EP0501465A1 - Silver halide color photographic light sensitive material - Google Patents

Silver halide color photographic light sensitive material Download PDF

Info

Publication number
EP0501465A1
EP0501465A1 EP92103312A EP92103312A EP0501465A1 EP 0501465 A1 EP0501465 A1 EP 0501465A1 EP 92103312 A EP92103312 A EP 92103312A EP 92103312 A EP92103312 A EP 92103312A EP 0501465 A1 EP0501465 A1 EP 0501465A1
Authority
EP
European Patent Office
Prior art keywords
group
red
light
atom
sensitive material
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.)
Withdrawn
Application number
EP92103312A
Other languages
German (de)
English (en)
French (fr)
Inventor
Kuniaki Konica Corporation Uezawa
Hiroshi Konica Corporation Shimazaki
Yoshitaka Konica Corporation Yamada
Kenji Konica Corporation Michiue
Satoru Konica Corporation Shimba
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Konica Minolta Inc
Original Assignee
Konica Minolta Inc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Konica Minolta Inc filed Critical Konica Minolta Inc
Publication of EP0501465A1 publication Critical patent/EP0501465A1/en
Withdrawn legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03CPHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C7/00Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
    • G03C7/30Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
    • G03C7/3041Materials with specific sensitometric characteristics, e.g. gamma, density

Definitions

  • the present invention relates to a silver halide color photographic light-sensitive material with improved color reproducibility, specifically to a silver halide color photographic light-sensitive material improved in reproducibility for red.
  • U.S. Patent No. 3,672,898 discloses a silver halide color photographic light-sensitive material having a specific spectral sensitivity distribution, with which a variation in color balance caused by a change in light source (e.g. sun, fluorescent lamp, tungsten lamp) can be minimized. It is also known in the art that the saturation of a primary color, such as red, green and blue, can be recorded accurately when the color-sensitive layers of a light-sensitive material each have a sharp spectral sensitivity distribution.
  • a primary color such as red, green and blue
  • Interimage effect or sharp spectral distribution allows the saturation of a color to be reproduced faithfully, but, at the same time, hinders the exact reproduction of delicate shades of a primary color.
  • the gradation of its complementary color tends to be lost or get softer due to the manifestation of interimage effect. This is the serious disadvantage of interimage effect.
  • D N2 -D R2 and D N16 -D R16 (which will be defined later) are adjusted to specific values.
  • D N2 -D R2 and D N16 -D R16 are adjusted to specific values.
  • the object of the invention is to provide a silver halide color photographic light-sensitive material which can reproduce red in a lower to medium density region accurately with a higher saturation, and, at the same time, can reproduce the delicate shades of red in a higher density region.
  • a silver halide photographic light-sensitive material comprising a support and provided thereon at least one red-sensitive silver halide emulsion layer, at least one green-sensitive silver halide emulsion layer and at least one blue-sensitive silver halide emulsion layer, wherein red density D N2 obtained after exposing said light-sensitive material to 2/S ⁇ lux ⁇ sec (wherein S is the ISO sensitivity of said light-sensitive material) of white light and red density D R2 obtained after exposing said light-sensitive material to 2/S ⁇ lux ⁇ sec (wherein S is as defined above) of white light through a red filter satisfy the following inequality: 2.0 ⁇ D N2 -D R2 ⁇ 0.13; and red density D N16 obtained after exposing said light-sensitive material to 16/S ⁇ lux ⁇ sec (wherein S is as defined above) of white light and red density D R16 obtained after exposing said light-sensitive material to 16 / S ⁇ lux ⁇ sec (wherein S is as defined above) of white light through a red
  • Red density D N2 is defined as a density obtained by exposing a light-sensitive material having an ISO sensitivity of S to white light emitted from a light source having the same spectral energy distribution as that of a light source employed for the ISO sensitivity measurement under the following exposure conditions: shutter speed, same as that employed for the ISO sensitivity measurement; exposure, 2 ⁇ 1/S ⁇ lux ⁇ sec.
  • Red density D R2 is defined as a density which is obtained in the same manner as mentioned above, except that the exposure is performed using a red filter.
  • a red filter is a filter having a transmittance of 2% or less at 350 to 585 nm, 80% or more at 630 to 800 nm, and attaining a 50% transmittance at a certain point in the wavelength region 600 to 610 nm.
  • Wratten (gelatin) filter No. 26 manufactured and sold by Eastman Kodak Co., Ltd. is one example of commercially available red filters.
  • Red density D N16 is defined as a density obtained in the same manner as that employed for the D N2 measurement, except that the exposure is 16 ⁇ 1/S ⁇ lux ⁇ sec.
  • Red density D R16 is defined as a density obtained in the same manner as that employed for the D N16 measurement, except that the exposure is conducted through a red filter.
  • a light-sensitive material is left at 20 ⁇ 5°C and RH60 ⁇ 10%, and then processed for 0.5 to 6 hours by processing methods recommended by film manufacturers.
  • the density is the Status M density prescribed in 1505/3-1984 (E).
  • the density measurement is conducted by the method prescribed by ISO, using a densitometer manufactured and sold by X-RITE Co., Ltd. (Model 310).
  • red sensitivities D N2 , D R2 , D N16 and D R16 should satisfy the following inequalities: 2.0 ⁇ D N2 -D R2 ⁇ 0.13; and 0.06 ⁇ D N16 -D R16 ⁇ 0
  • D N2 -D R2 and D N16 -D R16 are adjusted to such values, a light-sensitive material can reproduce red in a lower to medium density region accurately with a higher saturation, and at the same time, can reproduce faithfully the delicate shades of red in a higher density region.
  • the resulting negative image has a gradation.
  • gradation tends to be lost during the printing of the negative image on color paper, since the density of the negative image is likely to change by an amount that is beyond the latitude of the color paper.
  • Such loss of gradation can be avoided by making the gradation and density of a negative image softer and lower, respectively.
  • a negative image has a softer gradation and a lower density, red, in particular, skin color of a subject reproduced on color paper inevitably has a lower saturation.
  • the inventors have found that the above problem can be solved by adequately controlling the spectral sensitivity distribution of the red-sensitive layer and the interimage effect in the blue-, green-, and red-sensitive layers.
  • the spectral sensitivity distribution of the red-sensitive layer can be adjusted, for example, by the use of a spectral sensitizing dye.
  • the red-sensitive emulsion be spectrally sensitized with at least one sensitizing dye represented by Formula 1 and at least one sensitizing dye represented by Formula 2 or 3.
  • R1 represents a hydrogen atom, an alkyl group or an aryl group
  • R2 and R3 each represent an alkyl group
  • Y1 and Y2 each represent a sulfur atom or a selenium atom
  • Z1, Z2, Z3 and Z4 each represent a hydrogen atom, a halogen atom, a hydroxy group, an alkoxy group, an amino group, an acyl group, an acylamino group, an acyloxy group, an aryloxy group, an alkoxycarbonyl group, an aryloxycarbonyl group, an alkoxycarbonyl group, a sulfonyl group, a carbamoyl group, an aryl group, an alkyl group or a cyano group
  • X1 represents a cation
  • m represents an integer of 1 or 2.
  • Z1 and Z2 may combine with each other to form a ring. The same can be applied to Z3 and Z4.
  • R4 represents a hydrogen atom, an alkyl group or an aryl group
  • R5, R6, R7 and R8 each represent an alkyl group
  • Y3 represents a nitrogen atom, a sulfur atom or a selenium atom
  • z5, z6, Z7 and Z8 each represent a hydrogen atom, a halogen atom, a hydroxy group, an alkoxy group, an amino group, an acyl group, an acylamino group, an acyloxy group, an aryloxy group, an alkoxycarbonyl group, an aryloxycarbonyl group, an alkoxycarbonylamino group, a carbamoyl group, an aryl group, an alkyl group, a cyano group or a sulfonyl group
  • X2 represents a cation
  • n represents an integer of 1 or 2.
  • n 1
  • Y5 represents a sulfur atom or a selenium atom
  • R18 represents a hydrogen atom, a lower alkyl group or an aryl group
  • R10 and R20 each represent a substituted or unsubstituted alkyl group
  • Z17, Z18, Z19 and Z20 each represent a hydrogen atom, a halogen atom, a hydroxy group, an alkoxy group, an amino group, an acylamino group, an acyloxy group, an alkoxycarbonyl group, an alkoxycarbonylamino group or a lower alkyl group
  • X5 represents a cation
  • Q represents an integer of 1 or 2.
  • Z17, Z18, Z19 or Z20 Specific examples of the groups represented by Z17, Z18, Z19 or Z20 include those described in various publications published in the photographic industry. Z17 and Z18 may combine with each other to form a ring. The same can be applied to Z19 and Z20. Examples of such ring include a benzene ring. When the sensitizing dye forms an intramolecular salt, Q is 1.
  • sensitizing dyes represented by Formula 1, 2 or 3 benzothiazoles and quinolones described in Japanese Patent Examined Publication No. 24533/1982 and quinoline derivatives described in Japanese Patent Examined Publication No. 24899/1982 may optionally be employed as a supersensitizer.
  • the sensitizing dye for the red-sensitive layer it is preferred that at least one sensitizing dye represented by Formula 1 and at least one sensitizing dye represented by Formula 2 be employed in combination.
  • a DIR compound is defined as a compound that can release, upon a coupling reaction with an oxidized development agent, development inhibitor or a compound capable of releasing a development inhibitor.
  • Examples of usable DIR compounds include Example Compound Nos. D-1 to 37 described in Japanese Patent Publication Open to Public Inspection (hereinafter referred to as Japanese Patent O.P.I. Publication) No. 77056/1989, pp. 36-64.
  • at least one DIR compound is contained in at least one light-sensitive layer, preferably in at least two light-sensitive layers differing in sensitivity.
  • a development inhibitor to be released from a DIR compound contained in the green-sensitive layer preferably has a diffusibility of 0.34 to 0.60.
  • a development inhibitor to be released from a DIR compound contained in the blue-sensitive layer preferably has a diffusibility of 0.40 to 0.70.
  • the diffusibility of a development inhibitor can be measured by the method described in Japanese Patent O.P.I. Publication No. 77056/1989, pp. 36-42
  • the amount of a DIR compound is 1.0 ⁇ 10 ⁇ 4 to 1.0 ⁇ 10 ⁇ 1 mol, preferably 4.0 ⁇ 10 ⁇ 4 to 5.0 ⁇ 10 ⁇ 2 mol, still preferably 8.0 ⁇ 10 ⁇ 4 to 2.0 ⁇ 10 ⁇ 2 mol, per mol silver halide.
  • the average grain size d of silver halide grains contained in the high-speed light-sensitive layer is preferably 0.55 ⁇ m or less, still preferably 0.47 ⁇ m or less, further preferably 0.38 ⁇ m or less.
  • An average grain size d is defined as a diameter d i that maximizes the product of n i and d i 3 (wherein n i means the number of grains having a diameter of d i ). The significant figure is calculated down to the third decimal place and the fourth digit is rounded to the nearest whole number.
  • the size of a grain is defined as the length of a side of a cube having the same volume as that of the grain.
  • a silver halide emulsion to be employed in the invention is preferably monodispersed.
  • the "monodispersed emulsion” is defined as an emulsion containing 70% by weight more, preferably 80% by weight or more, still preferably 90% by weight or more, of grains with sizes falling within the range of 80 to 120% of the average grain size d.
  • an emulsion consisting of silver halide grains each having in its interior portion a high silver iodide phase.
  • the high silver iodide content phase is covered with a phase containing a smaller amount of silver iodide or a phase containing no silver iodide such as silver chloride phase (these two phases will be referred to as low silver iodide content phases).
  • the silver iodide content of the high iodide content phase is preferably 15 to 45 mol%, still preferably 20 to 42 mol%, most preferably 25 to 40 mol%.
  • the low silver iodide content phase may constitute the outermost layer of a silver halide grain.
  • the average silver iodide content of the low silver iodide content phase is preferably 6 mol% or more, still preferably 0 to 4 mol%.
  • Another silver iodide-containing phase e.g. a phase with a silver iodide content which is between the silver iodide content of the high silver iodide content phase and that of the low silver iodide content phase
  • a silver halide emulsion to be employed in the invention may consist of either regular or twin silver halide crystals. It is also possible to employ tabular silver halide crystals with an aspect ratio of 2 or more. Here, an aspect ratio is defined as a grain size/grain thickness ratio (wherein a grain size is defined as the diameter of a circle having the same projection area).
  • a silver halide emulsion to be used in the invention may be chemically sensitized in the usual way.
  • a silver halide emulsion may contain additives such as an antifoggant and a stabilizer.
  • Gelatin is useful as the binder for a silver halide emulsion, but other substances may also be employed.
  • Emulsion layers and other hydrophilic colloidal layers may be hardened, and may contain a plasticizer and a dispersion (latex) of a polymer which is soluble or sparingly soluble in water.
  • Emulsion layers of the silver halide light-sensitive material of the present invention each contain a color-forming coupler. Each of them may also contain a colored coupler for color compensation, a competitive coupler and a compound which can release, upon a coupling reaction with an oxidized developing agent, a photographically effective fragment such as a development accelerator, a bleaching accelerator, a developing agent, a silver halide solvent, a toning agent, a hardener, a foggant, an anti-foggant, a chemical sensitizer and a desensitizer.
  • a development accelerator a bleaching accelerator, a developing agent, a silver halide solvent, a toning agent, a hardener, a foggant, an anti-foggant, a chemical sensitizer and a desensitizer.
  • the light-sensitive material of the invention may be provided with auxiliary layers such as a filter layer, an anti-halation layer and an anti-irradiation layer.
  • auxiliary layers such as a filter layer, an anti-halation layer and an anti-irradiation layer.
  • These layers and/or silver halide emulsion layers each may contain a dye which can be removed therefrom or bleached out during development.
  • silver halide emulsions described in Research Disclosure No. 308119 may also be employed.
  • Silver halide emulsions to be employed in the invention are subjected to physical ripening, chemical ripening and spectral sensitization. Additives to be used in these processes are described in Research Disclosure Nos. 17643, 18716 and 308119.
  • Additives may be added, for instance, by the dispersion method described in Research Disclosure No. RD308119XIV.
  • the order of layers may be either conventional or inverted.
  • the light-sensitive material of the invention may be of unit structure. (For the layer order or the structure of a light-sensitive material, see Research Disclosure No. 308119VII-K).
  • polyethylene-coated paper As the support, use can be made of polyethylene-coated paper, polyethylene terephthalate films, baryta paper and cellulose triacetate films.
  • the present invention can be applied to color negative films for normal photography and cinematography, color reversal films for slide projection and telecasting, color paper, color positive films and color reversal paper.
  • the light-sensitive material of the present invention is, after exposure to light, processed by conventional methods described in Research Disclosure No. 17643, pp. 28-29, Research Disclosure No. 18716. p. 647 and Research Disclosure No. 308119, sec. XIX, whereby a dye image can be obtained.
  • the amounts of ingredients are expressed in terms of gram per square meter of a light-sensitive material, unless otherwise indicated.
  • the amounts of silver halide and colloidal silver are converted into the amounts of silver.
  • the amount of a sensitizing dye is expressed in terms of mol per mol of a silver halide contained in the same layer.
  • Example No. 101 On a cellulose triacetate film support, layers of the following compositions were provided in sequence, whereby a multilayer color photographic light-sensitive material (Sample No. 101) was obtained.
  • Second layer (intermediate layer) Gelatin 1.30 Third layer (low-speed red-sensitive layer) Silver iodobromide emulsion (average grain size: 0.27 ⁇ m, average silver iodide content: 7 mol%) 0.80 Sensitizing dye (I-34) 1.31 ⁇ 10 ⁇ 4 Sensitizing dye (I-6) 6.55 ⁇ 10 ⁇ 4 Sensitizing dye (III-11) 6.55 ⁇ 10 ⁇ 4 Cyan coupler (C-1) 0.60 Colored cyan coupler (CC-1) 0.10 DIR compound (D-25) 0.25 DIR compound (D-23) 0.004 High-boiling solvent (Oil-1) 0.50 Gelatin 0.90 Fourth layer (intermediate layer) Gelatin 1.00 Fifth layer (high-speed red-sensitive emulsion layer) Silver iodobromide emulsion (average grain
  • coating aids Su-1 and Su-2 Besides the above ingredients, coating aids Su-1 and Su-2, a viscosity controller, hardeners H-1 and H-2, a stabilizer ST-1 and anti-foggants AF-1 and AF-2 (two kinds AF-2 were employed. One had a molecular weight of 100,000 and the other had 1,100,000) were added.
  • Sample Nos. 102 to 106 were each prepared in substantially the same manner as in the preparation of Sample No. 101, except that the type and amount of the sensitizing dye and the DIR compound in the 3rd and 5th layers, as well as the type and amount of the DIR compound in the 7th and 8th layers were varied to those shown in Table 1.
  • each of the so-prepared samples was examined for ISO sensitivity S and red densities D N2 , D N16 , D R2 and D R16 .
  • As the red filter use was made of Wratten filter No. 26 (manufactured by Eastman Kodak Co., Ltd.). Using each sample, a color rendition chart (manufactured by Macbeth) and a red sweater were photographed. Then, each sample was processed according to the following procedure. Processing procedure (38°C) Color developing 3 min 10 sec Bleaching 6 min 30 sec Fixing 3 min 15 sec Rinsing 6 min 30 sec Stabilizing 3 min 15 sec Drying 1 min 30 sec
  • the processing liquids had the following compositions: ⁇ Color Developer ⁇ 4-amino-3-methyl-N-ethyl-N-( ⁇ -hydroxyethyl) aniline sulfate 4.75 g Anhydrous ⁇ sodium sulfite 4.24 g Hydroxylamine 1/2 sulfate 2.0 g Anhydrous potassium carbonate 37.5 g Sodium bromide 1.3 g Trisodium nitrilotriacetate (monohydrate) 2.5 g Potassium hydroxide 1.0 g Water was added to make the total quantity 1 liter.
  • each of the samples of the invention could reproduce red with a high saturation, and could reproduce accurately the delicate shades of red.

Landscapes

  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Silver Salt Photography Or Processing Solution Therefor (AREA)
EP92103312A 1991-03-01 1992-02-27 Silver halide color photographic light sensitive material Withdrawn EP0501465A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5954191A JPH04274422A (ja) 1991-03-01 1991-03-01 ハロゲン化銀写真感光材料

Publications (1)

Publication Number Publication Date
EP0501465A1 true EP0501465A1 (en) 1992-09-02

Family

ID=13116227

Family Applications (1)

Application Number Title Priority Date Filing Date
EP92103312A Withdrawn EP0501465A1 (en) 1991-03-01 1992-02-27 Silver halide color photographic light sensitive material

Country Status (2)

Country Link
EP (1) EP0501465A1 (ja)
JP (1) JPH04274422A (ja)

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4028115A (en) * 1975-08-26 1977-06-07 Fuji Photo Film Co., Ltd. Silver halide photographic emulsion sensitized to red with four carbocyanine dyes
JPS62160449A (ja) * 1986-01-08 1987-07-16 Fuji Photo Film Co Ltd カラ−写真感光材料
EP0283242A2 (en) * 1987-03-17 1988-09-21 Konica Corporation Silver halide colour photographic light-sensitive material

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4028115A (en) * 1975-08-26 1977-06-07 Fuji Photo Film Co., Ltd. Silver halide photographic emulsion sensitized to red with four carbocyanine dyes
JPS62160449A (ja) * 1986-01-08 1987-07-16 Fuji Photo Film Co Ltd カラ−写真感光材料
EP0283242A2 (en) * 1987-03-17 1988-09-21 Konica Corporation Silver halide colour photographic light-sensitive material

Also Published As

Publication number Publication date
JPH04274422A (ja) 1992-09-30

Similar Documents

Publication Publication Date Title
US5252444A (en) Silver halide color photographic light-sensitive material offering excellent hue reproduction
US5180657A (en) Color photographic light-sensitive material offering excellent hue reproduction
EP0492443B1 (en) Color photographic silver halide duplicating element and process
US5206126A (en) Color photographic light-sensitive material offering excellent hue reproduction
US5436116A (en) Silver halide color photographic photosensitive material and color proof preparation process
JP2884371B2 (ja) ハロゲン化銀カラー写真感光材料
US5206124A (en) Light-sensitive silver halide color photographic material
EP0588649B1 (en) Positive type color light sensitive material and the image forming process therefor
JP3391599B2 (ja) 写真要素および可視画像提供方法
EP0502491A1 (en) Method for forming a silver halide color photographic image
EP1033619B1 (en) Photographic film element containing an emulsion with broadened green responsivity
EP0501465A1 (en) Silver halide color photographic light sensitive material
USH1196H (en) Color photographic light-sensitive material excellent in color reproduction
US5302500A (en) Silver halide color photographic light-sensitive material offering excellent hue reproduction
JP2881330B2 (ja) 色相再現に優れたカラー写真感光材料
JP2881329B2 (ja) 色相再現性に優れたカラー写真感光材料
JPH08328216A (ja) 改良された感度を有するハロゲン化銀写真成分
JPH05249626A (ja) ハロゲン化銀カラー写真感光材料
JP3020105B2 (ja) 色相再現性に優れたカラー写真感光材料
JP2881327B2 (ja) 色相再現性に優れたカラー写真感光材料
JP3189102B2 (ja) ハロゲン化銀カラー写真感光材料
JP2843876B2 (ja) ハロゲン化銀カラー写真感光材料
JPH03264955A (ja) 色相再現性に優れたカラー写真感光材料
JPH03107139A (ja) 色相再現性に優れたカラー写真感光材料
JP2000221638A (ja) ハロゲン化銀カラー写真感光材料及びカラープルーフ作製方法

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): DE FR GB NL

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 19930303