DE2236947A1 - Lichtempfindliches, farbphotographisches aufzeichnungsmaterial - Google Patents
Lichtempfindliches, farbphotographisches aufzeichnungsmaterialInfo
- Publication number
- DE2236947A1 DE2236947A1 DE2236947A DE2236947A DE2236947A1 DE 2236947 A1 DE2236947 A1 DE 2236947A1 DE 2236947 A DE2236947 A DE 2236947A DE 2236947 A DE2236947 A DE 2236947A DE 2236947 A1 DE2236947 A1 DE 2236947A1
- Authority
- DE
- Germany
- Prior art keywords
- coupler
- recording material
- blue
- tert
- green
- 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
Links
- 239000000463 material Substances 0.000 title claims description 24
- -1 silver halide Chemical class 0.000 claims description 19
- 150000001875 compounds Chemical class 0.000 claims description 14
- 239000000839 emulsion Substances 0.000 claims description 6
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical group [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 5
- 108010010803 Gelatin Proteins 0.000 claims description 2
- 229920000159 gelatin Polymers 0.000 claims description 2
- 239000008273 gelatin Substances 0.000 claims description 2
- 235000019322 gelatine Nutrition 0.000 claims description 2
- 235000011852 gelatine desserts Nutrition 0.000 claims description 2
- 229910052709 silver Inorganic materials 0.000 claims 4
- 239000004332 silver Substances 0.000 claims 4
- 125000002723 alicyclic group Chemical group 0.000 claims 1
- 125000005037 alkyl phenyl group Chemical group 0.000 claims 1
- 125000000068 chlorophenyl group Chemical group 0.000 claims 1
- 238000002844 melting Methods 0.000 description 17
- 230000008018 melting Effects 0.000 description 17
- 239000000203 mixture Substances 0.000 description 11
- 239000000243 solution Substances 0.000 description 11
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 9
- 229940126062 Compound A Drugs 0.000 description 7
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 7
- 238000003786 synthesis reaction Methods 0.000 description 6
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 238000000921 elemental analysis Methods 0.000 description 4
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 230000003595 spectral effect Effects 0.000 description 3
- JXHXZEWREZILOO-UHFFFAOYSA-N (2-aminophenyl)-cyclohexylmethanone Chemical compound NC1=CC=CC=C1C(=O)C1CCCCC1 JXHXZEWREZILOO-UHFFFAOYSA-N 0.000 description 2
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- WTDHULULXKLSOZ-UHFFFAOYSA-N Hydroxylamine hydrochloride Chemical compound Cl.ON WTDHULULXKLSOZ-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 description 2
- 239000000084 colloidal system Substances 0.000 description 2
- 150000008049 diazo compounds Chemical class 0.000 description 2
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000000873 masking effect Effects 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- 230000001235 sensitizing effect Effects 0.000 description 2
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- OORHHPHMDCWJPG-UHFFFAOYSA-N 1-(2-aminophenyl)-3-phenylpropan-1-one Chemical compound NC1=CC=CC=C1C(=O)CCC1=CC=CC=C1 OORHHPHMDCWJPG-UHFFFAOYSA-N 0.000 description 1
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 1
- FLVSDXZOBZUNOB-UHFFFAOYSA-N 2-amino-1,3-diphenylpropan-1-one Chemical compound C=1C=CC=CC=1C(=O)C(N)CC1=CC=CC=C1 FLVSDXZOBZUNOB-UHFFFAOYSA-N 0.000 description 1
- 241001071861 Lethrinus genivittatus Species 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 239000007844 bleaching agent Substances 0.000 description 1
- 229960002380 dibutyl phthalate Drugs 0.000 description 1
- MQRJBSHKWOFOGF-UHFFFAOYSA-L disodium;carbonate;hydrate Chemical compound O.[Na+].[Na+].[O-]C([O-])=O MQRJBSHKWOFOGF-UHFFFAOYSA-L 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- RMHJJUOPOWPRBP-UHFFFAOYSA-N naphthalene-1-carboxamide Chemical compound C1=CC=C2C(C(=O)N)=CC=CC2=C1 RMHJJUOPOWPRBP-UHFFFAOYSA-N 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 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
- G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
- G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
- G03C7/32—Colour coupling substances
- G03C7/333—Coloured coupling substances, e.g. for the correction of the coloured image
- G03C7/3335—Coloured coupling substances, e.g. for the correction of the coloured image containing an azo chromophore
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP46055665A JPS5010729B1 (enrdf_load_stackoverflow) | 1971-07-27 | 1971-07-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2236947A1 true DE2236947A1 (de) | 1973-02-22 |
Family
ID=13005135
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2236947A Pending DE2236947A1 (de) | 1971-07-27 | 1972-07-27 | Lichtempfindliches, farbphotographisches aufzeichnungsmaterial |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US3811892A (enrdf_load_stackoverflow) |
| JP (1) | JPS5010729B1 (enrdf_load_stackoverflow) |
| DE (1) | DE2236947A1 (enrdf_load_stackoverflow) |
| GB (1) | GB1397628A (enrdf_load_stackoverflow) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5337019B2 (enrdf_load_stackoverflow) * | 1973-12-21 | 1978-10-06 | ||
| US4138258A (en) * | 1974-08-28 | 1979-02-06 | Fuji Photo Film Co., Ltd. | Multi-layered color photographic materials |
-
1971
- 1971-07-27 JP JP46055665A patent/JPS5010729B1/ja active Pending
-
1972
- 1972-07-24 US US00275211A patent/US3811892A/en not_active Expired - Lifetime
- 1972-07-26 GB GB3499572A patent/GB1397628A/en not_active Expired
- 1972-07-27 DE DE2236947A patent/DE2236947A1/de active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| GB1397628A (en) | 1975-06-11 |
| US3811892A (en) | 1974-05-21 |
| JPS5010729B1 (enrdf_load_stackoverflow) | 1975-04-24 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE1597572C3 (de) | Farbpholographische Silberhalogenidemulsion | |
| DE2362752C2 (de) | Einen photographischen Entwicklungsinhibitor abspaltende Verbindung und ihre Verwendung | |
| DE2250050A1 (de) | Farbphotographisches aufzeichnungsmaterial | |
| DE2421544C2 (de) | Mehrschichtiges farbphotographisches Aufzeichnungsmaterial mit einverleibten Kupplern | |
| DE1254463B (de) | Farbphotographisches Material | |
| DE2502820C3 (de) | Farbfotografisches Verfahren zur Herstellung von Cyanbildern | |
| EP0011051A2 (de) | Farbphotographisches Aufzeichnungsmaterial, Verfahren zu seiner Stabilisierung und Herstellung photographischer Farbbilder | |
| DE69328335T2 (de) | Verfahren zur Herstellung eines photographischen Farbbildes | |
| DE2429892A1 (de) | Verfahren zum entwickeln eines lichtempfindlichen photographischen silberhalogenidmaterials | |
| DE2604804C2 (de) | Fotografischer Farbentwickler | |
| DE2456076C3 (de) | Farbphotographisches mehrschichtiges Aufzeichnungsmaterial | |
| DE2016587B2 (de) | Farbentwickler | |
| DE2515771A1 (de) | Verfahren zur erzeugung eines farbphotographischen bildes | |
| DE3630564A1 (de) | Farbfotografisches aufzeichnungsmaterial mit einem gelb-dir-kuppler | |
| DE2236947A1 (de) | Lichtempfindliches, farbphotographisches aufzeichnungsmaterial | |
| DE3626219A1 (de) | Farbfotografisches aufzeichnungsmaterial mit einem gelb-dir-kuppler | |
| DE2163811A1 (de) | Verfahren zur Herstellung von Cyanbildern | |
| DE3316887A1 (de) | Photographisches aufzeichnungsmaterial und neue azofarbstoffe | |
| DE1547868B2 (de) | Farbphotographisches Aufzeichungs material | |
| DE1931122C3 (de) | Photographischer Farbentwickler | |
| DE2724488C2 (de) | Farbphotographisches Aufzeichnungsmaterial | |
| DE1140455B (de) | Verfahren zur Herstellung von farbmaskierten photographischen subtraktiven Ein- oder Mehrfarbenbildern durch Farbentwicklung | |
| DE1770014A1 (de) | Neue 5-Pyrazolon-Derivate und Magenta-Kuppler | |
| DE1949591A1 (de) | Verfahren zum Entwickeln eines photographischen Aufzeichnungsmaterials | |
| DE1931333A1 (de) | Farbbildentwicklermasse und Verfahren zur Farbentwicklung |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| OHW | Rejection |