Colour photographic silver halide material

Abstract

A color photographic silver halide material which can be developed to form a negative, at least 95 mol % of the silver halides of which consist of AgCl, and which contains at least one light-sensitive silver halide emulsion layer, the silver halide of which contains at least one compound of formulae (I), (II) and (III):

Description

[0001] This invention relates to a color photographic silver halide material which can be developed to form a negative, and which comprises a support, at least one blue-sensitive silver halide emulsion layer which contains at least one yellow coupler, at least one green-sensitive silver halide emulsion layer which contains at least one magenta coupler, and at least one red-sensitive silver halide emulsion layer which contains at least one cyan coupler, at least 95% of the silver halide emulsions of which consist of AgCl, and which under scanning exposure and under analogue exposure is distinguished by sharp contrast which is independent of exposure time, and by a stable latent image.

[0002] In order to produce “digital prints”, photographic material is inserted in scanning photographic exposure devices in which the exposure unit exposes the image information material on to the photographic material pixel by pixel, line by line or area by area, using directed light of high intensity (typically from lasers, from light-emitting diodes (LEDs), from devices which are termed DMDs (digital micromirror devices) or from comparable devices) and with very short exposure times per pixel (of the order of nano- to microseconds). At high densities in particular, the problem of line obliteration occurs. This is manifested in the image by a blurred depiction of the edges where there is a large difference in density (e.g. written characters) in the subject, and is a graphically described as “bloom”, “color fringe formation”, “blurring”, etc. This limits the usable range of densities of the photographic material. Therefore, photographic materials for the production of “digital prints” of high image quality in scanning photographic exposure devices comprising LEDs or lasers have to exhibit only a slight extent of line obliteration at high color density (blackening).

PRIOR ART, AND OBJECT OF THE PRESENT INVENTION

[0003] It is known of from EP 774 689 that in order to achieve a higher color density without color fringe formation during pixel by pixel exposure with directed light of high intensity (typically from gas or diode lasers, from LEDs or from comparable devices) and at very short exposure times per pixel (typically of the order of nano- to microseconds), the gradation of the light-sensitive layers of the color negative paper used should be as steep as possible over the range of exposure times used.

[0004] It is known from EP 350 046 and from U.S. Pat. No. 5,500,329 that the gradation within the exposure range of seconds or milliseconds can be steepened by doping the silver halides with metal ions of transition metals of Group II and of Group VIII of the periodic table of the elements.

[0005] Moreover, it is known from EP 350 046 that doping of silver chloride or silver chloride-bromide emulsions with compounds of iridium and iron can reduce the fluctuation of photographic properties during a continuous chemical process.

[0006] Furthermore, it is known from JP 3 188 437, EP 476 602, JP 4 204 941, JP 4 305 644, EP 816 918 and EP 952 484 that doping silver chloride or silver chloride bromide emulsions with compounds of iridium and iron, in combination with other compounds or with other measures, can reduce the reciprocity failure of the emulsions.

[0007] It has been found, however, that when using these measures one of the most important photographic properties, namely the latent image stability, is not satisfactory.

[0008] The object of the present invention was to provide a material which is suitable for digital exposure and for analogue exposure and which is distinguished by steep gradation, irrespective of exposure times, and by stable latent image properties.

SUBJECT MATTER OF THE PRESENT INVENTION

[0009] This object is surprisingly achieved if the color photographic material described at the outset contains at least one light-sensitive silver halide emulsion layer, which contains at least one compound of formulae (I) (II) and (III):

[IrClnF6-n]2−M2+  (I)

[0010] wherein n denotes 0 or an integer from 1 to 6 and M2+ denotes 1 or 2 cations with a total number of 2 positive charges,

[Fe(CN)6]m−Mm+  (II

[0011] wherein m denotes 2 or 3 and M+ denotes 1 to 3 cations with a total number of m positive charges, 2

[0012] wherein o denotes 0, 1 or 2 and R denotes an alkyl, aryl or aralkyl.

[0013] The emulsion which is used according to the invention is preferably produced either by a simple double-jet method, by a double-jet method with pre-precipitation and precipitation, or by a combined double-jet-redissolution method.

[0014] The silver halide emulsion preferably contains silver halide grains comprising at least two different zones, wherein the nucleus is produced by a double-jet method using an AgNO3 solution and a halide solution, essentially a chloride solution, and the precipitate is produced by redissolving a very fine-grained silver halide emulsion (a so-called micrate emulsion) on to the pre-precipitate.

[0015] In the double-jet method, the compounds of formulae (I) and (II) are preferably introduced via the halide solution.

[0016] In the double-jet-redissolution method, the compound of formula (I) is introduced via the micrate emulsion, and the compound of formula (II) is introduced via the halide solution during the double-jet precipitation or both compounds are introduced via the micrate emulsion.

[0017] The compound of formula (III) is preferably added before or during chemical ripening.

[0018] The following amounts are preferably used per mol Ag of silver halide emulsion:

[0019] 10 nmol to 5 pmol of the compound of formula (I)

[0020] 10 nmol to 10 μmol of the compound of formula (II)

[0021] 0.1 nmol to 5 μmol of the compound of formula (III).

[0022] In one preferred embodiment, yellow couplers, magenta couplers and cyan couplers of formulae (IV), (V), (VI) and (VII) are used.

Yellow Couplers

[0023] 3

[0024] wherein

[0025] R1 denotes an alkyl, alkoxy, aryl or hetaryl,

[0026] R2 denotes an alkoxy, an aryloxy or a halogen,

[0027] R3 denotes —CO2R6—CONR6R7, —NHCO2R6, —NHSO2-R6, —SO2NR6R7, —SO2NHCOR6 or —NHCOR6,

[0028] R4 denotes hydrogen or a substituent,

[0029] R5 denotes hydrogen or a radical which can be split off during coupling,

[0030] R6 and R7, independently of each other, denote hydrogen, alkyl or aryl and one of the

[0031] R2, R3 and R4 radicals is a ballast radical.

Magenta Couplers

[0032] 4

[0033] wherein

[0034] R8 and R9, independently of each other, denote hydrogen, alkyl, aralkyl, aryl, aryloxy, alkylthio, arylthio, amino, anilino, acylamino cyano, alkoxycarbonyl, alkyl-carbamoyl or alkylsulphamoyl, wherein these radicals can be further substituted and wherein at least one of these radicals contains a ballast group, and

[0035] R10 denotes hydrogen or a radical which can be split off during chromogenic coupling.

[0036] R8 is preferably tert.-butyl; R10 is preferably chlorine.

Cyan Couplers

[0037] 5

[0038] wherein

[0039] R11, R12, R13 and R14, independently of each other, denote hydrogen or a C1-C6 alkyl.

[0040] R11 is preferably CH3 or C2H5.

[0041] R12 is preferably a C2-C6 alkyl,

[0042] R13 and R14 are preferably t-C4H9 or t-C5H11. 6

[0043] wherein

[0044] R15 denotes alkyl, alkenyl, aryl or hetaryl,

[0045] R16 and R17 denote H, alkyl, alkenyl, aryl or hetaryl,

[0046] R18 denotes H or a group which can be split off under the conditions of chromogenic development,

[0047] R19 denotes —COR20, —CO2R20, —CONR20R21, —SO20R21, —CO—CO2R20, —COCONR 20R21, or a group of formula 7

[0048] R20 denotes alkyl, alkenyl, aryl or hetaryl,

[0049] R21 denotes H or R20,

[0050] R22 denotes —N═or —C(R25)═,

[0051] R23, R24 and R25 denote OR21, —SR21, —NR20R21, —R21 or Cl, and

[0052] p denotes 1 or 2.

[0053] Within formula (VIII), the following groups of couplers are preferred:

[0054] (1) couplers in which p denotes 1 and R15 to R25 have the aforementioned meanings.

[0055] (2) couplers in which p denotes 2, R19 denotes —CO—R26 and R26 denotes an alkenyl or hetaryl, and R15 to R18 have the aforementioned meanings.

[0056] (3) couplers in which p denotes 2, R19 denotes —SO2R27, —SO2N(R27)2, —CO2R27, —COCO2—R27 or —COCO—N(R27)2 and R27 denotes an alkyl, aryl, alkenyl or hetaryl, and R15 to R18 have the aforementioned meanings.

[0057] (4) couplers in which p denotes 2, and R19 denotes a radical of formula 8

[0058]  and R15 to R18 and R22 to R24 have the aforementioned meanings.

[0059] (5) couplers in which p denotes 2 and R19 denotes a radical of formula 9

[0060]  wherein

[0061] R28 denotes H, Cl, CN, Br, F, —COR29, —CONHR29 or CO2R29, and

[0062] R29 denotes an alkyl or aryl.

[0063] In formula (VIII) and compounds (1) to (5), the substituents have the following preferred meanings:

[0064] R15 denotes alkyl or aryl,

[0065] R16 and R17 denote H, alkyl or aryl,

[0066] R18 denotes H, Cl, alkoxy, aryloxy, alkylthio or arylthio,

[0067] R22 denotes —N═,

[0068] R23 and R24 denote —OR21, —NR20R21, —Cl.

[0069] The following meanings are quite particularly preferred:

[0070] R17 denotes H, and

[0071] R20 denotes an alkyl or aryl.

[0072] The alkyl and alkenyl radicals can be straight chain, branched or cyclic and can themselves be substituted.

[0073] The aryl and hetaryl radicals can themselves be substituted, wherein aryl denotes phenyl in particular.

[0074] Possible substituents for alkyl, alkenyl, aryl or hetaryl radicals include: alkyl, alkenyl, aryl, hetaryl, alkoxy, aryloxy, alkenyloxy, hydroxy, alkylthio, arylthio, a halogen, cyano, acyl, acyloxy and acylamino, wherein an acyl radical can originate from an aliphatic olefinic or from an aromatic carboxylic, carbonic, carbamic, sulphonic, sulphonamido, sulphinic, phosphoric, phosphonic or phosphorous acid.

[0075] Examples of cyan couplers of formula VII include:

[0076] VII-1, where R11═C2H5, R12═n-C4H9, R3═R14=t-C4H9,

[0077] VII-2, where R11═R12═C2H5, R13═R14=t-C5H11,

[0078] VII-3, where R11=C2H5, R12=n-C3H7, R13=R14═t-C5H11,

[0079] VII-4, where R11═CH3, R12═C2H5, R13═R14=t-C5H11.

[0080] Examples of cyan couplers of formula (VIII) where p═2 include:

No.	R16	R17	R15	R19	R18
VIII-1	—C2H5	H	10	11	—Cl
VIII-2	—C2H5	H	12	13	—H
VIII-3	—C6H13	H	14	15	—OCH2CH2—SCH2COOH
VIII-4	-Phenyl	H	16	17	—Cl
VIII-5	—CH3	—CH3	—C16H33	18	—Cl
VIII-6	-Phenyl	H	—C12H27	19	—SCH2CH2—COOH
VIII-7	—C2H5	H	20	21	—O—CH2—COOCH3
VIII-8	C12H25	H	22	23	—Cl
VIII-9	—C3H7-i	H	24	25	—Cl
VIII-10	—CH3	—CH3	26	27	28
VIII-11	—C2H5	H	29	30	—Cl
VIII-12	-Phenyl	H	—C16H33	31	H
VIII-13	—C12H25	H	32	33	—Cl
VIII-14	—C4H9	H	34	35	—OCH2COOCH3
VIII-15	—CH3	—CH3	36	37	—Cl
VIII-16	—C2H5	H	38	—SO2—C4H9	—Cl
VIII-17	—C2H5	H	39	—CO—O—C4H9-i	—Cl
VIII-18	—C3H7-i	H	40	41	—OCH2—COOCH3
VIII-19	-Phenyl	H	42	—SO2—NH—C4H9-t	H
VIII-20	—C6H13	H	43	44	H
VIII-21	—CH3	—CH3	45	—CO—CO—OC2H5	—Cl
VIII-22	—C4H9	H	46	—SO2—CH3	—Cl
VIII-23	-Phenyl	-Phenyl	—C12H25	—SO2—C4H9	—SCH2CH2—COOH
VIII-24	—C12H25	H	47	—CO—O—C2H5	—Cl
VIII-25	—C2H5	H	48	49	Cl
VIII-26	—CH3	H	50	51	Cl
VIII-27	—C2H5	H	52	53	Cl
Examples of cyan couplers of formula (VIII), where p = 2 and
54
include:
No.	R16	R17	R15	R23	R24	R22	R18
VIII-28	—C2H5	H	55	—N(C4H9)2	—N(C4H9)2	—N═	—C—
VIII-29	—C2H5	H	56	57	58	—N═	—Cl
VIII-30	—C2H5	H	59	—OCH3	—OCH3	—N═	—Cl
VIII-31	—C6H13	H	60	—Cl	—NH—C4H9	—C(NHC4H9)═	H
VIII-32	-Phenyl	H	—C12H25	—OCH3	—N(C4H9)2	—N═	—OCH2COOCH3—
VIII-33	—CH3	—CH3	61	—NH—C4H9	—NH—C4H9	—C(N(C2H5)2)═	—Cl
VIII-34	H	H	62	—OCH3	—NH—C4H9	—N═	—S—CH2CH2—COOH
VIII-35	—CH3	H	63	—Cl	64	—N═	—Cl
Examples of cyan couplers, where p = 1, include:
Nr.	R16	R17	R15	R19	R18
VIII-36	—C2H5	H	65	66	—Cl
VIII-37	—C4H9	H	67	—CO—C3F7	—Cl
VIII-38	—C6H13	H	68	69	—OCH2CH2—S—CH2COOH
VIII-39	—CH3	—CH3	70	71	H
VIII-40	-Phenyl	H	72	73	—Cl
VIII-41	—C2H5	H	74	75	H
VIII-42	—C12H25	H	76	77	78
VIII-43	—C4H9	H	—C12H25	79	—Cl
VIII-44	—C2H5	H	80	—SO2—C4H9	—Cl
VIII-45	—C3H7-i	H	—C16H33	81	—O—CH2—COO—CH3
VIII-46	—CH2CH2CH2CH2—	82	83	—Cl
VIII-47	—C2H5	—C2H5	84	—CO—O—C4H9-i	H
VIII-48	-Phenyl	H	—C12H25	—CO—CO—N(C4H9)2	85
VIII-49	—C12H25	H	86	—CO—CH═CH—CO—N(C2H5)2	—Cl
VIII-50	—C2H5	H	87	88	—Cl
VIII-51	—C6H13	H	89	90	H
VIII-52	—C4H9	H	91	92	—Cl
VIII-53	—CH3	H	93	94	—Cl
VIII-54	-Phenyl	H	95	96	H
VIII-55	—C2H5	H	97	98	—Cl
VIII-56	—C2H5	H	99	100	Cl
VIII-57	—C3H7	H	101	102	Cl
VIII-58	—C2H5	H	103	104	H
VIII-59	—H	H	105	106	Cl
VIII-60	—C2H5	H	107	108	Cl
Cyan couplers of formula (VIII) are produced by the procedure given in US 5 686 235.

[0081] Cyan couples of formula (VIII) are produced by the procedure given in U.S. Pat. No. 5,686,235.

[0082] Examples of magenta couplers of formula (V) include:

109
Coupler R9
V-1     —C13H27
V-2     —(CH2)3SO2C12H25
V-3     110
V-4     111
V-5     112
V-6     113
V-7     —(CH2)2NHCOC13H27
V-8     114
V-9     115
V-10    116
V-11    117
V-12    —CH2CH2NHSO2C16H33
V-13    —CH2CH2NHCONHC12H25
V-14    —(CH2)3NHSO2C12H25
V-15    118
V-16    119
V-17    120
V-18    121
V-19    122
V-20    123
V-21    —CH2CH2NHCOOC12H25
as well as
V-22    124
V-23    125
V-24    126
V-25    127

[0083] Examples of magenta couplers of formula (VI) include:

128
Coupler R9
VI-1    129
VI-2    130
VI-3    131
VI-4    132
VI-5    133
VI-6    134
VI-7    135
VI-8    136
VI-9    —CH2CH2NHCOC13H27
VI-10   137
VI-11   —(CH2)3SO2C12H25
VI-12   138
VI-13   139
VI-14   140
VI-15   141
VI-16   142
VI-17   143
VI-18   144
VI-19   145
VI-20   146
VI-21   147
VI-22   148
VI-23   149
VI-24   150

[0084] as well as

[0085] Examples of yellow couplers of formula (IV) include:

IV-1  151
IV-2  152
IV-3  153
IV-4  154
IV-5  155
IV-6  156
IV-7  157
IV-8  158
IV-9  159
IV-10 160
IV-11 161
IV-12 162
IV-13 163
IV-14 164
IV-15 165
IV-16 166
IV-17 167
IV-18 168
IV-19 169
IV-20 170
IV-21 171
IV-22 172
IV-23 173
IV-24 174
IV-25 175
IV-26 176
IV-27 177
IV-28 178
IV-29 179
IV-30 180
IV-31 181
IV-32 182
IV-33 183
IV-34 184
IV-35 185
IV-36 186
IV-37 187
IV-38 188
IV-39 189
IV-40 190
IV-41 191
IV-42 192
IV-43 193
IV-44 194
IV-45 195
IV-46 196
IV-47 197
IV-48 198
IV-49 199
IV-50 200
IV-51 201
IV-52 202
IV-53 203
IV-54 204

[0086] Compounds of formula IX are used in particular as blue sensitisers 205

[0087] wherein

[0088] X1 and X2 independently of each other, denote S or Se,

[0089] R31 to R36 independently of each other, denote a hydrogen atom or a halogen atom, an alkyl, alkoxy, aryl or hetaryl group, or R31 and R32 or R32 and R33, R34 and R35 or R35 and R36 denote the remaining members of a condensed-on benzene, naphthalene or heterocyclic ring,

[0090] R37 and R38 independently of each other, denote an alkyl, sulphoalkyl, carboxyalkyl, —(CH2)1SO2R39SO2-alkyl, —(CH2)1SO2R39CO-alkyl, —(CH2)1COR39SO2-alkyl or —(CH2)1—COR39CO-alkyl group,

[0091] R39 denotes —N— or —NH—,

[0092] 1 denotes an integer from 1 to 6, and

[0093] M denotes a counterion which may be necessary for charge equalisation.

[0094] R31 to R36, independently of each other, preferably denote H, alkyl, F, Cl, Br, CF3, OCH3, phenyl, or R31 and R32 or R32 and R33, R34 and R35 or R35 and R36 denote the remaining members of a condensed-on benzene or naphthalene ring.

[0095] Examples of suitable blue sensitisers include the following compounds, wherein “Et” represents ethyl: 206

[0096] Suitable red sensitisers correspond to general formulae X or XI 207

[0097] wherein

[0098] R41 to R46, independently of each other, have the same meanings as R31 to R36,

[0099] R47 and R48, independently of each other, have the same meanings as R37 and R38,

[0100] R49 and R50, independently of each other, denote a hydrogen atom or an alkyl or aryl group,

[0101] R51 denotes a hydrogen atom, a halogen atom or an alkyl group, and

[0102] M denotes a counterion which may be necessary for charge equalisation.

[0103] Examples of red sensitisers are listed below, wherein “Et” represents ethyl: 208

[0104] Other preferred embodiments of the invention are given in the subsidiary claims.

[0105] The photographic material is preferably a color print material.

[0106] Photographic color print materials consist of a support on which at least one light-sensitive silver halide emulsion layer is deposited. Thin films and foils are particularly suitable as supports, as is paper which is coated with polyethylene or with polyethylene terephthalate. A review of support materials and of the auxiliary layers which are deposited on the front and back thereof is given in Research Disclosure 37254, Part 1 (1995), page 285.

[0107] Color photographic color print materials usually contain, in the following sequence on their support, at least one blue-sensitive, yellow-coupling silver halide emulsion layer, at least one green-sensitive, magenta-coupling silver halide emulsion layer, and at least one red-sensitive, cyan-coupling silver halide emulsion layer. These layers can be interchanged with each other.

[0108] The essential constituents of the photographic emulsion layer are binders, silver halide grains and color couplers.

[0109] Information on suitable binders is given in Research Disclosure 37254, Part 2 (1995), page 286.

[0110] Information on suitable silver halide emulsions, their production, ripening, stabilisation and spectral sensitisation, including suitable spectral sensitisers, is given in Research Disclosure 37254, Part 3 (1995), page 286, and in Research Disclosure 37038, Part XV (1995), page 89.

[0111] Precipitation can also be conducted in the presence of sensitising dyes. Complexing agents and/or dyes can be made ineffective at any desired point in time, e.g. by altering the pH or by an oxidising treatment.

[0112] Information on color couplers is to be found in Research Disclosure 37254, Part 4 (1995), page 288, and in Research Disclosure 37038, Part II (1995), page 80. The maximum absorption of the dyes formed from the couplers and from the color developer oxidation product preferably falls within the following ranges: yellow couplers 430 to 460 mn, magenta couplers 540 to 560 nm, cyan couplers 630 to 700 nm.

[0113] The color couplers, which are mostly hydrophobic, and other hydrophobic constituents of the layers also, are usually dissolved or dispersed in high-boiling organic solvents. These solutions or dispersions are then emulsified in an aqueous binder solution (usually a gelatine solution), and after the layers have been dried are present as fine droplets (0.05 to 0.8 μm diameter) in the layers.

[0114] Suitable high-boiling organic solvents, methods of introduction into the layers of a photographic material, and other methods of introducing chemical compounds into photographic layers, are described in Research Disclosure 37254, Part 6 (1995), page 292.

[0115] The light-insensitive intermediate layers which are generally disposed between layers of different spectral sensitivity may contain media which prevent the unwanted diffusion of developer oxidation products from one light-sensitive layer into another light-sensitive layer which has a different spectral sensitivity.

[0116] Suitable compounds (white couplers, scavengers or DOP scavengers) are described in Research Disclosure 37254, Part 7 (1995), page 292, and in Research Disclosure 37038, Part III (1995), page 84.

[0117] The photographic material may additionally contain compounds which absorb UV light, brighteners, spacers, filter dyes, formalin scavengers, light stabilisers, anti-oxidants, DMin dyes, additives for improving the dye-, coupler- and white stability and to reduce color fogging, plasticisers (latices), biocides and other substances.

[0118] Suitable compounds are given in Research Disclosure 37254, Part 8 (1995), page 292, and in Research Disclosure 37038, Parts IV, V, VI, VII, X, XI and XIII (1995), pages 84 et seq.

[0119] The layers of color photographic materials are usually hardened, i.e. the binder used, preferably gelatine, is crosslinked by suitable chemical methods.

[0120] Instant or rapid hardeners are preferably used. Instant or rapid hardeners are to be understood as compounds which crosslink gelatine so that immediately after coating, or no later than a few days after coating, hardening has proceeded to such an extent that there is no further change in sensitometry and in the swelling of the layer composite due to the crosslinking reaction. Swelling is to be understood as the difference between the wet film density and the dry film density during the aqueous processing of the material.

[0121] Suitable rapid and instant hardener substances are described in Research Disclosure 37254, Part 9 (1995), page 294, and in Research Disclosure 37038, Part XII (1995), page 86.

[0122] After image-by-image exposure, color photographic materials are processed by different methods corresponding to their character. Details on the procedures used and the chemicals required therefor are published in Research Disclosure 37254, Part 10 (1995), page 294, and in Research Disclosure 37038, Parts XV1 to XXIII (1995), page 95 et seq., together with examples of materials. The color photographic material according to the invention is particularly suitable for rapid processing with development times of 10 to 30 seconds.

[0123] Halogen lamps or laser illumination devices are particularly suitable as light sources for exposure.

Production of Silver Halide Emulsions

Micrate Emulsion (EmM1) (Dopant-free Micrate Emulsion)

[0124] The following solutions were made up using demineralised water:

	Solution 01	5500	g	water
		700	g	gelatine
		5	g	n-decanol
		20	g	NaCl
	Solution 02	9300	g	water
		1800	g	NaCl
	Solution 03	9000	g	water
		5000	g	AgNO3

[0125] Solutions 02 and 03 were added, simultaneously and with intensive stirring, to solution 01 at 40° C. over 30 minutes at a constant rate of addition at pAg 7.7 and pH 6.0. During precipitation, the pAg in the precipitation vessel was held constant by adding a NaCl solution and the pH in the precipitation vessel was held constant by adding H2SO4. An AgCl emulsion with an average particle diameter of 0.10 μm was obtained. The ratio by weight of gelatine to AgNO3 (the amount of AgCl in the emulsion is converted below into AgNO3) was 0.14. The emulsion was ultrafiltered at 50° C. and was redispersed with an amount of gelatine and water such that the ratio by weight of gelatine to AgNO3 was 0.3 and the emulsion contained 200 g AgCl per kg. After redispersion, the grain size was 0.13 μm.

Micrate Emulsion EmM2 (Ir- and Fe-doped Micrate Emulsion)

[0126] The procedure was as for EmMl, except that 7150 μg K2IrCl6 and 21.33 mg K4Fe(CN)6 were additionally added to solution 02. The emulsion accordingly contained 500 nmol K2IrCl6 and 2500 nmol K4Fe(CN)6 per mol Ag.

Pre-precipitation for Blue-sensitive Emulsion EmB

[0127] The following solutions were made up with demineralised water:

	Solution 11	5500	g	water
		680	g	gelatine
		5	g	n-decanol
		20	g	NaCl
		325	g	EmMl
	Solution 12	9300	g	water
		1800	g	NaCl
	Solution 13	9000	g	water
		5000	g	AgNO3

[0128] Solutions 12 and 13 were added simultaneously and with intensive stirring to solution 11, which had been placed in the precipitation vessel, at 50° C. over 150 minutes at a pAg of 7.7. The pAg and pH were controlled as for the precipitation of the emulsion (EmM1). The addition was controlled so that over the first 100 minutes the flow rate of solutions 12 and 13 increased linearly from 10 ml/min to 90 ml/min; over the remaining 50 minutes a constant flow rate of 100 ml/min was employed. An AgCl emulsion with an average particle diameter of 0.70 μm was obtained. The ratio by weight of gelatine to AgNO3 (the amount of AgCl in the emulsion is converted below into AgNO3) was 0.14. The emulsion was ultrafiltered and was redispersed with an amount of gelatine and water such that the ratio by weight of gelatine to AgNO3 was 0.56 and the emulsion contained 200 g AgNO3 per kg.

Blue-sensitive Emulsions

EmB1

[0129] 4.50 kg of the pre-precipitate (corresponding to 900 g AgNO3) were melted at 40° C. in a precipitation vessel. 0.5 kg micrate emulsion EmM2 (corresponding to 100 g AgNO3) were melted at 40° C. a second inflow vessel equipped with a stirrer. 10 mg bisthioether 1 were added, with intensive stirring, to pre-precipitate EmV. After 5 minutes, micrate emulsion EmM2 was added at a constant rate over 25 minutes. After 10 minutes, the emulsion was redispersed with an amount of gelatine such that the ratio by weight of gelatine to AgNO3 was 0.56. An AgCl emulsion with an average particle diameter of 0.725 μm was obtained. The emulsion contained 50 nmol K2IrCl6 and 250 nmol K4Fe(CN)6 per mol Ag.

[0130] The emulsion was ripened at a pH of 5.3 with the optimum amount of gold(III) chloride and Na2S2O3, at a temperature of 50° C. for 2 hours. After chemical ripening, the emulsion was, per mol AgCl, spectrally sensitised at 40° C. with 0.3 mmol of compound (IX-17), was stabilised with 0.5 mmol of compound (Stab 1) and subsequently treated with 0.6 mmol KBr. 209

[0131] Stab-1:

[0132] bisthioether: H5C2SCH2CH2SCH2CH2NHCONH2

EmB2

[0133] Precipitation, redispersion, chemical ripening and spectral sensitisation were carried out as for EmB1. After sensitisation, the emulsion was stabilised with 0.5 mmol of compound (Stab 2) per mol AgCl instead of compound (Stab 1). 210

[0134] Stab-2:

Green-sensitive Emulsions EmGI-EmG3

EmG1

[0135] The following solutions were made up with demineralised water:

	Solution 21	1100	g	water
		136	g	gelatine
		1	g	n-decanol
		4	g	NaCl
		186	g	EmMl
	Solution 22	1860	g	water
		360	g	NaCl
		565.4	μg	K2IrCl6
		3414	μg	K4Fe(CN)6
	Solution 23	1800	g	water
		1000	g	AgNO3

[0136] Solutions 22 and 23 were added simultaneously and with intensive stirring to solution 21, which had been placed in the precipitation vessel, at 40° C. over 75 minutes at pAg 7.7. The pAg and pH were controlled as for the precipitation of emulsion EmM1. The addition was controlled so that during the first 50 minutes the flow rate of solutions 22 and 23 increased linearly from 4 ml/min to 36 m/min; during the remaining 25 minutes a constant flow rate of 40 ml/min was employed. An AgCl emulsion with an average particle diameter of 0.52 μm was obtained. The emulsion contained 200 mmol Ir4+ and 2 μmol K4Fe(CN)6 per mol AgCl. The ratio by weight of gelatine to AgNO3 was 0.14. The emulsion was ultrafiltered, washed and redispersed with an amount of gelatine and water such that the ratio by weight of gelatine to AgNO3 was 0.56 and the emulsion contained 200 g AgNO3 per kg.

[0137] 1.25 kg of the emulsion (corresponding to 250 g AgNO3) was subjected to the optimum ripening procedure at a pH of 5.3 with gold(III) chloride and Na2S2O3 at a temperature of 60° C. for 2 hours. After chemical ripening, the emulsion was, per mol AgCl, spectrally sensitised with 0.6 mmol of compound (Sens G) at 50° C., was stabilised with 1.2 mmol of compound (Stab 3) and was subsequently treated with with 1 mmol KBr. 211

EmG2

[0138] The procedure was as for EmG1, except that Stab-3 was replaced by 0.6 mmol Stab-2 per mol AgCl.

EmG3

[0139] The procedure was as for EmG1, except that Stab-3 was replaced by 0.6 mmol Stab-4 per AgCl. 212

[0140] Stab-4:

Red-sensitive Emulsions EmR1 and EmR2

EmR1

[0141] Precipitation, desalination and redispersion were effected as for the green-sensitive emulsion EmG1, except that the compound K2IrCl6 in solution 22 was replaced by 5654 μg K2IrCl4F2. The emulsion was chemically ripened with the optimum amount of gold(III) chloride and Na2S2O3 for 2 hours at a temperature of 75° C. After chemical ripening, the emulsion was spectrally sensitised at 40° C. with 50 μmol of compound (X-1) and with 25 μmol of compound (XI-12) per mol AgCl, and was stabilised with 1 mmol (Stab 1) and 2.5 mmol (Stab 5) per mol AgNO3. 3 mmol per mol AgCl KBr were subsequently added.

[0142] Stab-5: 213

EmR2

[0143] As for EMRI, except that Stab-1 was replaced by 0.6 mmol Stab-4 per mol AgCl

Layer Structures

[0144] A color photographic recording material was produced by coating the following layers in the given sequence on a paper base coated on both sides with polyethylene. The quantitative data are given with respect to 1 m2 in each case. The corresponding amounts of AgNO3 are quoted for silver halide deposition.

Layer Structure 1

[0145] 1 st Layer (substrate layer)

[0146] 0.3 g gelatine p0 2nd layer (blue-sensitive layer):

[0147] EmB1 comprising 0.35 g AgNO3

[0148] 0.635 g gelatine

[0149] 0.45 g yellow coupler IV-11

[0150] 0.25 g tricresyl phosphate (TCP)

[0151] 25 3rd layer (intermediate layer):

[0152] 1.1 g gelatine

[0153] 0.2 g scavenger SC

[0154] 0.2 g TCP

[0155] 4th layer (green-sensitive layer):

[0156] EmG comprising 0.14 g AgNO3

[0157] 1.2 g gelatine

[0158] 0.14 g magenta coupler III-2

[0159] 0.20 g color stabiliser ST-1

[0160] 0.10 g color stabiliser ST-2

[0161] 0.19 g of a polymer of trimethylolpropane and caprolactone

[0162] 0.19 g of a mixture comprising 75% by weight dodecanol and 25% by weight tetradecanol

[0163] 5th layer (UV protection layer):

[0164] 1.1 g gelatine

[0165] 0.125 g SC

[0166] 0.0125 g white coupler

[0167] 0.418 g V absorber UV

[0168] 0.1375 g TCP

[0169] 0.266 g solvent O-1

[0170] 6th layer (red-sensitive layer):

[0171] EmR1 comprising 0.24 g AgNO3 with

[0172] 0.75 g gelatine

[0173] 0.38 g cyan coupler VI-2

[0174] 0.42 g TCP

[0175] 7th layer (UV protection layer):

[0176] 0.35 g gelatine

[0177] 0.18 g UV absorber UV-1

[0178] 0.098 g solvent O-1

[0179] 8th layer

[0180] 0.28 g hardener HM

Layer Structure 2

[0181] As layer structure 1, except that the blue-sensitive emulsion in the 2nd layer was EmB2 comprising 0.35 g AgNO3/m2.

Layer Structure 3

[0182] As layer structure 1, except that the green-sensitive emulsion in the 4th layer was EmG2 comprising 0.14 g AgNO3/m2.

Layer structure 4

[0183] As layer structure 1, except that the green-sensitive emulsion in the 4th layer was EmG3 comprising 0.14 g AgNO3/m2.

Layer Structure 5

[0184] As layer structure 1, except that the red-sensitive emulsion in the 6th layer was EmG5 comprising 0.24 g AgNO3/m2. 214

[0185] Compounds used for the first time in layer structures 1 to 5:

Processing

[0186] 1. Analogue Exposure

[0187] Samples were exposed behind a graduated neutral wedge filter with a density gradation of 0.1/step for 40 msec and 5 sec under a constant amount of light from a halogen lamp.

[0188] 2. Laser Exposure

[0189] The following laser exposure devices were used

[0190] red laser: a laser diode with wavelength of 683 nm

[0191] green laser: a 514 nm argon gas laser

[0192] blue laser: a 458 nm argon gas laser

[0193] optical resolution: 400 dpi

[0194] pixel exposure time: 131 nsec

[0195] color gradations produced: 256 per channel

[0196] An area of the samples was first exposed for the given exposure time (131 nsec) at a luminous intensity I such that the density D after processing (see below) corresponded to about 0.6 (by X-Rite Status A measurement). The luminous intensity I was subsequently reduced or increased so that the logarithm of the amount of light log I.t was 0.1 less or 0.1 greater than that of the preceding step. This procedure was continued until a total of 29 steps had been exposed. The lowest step corresponded to a luminous intensity equal to zero.

Processing

[0197] The exposed samples were processed as follows, using Process AP 49:

	a)	Colour developer-45 sec.-35° C.
		triethanolamine	9.0	g
		N,N-diethylhydroxylamine	4.0	g
		diethylene glycol	0.05	g
		3-methyl-4-amino-N-ethyl-N-methane-	5.0	g
		sulphonamidoethyl-aniline sulphate
		potassium sulphite	0.2	g
		triethylene glycol	0.05	g
		potassium carbonate	22	g
		potassium hydroxide	0.4	g
		ethylenediaminetetraacetic acid,	2.2	g
		di-Na salt
		potassium chloride	2.5	g
		1,2-dihydroxybenzene-3,4,6-	0.3	g
		trisulphonic acid, trisodium salt
		made up with water to 1000 ml; pH 10.0
	b)	Bleach hardener-45 sec.-35° C.
		ammonium thiosulphate	75	g
		sodium hydrogen sulphite	13.5	g
		ammonium acetate	2.0	g
		ethylenediaminetetraacetic acid	57	g
		(iron ammonium salt)
		25% ammonia	9.5	g

[0198] made up with water to 1000 ml; pH adjusted to 5.5 with acetic acid

[0199] c) Washing-2 min-33° C.

[0200] d) Drying

[0201] The results of integral analogue exposure and laser exposure are presented in the form of the following parameters:

[0202] Dmin: density in the unexposed region

[0203] sensitivity E: abscissa to the density =0.6 the density is given as the abscissa value (relative sensitivity value)

[0204] Gamma value G2: shoulder gradation: is the gradient of the secant between the sensitivity point at density D=Dmin +0.85 and the point on the curve at which the density D =Dmin +1.60.

Latent Image Behaviour

Experimental:

[0205] Unprocessed samples with layer structures 1 to 5 were subjected to analogue exposure in a sensitometer. After 5 min, 30 min, 6 hours and 24 hours, the exposed samples were processed using the AP 94 process described above. The yellow, magenta and cyan color densities of a grey area with a density of about 0.5 were subsequently measured. The change in density as a function of the delay between exposure and processing corresponded to the latent image behaviour of the material.

Results
		Latent
Layer	Light-	image behaviour
struc-	sensitive	131	40	4.91	30′-	6h-	24h-	Re-
ture	layer	nsec	msec	sec	1.5′	1.5′	1.5′	marks
1	yellow	2.85	2.92	2.90	0.10	0.12	0.12	com-
	magenta	3.15	3.14	3.12	0.14	0.15	0.17	parison
	cyan	3.67	3.34	3.32	0.15	0.20	0.19
2	yellow	2.90	2.98	2.95	0.05	0.03	0.04	inven-
	magenta	3.16	3.15	3.11	0.13	0.13	0.16	tion
	cyan	3.67	3.34	3.32	0.15	0.20	0.19
3	yellow	2.87	2.92	2.91	0.09	0.10	0.12
	magenta	3.20	3.20	3.18	0.03	0.02	0.05	inven-
	cyan	3.68	3.36	3.33	0.13	0.17	0.16	tion
4	yellow	2.88	2.89	2.88	0.08	0.10	0.11
	magenta	3.10	3.12	3.14	0.04	0.05	0.07	inven-
	cyan	3.67	3.34	3.32	0.14	0.19	0.18	tion
5	yellow	2.99	2.96	2.95	0.09	0.10	0.11
	magenta	3.20	3.18	3.17	0.13	0.14	0.16
	cyan	3.87	3.54	3.50	−0.02	−0.03	−0.02	inven-
								tion

[0206] It is clear that emulsions which contain the compound of formula (III) exhibit a d change in density and thus exhibit improved latent image stability.

Claims

1. A color photographic silver halide material which can be developed to form a negative, and which comprises a support, at least one blue-sensitive silver halide emulsion layer which contains at least one yellow coupler, at least one green-sensitive silver halide emulsion layer which contains at least one magenta coupler, and at least one red-sensitive silver halide emulsion layer which contains at least one cyan coupler, at least 95 mol % of the silver halides of which consist of AgCl, characterised in that the material contains at least one light-sensitive silver halide emulsion layer which contains at least one compound of formulae (I) (II) and (III):

2. A color photographic silver halide material according to claim 1, characterised in that the amount of compound (I) ranges from 10 nmol to 5 mol per mol AgCl, the amount of compound (II) ranges from 10 nmol to 10 μmol per mol AgCl and the amount of compound (III) ranges from 0.1 mmol to 5 mmol per mol AgCl.

3. A color photographic silver halide material according to claims 1 and 2, characterised in that the silver halide is additionally doped with at least one metal of group IVA, with a further metal of group VIIIB, or with a metal of group IIB of the periodic table of the elements, or with Ga, In, Tl, Ge, Sn, Pb, Re, Au, Pr or Ce.

4. A color photographic silver halide material according to any one of the preceding claims, characterised in that the silver halide emulsion is blue-sensitive and contains at least one compound of formula IX

5. A color photographic silver halide material according to any one of the preceding claims, characterised in that the at least one blue-sensitive layer contains at least one yellow coupler of formula IV

6. A color photographic silver halide material according to any one of the preceding claims, characterised in that the silver halide emulsion is red-sensitive and contains at least one compound of formulae X or XI

7. A color photographic silver halide material according to any one of the preceding claims, characterised in that the at least one green-sensitive layer contains at least one magenta coupler of formulae V or VI,

8. A color photographic silver halide material according to any one of the preceding claims, characterised in that the at least one red-sensitive layer contains at least one cyan coupler of formulae VII or VIII