GB1465183A - Photographic silver halide elements useful in colour diffusion transfer processes and chemical compounds useful in said elements - Google Patents
Photographic silver halide elements useful in colour diffusion transfer processes and chemical compounds useful in said elementsInfo
- Publication number
- GB1465183A GB1465183A GB624874A GB624874A GB1465183A GB 1465183 A GB1465183 A GB 1465183A GB 624874 A GB624874 A GB 624874A GB 624874 A GB624874 A GB 624874A GB 1465183 A GB1465183 A GB 1465183A
- Authority
- GB
- United Kingdom
- Prior art keywords
- hydroxy
- alkyl
- optionally substituted
- formula
- compound
- 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.)
- Expired
Links
- 150000001875 compounds Chemical class 0.000 title abstract 10
- -1 silver halide Chemical class 0.000 title abstract 4
- 238000000034 method Methods 0.000 title abstract 3
- 238000009792 diffusion process Methods 0.000 title abstract 2
- 229910052709 silver Inorganic materials 0.000 title 1
- 239000004332 silver Substances 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 7
- 125000003118 aryl group Chemical group 0.000 abstract 4
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 abstract 4
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 abstract 4
- 125000002947 alkylene group Chemical group 0.000 abstract 3
- 230000008878 coupling Effects 0.000 abstract 3
- 238000010168 coupling process Methods 0.000 abstract 3
- 238000005859 coupling reaction Methods 0.000 abstract 3
- 150000003839 salts Chemical class 0.000 abstract 3
- QTAFTMYOVKQYMG-UHFFFAOYSA-N 4-acetamido-5-hydroxy-6-[(2-methoxyphenyl)diazenyl]naphthalene-1-sulfonyl chloride Chemical compound COC1=CC=CC=C1N=NC1=CC=C(C(=CC=C2NC(C)=O)S(Cl)(=O)=O)C2=C1O QTAFTMYOVKQYMG-UHFFFAOYSA-N 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 125000000732 arylene group Chemical group 0.000 abstract 2
- 239000000987 azo dye Substances 0.000 abstract 2
- 238000006193 diazotization reaction Methods 0.000 abstract 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 235000019260 propionic acid Nutrition 0.000 abstract 2
- 125000001424 substituent group Chemical group 0.000 abstract 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 abstract 2
- KAIPJAQPXZADEK-UHFFFAOYSA-N 2-[3-[(2,5-dimethoxy-4-sulfamoylphenyl)diazenyl]-4-hydroxynaphthalen-1-yl]oxypropanoic acid Chemical compound COC1=C(C=C(C(=C1)S(N)(=O)=O)OC)N=NC=1C=C(C2=CC=CC=C2C=1O)OC(C(=O)O)C KAIPJAQPXZADEK-UHFFFAOYSA-N 0.000 abstract 1
- GJRPDPRUUNLNSP-UHFFFAOYSA-N 4-(3-aminopropylsulfonylamino)-n-[4-(2,4-ditert-butylphenoxy)butyl]-1-hydroxynaphthalene-2-carboxamide Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC=C1OCCCCNC(=O)C1=CC(NS(=O)(=O)CCCN)=C(C=CC=C2)C2=C1O GJRPDPRUUNLNSP-UHFFFAOYSA-N 0.000 abstract 1
- GYVABUSMWJYZKN-UHFFFAOYSA-N 4-[(3-aminophenyl)sulfonylamino]-n-[4-[2,4-bis(2-methylbutan-2-yl)phenoxy]butyl]-1-hydroxynaphthalene-2-carboxamide Chemical compound CCC(C)(C)C1=CC(C(C)(C)CC)=CC=C1OCCCCNC(=O)C1=CC(NS(=O)(=O)C=2C=C(N)C=CC=2)=C(C=CC=C2)C2=C1O GYVABUSMWJYZKN-UHFFFAOYSA-N 0.000 abstract 1
- IARLJPWFLRVFST-UHFFFAOYSA-N 4-acetamido-5-acetyloxynaphthalene-1-sulfonic acid pyridine Chemical compound C1=CC=NC=C1.CC(=O)NC1=C2C(OC(C)=O)=CC=CC2=C(C=C1)S(O)(=O)=O IARLJPWFLRVFST-UHFFFAOYSA-N 0.000 abstract 1
- LQPYPLBCZNOKKA-UHFFFAOYSA-N 4-amino-n-[4-[2,4-bis(2-methylbutan-2-yl)phenoxy]butyl]-1-hydroxynaphthalene-2-carboxamide Chemical compound CCC(C)(C)C1=CC(C(C)(C)CC)=CC=C1OCCCCNC(=O)C1=CC(N)=C(C=CC=C2)C2=C1O LQPYPLBCZNOKKA-UHFFFAOYSA-N 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- 239000005864 Sulphur Substances 0.000 abstract 1
- 230000021736 acetylation Effects 0.000 abstract 1
- 238000006640 acetylation reaction Methods 0.000 abstract 1
- 125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 125000004442 acylamino group Chemical group 0.000 abstract 1
- 125000004423 acyloxy group Chemical group 0.000 abstract 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 1
- 125000005129 aryl carbonyl group Chemical group 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- SOYBJIUDKRLQTA-UHFFFAOYSA-N benzene;dinaphthalen-1-yldiazene Chemical compound C1=CC=CC=C1.C1=CC=C2C(N=NC=3C4=CC=CC=C4C=CC=3)=CC=CC2=C1 SOYBJIUDKRLQTA-UHFFFAOYSA-N 0.000 abstract 1
- 150000001555 benzenes Chemical class 0.000 abstract 1
- 125000006367 bivalent amino carbonyl group Chemical group [H]N([*:1])C([*:2])=O 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 230000007062 hydrolysis Effects 0.000 abstract 1
- 238000006460 hydrolysis reaction Methods 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- UFWIBTONFRDIAS-UHFFFAOYSA-N naphthalene-acid Natural products C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 abstract 1
- 150000002790 naphthalenes Chemical class 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical class ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C8/00—Diffusion transfer processes or agents therefor; Photosensitive materials for such processes
- G03C8/02—Photosensitive materials characterised by the image-forming section
- G03C8/08—Photosensitive materials characterised by the image-forming section the substances transferred by diffusion consisting of organic compounds
- G03C8/10—Photosensitive materials characterised by the image-forming section the substances transferred by diffusion consisting of organic compounds of dyes or their precursors
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US33172873A | 1973-02-12 | 1973-02-12 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1465183A true GB1465183A (en) | 1977-02-23 |
Family
ID=23295129
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB624874A Expired GB1465183A (en) | 1973-02-12 | 1974-02-12 | Photographic silver halide elements useful in colour diffusion transfer processes and chemical compounds useful in said elements |
Country Status (7)
Country | Link |
---|---|
JP (1) | JPS49114424A (enrdf_load_stackoverflow) |
BE (1) | BE796040A (enrdf_load_stackoverflow) |
CH (1) | CH588095A5 (enrdf_load_stackoverflow) |
DE (2) | DE2406627A1 (enrdf_load_stackoverflow) |
FR (1) | FR2217725A1 (enrdf_load_stackoverflow) |
GB (1) | GB1465183A (enrdf_load_stackoverflow) |
NL (1) | NL7401910A (enrdf_load_stackoverflow) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4585483A (en) * | 1983-05-20 | 1986-04-29 | Fuji Photo Film Co., Ltd. | Recording materials |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2505248C2 (de) * | 1975-02-07 | 1982-11-25 | Agfa-Gevaert Ag, 5090 Leverkusen | Photographisches Farbdiffusionsübertragungsverfahren und farbphotographisches Aufzeichnungsmaterial für das Diffusionsübertragungsverfahren |
JP4022271B2 (ja) | 1995-10-31 | 2007-12-12 | 富士フイルム株式会社 | ピラゾリルアゾフエノール色素 |
-
1973
- 1973-02-26 FR FR7306644A patent/FR2217725A1/fr not_active Withdrawn
- 1973-02-27 BE BE128171A patent/BE796040A/xx unknown
-
1974
- 1974-02-11 CH CH185374A patent/CH588095A5/xx not_active IP Right Cessation
- 1974-02-12 NL NL7401910A patent/NL7401910A/xx not_active Application Discontinuation
- 1974-02-12 GB GB624874A patent/GB1465183A/en not_active Expired
- 1974-02-12 JP JP1706274A patent/JPS49114424A/ja active Pending
- 1974-02-12 DE DE19742406627 patent/DE2406627A1/de active Pending
- 1974-02-12 DE DE19742462061 patent/DE2462061A1/de active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4585483A (en) * | 1983-05-20 | 1986-04-29 | Fuji Photo Film Co., Ltd. | Recording materials |
Also Published As
Publication number | Publication date |
---|---|
DE2406627A1 (de) | 1974-08-29 |
AU6548974A (en) | 1975-08-14 |
DE2462061A1 (de) | 1975-12-18 |
BE796040A (fr) | 1973-08-27 |
CH588095A5 (enrdf_load_stackoverflow) | 1977-05-31 |
JPS49114424A (enrdf_load_stackoverflow) | 1974-10-31 |
NL7401910A (enrdf_load_stackoverflow) | 1974-08-14 |
FR2217725A1 (enrdf_load_stackoverflow) | 1974-09-06 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PCNP | Patent ceased through non-payment of renewal fee |