Photographic material having enhanced light absorption

[0006] This invention relates to silver halide photographic material containing at least one silver halide emulsion which has enhanced light absorption.

[0007] J-aggregating cyanine dyes are used in many photographic systems. It is believed that these dyes adsorb to a silver halide emulsion and pack together on their “edge” which allows the maximum number of dye molecules to be placed on the surface. However, a monolayer of dye, even one with as high an extinction coefficient as a J-aggregated cyanine dye, absorbs only a small fraction of the light impinging on it per unit area. The advent of tabular emulsions allowed more dye to be put on the grains due to increased surface area. However, in most photographic systems, it is still the case that not all the available light is being collected.

[0008] Increasing the absorption cross-section of the emulsion grains should lead to an increased photographic sensitivity. The need is especially great in the blue spectral region where a combination of low source intensity and relatively low dye extinction result in deficient photoresponse. The need for increased light absorption is also great in the green sensitization of the magenta layer of color negative photographic elements. The eye is most sensitive to the magenta image dye and this layer has the largest impact on color reproduction. Higher speed from increased light absorption in this layer can allow the use of smaller emulsions to obtain improved color and image quality characteristics and reduce radiation sensitivity. The cyan layer can also benefit from improved spectral sensitivity and lower radiation sensitivity that can be obtained by enhanced red-light absorption. For certain applications it may be useful to enhance infrared light absorption in infrared sensitized photographic elements to achieve greater sensitivity and image quality characteristics.

[0009] One way to achieve greater light absorption is to increase the amount of spectral sensitizing dye associated with the individual grains beyond monolayer coverage of dye (some proposed approaches are described in the literature, G. R. Bird, Photogr. Sci. Eng., 18, 562 (1974)). One method is to synthesize molecules in which two dye chromophores are covalently connected by a linking group (see U.S. Pat. No. 2,518,731, U.S. Pat. No. 3,976,493, U.S. Pat. No. 3,976,640, U.S. Pat. No. 3,622,316, Kokai Sho 64(1989)91134, and EP 565,074). This approach suffers from the fact that when the two dyes are connected they can interfere with each other's performance, e.g., not aggregating on or adsorbing to the silver halide grain properly.

[0010] In a similar approach, several dye polymers were synthesized in which cyanine dyes were tethered to poly-L-lysine (U.S. Pat. No. 4,950,587). These polymers could be combined with a silver halide emulsion, however, they tended to sensitize poorly and dye stain (an unwanted increase in D-min due to retained sensitizing dye after processing) was severe in this system and unacceptable.

[0011] A different strategy involves the use of two dyes that are not connected to one another. In this approach the dyes can be added sequentially and are less likely to interfere with one another. Miysaka et al. in EP 270 079 and EP 270 082 describe silver halide photographic material having an emulsion spectrally sensitized with an adsorable sensitizing dye used in combination with a non-adsorable luminescent dye which is located in the gelatin phase of the element. Steiger et al. in U.S. Pat. No. 4,040,825 and U.S. Pat. No. 4,138,551 describe silver halide photographic material having an emulsion spectrally sensitized with an adsorable sensitizing dye used in combination with second dye which is bonded to gelatin. The problem with these approaches is that unless the dye not adsorbed to the grain is in close proximity to the dye adsorbed on the grain (less than 50 angstroms separation) efficient energy transfer will not occur (see T. Förster, Disc. Faraday Soc., 27, 7 (1959)). Most dye off-the-grain in these systems will not be close enough to the silver halide grain for energy transfer, but will instead absorb light and act as a filter dye leading to a speed loss. A good analysis of the problem with this approach is given by Steiger et al. (Photogr. Sci. Eng., 27, 59 (1983)).

[0012] A more useful method is to have two or more dyes form layers on the silver halide grain. Penner and Gilman described the occurrence of greater than monolayer levels of cyanine dye on emulsion grains, Photogr. Sci. Eng., 20, 97 (1976); see also Penner, Photogr. Sci. Eng., 21, 32 (1977). In these cases , the outer dye layer absorbed light at a longer wavelength than the inner dye layer (the layer adsorbed to the silver halide grain). Bird et al. in U.S. Pat. No. 3,622,316 describe a similar system. A requirement was that the outer dye layer absorb light at a shorter wavelength than the inner layer. The problem with prior art dye layering approaches was that the dye layers described produced a very broad sensitization envelope. This would lead to poor color reproduction since, for example, the silver halide grains in the same color record would be sensitive to both green and red light.

[0013] Yamashita et. al. (EP 838 719 A2) describes the use of two or more cyanine dyes to form dye layers on silver halide emulsions. The preferred dyes are required to have at least one aromatic or heteroaromatic substitutent attached to the chromophore via the nitrogen atoms of the dye. This is undesirable because such substitutents can lead to large amounts of retained dye after processing (dye stain) which affords increased D-min. We have found that this is not necessary and that neither dye is required to have a at least one aromatic or heteroaromatic substitute attached to the chromophore via the nitrogen atoms of the dye. The dyes of our invention give increased photographic sensitivity.

[0014] Not all the available light is being collected in many photographic systems. The need is especially great in the blue spectral region where a combination of low source intensity and relatively low dye extinction result in deficient photoresponse. The need for increased light absorption is also great in the green sensitization of the magenta layer of color negative photographic elements. The eye is most sensitive to the magenta image dye and this layer has the largest impact on color reproduction. Higher speed from increased light absorption in this layer can allow the use of smaller emulsions to obtain improved color and image quality characteristics. The cyan layer could also benefit from increased red-light absorption which could allow the use of smaller emulsions with less radiation sensitivity and improved color and image quality characteristics. For certain applications, it may be useful to enhance infrared light absorption in infrared sensitized photographic elements to achieve greater sensitivity and image quality characteristics. Further, the invention provides increased photographic sensitivity without development inhibition as observed with other silver halide emulsions.

[0015] One aspect of the invention comprises a silver halide photographic material comprising at least one silver halide emulsion comprising tabular silver halide grains having associated therewith at least two dye layers comprising

[0016] (a) an inner dye layer adjacent to the silver halide grain and comprising at least one dye that is capable of spectrally sensitizing silver halide and

[0017] (b) an outer dye layer adjacent to the inner dye layer and comprising at least one dye,

[0018] wherein the dye layers are held together by non-covalent forces or by in situ bond formation; the outer dye layer adsorbs light at equal or higher energy than the inner dye layer; and the energy emission wavelength of the outer dye layer overlaps with the energy absorption wavelength of the inner dye layer.

[0019] We have also found that silver halide tabular grains sensitized with at least one dye containing at least one anionic substituent and at least one dye containing at least one cationic substituent provides increased light absorption. Further, the invention provides increased photographic sensitivity with little if any development inhibition.

[0020] The invention increases light absorption and photographic sensitivity with little, if any, development inhibition. The increased sensitivity can also provide improved granularity by enabling the use of smaller grain size emulsions. The relatively slow speed of the small grain emulsions is compensated for by the increased light absorption of the dye layers of the invention. In addition to improved granularity, the smaller emulsions would have lower ionizing radiation sensitivity which is determined by the mass of silver halide per grain.

[0021] As mentioned above, in preferred embodiments of the invention silver halide grains have associated therewith dyes layers that are held together by non-covalent attractive forces. Examples of non-covalent attractive forces include electrostatic attraction, hydrophobic interactions, hydrogen-bonding, van der Waals interactions, dipole-dipole interactions, dipole-induced dipole interactions, London dispersion forces, cation-π interactions or any combinations of these. In addition, in situ bond formation between complementary chemical groups is valuable for this invention. For example, one layer of dye containing at least one boronic acid substituent can be formed. Addition of a second dye having at least one diol substituent results in the formation of two dye layers by the in situ formation of boron-diol bonds between the dyes of the two layers. Another example of in situ bond formation is the formation of a metal complex between dyes that are adsorbed to silver halide and dyes that can form a second or subsequent layer. For example, zirconium could be useful for binding dyes with phosphonate substitutents into dye layers. For a non-silver halide example see H. E. Katz et. al., Science, 254, 1485, (1991). Also see A. Shanzer et. al., Chem. Eur. J., 4, 502, (1998).

[0022] The photographic materials of the invention employ radiation-sensitive tabular grain silver halide emulsions. Tabular grains are silver halide grains having parallel major faces and an aspect ratio of at least 2, where aspect ratio is the ratio of grain equivalent circular diameter (ECD) divided by grain thickness (t). The equivalent circular diameter of a grain is the diameter of a circle having an average equal to the projected area of the grain. A tabular grain emulsion is one in which tabular grains account for greater than 50 percent of total grain projected area. In preferred tabular grain emulsions tabular grains account for at least 70 percent of total grain projected area and optimally at least 90 percent of total grain projected area. It is possible to prepare tabular grain emulsions in which substantially all (>97%) of the grain projected area is accounted for by tabular grains. The non-tabular grains in a tabular grain emulsion can take any convenient conventional form. When coprecipitated with the tabular grains, the non-tabular grains typically exhibit a silver halide composition as the tabular grains.

[0023] The tabular grain emulsions can be either high bromide or high chloride emulsions. High bromide emulsions are those in which silver bromide accounts for greater than 50 mole percent of total halide, based on silver. High chloride emulsions are those in which silver chloride accounts for greater than 50 mole percent of total halide, based on silver. Silver bromide and silver chloride both form a face centered cubic crystal lattice structure. This silver halide crystal lattice structure can accommodate all proportions of bromide and chloride ranging from silver bromide with no chloride present to silver chloride with no bromide present. Thus, silver bromide, silver chloride, silver bromochloride and silver chlorobromide tabular grain emulsions are all specifically contemplated. In naming grains and emulsions containing two or more halides, the halides are named in order of ascending concentrations. Usually high chloride and high bromide grains that contain bromide or chloride, respectively, contain the lower level halide in a more or less uniform distribution. However, non-uniform distributions of chloride and bromide are known, as illustrated by Maskasky U.S. Pat. Nos. 5,508,160 and 5,512,427 and Delton U.S. Pat. Nos. 5,372,927 and 5,460,934, the disclosures of which are here incorporated by reference.

[0024] It is recognized that the tabular grains can accommodate iodide up to its solubility limit in the face centered cubic crystal lattice structure of the grains. The solubility limit of iodide in a silver bromide crystal lattice structure is approximately 40 mole percent, based on silver. The solubility limit of iodide in a silver chloride crystal lattice structure is approximately 11 mole percent, based on silver. The exact limits of iodide incorporation can be somewhat higher or lower, depending upon the specific technique employed for silver halide grain preparation. In practice, useful photographic performance advantages can be realized with iodide concentrations as low as 0.1 mole percent, based on silver. It. is usually preferred to incorporate at least 0.5 (optimally at least 1.0) mole percent iodide, based on silver. Only low levels of iodide are required to realize significant emulsion speed increases. Higher levels of iodide are commonly incorporated to achieve other photographic effects, such as interimage effects. Overall iodide concentrations of up to 20 mole percent, based on silver, are well known, but it is generally preferred to limit iodide to 15 mole percent, more preferably 10 mole percent, or less, based on silver. Higher than needed iodide levels are generally avoided, since it is well recognized that iodide slows the rate of silver halide development.

[0025] Iodide can be uniformly or non-uniformly distributed within the tabular grains. Both uniform and non-uniform iodide concentrations are known to contribute to photographic speed. For maximum speed it is common practice to distribute iodide over a large portion of a tabular grain while increasing the local iodide concentration within a limited portion of the grain. It is also common practice to limit the concentration of iodide at the surface of the grains. Preferably the surface iodide concentration of the grains is less than 5 mole percent, based on silver. Surface iodide is the iodide that lies within 0.02 nm of the grain surface.

[0026] With iodide incorporation in the grains, the high chloride and high bromide tabular grain emulsions within the contemplated of the invention extend to silver iodobromide, silver iodochloride, silver iodochlorobromide and silver iodobromochloride tabular grain emulsions.

[0027] When tabular grain emulsions are spectrally sensitized, as herein contemplated, it is preferred to limit the average thickness of the tabular grains to less than 0.3 μm. Most preferably the average thickness of the tabular grains is less than 0.2 μm. In a specific preferred form the tabular grains are ultrathin—that is, their average thickness is less than 0.07 μm.

[0028] The useful average grain ECD of a tabular grain emulsion can range up to about 15 μm. Except for a very few high speed applications, the average grain ECD of a tabular grain emulsion is conventionally less than 10 μm, with the average grain ECD for most tabular grain emulsions being less than 5 μm.

[0029] The average aspect ratio of the tabular grain emulsions can vary widely, since it is quotient of ECD divided grain thickness. Most tabular grain emulsions have average aspect ratios of greater than 5, with high (>8) average aspect ratio emulsions being generally preferred. Average aspect ratios ranging up to 50 are common, with average aspect ratios ranging up to 100 and even higher, being known. The tabular grains can have parallel major faces that lie in either {100} or {111} crystal lattice planes. In other words, both {111} tabular grain emulsions and {100} tabular grain emulsions are within the specific contemplation of this invention. The {111} major faces of {111} tabular grains appear triangular or hexagonal in photomicrographs while the {100} major faces of {100} tabular grains appear square or rectangular.

[0030] High chloride {111} tabular grain emulsions are specifically contemplated, as illustrated by the following patents here incorporated by reference:

[0031] Wey et al U.S. Pat. No. 4,414,306;

[0032] Maskasky U.S. Pat. No. 4,400,463;

[0033] Maskasky U.S. Pat. No. 4,713,323;

[0034] Takada et al U.S. Pat. No. 4,783,398;

[0035] Nishikawa et al U.S. Pat. No. 4,952,508;

[0036] Ishiguro et al U.S. Pat. No. 4,983,508;

[0037] Tufano et al U.S. Pat. No. 4,804,621;

[0038] Maskasky U.S. Pat. No. 5,061,617;

[0039] Maskasky U.S. Pat. No. 5,178,997;

[0040] Maskasky and Chang U.S. Pat. No. 5,178,998;

[0041] Maskasky U.S. Pat. No. 5,183,732;

[0042] Maskasky U.S. Pat. No. 5,185,239;

[0043] Maskasky U.S. Pat. No. 5,217,858; and

[0044] Chang et al U.S. Pat. No. 5,252,452.

[0045] Since silver chloride grains are most stable in terms of crystal shape with {100} crystal faces, it is common practice to employ one or more grain growth modifiers during the formation of high chloride {111} tabular grain emulsions. Typically the grain growth modifier is displaced prior to or during subsequent spectral sensitization, as illustrated by Jones et al U.S. Pat. No. 5,176,991 and Maskasky U.S. Pat. Nos. 5,176,992, 5,221,602, 5,298,387 and 5,298,388, the disclosures of which are here incorporated by reference.

[0046] Preferred high chloride tabular grain emulsions are {100} tabular grain emulsions, as illustrated by the following patents, here incorporated by reference:

[0047] Maskasky U.S. Pat. No. 5,264,337;

[0048] Maskasky U.S. Pat. No. 5,292,632;

[0049] House et al U.S. Pat. No. 5,320,938;

[0050] Maskasky U.S. Pat. No. 5,275,930;

[0051] Brust et al U.S. Pat. No. 5,314,798;

[0052] Chang et al U.S. Pat. No. 5,413,904;

[0053] Budz et al U.S. Pat. No. 5,451,490;

[0054] Maskasky U.S. Pat. No. 5,607,828;

[0055] Chang et al U.S. Pat. No. 5,663,041;

[0056] Reed et al U.S. Pat. No. 5,695,922; and

[0057] Chang et al U.S. Pat. No. 5,744,297.

[0058] Since high chloride {100} tabular grains have {100} major faces and are, in most instances, entirely bounded by {100} grain faces, these grains exhibit a high degree of grain shape stability and do not require the presence of any grain growth modifier for the grains to remain in a tabular form following their precipitation.

[0059] High bromide {100}tabular grain emulsions are known, as illustrated by Mignot U.S. Pat. No. 4,386,156 and Gourlaouen et al U.S. Pat. No. 5,726,006, the disclosures of which are here incorporated by reference. It is, however, generally preferred to employ high bromide tabular grain emulsions in the form of {111} tabular grain emulsions, as illustrated by the following patents, here incorporated by reference:

[0060] Kofron et al U.S. Pat. No. 4,439,520;

[0061] Wilgus et al U.S. Pat. No. 4,434,226;

[0062] Solberg et al U.S. Pat. No. 4,433,048;

[0063] Maskasky U.S. Pat. No. 4,435,501;

[0064] Maskasky U.S. Pat. No. 4,463,087;

[0065] Daubendiek et al U.S. Pat. No. 4,414,310;

[0066] Daubendiek et al U.S. Pat. No. 4,672,027;

[0067] Daubendiek et al U.S. Pat. No. 4,693,964;

[0068] Maskasky U.S. Pat. No. 4,713,320;

[0069] Daubendiek et al U.S. Pat. No. 4,914,014;

[0070] Piggin et al U.S. Pat. No. 5,061,616;

[0071] Piggin et al U.S. Pat. No. 5,061,609;

[0072] Bell et al U.S. Pat. No. 5,132,203;

[0073] Antoniades et al U.S. Pat. No. 5,250,403;

[0074] Tsaur et al U.S. Pat. No. 5,147,771;

[0075] Tsaur et al U.S. Pat. No. 5,147,772;

[0076] Tsaur et al U.S. Pat. No. 5,147,773;

[0077] Tsaur et al U.S. Pat. No. 5,171,659;

[0078] Tsaur et al U.S. Pat. No. 5,252,453,

[0079] Brust U.S. Pat. No. 5,248,587;

[0080] Black et al U.S. Pat. No. 5,337,495;

[0081] Black et al U.S. Pat. No. 5,219,720;

[0082] Delton U.S. Pat. No. 5,310,644;

[0083] Chaffee et al U.S. Pat. No. 5,358,840;

[0084] Maskasky U.S. Pat. No. 5,411,851;

[0085] Maskasky U.S. Pat. No. 5,418,125;

[0086] Wen U.S. Pat. No. 5,470,698;

[0087] Mignot et al U.S. Pat. No. 5,484,697;

[0088] Olm et al U.S. Pat. No. 5,576,172;

[0089] Maskasky U.S. Pat. No. 5,492,801;

[0090] Daubendiek et al U.S. Pat. No. 5,494,789;

[0091] King et al U.S. Pat. No. 5,518,872;

[0092] Maskasky U.S. Pat. No. 5,604,085;

[0093] Reed et al U.S. Pat. No. 5,604,086;

[0094] Eshelman et al U.S. Pat. No. 5,612,175;

[0095] Eshelman et al U.S. Pat. No. 5,612,176;

[0096] Levy et al U.S. Pat. No. 5,612,177;

[0097] Eshelman et al U.S. Pat. No. 5,14,359;

[0098] Maskasky U.S. Pat. No. 5,620,840;

[0099] Irving et al U.S. Pat. No. 5,667,954;

[0100] Maskasky U.S. Pat. No. 5,667,955;

[0101] Maskasky U.S. Pat. No. 5,693,459;

[0102] Irving et al U.S. Pat. No. 5,695,923;

[0103] Reed et al U.S. Pat. No. 5,698,387;

[0104] Deaton et al U.S. Pat. No. 5,726,007;

[0105] Irving et al U.S. Pat. No. 5,728,515;

[0106] Maskasky U.S. Pat. No. 5,733,718; and

[0107] Brust U.S. Pat. No. 5,763,151.

[0108] In many of the patents listed above (starting with Kofron et al, Wilgus et al and Solberg et al, cited above) speed increases without accompanying increases in granularity are realized by the rapid (a.k.a. dump) addition of iodide for a portion of grain growth. Chang et al U.S. Pat. No. 5,314,793 correlates rapid iodide addition with crystal lattice disruptions observable by stimulated X-ray emission profiles.

[0109] Localized peripheral incorporations of higher iodide concentrations can also be created by halide conversion. By controlling the conditions of halide conversion by iodide, differences in peripheral iodide concentrations at the grain corners and elsewhere along the edges can be realized. For example, Fenton et al U.S. Pat. No. 5,476,76 discloses lower iodide concentrations at the corners of the tabular grains than elsewhere along their edges. Jagannathan et al U.S. Pat. Nos. 5,723,278 and 5,736,312 disclose halide conversion by iodide in the corner regions of tabular grains.

[0110] Crystal lattice dislocations, although seldom specifically discussed, are a common occurrence in tabular grains. For example, examinations of the earliest reported high aspect ratio tabular grain emulsions (e.g., those of Kofron et al, Wilgus et al and Solberg et al, cited above) reveal high levels of crystal lattice dislocations. Black et al U.S. Pat. No. 5,709,988 correlates the presence of peripheral crystal lattice dislocations in tabular grains with improved speed-granularity relationships. Ikeda et al U.S. Pat. No. 4,806,461 advocates employing tabular grain emulsions in which at least 50 percent of the tabular grains contain or more dislocations. For improving speed-granularity characteristics, it is preferred that at least 70 percent and optimally at least 90 percent of the tabular grains contain 10 or more peripheral crystal lattice dislocations.

[0111] In a preferred embodiment of the invention the silver halide emulsion comprises tabular silver halide grains that:

[0112] (a) have {111} major faces and

[0113] (b) comprise greater than 50 percent of total grain projected area and

[0114] (c) have latent image-forming chemical sensitization sites on the surfaces thereof;

[0115] wherein the surface chemical sensitization sites include at least one silver salt forming epitaxial junctions with the tabular grains and being restricted to those portions of the tabular grains located nearest peripheral edges of and accounting for less than 50 percent of the {111} major faces of the tabular grains.

[0116] In another embodiment of the invention the silver halide tabular grains of the photographic material have a maximum surface iodide concentration along the edges and a lower surface iodide concentration within the corners than elsewhere along the edges.

[0117] In yet another embodiment of the invention, the silver halide emulsion comprises tabular grains having:

[0118] (a) {11} major faces and

[0119] (b) a central region extending between the {111} major faces and at least one laterally displaced region also extending between the {111} major faces having an abruptly higher iodide concentration than the central region.

[0120] In one preferred embodiment of the invention the silver halide emulsion is dyed with a saturation or near saturation monolayer of one or more cyanine dyes which have either a positive or negative net charge or the net charge can be zero if one of the substitutents has a negative charge. The area a dye covers on the silver halide surface can be determined by preparing a dye concentration series and choosing the dye level for optimum performance or by well-known techniques such as dye adsorption isotherms (for example see W. West, B. H. Carroll, and D. H. Whitcomb, J. Phys. Chem, 56, 1054 (1962)). The second layer consists of dyes which have a net charge of opposite sign compared to the dyes of the first layer.

[0121] In another preferred embodiment, the dye or dyes of the outer dye layer and the dye or dyes of the inner dye layer have their maximum light absorption either between 400 to 500 nm or between 500 to 600 nm or between 600 and 700 nm.

[0122] In another preferred embodiment the silver halide emulsion is dyed with a saturation monolayer of negatively charged cyanine dye. The second layer consists of dyes with positive charges. In another preferred embodiment the second layer consists of cyanine dyes with at least one substituent that has a positive charge. In another preferred embodiment the second layer consists of a combination of dyes with at with at least one cationic substituent and dyes with at least one anionic substituent. Speed increases of greater than 0.15 log E (40% increase) for daylight type exposures were observed.

[0123] To determine the increased light absorption by the photographic element as a result of forming an outer dye layer in addition to the inner dye layer, it is necessary to compare the overall absorption of the emulsion subsequent to the addition of the dye or dyes of the inner dye layer with the overall absorption of the emulsion subsequent to the further addition of the dye or dyes of the outer dye layer. This measurement of absorption can be done in a variety of ways known in the art, but a particularly convenient and directly applicable method is to measure the absorption spectrum as a function of wavelength of a coating prepared on a planar support from the liquid emulsion in the same manner as is conventionally done for photographic exposure evaluation. The methods of measurement of the total absorption spectrum, in which the absorbed fraction of light incident in a defined manner on a sample as a function of the wavelength of the impinging light for a turbid material such as a photographic emulsion coated onto a planar support, has been described in detail (for example see F. Grum and R. J. Becherer, “Optical Radiation Measurements, Vol. 1, Radiometry”, Academic Press, New York, 1979). The absorbed fraction of incident light can be designated by A(λ), where A is the fraction of incident light absorbed and λ is the corresponding wavelength of light. Although A(λ) is itself a useful parameter allowing graphical demonstration of the increase in light absorption resulting from the formation of additional dye layers described in this invention, it is desirable to replace such a graphical comparison with a numerical one. Further, the effectiveness with which the light absorption capability of an emulsion coated on a planar support is converted to photographic image depends, in addition to A(λ), on the wavelength distribution of the irradiance I(λ) of the exposing light source. (Irradiance at different wavelengths of light sources can be obtained by well-known measurement techniques. See, for example, F. Grum and R. J. Becherer, “Optical Radiation Measurements, Vol. 1, Radiometry”, Academic Press, New York, 1979.) A further refinement follows from the fact that photographic image formation is, like other photochemical processes, a quantum effect so that the irradiance, which is usually measured in units of energy per unit time per unit area, needs to be converted into quanta of light N(λ) via the formula N(λ)=I(λ)λ/hc where h is Planck's constant and c is the speed of light. Then the number of absorbed photons per unit time per unit area at a given wavelength for a photographic coating is given by: N_a(λ)=A(λ)N(λ). In most instances, including the experiments described in the Examples of this invention, photographic exposures are not performed at a single or narrow range of wavelengths but rather simultaneously over a broad spectrum of wavelengths designed to simulate a particular illuminant found in real photographic situations, for example daylight. Therefore the total number of photons of light absorbed per unit time per unit area from such an illuminant consists of a summation or integration of all the values of he individual wavelengths, that is: N_a=∫A(λ)N(λ)dλ, where the limits of integration correspond to the wavelength limits of the specified illuminant. In the Examples of this invention, comparison is made on a relative basis between the values of the total number of photons of light absorbed per unit time per unit area of the coating of emulsion containing the sensitizing inner dye layer alone set to a value of 100 and the total number of photons of light absorbed per unit time of the coatings containing a sensitizing outer dye layer in addition to inner dye layer. These relative values of N_aare designated as Normalized Relative Absorption and are tabulated in the Examples. Enhancement of the Normalized Relative Absorption is a quantitative measure of the advantageous light absorption effect of this invention.

[0124] As stated in the Background of the Invention, some previous attempts to increase light absorption of emulsions resulted in the presence of dye that was too remote from the emulsion grains to effect energy transfer to the dye adsorbed to the grains, so that a significant increase in photographic sensitivity was not realized. Thus an enhancement in Relative Absorption by an emulsion is alone not a sufficient measurement of the effectiveness of additional dye layers. For this purpose a metric must be defined that relates the enhanced absorption to the resulting increase in photographic sensitivity. Such a parameter is now described.

[0125] Photographic sensitivity can be measured in various ways. One method commonly practiced in the art and described in numerous references (for example in The Theory of the Photographic Process, 4^thedition, T. H. James, editor, Macmillan Publishing Co., New York, 1977) is to expose an emulsion coated onto a planar substrate for a specified length of time through a filtering element, or tablet interposed between the coated emulsion and light source which modulates the light intensity in a series of uniform steps of constant factors by means of the constructed increasing opacity of the filter elements of the tablet. As a result the exposure of the emulsion coating is spatially reduced by this factor in discontinuous steps in one direction, remaining constant in the orthogonal direction. After exposure for a time required to cause the formation of developable image through a portion but not all the exposure steps, the emulsion coating is processed in an appropriate developer, either black and white or color, and the densities of the image steps are measured with a densitometer. A graph of exposure on a relative or absolute scale, usually in logarithmic form, defined as the irradiance multiplied by the exposure time, plotted against the measured image density can then be constructed. Depending on the purpose, a suitable image density is chosen as reference (for example 0.15 density above that formed in a step which received too low an exposure to form detectable exposure-related image). The exposure required to achieve that reference density can then be determined from the constructed graph, or its electronic counterpart. The inverse of the exposure to reach the reference density is designated as the emulsion coating sensitivity S. The value of Log₁₀S is termed the speed. The exposure can be either monochromatic over a small wavelength range or consist of many wavelengths over a broad spectrum as already described. The film sensitivity of emulsion coatings containing only the inner dye layer or, alternatively, inner dye layer plus outer dye layer can be measured as described using a specified light source, for example a simulation of daylight. The photographic sensitivity of a particular example of an emulsion coating containing the inner dye layer plus an outer dye layer can be compared on a relative basis with a corresponding reference of an emulsion coating containing only the inner dye layer by setting S for the latter equal to 100 and multiplying this times the ratio of S for the invention example coating containing the inner dye layer plus an outer dye layer to S for the comparison example containing only inner dye layer. These values are designated as Normalized Relative Sensitivity. They are tabulated in the Examples along with the corresponding speed values. Enhancement of the Normalized Relative Sensitivity is a quantitative measure of the advantageous photographic sensitivity effect of this invention.

[0126] As a result of these measurements of emulsion coating absorption and photographic sensitivity, one obtains two sets of parameters for each example, N_aand S, each relative to 100 for the comparison example containing only the inner dye layer. The exposure source used to calculate N_ashould be the same as that used to obtain S. The increase in these parameters N_aand S over the value of 100 then represent respectively the increase in absorbed photons and in photographic sensitivity resulting from the addition of an outer dye layer of this invention. These increases are labeled respectively ΔN_aand ΔS. It is the ratio of ΔS/ΔN_athat measures the effectiveness of the outer dye layer to increase photographic sensitivity. This ratio, multiplied by 100 to convert to a percentage, is designated the Layering Efficiency, designated E, and is tabulated in the Examples, set forth below along with S and N_a. The Layering Efficiency measures the effectiveness of the increased absorption of this invention to increase photographic sensitivity. When either ΔS or ΔNa is zero, then the Layering Efficiency is effectively zero.

[0127] In preferred embodiments, the following relationship is met:

[0128] E=100ΔS/ΔN_a≧10 and ΔN_a≧10

[0129] wherein

[0130] E is the layering efficiency;

[0131] ΔS is the difference between the Normalized Relative Sensitivity (S) of an emulsion sensitized with the inner dye layer and the Normalized Relative Absorption of an emulsion sensitized with both the inner dye layer and the outer dye layer; and

[0132] ΔN_ais the difference between the Normalized Relative Absorption (N_a) of an emulsion sensitized with the inner dye layer and the Normalized Relative Absorption of an emulsion sensitized with both the inner dye layer and the outer dye layer.

[0133] In another preferred embodiment, the dye or dyes of the outer layer forms a well-ordered liquid-crystalline phase (a lyotropic mesophase) in a solvent, typically an aqueous medium (for example, water, aqueous gelatin, methanolic aqueous gelatin, etc.), and preferably forms a smectic liquid-crystalline phase (W. J. Harrison, D. L. Mateer & G. J. T. Tiddy, J.Phys.Chem. 1996, 100, pp 2310-2321). More specifically, in one embodiment preferred outer layer dyes will form liquid-crystalline J-aggregates in aqueous-based media (in the absence of silver halide grains) at any equivalent molar concentration equal to, or up to 4 orders of magnitude greater than, but more preferably at any equivalent molar concentration equal to or less than, the optimum level of the inner layer dye deployed for conventional sensitization (see The Theory of the Photographic Process, 4^thedition, T. H. James, editor, Macmillan Publishing Co., New York, 1977, for a discussion of aggregation).

[0134] Mesophase-forming dyes may be readily identified by someone skilled in the art using polarized-light optical microscopy as described by N. H. Hartshorne in The Microscopy of Liquid Crystals, Microscope Publications Ltd., London, 1974. In one embodiment, preferred outer layer dyes when dispersed in the aqueous medium of choice (including water, aqueous gelatin, aqueous methanol etc. with or without dissolved electrolytes, buffers, surfactants and other common sensitization addenda) at optimum concentration and temperature and viewed in polarized light as thin films sandwiched between a glass microscope slide and cover slip display the birefringent textures, patterns and flow rheology characteristic of distinct and readily identifiable structural types of mesophase (e.g. smectic, nematic, hexagonal). Furthermore, in one embodiment, the preferred dyes when dispersed in the aqueous medium as a liquid-crystalline phase generally exhibit J-aggregation resulting in a unique bathochromically shifted spectral absorption band yielding high fluorescence intensity. In another embodiment useful hypsochromically shifted spectral absorption bands may also result from the stabilization of a liquid-crystalline phase of certain other preferred dyes. In certain other embodiments of dye layering, especially in the case of dye layering via in situ bond formation, it may be desirable to use outer layer dyes that do not aggregate. In particularly preferred embodiments of the invention, the dye or dyes of the outer dye layer form a liquid-crystalline phase in aqueous gelatin at a concentration of 1 weight percent or less.

[0135] In one preferred embodiment, a molecule containing a group that strongly bonds to silver halide, such as a mercapto group (or a molecule that forms a mercapto group under alkaline or acidic conditions) or a thiocarbonyl group is added after the first dye layer has been formed and before the second dye layer is formed. Mercapto compounds represented by the following formula (A) are particularly preferred.

[0136] wherein R₆represents an alkyl group, an alkenyl group or an aryl group and Z₄represents a hydrogen atom, an alkali metal atom, an ammonium group or a protecting group that can be removed under alkaline or acidic conditions.

[0137] Examples of some preferred mercapto compounds are shown below.

[0138] In describing preferred embodiments of the invention, one dye layer is described as an inner layer and one dye layer is described as an outer layer. It is to be understood that one or more intermediate dye layers may be present between the inner and outer dye layers, in which all of the layers are held together by non-covalent forces, as discussed in more detail above. Further, the dye layers need not completely encompass the silver halide grains or underlying dye layer(s). Also some mixing of the dyes between layers is possible.

[0139] The dyes of the inner dye layer are preferably any dyes capable of spectral sensitization, for example, a cyanine dye, merocyanine dye, complex cyanine dye, complex merocyanine dye, homopolar cyanine dye, or hemicyanine dye, etc. Of these dyes, merocyanine dyes containing a thiocarbonyl group and cyanine dyes are particularly useful. Of these cyanine dyes are especially useful. Particularly preferred is a cyanine dye of Formula Ia or a merocyanine dye of Formula Ib.

[0140] wherein:

[0141] E₁and E₂may be the same or different and represent the atoms necessary to form a substituted or unsubstituted heterocyclic ring which is a basic nucleus (see The Theory of the Photographic Process, 4^thedition, T. H. James, editor, Macmillan Publishing Co., New York, 1977 for a definition of basic and acidic nucleus),

[0142] each J independently represents a substituted or unsubstituted methine group,

[0143] q is a positive integer of from 1 to 4,

[0144] p and r each independently represents 0 or 1,

[0145] D₁and D₂each independently represents substituted or unsubstituted alkyl or substituted or unsubstituted aryl and at least one of D₁and D₂contains an anionic substituent; and

[0146] W₂is one or more a counterions as necessary to balance the charge;

[0147] wherein E₁, D₁, J, p, q and W₂are as defined above for formula (Ia) wherein E₄represents the atoms necessary to complete a substituted or unsubstituted heterocyclic acidic nucleus which preferably contains a thiocarbonyl group.

[0148] The dyes of the outer dye layer are not necessarily spectral sensitizers. Examples of preferred outer layer dyes are a cyanine dye, merocyanine dye, arylidene dye, complex cyanine dye, complex merocyanine dye, homopolar cyanine dye, hemicyanine dye, styryl dye, hemioxonol dye, oxonol dye, anthraquinone dye, triphenylmethane dye, azo dye type, azomethines, coumarin dye or combinations of dyes from these classes. Particularly preferred are dyes having structure IIa, IIb, and IIc,

[0149] wherein:

[0150] E₁, E₂, J, p, q and W₂are as defined above for Formula (Ia),

[0151] D₃and D₄each independently represents substituted or unsubstituted alkyl or unsubstituted aryl and at least one of E₁, E₂, J or D₃and D₄contains a cationic substituent;

[0152] wherein E₁, D₃, J, p, q and W₂are as defined above for Formula (D) and G represents

[0153] wherein E₄represents the atoms necessary to complete a substituted or unsubstituted heterocyclic acidic nucleus which preferably does not contain a thiocarbonyl, and F and F′ each independently represents a cyano radical, an ester radical, an acyl radical, a carbamoyl radical or an alkylsulfonyl radical, and at least one of E₁, G, J or D₃contains a cationic substituent,

[0154] wherein J and W₂are as defined above for Formula (I) above and q is 2, 3 or 4, and E₅and E₆independently represent the atoms necessary to complete a substituted or unsubstituted acidic heterocyclic nucleus and at least one of J, E₅, or E₆contains a cationic substituent.

[0155] In embodiments of the invention in which the inner dye is of formula (Ia) and the outer dye is of formula (IIa), if either D₁or D₂contains an aromatic or heteroaromatic group then D₃and D₄do not contain an aromatic or heteroaromatic group.

[0156] Particularly preferred is a photographic material in which the inner dye layer comprises a cyanine dye of formula (Ic) and the outer dye layer comprises a dye of formula (IId):

[0157] wherein:

[0158] G₁and G₁′ independently represent the atoms necessary to complete a benzothiazole nucleus, benzoxazole nucleus, benz oselenazole nucleus, benzotellurazole nucleus, quinoline nucleus, or benzimidazole nucleus in which G₁and G₁′ independently may be substituted or unsubstituted;

[0159] G₂and G₂′ independently represent the atoms necessary to complete a benzothiazole nucleus, benzoxazole nucleus, benzoselenazole nucleus, benzotellurazole nucleus, quinoline nucleus, indole nucleus, or benzimidazole nucleus in which G2, and G₂′ independently may be substituted or unsubstituted;

[0160] n and n′ are independently a positive integer from 1 to 4,

[0161] each L and L′ independently represent a substituted or unsubstituted methine group,

[0162] R₁and R₁′ each independently represents substituted or unsubstituted aryl or substituted or unsubstituted aliphatic group, at least one of R₁and R₁′ has a negative charge,

[0163] W₁is a cationic counterion to balance the charge if necessary,

[0164] R₂and R₂′ each independently represents substituted or unsubstituted aryl or substituted or unsubstituted aliphatic group and preferably at least one of R₂and R₂′ has a positive charge; such that the net charge of IId is +1, +2, +3, +4, or +5,

[0165] W₂is one or more anionic counterions to balance the charge.

[0166] In a preferred embodiment the silver halide emulsion is dyed with a saturation or near saturation monolayer of one or more dyes wherein at least one dye is a cyanine dye with an anionic substituent. The second layer consists of one or more dyes wherein at least one dye has a substituent that contains a positive charge. In another preferred embodiment the second layer comprises at least one cyanine dye with at least one substituent that contains a positive charge. In one preferred embodiment the substituent that contains positive charges is connected to the cyanine dye via the nitrogen atoms of the cyanine dye chromophore. However, preferably the anionic and cationic dyes of the invention do not both have an aromatic or heteroaromatic group attached to the dye by means of the nitrogen atoms of the cyanine chromophore.

[0167] Examples of positively charged substituents are 3-(trimethylammonio)propyl), 3-(4-ammoniobutyl), 3-(4-guanidinobutyl) etc. Other examples are any substitutents that take on a positive charge in the silver halide emulsion melt, for example, by protonation such as aminoalkyl substitutents, e.g. 3-(3-aminopropyl), 3-(3-dimethylaminopropyl), 4-(4-methylaminopropyl), etc. Examples of negatively charged substituents are 3-sulfopropyl, 2-carboxyethyl, 4-sulfobutyl, etc.

[0168] When reference in this application is made to a particular moiety as a “group”, this means that the moiety may itself be unsubstituted or substituted with one or more substituents (up to the maximum possible number). For example, “alkyl group” refers to a substituted or unsubstituted alkyl, while “benzene group” refers to a substituted or unsubstituted benzene (with up to six substituents). Generally, unless otherwise specifically stated, substituent groups usable on molecules herein include any groups, whether substituted or unsubstituted, which do not destroy properties necessary for the photographic utility. Examples of substituents on any of the mentioned groups can include known substituents, such as: halogen, for example, chloro, fluoro, bromo, iodo; alkoxy, particularly those “lower alkyl” (that is, with 1 to 6 carbon atoms, for example, methoxy, ethoxy; substituted or unsubstituted alkyl, particularly lower alkyl (for example, methyl, trifluoromethyl); thioalkyl (for example, methylthio or ethylthio), particularly either of those with 1 to 6 carbon atoms; substituted and unsubstituted aryl, particularly those having from 6 to 20 carbon atoms (for example, phenyl); and substituted or unsubstituted heteroaryl, particularly those having a 5 or 6-membered ring containing 1 to 3 heteroatoms selected from N, 0, or S (for example, pyridyl, thienyl, furyl, pyrrolyl); acid or acid salt groups such as any of those described below; and others known in the art. Alkyl substituents may specifically include “lower alkyl” (that is, having 1-6 carbon atoms), for example, methyl, ethyl, and the like. Further, with regard to any alkyl group or alkylene group, it will be understood that these can be branched or unbranched and include ring structures.

[0169] Particularly preferred dyes for use in accordance with this invention are give in Table I.

[0170]

[0171] Other non-cyanine dyes that can be used for the outer dye layer in accordance with this invention include, for example:

[0172] an oxonol dye of Formula IV:

[0173] wherein A¹and A²are ketomethylene or activated methylene moieties, L¹-L⁷are substituted or unsubstituted methine groups, (including the possibility of any of them being members of a five or six-membered ring where at least one and preferably more than one of p, q, or r is 1); M⁺ is a cation, and p, q and r are independently 0 or 1;

[0174] an oxonol dye of Formulae IV-A or IV-B:

[0175] Wherein W¹and Y₁are the atoms required to form a cyclic activated methylene/ketomethylene moiety; R³and R⁵are aromatic or heteroaromatic groups; R⁴and R₆are electron-withdrawing groups; G¹to G₄is O or dicyanovinyl (—C(CN)₂)) and p, q, and r are defined as above, and L¹to L⁷are defined as above;

[0176] An oxonol dye of Formula V

[0177] wherein X is oxygen or sulfur; R⁷-R¹⁰each independently represent an unsubstituted or substituted alkyl group, an unsubstituted or substituted aryl group or an unsubstituted or substituted heteroaryl group; L¹, L²and L³each independently represent substituted or unsubstituted methine groups; M+ represents a proton or an inorganic or organic cation; and n is 0, 1, 2 or 3;

[0178] a merocyanine of Formula VI:

[0179] wherein A³is a ketomethylene or activated methylene moiety as described above; each L⁸to L¹⁵are substituted or unsubstituted methine groups (including the possibility of any of them being members of a five or six-membered ring where at least one and preferably more than 1 of s, t, v or w is 1); Z¹represents the non-metallic atoms necessary to complete a substituted or unsubstituted ring system containing at least one 5 or 6-membered heterocyclic nucleus; R¹⁷represents a substituted or unsubstituted alkyl, aryl, or aralkyl group;

[0180] a merocyanine dye of Formula VII-A:

[0181] wherein A⁴is an activated methylene moeity or a ketomethylene moeity as described above, R¹⁸is substituted or unsubstituted aryl, alkyl or aralkyl, R¹⁹to R₂₂each individually represent hydrogen, alkyl, cycloalkyl, alkeneyl, substituted or unsubstituted aryl, heteroaryl or aralkyl, alkylthio, hydroxy, hydroxylate, alkoxy, amino, alkylamino, halogen, cyano, nitro, carboxy, acyl, alkoxycarbonyl, aminocarbonyl, sulfonamido, sulfamoyl, including the atoms required to form fused aromatic or heteroaromatic rings, or groups containing solubilizing substituents as described above for Y. L⁸through L¹³are methine groups as described above for L¹through L⁷, Y²is O, S, Te, Se, NR_x, or CR_yR_z(where Rx, Ry and Rz are alkyl groups with 1-5 carbons), and s and t and v are independently 0 or 1;

[0182] a merocyanine dye of Formula VIII-A:

[0183] wherein R²³is a substituted or unsubstituted aryl, heteroaryl, or a substituted or unsubstituted amino group; G⁵is O or dicyanovinyl (C(CN)₂),E¹is an electron-withdrawing group, R¹⁸to R²², L⁸to L¹³, Y², and s, t and v are as described above;

[0184] a dye of Formula VIII-B:

[0185] wherein G⁶is oxygen (O) or dicyanovinyl (C(CN)₂),R⁹to R¹²groups each individually represent groups as described above, and R¹⁸, R¹⁹through R₂₂, Y², L⁸through L¹³, and s, t and v are as described above,

[0186] a dye of Formula VIII-C:

[0187] wherein R²⁵groups each individually represent the groups described for R¹⁹through R₂₂above, Y³represents O , S, NR_x, or CR_yR_z(where Rx, Ry and Rz are alkyl groups with 1-5 carbons), x is 0, 1, 2, 3 or 4, R₂₄represents aryl, alkyl or acyl, and Y², R¹⁸, R¹⁹through R₂₂, L⁸through L¹³, and, s, t and v are as described above;

[0188] a dye of Formula VIII-D:

[0189] wherein E²represents an electron-withdrawing group, preferably cyano, R²⁶represents aryl, alkyl or acyl, and Y², R¹⁸, R¹⁹through R²², L⁸through L¹³, and, s, t and v are as described above;

[0190] a dye of Formula VIII-E:

[0191] wherein R²⁷is a hydrogen, substituted or unsubstituted alkyl, aryl or aralkyl, R²⁸is substituted or unsubstituted alkyl, aryl or aralkyl, alkoxy, amino, acyl, alkoxycarbonyl, carboxy, carboxylate, cyano, or nitro; R¹⁸to R²², L⁸to L¹³, Y², and s, t and v are as described above;

[0192] a dye of Formula VIII-F:

[0193] wherein R₂₉and R₃₀are each independently a hydrogen, substituted or unsubstituted alkyl, aryl or aralkyl, Y⁴is O or S, R¹⁸to R₂₂, L⁸to L¹³, Y², and s, t and v are as described above;

[0194] a dye of Formula IX:

[0195] wherein A⁵is a ketomethylene or activated methylene, L¹⁶through L¹⁸are substituted or unsubstituted methine, R³¹is alkyl, aryl or aralkyl, Q³represents the non-metallic atoms necessary to complete a substituted or unsubstituted ring system containing at least one 5- or 6-membered heterocyclic nucleus, R³²represents groups as described above for R¹⁹to R²², y is 0, 1, 2, 3 or 4, z is 0, 1 or 2;

[0196] a dye of Formula X:

[0197] wherein A⁶is a ketomethylene or activated methylene, L¹⁶through L¹⁸are methine groups as described above for L1 through L⁷, R³³is substituted or unsubstituted alkyl, aryl or aralkyl, R³⁴is substituted or unsubstituted aryl, alkyl or aralkyl, R³⁵groups each independently represent groups as described for R¹⁹through R²², z is 0, 1 or 2, and a is 0, 1, 2, 3 or 4;

[0198] a dye of Formula XI:

[0199] wherein A⁷represents a ketomethylene or activated methylene moiety, L¹⁹through L²¹represent methine groups as described above for L¹through L7, R₃₆groups each individually represent the groups as described above for R¹⁹through R²², b represents 0 or 1, and c represents 0, 1, 2, 3 or 4;

[0200] a dye of Formula XII:

[0201] wherein A⁸is a ketomethylene or activated methylene, L¹⁹through L²¹and b are as described above, R³⁹groups each individually represent the groups as described above for R¹⁹through R²², and R³⁷and R³⁸each individually represent the groups as described for R¹⁸above, and d represents 0, 1, 2, 3 or 4;

[0202] a dye of Formula XIII:

[0203] wherein A⁹is a ketomethylene or activated methylene moiety, L²²through L²⁴are methine groups as described above for L¹through L⁷, e is 0 or 1, R⁴⁰groups each individually represent the groups described above for R¹⁹through R²², and f is 0, 1, 2, 3 or 4;

[0204] a dye of Formula XIV:

[0205] wherein A¹⁰is a ketomethylene or activated methylene moiety, L²⁵through L²⁷are methine groups as described above for L¹through L⁷, g is 0, 1 or 2, and R³⁷and R³⁸each individually represent the groups described above for R¹⁸;

[0206] a dye of Formula XV:

[0207] wherein A¹¹is a ketomethylene or activated methylene moiety, R⁴¹groups each individually represent the groups described above for R¹⁹through R²², R³⁷and R³⁸each represent the groups described for R18, and h is 0, 1, 2, 3, or 4;

[0208] a dye of Formula XVI:

[0209] wherein Q⁴and Q⁵each represents the atoms necessary to form at least one heterocyclic or carbocyclic, fused or unfused 5 or 6-membered-ring conjugated with the azo linkage.

[0210] Dyes of Formula IV-XVI above are preferably substituted with either a cationic or an anionic group.

[0211] In a preferred embodiment of the invention, one of the dye layers comprises a dye of formula A and the other dye layer comprises a dye of formula B:

[0212] wherein

[0213] X, Y, represent independently O, S, NR₃, Se,—CH═CH—;

[0214] X′, Y′, represent independently O, S, NR₄, Se, —CH═CH—, or C(R₅)R₆;

[0215] R₃, R₄, R₅, R₆independently represent substituted or unsubstituted alkyl or substituted or unsubstituted aryl;

[0216] R₁and R₂are substituted or unsubstituted alkyl or substituted or unsubstituted aryl and at least one of R₁or R₂has an anionic substituent;

[0217] R₁′ and R₂′ are substituted or unsubstituted alkyl or substituted or unsubstituted aryl and at least one of R₁′ and R₂′ has a cationic substituent;

[0218] Z₁, Z₂, Z₁′, Z₂′ each independently represents hydrogen or one or more substituents which, optionally, may form fused aromatic rings;

[0219] W represents one or more cationic counterions if necessary; and

[0220] W′ represents one or more anionic counterions.

[0221] Dyes useful in the practice of this invention can be prepared according to techniques that are well-known in the art, such as described in F. M. Hamer, Cyanine Dyes and Related Compounds, 1964 (publisher John Wiley & Sons, New York, N.Y.) and The Theory of the Photographic Process, 4^thedition, T. H. James, editor, Macmillan Publishing Co., New York, 1977. The amount of sensitizing dye that is useful in the invention may be from 0.001 to 4 millimoles, but is preferably in the range of 0.01 to 4.0 millimoles per mole of silver halide and more preferably from 0.10 to 4.0 millimoles per mole of silver halide. Optimum dye concentrations can be determined by methods known in the art.

[0222] The dyes may be added to an emulsion of the silver halide grains and a hydrophilic colloid at any time prior to, during, or after chemical sensitization. Preferably the dye or dyes of the inner layer are added at a level such that, along with any other adsorbants (e.g., antifoggants), they will substantially cover at least 80% and more preferably 90% of the surface of the silver halide grain. The area a dye covers on the silver halide surface can be determined by preparing a dye concentration series and choosing the dye level for optimum performance or by well-known techniques such as dye adsorption isotherms (for example see W. West, B. H. Carroll, and D. H. Whitcomb, J. Phys. Chem, 56, 1054 (1962)).

[0223] In many cases it is preferable to add at least one dye, preferably an anionic dye, before the chemical sensitization. The dye forming the second layer, preferably the cationic dye, is added preferably either during or after the chemical sensitization. The level of the dye forming the second layer is such that it is preferably between 20%-300% of monolayer coverage and more preferably between 50%-150% of monolayer coverage. In some cases it is then desirable to have addition of at least a third dye (preferably an anionic dye). In some cases this can stabilize the dye layers. The third dye can be added before, during or after the chemical sensitization. Preferably it is added after the chemical sensitization and after the second dye addition. The third dye is preferably between 20%-300% of monolayer coverage and more preferably between 50%-150% of monolayer coverage.

[0224] The emulsion layer of the photographic element of the invention can comprise any one or more of the light sensitive layers of the photographic element. The photographic elements made in accordance with the present invention can be black and white elements, single color elements or multicolor elements. Multicolor elements contain dye image-forming units sensitive to each of the three primary regions of the spectrum. Each unit can be comprised of a single emulsion layer or of multiple emulsion layers sensitive to a given region of the spectrum. The layers of the element, including the layers of the image-forming units, can be arranged in various orders as known in the art. In an alternative format, the emulsions sensitive to each of the three primary regions of the spectrum can be disposed as a single segmented layer.

[0225] Photographic elements of the present invention may also usefully include a magnetic recording material as described in Research Disclosure, Item 34390, November 1992, or a transparent magnetic recording layer such as a layer containing magnetic particles on the underside of a transparent support as in U.S. Pat. No. 4,279,945 and U.S. Pat. No. 4,302,523. The element typically will have a total thickness (excluding the support) of from 5 to 30 microns. While the order of the color sensitive layers can be varied, they will normally be red-sensitive, green-sensitive and blue-sensitive, in that order on a transparent support, (that is, blue sensitive furthest from the support) and the reverse order on a reflective support being typical.

[0226] The present invention also contemplates the use of photographic elements of the present invention in what are often referred to as single use cameras (or “film with lens” units). These cameras are sold with film preloaded in them and the entire camera is returned to a processor with the exposed film remaining inside the camera. Such cameras may have glass or plastic lenses through which the photographic element is exposed.

[0227] In the following discussion of suitable materials for use in elements of this invention, reference will be made to Research Disclosure, September 1996, Number 389, Item 38957, which will be identified hereafter by the term “Research Disclosure I.” The Sections hereafter referred to are Sections of the Research Disclosure I unless otherwise indicated. All Research Disclosures referenced are published by Kenneth Mason Publications, Ltd., Dudley Annex, 12a North Street, Emsworth, Hampshire P010 7DQ, ENGLAND. The foregoing references and all other references cited in this application, are incorporated herein by reference.

[0228] The silver halide emulsions employed in the photographic elements of the present invention may be negative-working, such as surface-sensitive emulsions or unfogged internal latent image forming emulsions, or positive working emulsions of the internal latent image forming type (that are fogged during processing). Suitable emulsions and their preparation as well as methods of chemical and spectral sensitization are described in Sections I through V. Color materials and development modifiers are described in Sections V through XX. Vehicles which can be used in the photographic elements are described in Section II, and various additives such as brighteners, antifoggants, stabilizers, light absorbing and scattering materials, hardeners, coating aids, plasticizers, lubricants and matting agents are described, for example, in Sections VI through Xff. Manufacturing methods are described in all of the sections, layer arrangements particularly in Section XI, exposure alternatives in Section XVI, and processing methods and agents in Sections XLX and XX.

[0229] With negative working silver halide a negative image can be formed. Optionally a positive (or reversal) image can be formed although a negative image is typically first formed.

[0230] The photographic elements of the present invention may also use colored couplers (e.g. to adjust levels of interlayer correction) and masking couplers such as those described in EP 213 490; Japanese Published Application 58-172,647; U.S. Pat. No. 2,983,608; German Application DE 2,706,117C; U.K. Pat. No. 1,530,272; Japanese Application A-1 13935; U.S. Pat. No. 4,070,191 and German Application DE 2,643,965. The masking couplers may be shifted or blocked.

[0231] The photographic elements may also contain materials that accelerate or otherwise modify the processing steps of bleaching or fixing to improve the quality of the image. Bleach accelerators described in EP 193 389; EP 301 477; U.S. Pat. No. 4,163,669; U.S. Pat. No. 4,865,956; and U.S. Pat. No. 4,923,784 are particularly useful. Also contemplated is the use of nucleating agents, development accelerators or their precursors (UK Patent 2,097,140; U.K. Patent 2,131,188); development inhibitors and their precursors (U.S. Pat. No. 5,460,932; U.S. Pat. No. 5,478,711); electron transfer agents (U.S. Pat. No. 4,859,578; U.S. Pat. No. 4,912,025); antifogging and anti color-mixing agents such as derivatives of hydroquinones, aminophenols, amines, gallic acid; catechol; ascorbic acid; hydrazides; sulfonamido phenols; and non color-forming couplers.

[0232] The elements may also contain filter dye layers comprising colloidal silver sol or yellow and/or magenta filter dyes and/or antihalation dyes (particularly in an undercoat beneath all light sensitive layers or in the side of the support opposite that on which all light sensitive layers are located) either as oil-in-water dispersions, latex dispersions or as solid particle dispersions. Additionally, they may be used with “smearing” couplers (e.g. as described in U.S. Pat. No. 4,366,237; EP 096 570; U.S. Pat. No. 4,420,556; and U.S. Pat. No. 4,543,323.) Also, the couplers may be blocked or coated in protected form as described, for example, in Japanese Application 61/258,249 or U.S. Pat. No. 5,019,492.

[0233] The photographic elements may further contain other image-modifying compounds such as “Development Inhibitor-Releasing” compounds (DIR's). Useful additional DIR's for elements of the present invention, are known in the art and examples are described in U.S. Pat. Nos. 3,137,578; 3,148,022; 3,148,062; 3,227,554; 3,384,657; 3,379,529; 3,615,506; 3,617,291; 3,620,746; 3,701,783; 3,733,201; 4,049,455; 4,095,984; 4,126,459; 4,149,886; 4,150,228; 4,211,562; 4,248,962; 4,259,437; 4,362,878; 4,409,323; 4,477,563; 4,782,012; 4,962,018; 4,500,634; 4,579,816; 4,607,004; 4,618,571; 4,678,739; 4,746,600; 4,746,601; 4,791,049; 4,857,447; 4,865,959; 4,880,342; 4,886,736; 4,937,179; 4,946,767; 4,948,716; 4,952,485; 4,956,269; 4,959,299; 4,966,835; 4,985,336 as well as in patent publications GB 1,560,240; GB 2,007,662; GB 2,032,914; GB 2,099,167; DE 2,842,063, DE 2,937,127; DE 3,636,824; DE 3,644,416 as well as the following European Patent Publications: 272,573; 335,319; 336,411; 346,899; 362,870; 365,252; 365,346; 373,382; 376,212; 377,463; 378,236; 384,670; 396,486; 401,612; 401,613.

[0234] DIR compounds are also disclosed in “Developer-Inhibitor-Releasing (DIR) Couplers for Color Photography,” C. R. Barr, J. R. Thirtle and P. W. Vittum in Photographic Science and Engineering, Vol. 13, p. 174 (1969), incorporated herein by reference.

[0235] It is also contemplated that the concepts of the present invention may be employed to obtain reflection color prints as described in Research Disclosure, November 1979, Item 18716, available from Kenneth Mason Publications, Ltd, Dudley Annex, 12a North Street, Emsworth, Hampshire P0101 7DQ, England, incorporated herein by reference. The emulsions and materials to form elements of the present invention, may be coated on pH adjusted support as described in U.S. Pat. No. 4,917,994; with epoxy solvents (EP 0 164 961); with additional stabilizers (as described, for example, in U.S. Pat. No. 4,346,165; U.S. Pat. No. 4,540,653 and U.S. Pat. No. 4,906,559); with ballasted chelating agents such as those in U.S. Pat. No. 4,994,359 to reduce sensitivity to polyvalent cations such as calcium; and with stain reducing compounds such as described in U.S. Pat. No. 5,068,171 and U.S. Pat. No. 5,096,805. Other compounds which may be useful in the elements of the invention are disclosed in Japanese Published Applications 83-09,959; 83-62,586; 90-072,629; 90-072,630; 90-072,632; 90-072,633; 90-072,634; 90-077,82290-078,229; 90-078,230; 90-079,336; 90-079,338; 90-079,690; 90-079,691; 90-080,487; 90-080,489; 90-080,490; 90080,49 1; 90-080,492; 90-080,494; 90-085,928; 90-086,669; 90-086,670; 90-087,361; 90-087,362; 90-087,363; 90-087,364; 90-088,096; 90-088,097; 90-093,662; 90-093,663; 90-093,664; 90-093,665; 90-093,666; 90-093,668; 90-094,055; 90-094,056; 90-101,937; 90-103,409; 90-151,577.

[0236] The silver halide used in the photographic elements may be silver iodobromide, silver bromide, silver chloride, silver chlorobromide, silver chloroiodobromide, and the like. The grain size of the silver halide may have any distribution known to be useful in photographic compositions, and may be either polydipersed or monodispersed.

[0237] The silver halide grains to be used in the invention may be prepared according to methods known in the art, such as those described in Research Disclosure Iand The Theory of the Photographic Process, 4^thedition, T. H. James, editor, Macmillan Publishing Co., New York, 1977. These include methods such as ammoniacal emulsion making, neutral or acidic emulsion making, and others known in the art. These methods generally involve mixing a water soluble silver salt with a water soluble halide salt in the presence of a protective colloid, and controlling the temperature, pAg, pH values, etc, at suitable values during formation of the silver halide by precipitation.

[0238] In the course of grain precipitation one or more dopants (grain occlusions other than silver and halide) can be introduced to modify grain properties. For example, any of the various conventional dopants disclosed in Research Disclosure, Item 38957, Section I. Emulsion grains and their preparation, sub-section G. Grain modifying conditions and adjustments, paragraphs (3), (4) and (5), can be present in the emulsions of the invention. In addition it is specifically contemplated to dope the grains with transition metal hexaco-ordination complexes containing one or more organic ligands, as taught by Olm et al U.S. Pat. No. 5,360,712, the disclosure of which is here incorporated by reference.

[0239] It is specifically contemplated to incorporate in the face centered cubic crystal lattice of the grains a dopant capable of increasing imaging speed by forming a shallow electron trap (hereinafter also referred to as a SET) as discussed in Research Disclosure Item 36736 published November 1994, here incorporated by reference.

[0240] The SET dopants are effective at any location within the grains. Generally better results are obtained when the SET dopant is incorporated in the exterior 50 percent of the grain, based on silver. An optimum grain region for SET incorporation is that formed by silver ranging from 50 to 85 percent of total silver forming the grains. The SET can be introduced all at once or run into the reaction vessel over a period of time while grain precipitation is continuing. Generally SET forming dopants are contemplated to be incorporated in concentrations of at least 1×10⁻⁷mole per silver mole up to their solubility limit, typically up to about 5×10⁻⁴mole per silver mole.

[0241] SET dopants are known to be effective to reduce reciprocity failure. In particular the use of Ir⁺³or Ir⁺⁴hexacoordination complexes as SET dopants is advantageous.

[0242] Iridium dopants that are ineffective to provide shallow electron traps (non-SET dopants) can also be incorporated into the grains of the silver halide grain emulsions to reduce reciprocity failure.

[0243] To be effective for reciprocity improvement the Ir can be present at any location within the grain structure. A preferred location within the grain structure for Ir dopants to produce reciprocity improvement is in the region of the grains formed after the first 60 percent and before the final 1 percent (most preferably before the final 3 percent) of total silver forming the grains has been precipitated. The dopant can be introduced all at once or run into the reaction vessel over a period of time while grain precipitation is continuing. Generally reciprocity improving non-SET Ir dopants are contemplated to be incorporated at their lowest effective concentrations.

[0244] The contrast of the photographic element can be further increased by doping the grains with a hexacoordination complex containing a nitrosyl or thionitrosyl ligand (NZ dopants) as disclosed in McDugle et al U.S. Pat. No. 4,933,272, the disclosure of which is here incorporated by reference.

[0245] The contrast increasing dopants can be incorporated in the grain structure at any convenient location. However, if the NZ dopant is present at the surface of the grain, it can reduce the sensitivity of the grains. It is therefore preferred that the NZ dopants be located in the grain so that they are separated from the grain surface by at least 1 percent (most preferably at least 3 percent) of the total silver precipitated in forming the silver iodochloride grains. Preferred contrast enhancing concentrations of the NZ dopants range from 1×10⁻¹¹to 4×10⁻⁸mole per silver mole, with specifically preferred concentrations being in the range from 10⁻¹⁰to 10⁻⁸mole per silver mole.

[0246] Although generally preferred concentration ranges for the various SET, non-SET Ir and NZ dopants have been set out above, it is recognized that specific optimum concentration ranges within these general ranges can be identified for specific applications by routine testing. It is specifically contemplated to employ the SET, non-SET Ir and NZ dopants singly or in combination. For example, grains containing a combination of an SET dopant and a non-SET Ir dopant are specifically contemplated. Similarly SET and NZ dopants can be employed in combination. Also NZ and Ir dopants that are not SET dopants can be employed in combination. Finally, the combination of a non-SET Ir dopant with a SET dopant and an NZ dopant. For this latter three-way combination of dopants it is generally most convenient in terms of precipitation to incorporate the NZ dopant first, followed by the SET dopant, with the non-SET Ir dopant incorporated last.

[0247] The photographic elements of the present invention, as is typical, provide the silver halide in the form of an emulsion. Photographic emulsions generally include a vehicle for coating the emulsion as a layer of a photographic element. Useful vehicles include both naturally occurring substances such as proteins, protein derivatives, cellulose derivatives (e.g., cellulose esters), gelatin (e.g., alkali-treated gelatin such as cattle bone or hide gelatin, or acid treated gelatin such as pigskin gelatin), deionized gelatin, gelatin derivatives (e.g., acetylated gelatin, phthalated gelatin, and the like), and others as described in Research Disclosure I. Also useful as vehicles or vehicle extenders are hydrophilic water-permeable colloids. These include synthetic polymeric peptizers, carriers, and/or binders such as poly(vinyl alcohol), poly(vinyl lactams), acrylamide polymers, polyvinyl acetals, polymers of alkyl and sulfoalkyl acrylates and methacrylates, hydrolyzed polyvinyl acetates, polyamides, polyvinyl pyridine, methacrylamide copolymers, and the like, as described in Research Disclosure I. The vehicle can be present in the emulsion in any amount useful in photographic emulsions. The emulsion can also include any of the addenda known to be useful in photographic emulsions.

[0248] The silver halide to be used in the invention may be advantageously subjected to chemical sensitization. Compounds and techniques useful for chemical sensitization of silver halide are known in the art and described in Research Disclosure Iand the references cited therein. Compounds useful as chemical sensitizers, include, for example, active gelatin, sulfur, selenium, tellurium, gold, platinum, palladium, iridium, osmium, rhenium, phosphorous, or combinations thereof. Chemical sensitization is generally carried out at pAg levels of from 5 to 10, pH levels of from 4 to 8, and temperatures of from 30 to 80° C., as described in Research Disclosure I, Section IV (pages 510-511) and the references cited therein.

[0249] The silver halide may be sensitized by sensitizing dyes by any method known in the art, such as described in Research Disclosure I. The dyes may, for example, be added as a solution or dispersion in water, alcohol, aqueous gelatin, alcoholic aqueous gelatin, etc. The dye/silver halide emulsion may be mixed with a dispersion of color image-forming coupler immediately before coating or in advance of coating (for example, 2 hours).

[0250] Photographic elements of the present invention are preferably imagewise exposed using any of the known techniques, including those described in Research Disclosure I, section XVI. This typically involves exposure to light in the visible region of the spectrum, and typically such exposure is of a live image through a lens, although exposure can also be exposure to a stored image (such as a computer stored image) by means of light emitting devices (such as light emitting diodes, CRT and the like).

[0251] Photographic elements comprising the composition of the invention can be processed in any of a number of well-known photographic processes utilizing any of a number of well-known processing compositions, described, for example, in Research Disclosure I, or in The Theory of the Photographic Process, 4^thedition, T. H. James, editor, Macmillan Publishing Co., New York, 1977. In the case of processing a negative working element, the element is treated with a color developer (that is one which will form the colored image dyes with the color couplers), and then with a oxidizer and a solvent to remove silver and silver halide. In the case of processing a reversal color element, the element is first treated with a black and white developer (that is, a developer which does not form colored dyes with the coupler compounds) followed by a treatment to fog silver halide (usually chemical fogging or light fogging), followed by treatment with a color developer. Preferred color developing agents are p-phenylenediamines.

[0252] Especially preferred are:

[0253] 4-amino N,N-diethylaniline hydrochloride,

[0254] 4-amino-3-methyl-N,N-diethylaniline hydrochloride,

[0255] 4-amino-3-methyl-N-ethyl-N-((x-(methanesulfonamido) ethylaniline sesquisulfate hydrate,

[0256] 4-amino-3-methyl-N-ethyl-N-(oa-hydroxyethyl)aniline sulfate,

[0257] 4-amino-3-α(methanesulfonamido)ethyl-N,N-diethylaniline hydrochloride and 4-amino-N-ethyl-N-(2-methoxyethyl)-m-toluidine di-p-toluene sulfonic acid.

[0258] Dye images can be formed or amplified by processes which employ in combination with a dye-image-generating reducing agent an inert transition metal-ion complex oxidizing agent, as illustrated by Bissonette U.S. Pat. Nos. 3,748,138, 3,826,652, 3,862,842 and 3,989,526 and Travis U.S. Pat. No. 3,765,891, and/or a peroxide oxidizing agent as illustrated by Matejec U.S. Pat. No. 3,674,490, Research Disclosure, Vol. 116, December, 1973, Item 11660, and Bissonette Research Disclosure, Vol. 148, August, 1976, Items 14836, 14846 and 14847. The photographic elements can be particularly adapted to form dye images by such processes as illustrated by Dunn et al U.S. Pat. No. 3,822,129, Bissonette U.S. Pat. Nos. 3,834,907 and 3,902,905, Bissonette et al U.S. Pat. No. 3,847,619, Mowrey U.S. Pat. No. 3,904,413, Hirai et al U.S. Pat. No. 4,880,725, Iwano U.S. Pat. No. 4,954,425, Marsden et al U.S. Pat. No. 4,983,504, Evans et al U.S. Pat. No. 5,246,822, Twist U.S. Pat. No. 5,324,624, Fyson EPO 0 487 616, Tannahill et al WO 90/13059, Marsden et al WO 90/13061, Grimsey et al WO 91/16666, Fyson WO 91/17479, Marsden et al WO 92/01972. Tannahill WO 92/05471, Henson WO 92/07299, Twist WO 93/01524 and WO 93/11460 and Wingender et al German OLS 4,211,460.

[0259] Development is followed by bleach-fixing, to remove silver or silver halide, washing and drying.

[0260] (3-Bromopropyl)trimethylammonium bromide was obtained from Aldrich Chemical Company. The bromide salt was converted to the hexafluorophosphate salt to improve the compounds solubility in valeronitrile. Reaction of a heterocyclic base with 3-(bromopropyl)trimethylammonium hexafluorophosphate in valeronitrile gave the corresponding quaternary salt. For example, reaction of 2-methyl-5-phenylbenzothiazole with 3-(bromopropyl)trimethylammonium hexafluorophosphate gave 2-methyl-5-phenyl-3-(3-(trimethylammonio)propyl)benzothiazolium bromide hexafluorophosphate. Dyes were prepared from quaternary salt intermediates by standard methods such as described in F. M. Hamer, Cyanine Dyes and Related Compounds, 1964 (publisher John Wiley & Sons, New York, N.Y.) and The Theory of the Photographic Process, 4^thedition, T. H. James, editor, Macmillan Publishing Co., New York, 1977. For example reaction of 5-chloro-2-methyl-3-(3-(trimethylammonio)propyl)benzothiazolium bromide hexafluorophosphate with acetic anhydride, isoamyl nitrite, and triethylamine followed by treatment with tetrabutylammonium bromide gave 5,5′-dichloro-3,3′-di(3-(trimethylammonio)propyl)thiacyanine tribromide. Reaction of 5-chloro-2-methyl-3-(3-(trimethylammonio)propyl)benzothiazolium bromide hexafluorophosphate with anhydro-5-chloro-2-((hydroxyimino)methyl)-3-(3-sulfopropyl)benzothiazolium hydroxide, acetic anhydride, and triethylamine gave anhydro-5,5′-dichloro-3-(3-(trimethylammonio)propyl)-3′-(3-sulfopropyl) thiacyanine bromide hydroxide. Guanidinium substituted dyes can be prepared by reaction of the corresponding amino substituted dyes with 1-H-pyrazole-1-carboxamidine hydrochloride (S. Bernatowicz, Y. Wu, and G. R. Matsueda, J. Org. Chem. 2497 (1992)).

[0261] Dye dispersions (5.0 gram total weight) were prepared by combining known weights of water, deionized gelatin and solid dye into screw-capped glass vials which were then thoroughly mixed with agitation at 60° C.-80° C. for 1-2 hours in a Lauda model MA 6 digital water bath. Once homogenized, the dispersions were cooled to room temperature. Following thermal equilibration, a small aliquot of the liquid dispersion was tranferred to a thin-walled glass capillary cell (0.0066 cm pathlength) using a pasteur pipette. The thin-film dye dispersion was then viewed in polarized light at 16× objective magnification using a Zeiss Universal M microscope fitted with polarizing elements. Dyes forming a liquid-crystalline phase (i.e. a mesophase) in aqueous gelatin were readily identified microscopically from their characteristic birefringent type-textures, interference colours and shear-flow characteristics. (In some instances, polarized-light optical microscopy observations on thicker films of the dye dispersion, contained inside stoppered lmm pathlength glass cells, facilitated the identification of the dye liquid-crystalline phase). For example, dyes forming a lyotropic nematic mesophase typically display characteristic fluid, viscoelastic, birefringent textures including so-called Schlieren, Tiger-Skin, Reticulated, Homogeneous (Planar), Thread-Like, Droplet and Homeotropic (Pseudoisotropic). Dyes forming a lyotropic hexagonal mesophase typically display viscous, birefringent Herringone, Ribbon or Fan-Like textures. Dyes forming a lyotropic smectic mesophase typically display so-called Grainy-Mosaic, Spherulitic, Frond-Like (Pseudo-Schlieren) and Oily-Streak birefringent textures. Dyes forming an isotropic solution phase (non-liquid-crystalline) appeared black (i.e. non-birefringent) when viewed microscopically in polarized light. The same thin-film preparations were then used to determine the spectral absorption properties of the aqueous gelatin-dispersed dye using a Hewlett Packard 8453 UV-visible spectrophotometer. Representative data are shown in Table A.

[0262] The data clearly demonstrate that the thermodynamically stable form of most inventive dyes when dispersed in aqueous gelatin as described above (in the absence of silver halide grains) is liquid crystalline. Furthermore, the liquid-crystalline form of these inventive dyes is J-aggregated and exhibits a characteristically sharp, intense and bathochromically shifted J-band spectral absorption peak, generally yielding strong fluorescence. In some instances the inventive dyes possessing low gelatin solubility preferentially formed a H-aggregated dye solution when dispersed in aqueous gelatin, yielding a hysochromically-shifted H-band spectral absorption peak. Ionic dyes exhibiting the aforementioned aggregation properties were found to be particularly useful as antenna dyes for improved spectral sensitization when used in combination with an underlying silver halide-adsorbed dye of opposite charge.

[0263] Film coating evaluations were carried out in black and white format on a sulfur-and-gold sensitized 3.9 μm×0.11 μm silver bromide tabular emulsion containing iodide (3.6 mol %). Details of the precipitation of this emulsion can be found in Fenton, et al., U.S. Pat. No. 5,476,760. Briefly, 3.6% KI was run after precipitation of 70% of the total silver, followed by a silver over-run to complete the precipitation. The emulsion contained 50 molar ppm of tetrapotassium hexacyanoruthenate (K₄Ru(CN)₆) added between 66 and 67% of the silver precipitation. The emulsion (0.0143 mole Ag) was heated to 40° C. and sodium thiocyanate (120 mg/Ag mole) was added and after a 20′ hold the first sensitizing dye(see Table II for dye and level) was added. After an additional 20′ a sulfur agent (carboxymethyl-trimethyl-2-thiourea, sodium salt, 2.4 mg/ Ag mole), a gold salt (bis(1,3,5-trimethyl-1,2,4-triazolium-3-thiolate) gold(I) tetrafluoroborate, 2.0 mg/Ag mole), and an antifoggant (3-(3-((methylsulfonyl)amino)-3-oxopropyl)-benzothiazolium tetrafluoroborate), 45 mg/Ag mole) were added at 5′ intervals, the melt was held for 20′ and then heated to 60° C. for 20′. After cooling to 40° C. the second dye (see Table II for dye and level), when present, was added to the melt. After 30′ at 40° C., gelatin (647 g/Ag mole total), distilled water (sufficient to bring the final concentration to 0.11 Ag mmole/g of melt) and tetrazaindine (1.0 g/Ag mole) were added. Single-layer coatings were made on acetate support. Silver laydown was 0.5 g/m²(50 mg/ft²). Gelatin laydown was 3.2 g/m²(300 mg/ft²). A hardened overcoat was at 1.6 g/m²(150 mg/ft²) gelatin.

[0264] Sensitometric exposures (0.01 sec) were done using 365 nm Hg-line exposure or tungsten exposure with filtration to stimulate a daylight exposure. The elements were processed in Kodak RP X-OMAT™ chemistry. Results are shown in the Table II.

[0265] Film coating evaluations were carried out in black and white format on a sulfur-and-gold sensitized 3.9 μm×0.11 μm silver bromide tabular emulsion containing 3.6 mol % iodide (see Example 1). The emulsion (0.0143 mole Ag) was heated to 40° C. and sodium thiocyanate (120 mg/Ag mole) was added and after a 20′ hold the first sensitizing dye (see Table III for dye and level) was added. After an additional 20′ a gold salt (bis(1,3,5-trimethyl-1,2,4-triazolium-3-thiolate) gold(I) tetrafluoroborate, 2.0 mg/Ag mole), sulfur agent (carboxymethyl-trimethyl-2-thiourea, sodium salt, 2.4 mg/ Ag mole) and an antifoggant (3-(3-((methylsulfonyl)amino)-3-oxopropyl)-benzothiazolium tetrafluoroborate), 45 mg/Ag mole) were added at 5′ intervals, the melt was held for 20′ and then heated to 60° C. for 20′. After cooling to 40° C. the second dye (see Table III for dye and level), when present was added to the melt. After 30′ at 40° C., gelatin (647 g/Ag mole total), distilled water (sufficient to bring the final concentration to 0.11 Ag mmole/g of melt) and tetrazaindine (1.0 g/Ag mole) were added. Coating, exposure and processing, were carried out as described for Photographic Example 1. Results are shown in the Table III.

[0266] Film coating evaluations were carried out in black and white format on a sulfur-and-gold sensitized 3.9 μm×0.11 μm silver bromide tabular emulsion containing 3.6 mol % iodide (see Example 1). The emulsion (0.0143 mole Ag) was heated to 40° C. and sodium thiocyanate (100 mg/Ag mole) was added and after a 20′ hold the first sensitizing dye (see Table IV for dye and level) was added. After an additional 20′ a gold salt (bis(1,3,5-trimethyl-1,2,4-triazolium-3-thiolate) gold(I) tetrafluoroborate, 2.4 mg/Ag mole), sulfur agent (N-((carboxymethyl-trimethyl-2-thiourea, sodium salt, sodium salt, 2.3 mg/Ag mole) and an antifoggant (3-(3-((methylsulfonyl)amino)-3-oxopropyl)-benzothiazolium tetrafluoroborate), 37 mg/Ag mole) were added at 5′ intervals, the melt was held for 20′ and then heated to 60° C. for 20′. After cooling to 40° C. the second dye (see Table IV for dye and level), when present, was added to the melt. After 30′ at 40° C., gelatin (324 g/Ag mole total), distilled water (sufficient to bring the final concentration to 0.11 Ag mmole/g of melt) and tetrazaindine (1.0 g/Ag mole) were added. Single-layer coatings were made on acetate support. Silver laydown was 1.1 g/m²(100 mg/ft²). Gelatin laydown was 3.2 g/m²(300 mg/ft²). A hardened overcoat was at 1.6 g/m²(150 mg/ft²) gelatin.

[0267] Exposure and processing was carried out as described for Photographic Example 1. Results are shown in the Table IV.

[0268] Film coating evaluations were carried out in color format on a sulfur-and-gold sensitized 3.7 μm×0.11 μm silver bromide tabular emulsion containing iodide (3.6 mol %). Details of the precipitation of this emulsion can be found in Fenton, et al., U.S. Pat. No. 5,476,760. Briefly, 3.6% KI was run after precipitation of 70% of the total silver, followed by a silver over-run to complete the precipitation. The emulsion contained 50 molar ppm of tetrapotassium hexacyanoruthenate (K₄Ru(CN)₆) added between 66 and 67% of the silver precipitation. The emulsion (0.0143 mole Ag) was heated to 40° C. and sodium thiocyanate (120 mg/Ag mole) was added and after a 20′ hold the first sensitizing dye (see Table V for dye and level) was added. After another 20′ the second sensitizing dye (see Table V for dye and level), if present, was added. After an additional 20′ a gold salt (bis(1,3,5-trimethyl-1,2,4-triazolium-3-thiolate) gold(I) tetrafluoroborate, 2.2 mg/Ag mole), sulfur agent (N-((carboxymethyl-trimethyl-2-thiourea, sodium salt, 2.3 mg/ Ag mole) and an antifoggant (3-(3-((methylsulfonyl)amino)-3-oxopropyl)-benzothiazolium tetrafluoroborate), 45 mg/Ag mole) were added at 5′ intervals, the melt was held for 20′ and then heated to 60° C. for 20′. After cooling to 40° C. the third dye (see Table V for dye and level), when present, and in some cases a fourth dye (see Table V for dye and level), when present, was added to the melt. After 30′ at 40° C., gelatin (647 g/Ag mole total), distilled water (sufficient to bring the final concentration to 0.11 Ag mmole/g of melt) and tetrazaindine (1.0 g/Ag mole) were added. Coating, was carried out as described for Photographic Example 1 except the emulsion was combined with a coupler dispersion containing coupler C-1 just prior to coating. This is a cyan dye forming coupler and would normally be used in an emulsion layer with a red sensitizing dye. To facilitate analysis in a single layer coating, green sensitizing dyes were also being coated with this coupler. It is understood, however, that for traditional photographic applications the green sensitizing dyes of this invention would be used in combination with a magenta dye forming coupler.

[0269] Sensitometric exposures (0.01 sec) were done using 365 nm Hg-line exposure or tungsten exposure with filtration to stimulate a daylight exposure. The described elements were processed for 3.25′ in the known C-41 color process as described in Brit. J. Photog. Annualof 1988, p191-198 with the exception that the composition of the bleach solution was changed to comprise propylenediaminetetraacetic acid. Results are shown in the Table V.

[0270] Film coating evaluations were carried out in color format on a sulfur-and-gold sensitized 3.7 μm×0.11 μm silver bromide tabular emulsion containing iodide (3.6 mol %). Details of the precipitation of this emulsion can be found in Fenton, et al., U.S. Pat. No. 5,476,760. Briefly, 3.6% KI was run after precipitation of 70% of the total silver, followed by a silver over-run to complete the precipitation. The emulsion contained 50 molar ppm of tetrapotassium hexacyanoruthenate (K₄Ru(CN)₆) added between 66 and 67% of the silver precipitation. The emulsion (0.0143 mole Ag) was heated to 40° C. and sodium thiocyanate (120 mg/Ag mole) was added and after a 20′ hold the first sensitizing dye (see Table VI for dye and level) was added. After another 20′ the second sensitizing dye (see Table VI for dye and level), if present, was added. After an additional 20′ a gold salt (bis(1,3,5-trimethyl-1,2,4-triazolium-3-thiolate) gold(I) tetrafluoroborate, 2.2 mg/Ag mole), sulfur agent (N-((carboxymethyl-trimethyl-2-thiourea, sodium salt, 2.3 mg/ Ag mole) and an antifoggant (3-(3-((methylsulfonyl)amino)-3-oxopropyl)-benzothiazolium tetrafluoroborate), 45 mg/Ag mole) were added at 5′ intervals, the melt was held for 20′ and then heated to 60° C. for 20′. After cooling to 40° C., 75 mg/Ag mole of acetamidophenylmercaptotetrazole was added followed by addition of the third dye (see Table VI for dye and level), when present, and then a fourth dye (see Table VI for dye and level), when present, was added to the melt. After 30′ at 40 ° C., gelatin (647 g/Ag mole total), distilled water (sufficient to bring the final concentration to 0.11 Ag mmole/g of melt) and tetrazaindine (1.0 g/Ag mole) were added.

[0271] Single-layer coatings were made on acetate support. Total gelatin laydown was 4.8 g/m²(450 mg/ft²). Silver laydown was 0.5 g/m²(50 mg/ft²).

[0272] The emulsion was combined with a coupler dispersion containing coupler C-1 just prior to coating.

[0273] Sensitometric exposures (0.01 sec) were done using 365 nm Hg-line exposure or tungsten exposure with filtration to simulate a daylight exposure without the blue light. The described elements were processed for 3.25′ in the known C-41 color process as described in Brit. J. Photog. Annualof 1988, p 191-198 with the exception that the composition of the bleach solution was changed to comprise propylenediaminetetraacetic acid. Results are shown in the Table VI.

[0274] Emulsion sensitization, coating and evaluations were carried out in color format as described in Example 5 except that the emulsion was combined with a coupler dispersion containing coupler C-2 instead of C-1 just prior to coating. Results are described in Table VII.

[0275] Preparation of Emulsion A: The silver bromide tabular Emulsion A was prepared according to a formula based on Emulsion H of Deaton et. al., U.S. Pat. No. 5,726,007. Emulsion A had an ECD of 2.7 micron and thickness of 0.068 micron.

[0276] Example 7-1: A portion of Emulsion A was epitaxialy sensitized in the following manner: 5.3 ml/Ag mole of 3.76 M sodium chloride solution and 0.005 mole/Ag mole of a AgI Lippmann seed emulsion were added at 40° C. Then 0.005 mole/Ag mole each of AgNO3 (0.50 M solution) and NaBr (0.50 M solution) were simultaneously run into the emulsion over a period of approximately 1 min. Next, 0.0010 mole of the spectral sensitizing dye I-9 was added and held for 20 min. Then 4.46 mL/mole Ag of a 3.764 M NaCl solution, 33.60 mL/mole Ag of a 0.50 M NaBr solution, and 7.44 mL/Ag mole of a solution containing 1.00 g/L of K₄Ru(CN)₆were combined together and added to the emulsion. Then 0.0064 mole/Ag mole of the AgI Lippmann seed emulsion was also added. Next, 72 mL/mole Ag of a 0.5 M AgNO₃solution was added over a period of 1 min. The emulsion was further chemically sensitized with sodium thiocyanate (180 mg/mole Ag), 1,3-dicarboxymethyl-1,3-dimethyl-2-thiourea (10 μmole/mole Ag), and bis(1,3,5-trimethyl-1,2,4-triazolium-3-thiolate) gold(I) tetrafluoroborate (2 μmole/mole Ag). The antifoggant 1-(3-acetamidophenyl)-5-mercaptotetrazole (11.44 mg/Ag mole) was also added. Then the temperature was raised to 50° C. at a rate of 5° C. per 3 min interval and held for 15 min before cooling back to 40° C. at a rate of 6.6° C. per 3 min interval. Finally, an additional 114.4 mg/Ag mole of 1-(3-acetamidophenyl)-5-mercaptotetrazole was added.

[0277] Example 7-2: A portion of Emulsion A was sensitized in exactly the same manner as Example 7-1, except that after those steps were completed, an additional 0.5 mmole of dye I-9 was added and held for 20 min at 40° C.

[0278] Example 7-3: A portion of Emulsion A was sensitized in exactly the same manner as Example 7-1, except that after those steps were completed, an additional 0.5 mmole of dye II-31 was added and held 20 min at 40° C.

[0279] Example 7-4: A portion of Emulsion A was sensitized in exactly the same manner as Example 7-1, except that after those steps were completed, an additional 1.0 mmole of dye II-31 was added followed by 0.5 mmole of dye I-9 and held 20 min at 40 C.

[0280] The sensitized emulsion samples were coated on a cellulose acetate film support with antihalation backing. The coatings contained 8.07 mg/dm²silver, 32.30 mg/dm²gelatin, 16.15 mg/dm²cyan dye-forming coupler C1, 2 g/Ag mole 4-hydroxy-6-methyl-1,3,3a,7-tetraazaindene, and surfactants. A protective overcoat containing gelatin and hardener was also applied.

[0281] The dried coated samples were given sensitometric exposures (0.01 sec) using a 365 nm Hg-line exposure and using a Wratten 9™ filtered 5500 K daylight exposure through a 21 step calibrated neutral density step tablet. The exposed coatings were developed in the color negative Kodak Flexicolor™ C41 process. Speed was measured at a density of 0.15 above minimum density. Contrast was measured as mid-scale contrast (gamma). The sensitometric results are shown in Table VIII. Additional experimentation in which the levels of the dyes, sulfur, and gold sensitizers were systematically varied showed that the results given in the table are optimum for each Example.

[0282] It can be seen by comparing Invention Example 7-3 to Comparison Example 7-1 that a significant daylight exposure speed increase was obtained with no loss in gamma and no loss in the intrinsic sensitivity (365 nm exposure) by adding the second layer of dye having the cationic charge to the emulsion already dyed with the anionic dye. Comparison Example 7-2 shows that no speed increase relative to Example 7-1 could be obtained by simply adding more of the anionic dye I-9. Example 7-4 comprising the combination of the cationicndye II-31 with the anionic dye I-9 as a second dye layer to the epitaxially sensitized emulsion already spectrally sensitized with dye I-9 gave a substantially higher speed than what could be obtained by adding either II-31 or I-9 alone as the second layer (Examples 7-3 and 7-2).

[0283] A silver bromide tabular Emulsion A was prepared according to a formula based on Emulsion H of Deaton e t al, U.S. Pat. No. 5,276,007. Emulsion A had an ECD of 2.7 micron and thickness of 0.068 micron.

[0284] Example 8-1: A portion of Emulsion A was epitaxialy sensitized in the following manner: 5.3 mL/Ag mole of 3.76 M sodium chloride solution and 0.005 mole/Ag mole of a AgI Lippmann seed emulsion were added at 40 C. Then 0.005 mole/Ag mole each of AgNO3 (0.50 M solution) and NaBr (0.50 M solution) were simultaneously run into the emulsion over a period of approximately 1 min. Next, 1.221 mmol I-10 and 0.271 mmol I-18 were added and held for 20 min. Then 4.46 mL/mole Ag of a 3.764 M NaCl solution, 33.60 mL/mole Ag of a 0.50 M NaBr solution, and 7.44 mL/Ag mole of a solution containing 1.00 g/L of K₄Ru(CN)₆were combined together and added to the emulsion. Then 0.0064 mole/Ag mole of the AgI Lippmann seed emulsion was also added. Then 72 mL/mole Ag of a 0.5 M AgNO3 solution was added over a period of 1 min. The emulsion was further chemically sensitized with sodium thiocyanate (180 mg/mole Ag), 1,3-dicarboxymethyl-1,3-dimethyl-2-thiourea (10 μmole/mole Ag), and bis (1,3,5-trimethyl-1,2,4-triazolium-3-thiolate) gold(I) tetrafluoroborate (2 μmole/mole Ag). The antifoggant 1-(3-acetamidophenyl)-5-mercaptotetrazole (11.44 mg/Ag mole) was also added. Then the temperature was raised to 50° C. at a rate of 5° C. per 3 min interval and held for 15 min before cooling back to 40° C. at a rate of 6.6° C. per 3 min interval. Finally, an additional 114.4 mg/Ag mole of 1-(3-acetamidophenyl)-5-mercaptotetrazole was added.

[0285] Example 8-2: A portion of Emulsion A was sensitized in exactly the same manner as Example 8-1, except that after those steps were completed, 1.5 mmole each of dye II-57 and III-2 were added and held for 20 min at 40° C.

[0286] The sensitized emulsion samples were coated on a cellulose acetate film support with antihalation backing. The coatings contained 8.07 mg/dm2 Ag, 32.30 mg/dm2 gelatin, 16.15 mg/dm2 cyan dye-forming couple C-1, 2 g/Ag mole 4-hydroxy-6-methyl-1,3,3a,7-tetraazaindene, and surfactants. A protective overcoat containing gelatin and hardener was also applied.

[0287] The dried coated samples were given sensitometric exposures (0.01 sec) using a 365 nm Hg-line exposure and using a Wratten ₉™ filtered 5500 K daylight exposure through a 21 step calibrated neutral density step tablet. The exposed coatings were developed in the color negative Kodak Flexicolor™ C41 process. Speed was measured at a density of 0.15 above minimum density. The sensitometric results are shown in Table IX.

[0288] Film coating evaluations were carried out in color format on a sulfur-and-gold sensitized 3.7 μm×0.11 μm silver bromide tabular emulsion containing iodide (3.6 mol %). Details of the precipitation of this emulsion can be found in Fenton, et al., U.S. Pat. No. 5,476,760. Briefly, 3.6% KI was run after precipitation of 70% of the total silver, followed by a silver over-run to complete the precipitation. The emulsion contained 50 molar ppm of tetrapotassium hexacyanoruthenate (K₄Ru(CN)₆) added between 66 and 67% of the silver precipitation. The emulsion (0.0143 mole Ag) was heated to 40° C. and sodium thiocyanate (120 mg/Ag mole) was added and after a 20′ hold the first sensitizing dye (see Table X for dye and level) was added. After another 20′ the second sensitizing dye (see Table X for dye and level), if present, was added. After an additional 20′ a gold salt (bis[2,3-dihydro-1,4,5-trimethyl-3-(thioxo-κS)-1H-1,2,4-triazoliumato]-gold, tetrafluoroborate, 2.2 mg/Ag mole), sulfur agent (N-((dimethylamino)thioxomethyl)-N-methyl-glycine, sodium salt, 2.3 mg/ Ag mole) and an antifoggant (3-(3-((methylsulfonyl)amino)-3-oxopropyl)-benzothiazolium tetrafluoroborate), 45 mg/Ag mole) were added at 5′ intervals, the melt was held for 20′ and then heated to 60° C. for 20′. After cooling to 40° C. the third dye (see Table X for dye and level), when present, and then a fourth dye (see Table X for dye and level), when present, was added to the melt. After 30′ at 40° C., gelatin (647 g/Ag mole total), distilled water (sufficient to bring the final concentration to 0.11 Ag mmole/g of melt) and tetrazaindine (1.0 g/Ag mole) were added.

[0289] Single-layer coatings were made on acetate support. Total gelatin laydown was 4.8 g/m²(450 mg/ft²). Silver laydown was 0.5 g/m²(50 mg/ft²). The emulsion was combined with a coupler dispersion containing coupler C-1 just prior to coating. This is a cyan dye forming coupler and would normally be used in an emulsion layer with a red sensitizing dye. To facilitate analysis in a single layer coating, green sensitizing dyes were also being coated with this coupler. It is understood, however, that for traditional photographic applications the green sensitizing dyes of this invention would be used in combination with a magenta dye forming coupler.

[0290] Sensitometric exposures (0.01 sec) were done using 365 nm Hg-line exposure or tungsten exposure with filtration to simulate a daylight exposure and to remove the blue light component. The described elements were processed for 3.25′ in the known C-41 color process as described in Brit. J. Photog. Annualof 1988, p191-198 with the exception that the composition of the bleach solution was changed to comprise propylenediaminetetraacetic acid. Results are shown in the Table X.

[0291] Emulsion sensitization, coating and evaluations were carried out in color format as described in Example 9. Results are described in Table XI.

[0292] Emulsion sensitization, coating and evaluations were carried out in color format as described in Example 9. Unexposed coatings were processed. Absorptance measurements on these processed strips were made to determine the amount of retained sensitizing dye and results are described in Table XII.

[0293] Emulsion sensitization, coating and evaluations were carried out in color format as described in Example 9. Results are described in Table XIII.

[0294] Emulsion sensitization, coating and evaluations were carried out in color format as described in Example 9 except that the emulsion was combined with a coupler dispersion containing coupler C-2 instead of C-1 just prior to coating. Results are described in Table XIV.

[0295] Emulsion sensitization, coating and evaluations were carried out in color format as described in Example 9. Results are described in Table XV.

[0296] A 3.3×0.14 μm silver bromoiodide (overall iodide content 3.8%) tabular grain emulsion was prepared by the following method. To a 4.6 liter aqueous solution containing 0.4 weight percent bone gelatin and 7.3 g/L sodium bromide at 60.5 degrees ° C. with vigorous stirring in the reaction vessel was added by single jet addition of 0.21 M silver nitrate solution at constant flow rate over a 15-minute period, consuming 0.87% of total silver. Subsequently, 351 ml of an aqueous solution containing 25.8 g of ammonium sulfate was added to the vessel, followed by the addition of 158 ml of sodium hydroxide at 2.5 M. After 5 min, 99 mL nitric acid at 4.0 M was added. Then 2.4 liters of an aqueous solution containing 0.74% gelatin by weight and 40 degrees ° C. was added to the reaction vessel and held for 5 minutes. Then an aqueous 3.0M silver nitrate solution and an aqueous solution of 2.97M sodium bromide and 0.03M potassium iodide were added by double jet methods simultaneously to the reaction vessel utilizing accelerated flow rate over 46 minutes while controlling pBr at 0.74, consuming 67.5 mole percent of the total silver. At 44.5 minutes into this segment , a 75 mL of aqueous solution of potassium hexacyanoruthenate at 0.35 percent by weight was added to the reaction vessel. After the accelerated flow segment, both silver and salt solutions were halted and 279 ml of a solution containing 0.973 mg potassium selenocyanate and 10 g of potassium bromide was added. After two minutes the pBr of the vessel was adjusted to 1.21 by addition of sodium bromide salt. Silver iodide Lippmann seed at 3 percent of total silver was then added to the reaction vessel. After a two-minute halt, 3.0M sodium bromide solution was added simultaneously with the silver nitrate solution to the reaction vessel to control pBr at 2.48 until a total of 12.6 moles of silver halide was prepared. The emulsion was cooled to 40 degrees ° C. and washed by ultrafiltration methods.

[0297] The emulsion was heated to 43° C. and sodium thiocyanate (100 mg/Ag mole) was added. Then after 5 minutes an antifoggant, [(3-(3-((methylsulfonyl)amino)-3-oxopropyl)-benzothiazolium tetrafluoroborate] (35 mg/Ag-mole) was added and after a 5 minute hold the first sensitizing dye (see Table XVI for dye and level) was added. After another 20′ the second sensitizing dye (see Table XVI for dye and level) was added. After an additional 20′ a gold salt trisodium dithiosulfato gold (I) was added (2.24 mg/Ag mole) and two minutes later, sodium thiosulfate pentahydrate (1.11 mg/Ag-mole)was also added. The melt was held for 2′ and then heated to 65° C. for 5′ and then cooled to 40 degrees and tetra-azaindene (0.75 g/Ag-mole) was added. At 40° C. the third dye (see Table XVI for dye and level), and then a fourth dye (see Table XVI for dye and level), was added and then coated as described previously.

[0298] Film coating evaluations were carried out in color format on a sulfur-and-gold sensitized 0.2 μm cubic silver bromide emulsion containing iodide (2.5 mol %). This emulsion (0.0143 mole Ag) was heated to 40° C. The first sensitizing dye (see Table XVII for dye level) was added at approximately monolayer coverage and then the melt was heated to 60° C. for 15′. After cooling to 40° C., gelatin (647 g/Ag mole total) was added and then the second dye (see Table XVII for dye level), when present, was added to the melts.

[0299] Single-layer coatings were made on acetate support. Total gelatin laydown was 3.2 g/m²(300 mg/ft²). Silver laydown was 0.5 g/m²(50 mg/ft²). The emulsion was combined with a coupler dispersion containing C-1 just prior to coating.

[0300] Sensitometric exposures (1.0 sec) were done using 365 nm Hg-line exposure or tungsten exposure with filtration to stimulate a daylight exposure. The described elements were processed for 2′ in the known C-41 color process as described in Brit. J. Photog. Annualof 1988, p191-198 with the exception that the composition of the bleach solution was changed to comprise propylenediaminetetraacetic acid Results are shown in the Table XVII.

[0301] It can be seen from photographic examples 1-15 that the dye combinations of the invention give enhanced speed relative to the comparisons on various types of tabular grain emulsions. It can be seen from Example 16 that speed loss and development inhibition can occur on cubic emulsions.

[0302] The invention has been described in detail with particular reference to preferred embodiments, but it will be understood that variations and modifications can be effected within the spirit and scope of the invention.