US3694217A - Silver halide photographic emulsion - Google Patents
Silver halide photographic emulsion Download PDFInfo
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- US3694217A US3694217A US865545A US3694217DA US3694217A US 3694217 A US3694217 A US 3694217A US 865545 A US865545 A US 865545A US 3694217D A US3694217D A US 3694217DA US 3694217 A US3694217 A US 3694217A
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- 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
- G03C1/00—Photosensitive materials
- G03C1/005—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
- G03C1/06—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with non-macromolecular additives
- G03C1/08—Sensitivity-increasing substances
- G03C1/10—Organic substances
- G03C1/12—Methine and polymethine dyes
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- 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
- C09B23/00—Methine or polymethine dyes, e.g. cyanine dyes
- C09B23/02—Methine or polymethine dyes, e.g. cyanine dyes the polymethine chain containing an odd number of >CH- or >C[alkyl]- groups
- C09B23/06—Methine or polymethine dyes, e.g. cyanine dyes the polymethine chain containing an odd number of >CH- or >C[alkyl]- groups three >CH- groups, e.g. carbocyanines
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S430/00—Radiation imagery chemistry: process, composition, or product thereof
- Y10S430/134—Brightener containing
Definitions
- This invention relates to a spectrally sensitized silver halide photographic emulsion and, more particularly, to a silver halide photographic emulsion having a maximum spectral sensitization within the range of from about 620 my. to 645 mg and a high sensitivity to red light.
- the sensitizing effect in a. longer wave length region of a sensitizing dye having its maximum spectral sensitization in a longer wave length region is greatly affected by the other sensitizing dye having its spectral sensitivity in a shorter wave length region and, in general, the sensitization efiect (attributable to the aggregation of sensitizing dyes on particles of silver halide) in a longer wave length region is lowered.
- the principal object of the present invention is to provide a silver halide photographic emulsion containing a novel sensitizing dye which will aiford a high spectral sensitivity in a spectral sensitization wave length region of about 620 to 645 mp. without any decrease in either the total sensitivity and in the red sensitivity, even when used in combination with an ortho sensitizer, and further, which will not retain any stain in the sensitive material after development.
- FIGS. l-4 show spectral sensitization spectra obtained by employing a dye of the present invention alone, in combination with known dyes, and by employing a conventional dye alone and in combination with other known dyes, respectively.
- the special feature of the chemical structure of the sensitizing coloring matter used in the present invention consists of the substituents R and R. It has been found that the spectral sensitizing property of, especially, mesomethylthiacarbocyanines, mesomethylselenathiacarbocyanines and mesomethylselenacarbocyanines is affected to a great extent by the substituents R and R.
- mesomethylcarbocyanine dyes are used in combination with a known ortho sensitizing dye, such as thia-2'-cyanine or 2,2'-cyanine, its sensitizing property in a red region corresponding to the maximum spectral sensitization (approximately 620 to 645 m due to the aggregation of the mesomethylcarbocyanine dye on the silver halide particles is adversely affected, and, consequently, the red sensitivity of the emulsion is lowered to a great extent, so that the use of such mesomethylcarbocyanines is disadvantageous for the object of the present invention.
- a known ortho sensitizing dye such as thia-2'-cyanine or 2,2'-cyanine
- the sensitizing dye of the present invention is able to spectrally sensitize silver halide photographic emulsions.
- emulsion used in the present invention may be an emulsion which contains a mixed silver halide, such as silver iodobromide or silver chlorobromoiodide.
- the photoemulsion which is sensitized in accordance with the present invention may be prepared by incorporating one or more sensitizing dyes in a photographic emulsion in an ordinary manner.
- the dye is usually added to the emulsion while in solution in a suitable solvent, such as methanol or ethanol.
- the amount of the sensitizing dye to be incorporated in the emulsion may vary in a wide range of from 5 to 200 mg. per kg. of emulsion, depending on the required effect.
- the photographic emulsion used in accordance with the present invention may be, in addition, super-sensitized and hyper-sensitized according to conventional methods.
- the photographic emulsion in accordance with the present invention may be applied in the usual manner to a suitable support, such as, e.g., sheet glass, a film of cellulose derivative, a film of synthetic resin or baryta paper.
- a suitable support such as, e.g., sheet glass, a film of cellulose derivative, a film of synthetic resin or baryta paper.
- Fuji #7 filter made by Fuji Photo Film Co., Ltd., transmitting light having a wave length longer than 580 mg
- the developing solution used was of the formulation as indicated in Table 2.
- Table 3 is shown the degrees of color sensitization and maxima of sensitization obtained by separate addition of the sensitizing dyes as indicated in Table 1.
- Table 4 is shown the degrees of spectral sensitization and maxima of sensitization obtained by the separate addition of the sensitizing dyes indicated above as sensitizing dyes for comparison.
- Table 5 is shown the degrees of spectral sensitization and maxima of sensitization obtained by various combinations of sensitizing dyes selected from those listed in Table l and those as indicated above for comparison with a known green-sensitive sensitizing dye.
- the red sensitivities were indicated by terms of relative sensitivity, assuming that the red sensitivity of sensitizing coloring matter A was 100.
- sensitizing dye F 0. 015 AgBr/I 625 80
- the red sensitivities were indicated in terms of relative sensitivity, assuming that the red sensitivity of an emulsion having incorporated therein, by itself, sensitizing dye F was 100.
- FIG. 1 indicates a spectral sensitization spectrum obtained by using great extent when used in combination with green-sensitization spectrum obtained by using sensitizing dye 3 in combination with known green-sensitive coloring matter H and I;
- FIG. 3 indicates aspectral sensitization spectrum obtained by using sensitizing dye E alone;
- FIG. 4 indicates a spectral sensitization spectrum obtained by using sensitizing dye F in combination with the known green-sensitive sensitizing dyes H and I.
- sensitizing dye E was used for compan'sion purposes, its maximum sensitization in the red region (J-band) falls off to a great extent when used in combination witht green-sensitive sensitizing dye H and this causes a remarkable depression of the red sensitivity, while, when employing sensitizing dye 3 of the present invention, the phenomenon that will cause such a depression of red sensitivity does not occur even if it is used in combination with the green-sensitive sensitizing dyes H and I.
- the known green-sensitive sensitizing dyes used in combination with the sensitizing dye of the present in- The red sensitivities were indicated in terms of relative 75 vention are those having the following structures.
- Z and Z are individually selected from the group consisting of a sulfur and a selenium atom
- R is selected from the group consisting of an ethyl group, an n-propyl group, an n-butyl group and an allyl group
- R' is selected from the group consisting of an 'y-sulfopropyl group, a 'ysulfobutyl group, a a-sulfobutyl group, a B-carboxybutyl group and a w-carboxypentyl group
- X represents an anion
- n is or 1, n being 0 when the dye is an intramolecular salt.
- the silver halide photographic emulsion as in claim group consisting of p 1 Br CzHs l? CH N N Br- (5 2H5 2 5 8.
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- Spectroscopy & Molecular Physics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- General Physics & Mathematics (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
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Abstract
A SILVER HALIDE PHOTOGRAPHIC EMULSION HAVING THEREIN AT LEAST ONE SENSITIZING DYE REPRESENTED BY THE FOLLOWING FORMULA:
R-(+)N<(=C(-CH=C(-CH3)-CH=C<(-N(-R'')-(1,2-PHENYLENE)-Z''-))
-Z-(1,2-PHENYLENE)-) (X(-))N
WHEREIN Z AND Z'' ARE INDIVIDUALLY SELECTED FROM THE GROUP CONSISTING OF A SULFUR AND A SELENIUM ATOM, R IS SELECTED FROM THE GROUP CONSISTING OF AN ENTHYL GROUP, AN N-PROPYL GROUP, AN N-BUTYL GROUP AND AN ALLYL GROUP, R'' IS SELECTED FROM THE GROUP CONSISTING OF A Y-SULFOPROPYL GROUP, A Y-SULFOBUTYL GROUP, A 8-SULFOBUTYL GROUP, A 8-CARBOXYBUTYL GROUP AND AN W-CARBOXYPENTYL GROUP, X REPRESENTS AN ANION, AND N IS 0 OR 1, BEING 0 WHEN THE DYE IS AN INTRAMOLECULAR SALT.
R-(+)N<(=C(-CH=C(-CH3)-CH=C<(-N(-R'')-(1,2-PHENYLENE)-Z''-))
-Z-(1,2-PHENYLENE)-) (X(-))N
WHEREIN Z AND Z'' ARE INDIVIDUALLY SELECTED FROM THE GROUP CONSISTING OF A SULFUR AND A SELENIUM ATOM, R IS SELECTED FROM THE GROUP CONSISTING OF AN ENTHYL GROUP, AN N-PROPYL GROUP, AN N-BUTYL GROUP AND AN ALLYL GROUP, R'' IS SELECTED FROM THE GROUP CONSISTING OF A Y-SULFOPROPYL GROUP, A Y-SULFOBUTYL GROUP, A 8-SULFOBUTYL GROUP, A 8-CARBOXYBUTYL GROUP AND AN W-CARBOXYPENTYL GROUP, X REPRESENTS AN ANION, AND N IS 0 OR 1, BEING 0 WHEN THE DYE IS AN INTRAMOLECULAR SALT.
Description
Sept. 26, 1972 SENSITIVITY SENSITIVITY SENSITIVITY SENSITIVITY YOSHIKATA SAKAGUCHI HAL SILVER HALIDE PHOTOGRAPHIC EMULSION Filed Sept. 12, 1969 WAVE LENGTH (I00 AI FIGI WAVE LENGTH (I00 AI FIG. 2
WAVE LENGTH (IO0A) WAVE LENGTH (IO0A) FIG. 4
INVENTORS YOSHIKATA SAKAGUCHI MASAKADO SAKAI MASANAGA OHKI YASHUIIARU NAKAMURA MOTOHIKO TSUBOTA AKIRA SATO "United States Patent Oflice SILVER HALIDE PHOTOGRAPHIC EMULSION Yoshikata Sakaguchi, Masakado Sakai, Masanaga Ohki,
Yashuharu Nakamura, Motohiko Tsubota, and Akira Sato, Kanagawa, Japan, assignors to Fuji Photo Film Co., Ltd., Kanagawa, Japan Filed Sept. 12, 1969, Ser. No. 865,545 Claims priority, application Japan, Sept. 12, 1968,
/65,704 Int. Cl. C09b 23/06; G03c N18 US. Cl. 96-430 9 Claims ABSTRACT OF THE DISCLOSURE A silver halide photographic emulsion having therein at least one sensitizing dye represented by the following formula:
N. N/ i 1's wherein Z and Z are individually selected from the group consisting of a sulfur and a selenium atom, R is selected from the group consisting of an ethyl group, an n-propyl group, an n-butyl group and an allyl group, R is selected from the group consisting of a -sulfopropyl group, a 'y-sulfobutyl group, a a-sulfobutyl group, a a-carboxybutyl group and an w-carboxypentyl group, X represents an anion, and n is or 1, n being 0 when the dye is an intramolecular salt.
BACKGROUND OF THE INVENTION Field of the invention This invention relates to a spectrally sensitized silver halide photographic emulsion and, more particularly, to a silver halide photographic emulsion having a maximum spectral sensitization within the range of from about 620 my. to 645 mg and a high sensitivity to red light.
Description of the prior art It is well known in the manufacture of silver halide photographic emulsions that by the addition of a sensitizing dye to a silver halide photographic emulsion, the sensitive wave length region of the photographic emulsion is expanded and the emulsion is spectrally sensitized. In many cases, light sensitive photographic materials are incorporated with a single sensitizing dye so as to sensitize in a desired wave length region, while, in most cases, combinations of two or more sensitizing dyes are used. However, the total sensitivity obtained by the use of a combination of two or more sensitizing dyes is usually lower than the sum of the spectral sensitivities obtained by separate uses of the sensitizing dyes. For instance, in the case where a combination of two or more sensitizing dyes differing in spectral sensitizing wave length regions are used with each other for the purpose of sensitizing in a desired wave length region, the sensitizing effect in a. longer wave length region of a sensitizing dye having its maximum spectral sensitization in a longer wave length region is greatly affected by the other sensitizing dye having its spectral sensitivity in a shorter wave length region and, in general, the sensitization efiect (attributable to the aggregation of sensitizing dyes on particles of silver halide) in a longer wave length region is lowered.
Thus, a significant problem exists among various spectral sensitization techniques with respect to combinations of sensitizing dyes in which each sensitizer has no adverse eifect on the other and, preferably, there is obtained an increased spectral sensitivity.
The principal object of the present invention is to provide a silver halide photographic emulsion containing a novel sensitizing dye which will aiford a high spectral sensitivity in a spectral sensitization wave length region of about 620 to 645 mp. without any decrease in either the total sensitivity and in the red sensitivity, even when used in combination with an ortho sensitizer, and further, which will not retain any stain in the sensitive material after development.
SUMMARY OF THE INVENTION The object of the present invention is attained by incorporating in a silver halide photographic emulsion a mesomethylcarbocyanine dye represented by the For- BRIEF DESCRIPTION OF THE DRAWINGS FIGS. l-4 show spectral sensitization spectra obtained by employing a dye of the present invention alone, in combination with known dyes, and by employing a conventional dye alone and in combination with other known dyes, respectively.
DESCRIPTION OF THE PREFERRED EMBODIMENTS The special feature of the chemical structure of the sensitizing coloring matter used in the present invention consists of the substituents R and R. It has been found that the spectral sensitizing property of, especially, mesomethylthiacarbocyanines, mesomethylselenathiacarbocyanines and mesomethylselenacarbocyanines is affected to a great extent by the substituents R and R. Namely, we have found that only when a mesomethylcarbocyanine dye is incorporated in a silver halide photographic emulsion, in which R' is a sulfoalkyl or carboxyalkyl group, and R and R are as designated in the above general Formula I, it is possible to obtain an excellent spectral sensitization with the result that the object of the present invention is attainable. In cases where there is incorporated in a silver halide emulsion a mesomethylthiacarbocyanine, mesomethylselenathiacarbocyanine, or mesomethylselenacarbocyanine containing substituent R and R other than those as mentioned above, similarly, there is obtained a sensitized emulsion having a maximum spectral sensitization within the range of about 620 my. to 645 mg, and a high red sensitivity. However, if such mesomethylcarbocyanine dyes are used in combination with a known ortho sensitizing dye, such as thia-2'-cyanine or 2,2'-cyanine, its sensitizing property in a red region corresponding to the maximum spectral sensitization (approximately 620 to 645 m due to the aggregation of the mesomethylcarbocyanine dye on the silver halide particles is adversely affected, and, consequently, the red sensitivity of the emulsion is lowered to a great extent, so that the use of such mesomethylcarbocyanines is disadvantageous for the object of the present invention.
Patented Sept. 26, 1972 The mesomethylcarbocyanines of Formula I for use in the present invention may be synthesized by known processes. Namely, a sensitizing dye as in Formula I may be synthesized by reacting, in reflux, a compound of the general Formula II oH=e-sru" I X R (H) wherein Z, R and X have the same meanings as designated above and R" represents an alkyl group, such as methyl or ethyl, with a compound of the general Formula III following table.
B rl (CHz)aCOOH (ormasoan s s on; CH=JICH \N+ N/ (oHmoooH emhsozn-rj S was. S\ J s,
B r l (CHmCOOH (CHmCOOH The sensitizing dye of the present invention is able to spectrally sensitize silver halide photographic emulsions.
In particular, it is useful for expanding the spectral sensitive region of gelatino silver halide emulsions. In addition, it can sufiiciently sensitize emulsions of the type containing a hydrophilic colloid other than gelatin, such as, e.g., agar collodion, water soluble cellulose derivatives, polyvinyl alcohol or like natural or synthetic resinous materials. The emulsion used in the present invention may be an emulsion which contains a mixed silver halide, such as silver iodobromide or silver chlorobromoiodide. The photoemulsion which is sensitized in accordance with the present invention may be prepared by incorporating one or more sensitizing dyes in a photographic emulsion in an ordinary manner. In practice, the dye is usually added to the emulsion while in solution in a suitable solvent, such as methanol or ethanol. The amount of the sensitizing dye to be incorporated in the emulsion may vary in a wide range of from 5 to 200 mg. per kg. of emulsion, depending on the required effect.
The photographic emulsion used in accordance with the present invention may be, in addition, super-sensitized and hyper-sensitized according to conventional methods. In the manufacture of the photographic emulsions which may be used in accordance with the present invention, there may be incorporated therein by conventional methods one or more ordinarily used additives, such as sensitizers, stabilizers, anti-bronzing agents, hardeners, surface active agents, anti-foggants, plasticizers, developing promoters, color developers, or fluorescent whitening agents.
The photographic emulsion in accordance with the present invention may be applied in the usual manner to a suitable support, such as, e.g., sheet glass, a film of cellulose derivative, a film of synthetic resin or baryta paper.
The present invention will be further illustrated by the following examples.
Example 1.A silver halide photographic emulsion was prepared by incorporating one of the sensitizing dyes as indicated above in a silver iodobromide emulsion (AgI: AgBr-=7 moles; 93 moles). Separately, another silver halide photographic emulsion was prepared by incorporating a sensitizing dye of the present invention in combination with a known green-sensitive sensitizing dye. These emulsions were separately applied to a triacetylcellulose film base and, after drying, exposed through a Fuji #7 filter (made by Fuji Photo Film Co., Ltd., transmitting light having a wave length longer than 580 mg) to a daylight of 64 luxes (corresponding to 5,400 K.) and developed.
The developing solution used was of the formulation as indicated in Table 2.
Diluted with water to make 1 liter.
In Table 3 is shown the degrees of color sensitization and maxima of sensitization obtained by separate addition of the sensitizing dyes as indicated in Table 1. In Table 4 is shown the degrees of spectral sensitization and maxima of sensitization obtained by the separate addition of the sensitizing dyes indicated above as sensitizing dyes for comparison. In Table 5 is shown the degrees of spectral sensitization and maxima of sensitization obtained by various combinations of sensitizing dyes selected from those listed in Table l and those as indicated above for comparison with a known green-sensitive sensitizing dye.
TABLE3 Amountot sensitizing dyeadded sensitizing (millimole/ Maxima of Red sensi- Dye No. kg. emulsion) Emulsion sensitization tivities 0.06 AgBr/I 625-628 120 0.06 AgBr/I 625 150 0.06 AgBr/I 628 150 0.06 AgBr/I 628 150 0.06 AgBr/I 628-630 125 0.06 AgBr/I 640 130 0.06 AgBr/I 638 160 0.06 AgBr/I 640 160 0.06 AgBr/I 646 140 0.06 AgBr/I 625-628 140 0.06 AgBr/I 628 150 0.06 AgBr/I 625-628 130 0.06 AgBr/I 625 130 0.06 AgBr/I 625 130 0.06 AgBr/I 640 120 0.06 AgBr/I 625 120 0.06 AgBr/I 622 140 0.06 AgBr/I 625 140 0.06 AgBr/I 625 120 0.06 AgBr/I 638 130 0.06 AgBr/I 628 120 0.06 AgBr/I 624 13D sensitivity, assuming that the red sensitivity of sensitizing dye A was 100.
The red sensitivities were indicated by terms of relative sensitivity, assuming that the red sensitivity of sensitizing coloring matter A was 100.
TABLE 5 Amount of sensitizing dye added (millimolel Maxima oi sensitizing g. sensltiza- Red sensi- Dye No. emulsion) Emulsion tion tivltles }AgBr/I 628 100 0. 015 AgBr/I 628 100 0.06 AgBr/I 628 100 0. 053
0.015 AgBr/I 628 100 0. 06 AgBr/I 625 100 0. 053
0. 015 AgrB/I 620 0.06 AgBr/I 630 100 0. 053
0. 015 AgBr/I 625 0.06 }AgBr/I 628 0. 053
0. 015 AgBr/I 625 80 The red sensitivities were indicated in terms of relative sensitivity, assuming that the red sensitivity of an emulsion having incorporated therein, by itself, sensitizing dye F was 100.
In the accompanying drawings, FIG. 1 indicates a spectral sensitization spectrum obtained by using great extent when used in combination with green-sensitization spectrum obtained by using sensitizing dye 3 in combination with known green-sensitive coloring matter H and I; FIG. 3 indicates aspectral sensitization spectrum obtained by using sensitizing dye E alone; and FIG. 4 indicates a spectral sensitization spectrum obtained by using sensitizing dye F in combination with the known green-sensitive sensitizing dyes H and I.
As is evident from FIGS. 3 and 4, where sensitizing dye E was used for compan'sion purposes, its maximum sensitization in the red region (J-band) falls off to a great extent when used in combination witht green-sensitive sensitizing dye H and this causes a remarkable depression of the red sensitivity, while, when employing sensitizing dye 3 of the present invention, the phenomenon that will cause such a depression of red sensitivity does not occur even if it is used in combination with the green-sensitive sensitizing dyes H and I.
The known green-sensitive sensitizing dyes used in combination with the sensitizing dye of the present in- The red sensitivities were indicated in terms of relative 75 vention are those having the following structures.
What is claimed is:
1. A silver halide photographic emulsion having incorporated therein at least one sensitizing dye represented by the following formula:
wherein Z and Z are individually selected from the group consisting of a sulfur and a selenium atom, R is selected from the group consisting of an ethyl group, an n-propyl group, an n-butyl group and an allyl group, R' is selected from the group consisting of an 'y-sulfopropyl group, a 'ysulfobutyl group, a a-sulfobutyl group, a B-carboxybutyl group and a w-carboxypentyl group, X represents an anion, and n is or 1, n being 0 when the dye is an intramolecular salt.
2. The silver halide photographic emulsion as in claim 1, wherein said emulsion further contains a green sensitive sensitizing dye.
3. The silver halide photographic emulsion as in claim 1, wherein the maximum spectral sensitivity of said emulsion is from 620 to 645 m 4. The silver halide photographic emulsion as in claim 1, wherein the amount of said sensitizing dye varies from to 200 milligrams per kilogram of emulsion.
5. The silver halide photographic emulsion as in claim group consisting of p 1 Br CzHs l? CH N N Br- (5 2H5 2 5 8. The silver halide photographic emulsion as in claim 1, wherein said emulsion further contains an orthosensitizer.
9. The silver halide photographic emulsion as in claim 8, wherein said orthosensitizer comprises thia-2'-cyanine or 2,2'-cyanine.
References Cited UNITED STATES PATENTS 2,912,433 11/1959 Sprague 96106 3,288,610 11/1966 Gotze et al 96106 3,424,586 1/1969 Gotze et a1. 96-106 ROBERT F. BURNETT, Primary Examiner G. W. MOXON II, Assistant Examiner US. Cl. X.=R. '206240.6 R
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6570468 | 1968-09-12 |
Publications (1)
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US3694217A true US3694217A (en) | 1972-09-26 |
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US865545A Expired - Lifetime US3694217A (en) | 1968-09-12 | 1969-09-12 | Silver halide photographic emulsion |
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US (1) | US3694217A (en) |
DE (1) | DE1946307C2 (en) |
FR (1) | FR2019427B1 (en) |
GB (1) | GB1280016A (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3446962A1 (en) * | 1983-12-22 | 1985-07-04 | Fuji Photo Film Co., Ltd., Minami-Ashigara, Kanagawa | PHOTOGRAPHIC SILVER HALOGENIDE PRINT PAPER AND USE OF THE PAPER IN THE BLACK AND WHITE DEVELOPMENT PROCESS |
EP0202616A2 (en) | 1985-05-16 | 1986-11-26 | Konica Corporation | Method for color-developing a silver halide photographic light-sensitive material |
US4690883A (en) * | 1984-12-14 | 1987-09-01 | Fuji Photo Film Co., Ltd. | Image forming process |
JPH01302351A (en) * | 1988-05-31 | 1989-12-06 | Fuji Photo Film Co Ltd | Method for processing silver halide color photographic sensitive material |
US5354646A (en) * | 1986-03-26 | 1994-10-11 | Konishiroku Photo Industry Co., Ltd. | Method capable of rapidly processing a silver halide color photographic light-sensitive material |
US5456999A (en) * | 1991-11-29 | 1995-10-10 | Agfa-Gevaert, N.V. | Infrared sensitive silver halide photographic material |
WO1996013755A1 (en) | 1994-10-26 | 1996-05-09 | Eastman Kodak Company | Photographic emulsions of enhanced sensitivity |
US5582957A (en) * | 1995-03-28 | 1996-12-10 | Eastman Kodak Company | Resuspension optimization for photographic nanosuspensions |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB498290A (en) * | 1937-03-25 | 1938-12-28 | Eastman Kodak Co | Improvements in sensitised photographic emulsions |
DE917330C (en) * | 1940-10-22 | 1955-01-10 | Agfa Ag Fuer Photofabrikation | Process for the production of symmetrical and asymmetrical carbocyanines substituted on the middle carbon atom of the methine chain |
BE484580A (en) * | 1947-08-29 | |||
DE929080C (en) * | 1951-10-23 | 1955-08-16 | Agfa Ag Fuer Photofabrikation | Process for the production of betaine-cyanine dyes and betaine-styryl dyes |
BE548605A (en) * | 1956-03-07 | |||
GB841119A (en) * | 1957-09-02 | 1960-07-13 | Ici Ltd | New photographic sensitisers |
US2917516A (en) * | 1957-11-25 | 1959-12-15 | Eastman Kodak Co | Method of making thiazole or oxazole quaternary salts |
DE1113873B (en) * | 1959-01-17 | 1961-09-14 | Wolfen Filmfab Veb | Process for sensitizing halide silver emulsions |
GB1027053A (en) * | 1963-08-26 | 1966-04-20 | Ilford Ltd | Photographic light-sensitive materials |
-
1969
- 1969-09-11 FR FR696931013A patent/FR2019427B1/fr not_active Expired
- 1969-09-12 GB GB45170/69A patent/GB1280016A/en not_active Expired
- 1969-09-12 DE DE1946307A patent/DE1946307C2/en not_active Expired
- 1969-09-12 US US865545A patent/US3694217A/en not_active Expired - Lifetime
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3446962A1 (en) * | 1983-12-22 | 1985-07-04 | Fuji Photo Film Co., Ltd., Minami-Ashigara, Kanagawa | PHOTOGRAPHIC SILVER HALOGENIDE PRINT PAPER AND USE OF THE PAPER IN THE BLACK AND WHITE DEVELOPMENT PROCESS |
US4657846A (en) * | 1983-12-22 | 1987-04-14 | Fuji Photo Film Co., Ltd. | Silver halide photographic printing paper |
US4690883A (en) * | 1984-12-14 | 1987-09-01 | Fuji Photo Film Co., Ltd. | Image forming process |
EP0202616A2 (en) | 1985-05-16 | 1986-11-26 | Konica Corporation | Method for color-developing a silver halide photographic light-sensitive material |
US5354646A (en) * | 1986-03-26 | 1994-10-11 | Konishiroku Photo Industry Co., Ltd. | Method capable of rapidly processing a silver halide color photographic light-sensitive material |
JPH01302351A (en) * | 1988-05-31 | 1989-12-06 | Fuji Photo Film Co Ltd | Method for processing silver halide color photographic sensitive material |
US5456999A (en) * | 1991-11-29 | 1995-10-10 | Agfa-Gevaert, N.V. | Infrared sensitive silver halide photographic material |
WO1996013755A1 (en) | 1994-10-26 | 1996-05-09 | Eastman Kodak Company | Photographic emulsions of enhanced sensitivity |
US5582957A (en) * | 1995-03-28 | 1996-12-10 | Eastman Kodak Company | Resuspension optimization for photographic nanosuspensions |
Also Published As
Publication number | Publication date |
---|---|
DE1946307A1 (en) | 1970-05-14 |
FR2019427B1 (en) | 1973-05-11 |
GB1280016A (en) | 1972-07-05 |
FR2019427A1 (en) | 1970-07-03 |
DE1946307C2 (en) | 1983-10-20 |
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