US1996/008887 patent/WO1996039646A1/en active IP Right Grant
- 1996-06-05 BR BR9608367A patent/BR9608367A/pt not_active Application Discontinuation
- 1996-06-05 PL PL96323727A patent/PL323727A1/xx unknown
- 1996-06-05 CA CA002219450A patent/CA2219450A1/en not_active Abandoned
- 1996-06-05 AU AU63786/96A patent/AU6378696A/en not_active Abandoned
-
1998
- 1998-11-16 US US09/192,628 patent/US6063551A/en not_active Expired - Fee Related
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