JP2000181000A - Photographic recording element - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a photographic recording element having remarkably enhanced photographic characteristics. SOLUTION: The photographic recording element contains a substrate and at least one dye image forming layer unit containing (a) radiation sensitive silver halide grains, (b) a sensitizer for the silver halide grains, (c) a deflocculant for the silver halide grains, (d) at least one dye image providing coupler and (e) at least one dye image intensifying coupler. The silver halide grains include flat, plate-like grains having 111} principal face, containing >50 mol% bromide based on the amount of silver and occupying >50% of the total projection area of all the grains. The sensitizer includes a sensitizer that is an electron doner and can be fragmented. The deflocculant is water-dispersible cationic starch. The dye image providing coupler is a coupler capable of forming a dye image by reaction with an oxidizable primary amine color developing agent. The dye image intensifying coupler is a coupler capable of releasing an electron transfer agent by reaction with the oxidizable primary amine color developing agent.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0001]

The present invention relates to color photography. Specifically, the present invention relates to a color photographic element having a layer unit containing a radiation sensitive silver halide emulsion to produce a dye image.

[0002]

BACKGROUND OF THE INVENTION The most widely used forms of photographic elements are those containing one or more silver halide emulsions. Usually, silver halide emulsions are prepared by depositing the silver halide in the form of individual grains (microcrystals) in an aqueous medium. An organic peptizer is introduced into the aqueous medium to disperse the particles. Although various forms of hydrophilic colloids have been found to be useful as peptizers, by far the majority of silver halide emulsions use gelatino-peptizers. For an overview of conventional peptizers, including gelatino-peptizers, see Research Disclosur
e), Volume 389, 1996, Item 38957, II. "Vehicles, vehicle extenders, vehicle-like additives and vehicle-related additives";"Gelatin and hydrophilic colloid peptizers". Research disclosure is available from Kenneth Mason Publication Ltd., Dudley Annex, 1
2a North Street, Emsworth, Hampshire PO10 7DQ, Eng
Published by land. The term "vehicle" includes both peptizers used to disperse silver halide grains as they are formed and binders used in emulsion coating and processing solution permeable layers of photographic elements. . Gelatin and gelatin derivatives are commonly used to perform both peptizer and binder actions.

[0003] A major cause of the superiority of silver halide photography is the ability of silver halide grains to amplify images.
Upon imagewise exposure of a silver halide photographic element, incident light quanta are absorbed by the silver halide grains. When photons are absorbed,
The electrons of the silver halide crystal lattice structure of the grain are promoted from the valence band energy level to a higher conduction band energy level and can move within the grain lattice of the grain.
When some conduction band electrons are trapped by crystal lattice silver ions in close proximity, clusters of Ag ° atoms are created, which are commonly referred to as latent image sites. The latent image sites of the grains can catalyze the reduction of total silver ions within the grains to Ag °, and imagewise exposure creates a large amplification of very little original Ag ⁺ to Ag °. The developer is an aqueous solution containing a developing agent (a reducing agent capable of selectively reducing silver halide grains having a latent image to Ag °). Contacting a photographic element with an aqueous solution containing a developer to produce a visible image is called photographic processing.

While many factors play a role in obtaining the desired photographic image, the most fundamental is the sensitivity of the photographic element used. Silver halide photography with its inherent amplification mechanism shows much higher photographic sensitivity than other imaging systems, but has been up to 1 to date from its inception.
Over the centuries, there has been a continuing search for higher photographic sensitivity in silver halide photography. Photographic element sensitivity is measured by exposing sample portions of the photographic element to different levels and correlating with subsequent photographic image density. The characteristic curve is created by taking the logarithm of the image density (D) on the vertical axis and the log of the exposure amount (E) on the horizontal axis. Typically, the characteristic curve is a linear characteristic curve that changes with increasing exposure as a function of the exposure that changes with increasing exposure, from a portion that shows no density change (minimum density, Dmin). From the portion where the density increases as a function of increasing exposure, which often produces a portion (ie, ΔD / ΔE is constant), there is a portion (maximum density Dmax) where the density does not increase with increasing exposure. The speed of a photographic element is usually reported as the difference in LogE required to produce the same density in the compared elements.

[0005] Silver halide emulsions have an inherent sensitivity to light at wavelengths ranging from the ultraviolet to the blue region of the visible spectrum. Spectral sensitizing dyes are adsorbed on silver halide grain surfaces and extend sensitivity to longer parts of the spectrum. An overview of spectral sensitizing dyes is given in Research Disclosure, Item 38957, supra; "Spectral sensitization and desensitization", A.I.
"Sensitizing dyes". The action of the spectral sensitizer is
In order to form a latent image, it is to capture photons of a wavelength that cannot be captured by the silver halide grains themselves.

In order to increase the sensitivity of silver halide separately from spectral sensitization, the grain surface is treated with a chemical sensitizer. For an overview of chemical sensitizers, see Research Disclosure,
Item 38957, IV. It is described in "Chemical sensitization".

Recently, it has been found that further enhancement of photographic speed can be achieved by associating silver halide grains with a fragmentable electron donor (FED) sensitizer. The mechanism of FED sensitization has not yet been proven, but one good explanation is: As described above, photon trapping in particles causes electron promotion from the valence shell to the conduction energy band. Sometimes, the common loss factor is recombination. That is, the promoted electron simply returns to a hole in the valence shell created by the promotion of that electron or another electron to the conduction band. When recombination occurs, the energy of the captured photons is dissipated without contributing to latent image formation. It is believed that FED sensitizers reduce recombination by donating electrons to fill holes created by photon capture. Therefore, fewer conduction band electrons return to the hole site, and more electrons can participate in latent image formation.

[0008] When the FED sensitizer donates electrons to the silver halide grains, they fragment to form cations and free radicals. This free radical is a single atom or compound that has an unpaired valence shell electron and is therefore very unstable. If the oxidation potential of the free radical is equal to or less than -0.7 volts, the free radical will inject a second electron into the particle as soon as it is formed,
Eliminate its unvalence electron shell electrons. Also, when the free radicals supply electrons to the particles, apparently, the absorption of a single photon within the particles promotes the electrons to the conduction band and excites the FED sensitizer, which supplies the electrons that fill the remaining holes. Thus, this reduces hole-electron recombination and injects a second electron. Thus, FED sensitizers provide one or more electrons to silver halide that contribute directly or indirectly to forming a latent image.

FED sensitizers and their use to enhance photographic sensitivity are described in US Pat. No. 5,747,235 to Farid et al.
No. 5,747,236, and the following commonly assigned applications: U.S. Patent Application No. 08 to Lenhard et al.
No./739,911 (filed October 30, 1998) and US Patent Application No. 09 / 118,536 to Gould et al., US Patent Application No. 09 / 118,536, filed June 25, 1998, respectively. No. 09 / 118,552 and U.S. Patent Application No. 09 / 118,714 to Adin et al.

A dramatic increase in photographic speed began with the introduction of tabular grain emulsions in silver halide photographic products in 1982. Tabular grains are grains that have two parallel major faces that are clearly larger than the other crystal faces and have an aspect ratio of at least 2. The term "aspect ratio" is the ratio of the equivalent circular diameter (ECD) of a particle divided by its thickness (the distance separating the major surfaces). Tabular grain emulsions are emulsions in which tabular grains account for greater than 50% of total grain projected area.
U.S. Pat. No. 4,439,520 to Kofron et al. Describes the first tabular grain emulsions of high aspect ratio (average aspect ratio> 8) chemically and spectrally sensitized. In the most common form of use, tabular grain emulsions comprise tabular grains having a major surface in the {111} crystal plane and containing greater than 50 mole percent bromide, based on silver. An overview of tabular grain emulsions is described in Research Disclosure,
Item 38957, I.P. "Emulsion grains and their preparation";
"Particle morphology", especially described in subparagraphs (1) and (3).

The use of cationic starch as a peptizer for the precipitation of high bromide {111} tabular grain emulsions has been disclosed by Maskasky in US Pat. No. 5,604,085;
Nos. 5,620,840, 5,667,955, 5,691,131, and 5,733,718. Oxidized cationic starch has the advantage of exhibiting lower viscosity levels than gelatino-peptizers. This facilitates mixing. With cationic starch peptizers, higher photographic speeds can be achieved with comparable levels of chemical sensitizers. Alternatively, the same sensitivity as that obtained using a gelatino-peptizer can be achieved at lower precipitation and / or sensitization temperatures, thereby avoiding undesirable grain ripening.

When silver halide is reduced to silver during development, a black-and-white photographic image can be produced depending on the neutral density of the developed silver. An alternative to image formation is to use a primary amine color developing agent during development. The oxidized color developing agent then reacts (couples) with the dye image providing coupler to form an image dye. Form a so-called "dye-producing" black-and-white image that uses a combination with an image dye-forming coupler to produce a black dye image that can be used in place of or in combination with developed silver to produce a black-and-white image can do. Image hues other than black (generally subtractive three primary hues)
To achieve this, the neutral density of silver is removed by bleaching and fixing, relying exclusively on image dye formation on the dye formed by the reaction product of the image dye forming coupler with the color developing agent. A red, blue and deep mud recording layer unit capable of producing three types of spectrally distinct dye image records to obtain an acceptable photographic image of the neutral hues of the subject taken Is widely used for dye image formation.

In the last two decades, the enhancement of dye images due to the introduction of dye image improving couplers has become common. Photographically useful fragments, such as development accelerators, development inhibitors,
Bleach accelerators, bleach inhibitors, developing agents (eg, competing or auxiliary developing agents), silver complexing agents, fixing agents, toners, hardeners, tanning agents, stain inhibitors, stabilizers, antifoggants, competition To release couplers and chemical or spectral sensitizers or desensitizers immediately or in time, one can rely on these couplers, which often do not produce image dyes upon coupling.

An overview of the coupler is given in Research Disclosure, Item 38957, X. "Dye image forming and improving agents", especially B.I. "Image dye-forming couplers", and C.I. "Image dye improver".

[0015]

SUMMARY OF THE INVENTION In one aspect, the invention comprises a support, and (a) radiation-sensitive silver halide grains; (b) a sensitizer for said silver halide grains;
(C) a peptizer for the silver halide grains, (d)
At least one dye image providing coupler, and (e) at least one dye having at least one dye image enhancing coupler
A photographic recording element comprising two dye image forming layer units, wherein said radiation sensitive silver halide grains comprise:
A {111} major surface, (2) containing more than 50 mol% bromide based on silver, and (3) 50% of total grain projected area.
The sensitizer comprises a fragmentable electron-donating sensitizer, the peptizer is a water-dispersible cationic starch, and the dye image providing coupler comprises: Is a coupler capable of forming a dye image by reacting with an oxidized primary amine color developing agent, and wherein the dye image enhancing coupler reacts with the oxidized primary amine color developing agent to form an electron transfer agent. Directed to a photographic recording element that is a coupler capable of emitting a.

A high bromide {111} tabular grain emulsion precipitated in the presence of a cationic starch peptizer and sensitized with a fragmentable electron donating (FED) sensitizer;
When compared to the same emulsion except that it contained a gelatino-peptizer, it was found that the starch-peptized emulsion exhibited much higher sensitivity than the gelatino-peptized emulsion. FE
Repeating the comparison omitting the D sensitizer showed a relatively small sensitivity advantage for the starch peptized emulsion. FE to starch peptized high bromide {111} tabular grain emulsion
It was quite unexpected that great sensitivity advantages were achieved by adding the D sensitizer. This sensitivity advantage is
It is reported in the specification and in the aforementioned application I.

Furthermore, the introduction of an electron transfer agent releasing coupler leads to a much larger and unexpected increase in sensitivity. Starch or gelatin peptized FED sensitized high bromide # 11
Comparing color photographic elements containing 1 tabular grain emulsions with and without the introduction of an electron transfer agent releasing (ETARC) coupler, the presence of ETARC in a color element with a starch peptized emulsion was unexpected A great sensitivity advantage is realized.

[0018]

DETAILED DESCRIPTION OF THE INVENTION The present invention generally comprises at least one
Fragmentable electron donor (FED) sensitized, cationic starch peptized high bromide {111} tabular grain emulsion in one dye image forming layer unit, dye image providing coupler, electron transfer agent release (ETARC) couplers. High bromide {111} tabular grain emulsions have a total grain projected area of 5
More than 0% has {111} main surface and 50 mol% based on silver amount
Emulsion occupied by tabular grains containing extra bromide.

[0019] Any of the conventional cationic starches can be used as a peptizer. The term "starch" includes native starch and, for example, dextrinized, hydrolyzed, alkylated, hydroxyalkylated, acetylated or fractionated And both improved starch derivatives. The starch can be of any origin, such as corn starch, wheat starch, potato starch, tapioca starch, sago starch, rice starch, waxy corn starch or high amylose corn starch.

[0020] Starch generally consists of two structurally distinct polysaccharides, α-amylose and amylopectin. Both consist of α-D-glucopyranose units. In α-amylose, α-D-glucopyranose units form a 1,4-linear polymer. This repeating unit takes the following form:

Embedded image

In amylopectin, the repeating unit 1,4-
In addition to the binding, 6-position chain branching (above, at the site of the -CH ₂ OH groups) also appeared clearly produces a branched polymer. The repeating units of starch and cellulose are diastereoisomers that give their molecules an entirely different linkage configuration. The α anomer (found in starch and found in Formula I above) is crystallizable and capable of some hydrogen bonding between repeating units of adjacent molecules (provided that the β anomer repeating units of cellulose and cellulose derivatives are the same). To a lesser degree) polymer. The polymer molecules formed by the beta anomer show strong hydrogen bonding between adjacent molecules, causing aggregation of the polymer molecules and greater crystallinity. Lack of sequences of substituents that favor strong intermolecular bonds (found in cellulose repeating units), starch and starch derivatives disperse more readily in water.

[0022] The water-dispersible starch used in the practice of the present invention is cationic. That is, when dispersed in water, it has an overall positive net charge. Generally, the starch is rendered usually cationic by attaching a cationic substituent to the α-D-glucopyranose unit by esterification or etherification at one or more free hydroxyl sites. Reactive cation-forming reagents generally include primary, secondary, or tertiary amino groups (which can then be protonated to a cationic form under the conditions intended for use) or Includes quaternary ammonium, sulfonium or phosphonium groups.

To be useful as a peptizer, the cationic starch must be water-dispersible. Many starches disperse in water in a short time (eg, 5 to 30 minutes) when heated to a temperature to boiling. High shear mixers also promote starch dispersion. The presence of a cationic substituent increases the polarity of the starch molecule and promotes dispersion. The starch molecules achieve at least a colloidal level of dispersion, and are ideally dispersed (ie, dissolved) at the molecular level.

The following patent documents describe water-dispersible cationic starches within the intended scope of the present invention (incorporated herein by reference): * US Pat. No. 2,989 , 520 (Rutenberg
U.S. Pat. No. 3,017,294 (Meise).
l), U.S. Pat. No. 3,051,700 (Elizer
U.S. Pat. No. 3,077,469 (Aszolo).
s), U.S. Pat. No. 3,136,646 (Eizer
* U.S. Pat. No. 3,219,518 (Barb
er et al.), * U.S. Patent No. 3,320,080 (Ma
zzarella et al.), U.S. Patent No. 3,320,118 (Black et al.), U.S. Patent No. 3,243,426 (Caesar), U.S. Patent No. 3,336,292 (Kirby), U.S. Pat. No. 3,354,034 (Jarowenko), U.S. Pat. No. 3,422,087 (Caesar), * U.S. Pat. No. 3,467,608 (Dishburger et al.), * U.S. Pat. 3,467,647
Specification (Beaninga et al.), US Pat. No. 3,671,31.
No. 0 (Brown et al.), U.S. Pat. No. 3,706,58.
No. 4 (Cescato), U.S. Pat. No. 3,737,37.
No. 0 (Jarowenko et al.), * US Pat.
0,472 (Jarowenko), U.S. Pat.
42,005 (Moser et al.), U.S. Pat.
60,683 (Tessler); U.S. Pat.
No. 27,563 (Rankin et al.); U.S. Pat.
13,407 (Huchette et al.); U.S. Pat.
964,915 (Blixt et al.), * U.S. Pat. No. 5,227,481 (Tsai et al.), And * U.S. Pat. No. 5,349,089 (Tsai).

The use of oxidized cationic starch
Is preferred. Starch before adding cationic substituents
(Patent document marked with * above) or may be oxidized later
No. This is achieved by treating the starch with a strong oxidizer.
Done. In the preparation of commercial starch derivatives, hypochlorite
Acid ion (ClO^-) Or periodate ion (IO
_Four-) Has been widely used and studied, and this is preferred.
New Normal oxidant counterions can be used,
Preferred counterions are fully compatible with silver halide emulsion preparation.
Can be combined, for example, alkali and alkaline earth
Cations, most commonly sodium, potassium or
Is calcium.

When the oxidizing agent opens the α-D-glucopyranose ring, the oxidation site is usually at the 2- and 3-position carbon atoms forming the α-D-glucopyranose ring.

The 2- and 3-position groups:

Embedded image Is usually preferred as a glycol group. The carbon-carbon bond of the glycol group is replaced as follows:

[0028]

Embedded image (Where R represents an atomic group completing an aldehyde group or a carboxyl group).

For commercial applications, hypochlorite ion oxidation of starch is most widely used. A small amount of hypochlorite ion is used to modify starch impurities. At these low levels, starch modification is minimal and α-D-
It only affects, at best, the polymer chains with terminal aldehyde groups, rather than the glucopyranose repeating units themselves. At the oxidation level acting on the α-D-glucopyranose repeating unit, hypochlorite ion acts on the 2, 3 and 6 positions to form aldehyde groups at relatively low oxidation levels, Form carboxyl groups at high oxidation levels. Oxidation is moderately acidic to alkaline pH (eg,
> 5 to 11). The oxidation reaction is exothermic and requires cooling of the reaction mixture. It is preferred to maintain a temperature below 45 ° C. It has been found that using the hypobromite oxidizing agent gives the same results as hypochlorite.

Hypochlorite oxidation is catalyzed by the presence of bromide ions. Usually, a silver halide emulsion is precipitated in the presence of an excess of a stoichiometric amount of a halide in order to avoid accidental silver ion reduction (fogging). Therefore, in a dispersion medium of a high bromide silver halide emulsion, Bromide ions are commonly obtained. Thus, it is specifically contemplated to add bromide to the starch prior to performing the oxidation step at a concentration said to be useful in high bromide {111} tabular grain emulsions (eg, up to 3.0 pBr).

Cescato, US Pat. No. 3,706,574
The specification, incorporated herein by reference, discloses a technique for the hypochlorite oxidation of cationic starch. Instead of sodium hypochlorite, sodium bromite, sodium chlorite, and calcium hypochlorite are mentioned. An alternative method for the hypochlorite oxidation of starch is disclosed in the following document: RL
Whistler, EG Linke and S. Kazeniac, "Action
of Alkaline Hypochlorite on Corn Starch Amylose a
nd Methyl 4-O-Methyl-D-glucopyranosides ", Journa
l Amer. Chem. Soc., 78, 4704-9 (1956); L. Whist
ler and R. Schweiger, "Oxidation of Arnylopecti
n with Hypochlorite at Different Hydrogen lon Conc
entrations, JournalAmer. Chem. Soc., 79, 6460-646
P. 4 (1957); J. Schmorak, D. Mejzler and M. Lewi
n "A Kinetic Study of the Mild Oxidation of Whe
at Starch by Sodium Hypochloride in the Alkaline p
H Range ", Journal of Polymer Science, XLIX, 203-
216 (1961); J Schmorak and M. Lewin, "The Che
mical and Physico-chemical Properties of Wheat Sta
rch with Alkaline Sodium Hypochlorite ", Journal of
Polymer Science: Part A, Volume 1, 2601-2620 (1963)
KF Patel, HU Mehta and HC Srivastava,
"Kinetics and Mechanism of Oxidation of Starch wi
th Sodium Hypochlorite ", Journal of Applied Polymer
Science, 18, 389-399 (1974); RL Whistle
r, JNBemiller and EF Paschall, Starch: Chem
istry and Technology, Chapter X, Starch Derivatives: Pro
duction and Uses, II. Hypochlorite-Oxidized Starch
es, pp. 315-323, Academic Press, 1984; and OB W
urzburg, Modlfied Starches: Properties and Uses,
III. Oxidized or Hypochlorite-Modified Starches,
Pages 23-28 and 245-246, CRC Press (1986).

Hypochlorite oxidation is usually carried out using soluble salts and is described in ME McKillican and CBPurves, "Estimati.
on of Carboxyl, Aldehyde and Ketone Groups in Hypo
chlorous Acid Oxystarches ", Can. J Chem., 312-321
Alternatively, the free acid can be used, as described in Vol. (1954).

The periodate oxidizing agent is particularly important, as it is known to have high selectivity. The periodate oxidizing agent produces dialdehyde starch at the carbon atom at position 6 without significant oxidation by the reaction shown in formula (II) above. Unlike hypochlorite oxidation, periodate oxidation does not generate carboxyl groups and does not result in oxidation at the 6-position. US Patent No. 3,251,8 to Mehltretter
No. 26, incorporated herein by reference, discloses the use of periodic acid to produce a dialdehyde starch that has been modified to a substantially cationic form. Mehltretter also discloses solubilized salts of periodic acid and chlorine for use as oxidizing agents. In addition, techniques for periodate oxidation of starch are described in the following literature: VC Bany and PWD Mitchell, "Propertie
s of Periodate-oxidized Polysaccharides. Part II.
The Structure of some Nitrogen-containing Polymer
s ", Journal Amer. Chem. Soc., 1953, 3631-3635;
PJ Borchert and J. Mirza, "Cationic Dispersio
ns of Dialdehyde Starch I. Theory and Preparatio
n ", Tappi, Volume 47, No. 9, pp. 525-528 (1964); JE M
cCormick's "Properties of Periodate-oxidized Pol
ysaccharides. Part VII. The Structure of Nitrogen-
containing Derivatives as deduced from a Study of
MonosaccharideAnalogues ", Journal Amer. Chem. So
c., 2121-2127 (1966); and OB Wurzburg, M.
odlfied Starches; Properties and Uses, III. Oxidiz
ed or Hypochlorite-Modified Starches, pages 28-29, CRC
Press (1986).

Starch oxidation by electrolysis is carried out by FF Far
ley and RM Hixon's "Oxidation of Raw Starch G
ranules by Electrolysis in Alkaline Sodium Chlorid
e Solution ", Ind. Eng. Chem., 34, 677-681 (19
42).

Depending on the choice of oxidizing agent used, one or more soluble salts can be released in the oxidation step. The soluble salt or corresponding soluble salt is the same as that normally present during silver halide precipitation, and it is not necessary to separate this soluble salt from the oxidized starch prior to silver halide precipitation. Of course, it is also possible to separate the soluble salts from the oxidized starch prior to precipitation using conventional separation techniques. For example, removal of excess halide ions, which is preferably present at the time of grain precipitation, is also performed. A simple alternative is to simply decant the solute and dissolved salt from the oxidized cationic starch particles. Washing the oxidized cationic starch under non-dissolving conditions is also a preferred alternative. Even when the oxidized cationic starch is dispersed in solution during oxidation, there is a large difference in molecular size between the oxidized cationic starch and the soluble salt by-product of oxidation, so Can be separated using ultrafiltration techniques.

The carboxyl group formed by oxidation takes the form of -C (O) OH, but if necessary, the carboxyl group can be further processed to form -C (O) OR ', where R' Represents an atomic group forming a salt or an ester). The organic moiety added by esterification preferably has 1 to 6 carbon atoms, optimally 1 to 3 carbon atoms.

The minimum possible degree of oxidation is that required to reduce the viscosity of the starch. The opening of the α-D-glucopyranose ring of the starch molecule breaks down the helical structure of the linear repeating unit and reduces the viscosity of the solution. On average, it is possible to open at least one α-D-glucopyranose repeating unit per starch polymer in the oxidation step. Α-D-opened per polymer
About two to three glucopyranoses sufficiently affect the performance of the starch polymer and maintain a linear helical structure. Preferably, at least 1% of the glucopyranose rings are opened by oxidation.

A preferred goal is to reduce the viscosity of the cationic starch by oxidation to less than four times (400%) the viscosity of water at the starch concentration used for silver halide precipitation. Although this viscosity reduction goal can be achieved with lower degrees of oxidation, starch oxidation of up to 90% of α-D-glucopyranose repeating units has been reported (see above).
Wurzburg, p. 29). A typical conventional oxidative ring opening ratio is 3% of α-D-glucopyranose repeating units.
５０50%.

The water-dispersible cationic starch can be used during precipitation of high bromide {111} tabular grains (nucleation and grain growth,
Or during grain growth). It is preferred to effect precipitation by replacing all conventional gelatino-peptizers with this water-dispersible cationic starch. In replacing the conventional gelatino-peptizer with the selected cationic starch peptizer, the concentration and timing of addition of the selected peptizer (s)
Can correspond to the case where a gelatino-peptizer is used.

In addition, it was unexpected that emulsion precipitation was acceptable at higher concentrations of the selected peptizer. For example, it has been found that all selected peptizers required for the steps of chemical sensitization from emulsion precipitation can be placed in a reaction vessel prior to grain nucleation. This has the advantage that no peptizer needs to be injected after tabular grain precipitation has begun. The selected peptizer is 1-500 g (most preferably 5 g / mol silver) deposited.
〜100 g) is generally preferred in the reaction vessel prior to tabular grain nucleation.

In extreme cases, Mignot US Pat.
As described in US Pat. No. 334,012, which is incorporated herein by reference, the required peptizer is not present during particle nucleation and, if necessary, the selected peptizer It is of course also known to defer the addition of the agent until the grain growth has proceeded to the point where the peptizer actually needs it, to avoid tabular grain agglomeration.

High bromide to completion of tabular grain growth # 11
The procedure for preparing 1｝ tabular grain emulsions simply requires replacing the conventional gelatino-peptizer with the selected peptizer. The following high bromide {111} tabular grain emulsion precipitation procedure (herein incorporated by reference) is useful in the practice of this invention, subject to the selected peptizer improvement discussed above. It is believed that US Pat. No. 4,414,310 (Daubendiek)
Et al.), U.S. Pat. No. 4,425,426 (Abbott
Et al.), U.S. Pat. No. 4,434,226 (Wilgus
Et al.), U.S. Pat. No. 4,435,501 (Maskas
ky), U.S. Pat. No. 4,439,520 (Kofron
Et al.), U.S. Pat. No. 4,433,048 (Solber
g et al.), U.S. Pat. No. 4,504,570 (Evan
s et al.), U.S. Patent No. 4,647,528 (Yama
da et al.), U.S. Patent No. 4,672,027 (Daub
endiek et al.), U.S. Pat. No. 4,693,964 (Daubendiek et al.), U.S. Pat. No. 4,665,012 (Sugimoto et al.), U.S. Pat. No. 4,672,027 (Daubendiek et al.) ), U.S. Pat. No. 4,679,74.
No. 5, No. 5,693,96 (Yamada et al.).
No. 4 (Daubendiek et al.), U.S. Pat. No. 4,713,
320 (Maskasky); U.S. Pat.
886 (Nottorf), U.S. Pat.
No. 456 (Sugimoto), US Pat.
No. 617 (Goda), US Pat. No. 4,797,35.
No. 4 (Saitou et al.),

US Pat. No. 4,801,522 (Ellis), US Pat. No. 4,806,461 (Ikeda et al.), US Pat. No. 4,835,095 (Ohashi et al.), U.S. Pat. No. 4,835,322 (Makino et al.), U.S. Pat. No. 4,914,014 (Daubendiek et al.), U.S. Pat. No. 4,962,015 (Aida et al.), U.S. Pat. No. 4,985,350 (Ikeda et al.), U.S. Pat. No. 5,061,609 (Piggin et al.), U.S. Pat. No. 5,061,616 (Piggin et al.), U.S. Pat. No. 5,147,772 (Tsaur et al.), U.S. Pat. No. 5,147,773 (Tsaur et al.), U.S. Pat. No. 5,171. No. 5,659 (Tsaur et al.); U.S. Pat. No. 5,210,013. US Pat. No. 5,250,403 (Antoniades et al.), US Pat. No. 5,272,048 (Kim et al.), US Pat. No. 5,310,644 (Tsaur et al.) Delton), US Pat. No. 5,314,793 (Chang et al.), US Pat. No. 5,334,469 (Sutton et al.), US Pat. No. 5,334,495 (Black et al.) U.S. Pat. No. 5,358,840 (Chaffee et al.) And U.S. Pat. No. 5,372,927.
Issue Specification (Delton).

The resulting high bromide ultrathin {111} tabular grain emulsions preferably contain at least 70 mole%, optimally at least 90 mole% bromide, based on silver. Silver bromide, silver iodobromide, silver chlorobromide, silver iodochlorobromide, and silver chloroiodobromide tabular grain emulsions are specifically contemplated.
Silver chloride and silver bromide form tabular grains in all proportions, but it is preferred that the chloride be present at a concentration of 30 mole percent or less, based on silver. Iodide can be present in the tabular grains up to its solubility limit under the precipitation conditions selected for tabular grain precipitation.

Under normal precipitation conditions, silver iodide can be incorporated into the tabular grains at concentrations ranging up to about 40 mol%, based on silver. Iodide concentration is 20 mol% based on silver
It is generally preferred that it be less than. Typically, iodide concentrations are less than 10 mole percent, based on silver. To facilitate rapid processing (e.g., commonly done in radiography), it is preferred that the iodide concentration be limited to less than 4 mole percent, based on silver. Significant photographic advantages can be achieved with iodide concentrations as low as 0.5 mole percent based on silver, but iodide concentrations of at least 1 mole percent based on silver are preferred.

The high bromide {111} tabular grain emulsions can exhibit any conventional average grain ECD, with a maximum of 10
Over μm, this is generally accepted as the maximum average particle size compatible with photographic utility. In fact, the tabular grain emulsions of the present invention typically exhibit an average ECD ranging from 0.2 to 7.0. Tabular grain thickness is typically 0.0
It ranges from 3 to 0.3 μm. For the blue record, somewhat thicker grains (up to 0.5 μm) can be used. For minus blue (red and / or green) records, thin (<0.2μ
m) Tabular grains are preferred.

In general, as the average aspect ratio or tabularity of a tabular grain emulsion increases, the advantages that the tabular grains provide to the emulsion increase. As the average tabular grain thickness decreases, both the aspect ratio (ECD / t) and tabularity (ECD / t ² ) increase. Therefore, it is required that the thickness of the tabular grains be minimized to the full potential of photographic applications. 0.3 without prohibition of specific use
having a thickness of less than μm (preferably less than 0.2 μm and optimally less than 0.07 μm) and greater than 50% (preferably at least 70%, and optimally at least 90%) of the total grain projected area Is generally preferred to exhibit an average aspect ratio of greater than 5, most preferably greater than 8. Tabular grain average aspect ratios can range up to 100, 200 or more, but typically range from 12 to 80. A tabularity greater than 25 is generally preferred.

High bromide {111} tabular grain emulsions precipitated in the presence of cationic starch are disclosed in the following references (incorporated herein by reference): US Pat. 5,604,085, 5,62
0,840, 5,667,955, 5,691,
No. 131 and 5,733,718.

The above-cited patent specification and the above-mentioned Research Disclosure, Item 38957, Section I.
"Emulsion grains and their preparation"; As described in "Grain Improvement Conditions and Adjustments", paragraphs (3), (4), and (5), conventional dopants can be introduced into the tabular grains during their precipitation. Research Disclosure, Vol. 367, November 1994, Item 36736, and shallow electron trap (SET) sites on the tabular grains as described in Olm et al., US Pat. No. 5,576,171. It is particularly conceivable to introduce the providing dopant.

It is also observed that silver salts are grown epitaxially on the tabular grains during the precipitation process. Epitaxial deposition of tabular grains on sides and / or corners is described in Maskasky U.S. Pat. Nos. 4,435,501 and Daubendiek et al., 5,573,902 and 5,576,168 (cf. In particular, as described herein.

Epitaxy on host tabular grains is:
While capable of acting as a sensitizer per se, the emulsions of the present invention can provide epitaxy when chemically sensitized with one or a combination of noble metals, intermediate chalcogens and reduction chemical sensitization techniques without a gelatino-peptizer. It shows unexpected sensitivity enhancement with and without use. Conventional chemical sensitizations by these techniques are outlined in Research Disclosure, Item 38957, supra, Section IV, Chemical sensitization. It is preferred to use at least one of a noble metal (typically gold) and an intermediate chalcogen (typically sulfur), most preferably a combination of both in preparing the emulsions of the present invention for photographic applications. The use of cationic starch peptizers can provide significant advantages with respect to chemical sensitization. At comparable chemical sensitization levels, higher photographic speeds can be achieved with cationic starch peptizers. If you are looking for equivalent photographic speed,
Cationic peptizer without gelatin allows for the use of lower amounts of chemical sensitizer and provides good incubation storage. If the amount of chemical sensitizer is left unchanged, the same sensitivity can be achieved at lower precipitation and / or sensitization temperatures as is obtained with gelatino-peptizers, which is undesirable. Particle ripening can be avoided.

Between the precipitation of the emulsion and the chemical sensitization, a step which is preferably completed prior to the addition of gelatin or a gelatin derivative to the emulsion, comprises soluble reaction by-products (eg alkali and / or alkaline earth cations and nitrate anions).
It is common practice to wash the emulsion in order to remove. If necessary, US Pat. No. 4,334,012 (Mi
gnot) As taught in the specification, emulsion washing can be combined with emulsion precipitation using ultrafiltration during precipitation. Or, Research Disclosure, Volume 102, 1
Item 10208, October 972; Research Disclosure by Hagemaier et al., Volume 131, March 1975, Item 13
122; Research Disclosure such as Bonnet, 135
Volume, July 1975, item 13577; Germany, such as Berg O
LS 2,436,461; and emulsion washing by diafiltration after deposition and before chemical sensitization, as described in Bolton U.S. Pat. No. 2,495,918, using a semipermeable membrane. Or Maley U.S. Pat. No. 3,782,953 and Noble U.S. Pat.
Emulsion washing can be carried out using an ion exchange resin as described in US Pat. No. 7,428. Washing by these techniques does not have the potential to remove selected peptizers, since ion removal is inherently limited to removing lower molecular weight solute ions.

A particularly preferred technique for chemical sensitization employs a combination of a sulfur-containing ripener in combination with a middle chalcogen (typically sulfur) and a noble metal (typically gold) chemical sensitizer. Possible sulfur-containing ripening agents include:
U.S. Pat. No. 3,271,157 (McBride);
U.S. Pat. No. 3,574,628 (Jones) and U.S. Pat. No. 3,737,313 (Rosencrants)
And the like. Preferred sulfur-containing ripening agents are described in U.S. Pat. No. 2,222,264 (Nietz), U.S. Pat. No. 2,448,534 (Lowe et al.) And U.S. Pat. No. 3,320,069 ( Illingsworth). A preferred class of middle chalcogen sensitizers is disclosed in US Pat. No. 4,749,6.
No. 46 (Herz et al.) And 4,810,626 (Herz et al.) Are tetra-substituted middle chalcogen ureas.

Preferred compounds include those of the formula:

Embedded image Wherein X is sulfur, selenium or tellurium;
₁ , R ₂ , R ₃ and R ₄ are each independently alkylene,
Represents a cycloalkylene, alkarylene, aralkylene or heterocyclic arylene group or, together with the attached nitrogen atom, R ₁ and R ₂ or R ₃ and R ₄
Can complete a 5- to 7-membered heterocycle; and A
_1, each of A _2, A ₃ and A ₄ may represent a hydrogen or a radical comprising an acidic independently group, A ₁ R ₁ ~
At least one of A ₄ R ₄ contains an acid group which is bonded to the urea nitrogen through a carbon chain of 1 to 6 carbon atoms). X
Is preferably sulfur, and A ₁ R _{1 to} A ₄ R ₄ are
Preferably, it is methyl or carboxymethyl (provided that the carboxy group may be in an acid form or a salt form). Specifically preferred tetra-substituted thiourea sensitizers are 1,3-
Dicarboxymethyl-1,3-dimethylthiourea.

Preferred gold sensitizers are disclosed in US Pat.
No. 9,485 (Deatone), which is incorporated herein by reference. These compounds include those represented by the formula:

Embedded image Wherein L is a mesoionic compound; X is an anion; and L ₁ is a Lewis acid donor.

In another preferred form of the invention, sulfur sensitizers (eg, of formula III) and / or gold sensitizers (eg, of formula IV), US Pat. 2- [N- (2-alkynyl) amino] -meta-method described in 378,426 and 4,451,557 (herein incorporated by reference).
It is considered that calcoazoles are used alone or in combination.

Preferred 2- [N- (2-alkynyl) amino] -meta-calcoazoles can be represented by the formula:

Embedded image Wherein X = O, S, Se; R ₁ = (Va) hydrogen or (Vb) alkyl or substituted alkyl or aryl or substituted aryl; and Y ₁ and Y ₂
Represents, independently, hydrogen, an alkyl group or an aromatic nucleus, or taken together to complete an aromatic or alicyclic ring having an atom selected from carbon, oxygen, selenium, and nitrogen. Represents the atomic group required for).

The compounds of formula (V) are generally effective when present during the heating step (finishing) which results in chemical sensitization (the Vb form gives a very high sensitivity gain and exceptional latent image stability). . Fragmentable electron-donating sensitizers provide higher sensitivity when used in place of, or in combination with, one, some, or all of the conventional chemical sensitizers. Holding the emulsion at elevated temperature for a period of time to achieve chemical sensitization is a common practice when chemically sensitizing emulsions that are peptized. If the sensitizer is stable enough to withstand high temperatures without fragmentation, the FED sensitizer may be added before heating. However, if a heating step is intended to achieve conventional chemical sensitization, it is preferred to add an FED sensitizer at the end of the heating step. One of the great advantages of the present invention is that oxidized cationic starch peptized emulsions can be efficiently prepared at lower temperatures using conventional sensitizers such as formulas (III), (IV) and (V) above. That is, it can be chemically sensitized well.

For example, chemical sensitization can be achieved at a temperature lower than the temperature required for sensitization of the corresponding gelatinized peptized emulsion. Heating at a temperature below 40 ° C. can achieve chemical sensitization of oxidized cationic starch peptized tabular grain emulsions. Thus, the FED sensitizer can be added before, during, or after the addition of other conventional chemical sensitizers.

US Pat. No. 5,747,235 to Farid et al.
And U.S. Patent Application Serial No. 08 / 739,911 to Lenhard et al. (October 1996).
Gould et al., US patent application Ser. No. 09/11.
No. 8,536, Farid et al., US patent application Ser.
No. 118,552 and U.S. patent application Ser. No. 09 / 118,714 to Adin et al.
(Filed on the 25th) (The content of the present invention is incorporated by reference. 9
Fragmentable electron-donating (FED) sensitizers of the type disclosed in US Pat.

These FED sensitizers satisfy the formula XY ′, where XY ′ constitutes the entire sensitizer or a part of the sensitizer —XY ′. Wherein X is an electron donating compound moiety, Y 'is a proton or leaving group Y, and (1) XY' has an oxidation potential between 0 and 1.4V; (2) The oxidized form of XY ′ undergoes a bond cleavage reaction to produce a radical X ^· and a released fragment Y ′, and, optionally, (3) a radical X ^· with an oxidation potential ≦ −0.7 V (I.e., equal to or less than -0.7 V). In a preferred embodiment of the invention, Y 'is a proton and the base B ^- is directly or indirectly covalently linked to X.

[0062] Although the criteria (1) and (2) are satisfied,
Compounds that do not conform to (3) can donate one electron and are referred to herein as fragmentable one-electron donating compounds. Compounds that meet all three criteria can donate two electrons and are referred to herein as fragmentable two-electron donating compounds. As used herein, the oxidation potential is reported as "V", which represents the potential relative to a saturated calomel reference electrode.

[0063] In a preferred embodiment of Y 'is the invention which is a Y, the following expression, thought to undergo X-Y is oxidized and fragmentation occurs when the further radical X ^· generate undergo oxidation in a preferred embodiment Shows the reaction.

Embedded image Electron emission from compound XY occurs when the oxidation potential of XY is 1.4 volts or less. X
^· Occurs electron emission from the free radical X ^· if it is -0.7 volts or more negative.

The structural features of XY are defined by the features of the two parts (ie, fragment X and fragment Y). While the structural characteristics of fragment X determine the oxidation potential of the XY molecule and the oxidation potential of radical X. ^, both the X and Y fragments
Affects the fragmentation rate of -Y. ⁺ .

[0065] In a preferred embodiment of Y 'is the invention which are H, the following formula, Compound X-H is oxidized and base B ^- undergo deprotonation to the radical X ^· which in a preferred embodiment undergoes further oxidation Shows reactions that may occur when formed.

Embedded image

Preferred X groups have the general formula:

Embedded image The symbol "R" (R without a subscript) is used in all structural formulas herein to represent a hydrogen atom or an unsubstituted or substituted alkyl group.

In the structural formula (IV), m: 0, 1; Z: O, S, Se, Te; Ar: an aryl group (for example, phenyl, naphthyl, phenanthryl, anthryl); or a heterocyclic group (for example,
Pyridine, indole, benzimidazole, thiazole, benzothiazole, thiadiazole, etc.); R ₁ : R, carboxyl, amide, sulfonamide, halogen, NR ₂ , (OH) _n , (OR ′) _n , or (S)
R) _n; R ': alkyl or substituted _{alkyl; n: 1~3; R 2:} R, Ar'; R 3: R, Ar '; R 2 and R _3, 5-membered to 8-membered together R ₂ and Ar can combine to form a 5- to 8-membered ring; R ₃ and Ar can combine to form a 5- to 8-membered ring; Ar ′ is phenyl, substituted An aryl group such as phenyl or a heterocyclic group (for example, pyridine, benzothiazole, etc.); R: a hydrogen atom or an unsubstituted or substituted alkyl group.

In structural formula (VII), Ar is an aryl group (eg, phenyl, naphthyl, phenanthryl);
Or a heterocyclic group (eg, pyridine, benzothiazole, etc.); R ₄ has a Hammett sigma value of −1 to +1 and preferably −0.7 to +0.7, for example, R, O
R, SR, halogen, CHO, C (O) R, COOR,
CONR ₂ , SO ₃ R, SO ₂ NR ₂ , SO ₂ R, SO
R ₅ is a substituent such as R, C (S) R, etc .; R ₅ is R, Ar ′; R ₆ and R ₇ : R, Ar ′; R ₅ and Ar are combined to form a 5- to 8-membered ring R ₆ and Ar can combine to form a 5- to 8-membered ring (where R ₆ can be a heteroatom); R ₅ and R ₆ combine to form a 5-membered ring.
R ₆ and R ₇ can be joined to form a 5- to 8-membered ring;
Ar 'is an aryl group such as phenyl or substituted phenyl, or a heterocyclic group; R is a hydrogen atom or an unsubstituted or substituted alkyl group. For a discussion of Hammett sigma values, see Hansch and RW Taft, Ch.
em. Rev. 91, (1991), p. 165, which is incorporated herein by reference.

In the structural formula (VIII), W: O, S, Se; Ar: an aryl group (for example, phenyl, naphthyl, phenanthryl, anthryl); or a heterocyclic group (for example,
R ₈ : R, carboxyl, NR ₂ , (OR) _n , or (SR) _n (n = 1 to 3); R ₉ and R ₁₀ : R, Ar ′; R ₉ and Ar can combine to form a 5- to 8-membered ring;
Ar ′ is an aryl group such as phenyl or substituted phenyl, or a heterocyclic group; R: a hydrogen atom or an unsubstituted or substituted alkyl group.

In the structural formula (IX), “ring” represents a substituted or unsubstituted 5-, 6- or 7-membered unsaturated ring, preferably a heterocyclic ring.

The following represents examples of X in general structural formula VI:

Embedded imageIn the structure of the present specification, -OR (NR_Two )
Is -OR or -NR _Two That any of
Show that you can.

The following are specific examples of X in general structure VII:

Embedded image R ₁₁ and R ₁₂ are H, alkyl, alkoxy, alkylthio, halo, carbamoyl, carboxyl, amide, formyl, sulfonyl, sulfonamide, nitrile.

[0073]

Embedded image Z ₁ is a covalent bond, S, O, Se, NR, CR ₂ , CR
= CR, or CH ₂ CH _2.

[0074]

Embedded image Z ₂ is S, O, Se, NR, CR ₂ , CR = CR, R ₁₃ is alkyl, substituted alkyl or aryl, and R ₁₄ is H, alkyl, substituted alkyl or aryl.

The following are specific examples of X in general structure VIII:

Embedded image

The following are specific examples of X in general structure IX:

Embedded image Z ₃ is O, S, Se, NR, and R ₁₅ is R, O
R and NR ₂ , and R ₁₆ is alkyl or substituted alkyl.

Preferred Y 'groups are: (1) X', where X 'is an X group as defined in structural formulas VI to IX and is the same as or different from the X group to which it is attached. You may. (2)

Embedded image (3)

Embedded image Wherein M is Si, Sn or Ge, and R ′ is alkyl or substituted alkyl. (4)

Embedded image Wherein Ar ″ is aryl or substituted aryl. (5)

Embedded image

In a preferred embodiment of the present invention, Y 'is-
H, -COO ^- or -Si (R ') ₃ or -X'. Particularly preferred Y 'groups, -H, -COO ^- or -
Si (R ′) ₃ . In a preferred embodiment of the invention in which Y 'is a proton, the base B ^- is covalently linked directly or indirectly to X. The base preferably has a pKa of 1 to
8, preferably a conjugate base of 2 to 7 acids. Examples of pKa values are, for example, Dissociation Constants of Organic
Bases in Aqueous Solution, DDPeril (Butterworth,
London, 1965); CRC Handbook of Chemistry and Phys
ics, 77th, DRLide (CRC Press, Boca Raton, F1, 19
96).

Examples of useful bases are shown in Table I.

[Table 1]

Preferably, the base B ^- is a carboxylate, sulfate or amine oxide.

In some embodiments of the present invention, the fragmentable electron donating sensitizer is a light absorbing group Z directly or indirectly bonded to X, a silver halide adsorbing group directly or indirectly bonded to X. It has a chromophore-forming group Q bonded to A or X. Such a fragmentable electron donating sensitizer is preferably of the formula:

[0082]

Embedded image

Wherein Z is a light absorbing group, k is 1 or 2, and A is at least one of N, S, P, Se or Te which promotes adsorption to silver halide. L is a linking group having at least one C, N, S or O atom, and Q is an amidinium ion when bonded to XY ′
It represents an atomic group necessary for forming a chromophore including a carboxyl ion or amphoteric amide chromophore system.

Z is a light absorbing group, for example, cyanine dyes, complex cyanine dyes, merocyanine dyes, complex merocyanine dyes, amphoteric cyanine dyes, styryl dyes, oxonol dyes, hemioxonol dyes , And hemicyanine dyes.

Preferred Z groups are derived from the following dyes:

Embedded image

[0086]

Embedded image

The linking group L may be substituted at one (or more) heteroatom, at one (or more) aromatic or heterocyclic ring, at one (or more) atom of the polymethine chain. By the way, it can bind to a dye.
For simplicity and because of the multiple possible attachment sites, the attachment of the L group is not specifically indicated in the general structural formula.

The silver halide adsorptive group A is preferably a silver ion ligand moiety or a cationic surfactant moiety. In a preferred embodiment, A is i) sulfuric acids and their Se and Te analogs, ii) nitric acids, iii) thioethers and their Se and Te analogs, iv) phosphines, v) thionamides, selenamides , And telluramides, and vi) carbon acids.

Specific examples of group A are:

Embedded image

The point of attachment of the linking group L to the silver halide adsorptive group A depends on the structure of the adsorptive group, and one (or more) heteroatoms can be replaced by one (or more) heteroatoms.
Can be an aromatic or heterocyclic ring.

The linking group represented by L, which covalently bonds the light absorbing group to the fragmentable electron donating group XY, is preferably an organic group having at least one of C, N, S, or O atoms. A linking group. Also,
The linking group is not completely aromatic or unsaturated, resulting in π
It is preferred that a binding system cannot exist between the Z and XY moieties. Preferred examples of the linkage group include, an alkylene group, an arylene group, -O -, - S -, - C = O, -SO 2 -, - NH
-, -P = O, and -N =. Each of these binding components may be optionally substituted and may be used alone or in combination.

Preferred examples of combinations of these groups include
It is:

Embedded image

The length of the linking group can be limited to one atom or even longer, for example up to 30 atoms in length. Preferred lengths are from 2 to 20 atoms, most preferably 3 to 10 atoms.

Some preferred examples of L can be represented by the following general formula:

Embedded image

Q represents an atomic group necessary for forming a chromophore containing an amidinium ion, a carboxyl ion or an amphoteric amide chromophore system when bonded to XY ′. Preferably, the chromophore system is from The Cyanin of FM Hamer.
e Dyes and Related Compounds (Interscience Publish
ers, New York, 1964), cyanine,
It is a type commonly found in complex cyanine, hemicyanine, merocyanine, and complex merocyanine dyes.

Specific examples of the Q group are:

Embedded image

Particularly preferred are Q groups of the formula:

Embedded image

X ₂ is O, S, N, or C (OR ₁₉ ) ₂ , wherein R ₁₉ is a substituted or unsubstituted alkyl;
Each R ₁₇ is independently a hydrogen atom, a halogen atom, a substituted or unsubstituted alkyl group, or a substituted or unsubstituted aryl group, a is an integer of 1 to 4, and R ₁₈ is a substituted or unsubstituted Or a substituted or unsubstituted aryl.

Specific examples of fragmentable electron donating sensitizers include the following:

Embedded image

[0100]

Embedded image

[0101]

Embedded image

[0102]

Embedded image

[0103]

Embedded image

In a preferred embodiment of the invention, one or more spectral sensitizing dyes are adsorbed on the surface of high bromide {111} tabular grains. In one particular preferred embodiment of the present invention, F
ED sensitizers include the photon trapping ability of spectral sensitizing dyes and F
Dye chromophores that provide the additional electron-injection capability of the ED sensitizer are included. This allows the dye chromophore with the FED sensitizer to be replaced with a conventional spectral sensitizing dye. Conventional and conventional amounts of spectral sensitizing dyes are also contemplated for use with the FED sensitizer. When used in combination with one or more conventional spectral sensitizing dyes, an FED sensitizer having a chromophore can be used to absorb light in the same spectral range as the conventional spectral sensitizing dye or in a different spectral range. You can choose. As mentioned above, an overview of spectral sensitizing dyes can be found in Research Disclosure, Item 3895, supra.
7, V.I. "Spectral sensitization and desensitization", A.I. "Sensitizing dyes". Generally, spectral sensitizing dyes are adsorbed on the grain surface after chemical sensitization, but the advantage of adding the dye to high bromide {111} tabular grains before or during chemical sensitization has long been recognized. And described in U.S. Pat. No. 4,439,520 to Kofron et al. FED
The sensitizer can be added to the emulsion before, during, or after spectral sensitization.

The FED sensitizer can be incorporated into the emulsion by the usual techniques for dispersing spectral sensitizing dyes. That is, the FED sensitizer is directly added to the emulsion or a solvent such as water, methanol, or ethanol.
Alternatively, it can be added after being dissolved in a mixture of these solvents (for example, an aqueous alcohol solution). Also, FED
The sensitizer can also be added from a solution containing a base and / or a surfactant. The FED sensitizer can also be incorporated into the aqueous slurry or peptizer dispersion.

A FED sensitizer was added to the emulsion of the present invention,
It can be brought into uniform contact with high bromide {111} tabular grains. In a preferred form, the FED sensitizer is adsorbed on the grain surface. The concentration of the FED sensitizer in the emulsions of the present invention can range from at least 1.times.10.sup.- ⁸ mole per silver mole to 0.1 mole per maximum silver mole.
The preferred concentration range is from 5 × 10 ^-7 mole / silver mole to ^0.1 mole.
It is in the range of 0.05 mole / silver mole. It is also observed that lower concentrations of a more active form of the FED sensitizer (eg, those that can inject more electrons per molecule) achieve the same beneficial effects as the less active form. It is preferred that the FED sensitizer be added to the emulsion of the present invention before, during, and after the addition of other conventionally introduced sensitizers, but the addition of the FED sensitizer may be added after the emulsion is coated. Even when it was delayed, an increase in emulsion sensitivity was observed.

In addition to the high bromide {111} tabular grains, the cationic starch peptizer, and the FED sensitizer (usually combined with a chemical and / or spectral sensitizer), the emulsions of the present invention are preferably And one or more conventional antifoggants and stabilizers. For an overview of antifoggants and stabilizers, see Research Disclosure, Item 3895.
7, VII. It is described in "Anti-fogging agents and stabilizers".

The use of FED sensitizers in combination with cationic starch peptizers, even when conventional antifoggants and stabilizers are present in the emulsion, are less than when replaced with gelatino peptizers. It was found to produce a minimum concentration that was a minute higher. This minimum concentration increase may be reduced by treating the emulsion with an oxidizing agent during or after grain precipitation, or
It was found that it could be removed. Preferred oxidizing agents are those whose reduced form has little or no effect on the properties of the emulsion into which they are introduced.

The strong oxidizing agents mentioned above useful for the oxidation of cationic starch, such as hypochlorite (ClO ⁻ ) or periodate (IO ₄ ⁻ ), are particularly conceivable. Particularly preferred oxidizing agents are halogens, such as bromine (Br ₂ )
Or iodine (I ₂ ). When using a bromine or iodine as an oxidizing agent, bromine or iodine, Br ^- is reduced to ^- or I. These halide ions can remain in the dispersion medium of the emulsion with other excess halide ions or can be incorporated into the grains without adversely affecting photographic performance. Any concentration of oxidizing agent that is effective in reducing the minimum concentration can be used. The concentration of oxidizing agent added to the emulsion should be at least 1 per mole of silver.
× 10 ^-6 moles are possible. Since very low concentrations of Ag ° are responsible for the minimum density increase, there is no useful role by using oxidizing agents in concentrations greater than 0.1 mole per silver mole. A particularly preferred concentration range of the oxidizing agent is 1 × 10 ^−4.
The range is from mol / silver to 1.times.10.sup.- ² mol / silver mol. The silver basis is the total silver at the end of precipitation of the high bromide {111} tabular grain emulsion, whether the oxidizing agent is added during precipitation or after precipitation.

At least one dye image providing coupler and at least one electron transfer agent releasing (ETARC) coupler are present in the dye image forming layer unit. The term "coupler" is an art-recognized meaning that refers to a compound that selectively reacts with a primary amine color developing agent that has been oxidized (used as the opposite of the unoxidized) during development of the photographic element. Used. Dye image forming couplers
Complete the dye chromophore during coupling. ETARC
Releases an electron transfer agent. The term `` electron transfer agent '' or
"ETA" refers to silver halide Ag ⁺ ion of silver Ag °.
To provide electrons when oxidized, and then
A silver halide developing agent that is regenerated to its original non-oxidized state by entering a redox reaction with a primary amine color developing agent is used in its art-recognized meaning. In the redox reaction, the color developing agent is oxidized,
Activated for coupling. Since the ETA circulates during the reaction between the silver halide grains and the color developing agent during development, it does not disappear during use, and a very small amount of ETA is very effective.

In a general form, ETARC satisfies the formula: (X) COUP- (L) _n -ETA where COUP is an oxidized developing agent (preferably an oxidized primary amine color former). Is a coupler moiety capable of releasing-(L _n ) -ETA upon reaction with (a developing agent), n is 0, 1, or 2, and L is two or more L
When a moiety is present, it is a divalent linking group which may be the same or different, and ETA is an electron transfer agent, preferably a 1-aryl-3-pyrazolidinone derivative, -(L) _n-
When unreacted, the active electron transfer agent is unblocked and promotes development under the processing conditions used to obtain the desired dye image.

The electron transfer agent pyrazolidinone moiety is generally described in US Pat. Nos. 4,209,580 and 4,463.
Nos. 081, 4,471, 045 and 4,48
It is derived from compounds of the type described in U.S. Pat. No. 1,287 and JP-A-62-123172. Such compounds comprise a 3-pyrazolidinone structure having an unsubstituted or substituted aryl group at the 1-position. Preferably, those compounds have one or more alkyl groups at the 4- or 5-position of the pyrazolidinone ring.

Preferred electron transfer agents suitable for use in the present invention are represented by tautomeric structures XI and XII:

Embedded image Wherein R ¹ is hydrogen, and R ² and R ³ are independently hydrogen, substituted or unsubstituted alkyl having 1 to 8 carbon atoms (eg, hydroxyalkyl), carbamoyl, or substituted or An unsubstituted aryl group having 6 to 10 carbon atoms, wherein R ⁴ and R ⁵ are each independently hydrogen, substituted or unsubstituted alkyl having 1 to 8 carbon atoms, or substituted or unsubstituted 10 to 10 aryl groups, and R ⁶ is
It can be in the ortho, meta or para position of the benzene ring, and is halogen, substituted or unsubstituted.
Alkyl of 8 to 8 or substituted or unsubstituted 1 to 8 carbon atoms
Alkoxy or sulfonamides and m
Is 2 or more, the R ⁶ substituents may be different or the same, or may together form a carbocyclic or heterocyclic ring containing a benzene ring or an alkylenedioxy ring, and , M is 0 or 1-3).

When the R ² and R ³ groups are alkyl,
They preferably have 1 to 3 carbon atoms. If R ² and R ³ are aryl, they are preferably phenyl. Preferably, R ⁴ and R ⁵ are hydrogen. If R ⁶ is a sulfonamide, it can be, for example, methanesulfonamide, ethanesulfonamide or toluenesulfonamide.

The preferred amount of ETARC in the image forming layer unit is from 1.0 × 10 ^{-3 to} 1.0 per mol of silver.
Is a mole. A more preferred amount of ETARC is from 2.0 × 10 ^{-2 to} 5 × 10 ^-1 mole, and most preferably from 5 × 10 ^{-2 to} 4.0 × 10 ^-1 mole per silver mole.
The ETARC is disposed in the silver halide emulsion layer of the image forming layer unit or a layer adjacent to the layer (preferably the former).

It is suitable for the use of the present invention, and
Structural formulas XI and XII (where R ¹ , R^Four And R^Five water
Particularly preferred electron transfer agents that fall under
I.

[0117]

[Table 2]

ETA is inactive until released
A is attached to the coupler moiety at the position giving A. In the tautomeric form of structure XI, ETA has the coupler moiety COUP
Alternatively, the point at which R ¹ binds to COUP- (L) _n- is the point at which R ¹ binds after release. Such a bond is E
Since the TA moieties are inert, there is no potential for unwanted reactions during storage of the photographic element. However, the oxidized developing agent formed imagewise as a result of silver halide development reacts with the COUP moiety to cleave the bond between COUP and L. Thereafter, following the reaction, the linking group L and the blocked ET were added without the need for an oxidized developing agent.
The bond to A is broken, releasing the active ETA moiety.

The-(L)-moiety has 2
Including valence groups. In general, such groups can be:

Embedded image

In the above formula, each R ⁷ is independently hydrogen, alkyl having 1 to 12 carbons or aryl having 6 to 12 carbons, and R ⁸ is alkyl having 1 to 20 carbons. , Preferably lower alkyl having 1 to 4 carbons or aryl having 6 to 20 carbons, preferably 6 to 1 carbons
0 is aryl, X is, -NO _2, -CN, sulfone, halogen or alkoxycarbonyl and p is 0 or 1.

The linking group-(L) _n- (present in the compounds described herein) is used to achieve a fast silver halide development effect in a short time from a controlled coupler moiety. Provides release of the ETA pyrazolidinone moiety.

Various types of known linking groups can be used. These include quinone methide linking groups, for example,
U.S. Pat. No. 4,409,323, pyrazolone methide linking groups such as those described in U.S. Pat. No. 4,421,845, and intramolecular nucleophilicity. Substituted linking groups, for example, US Pat.
248,962 and EP 0 193 338
No. 9 and No. 0255085.

Typically useful linking groups include the following:

Embedded image

[0124]

Embedded image Where A is

Embedded image Wherein q is 1-4 and R ⁸ and p are as defined above.

The COUP moiety (where the electron transfer agent pyrazolidinone moiety is released) can be selected from the conventional COUP moiety of the image dye-forming coupler,
The COPU moiety found in couplers that do not produce image dyes can be selected because of the lower required amount of For example, the COUP moiety can be selected to yield a colorless product upon reaction with the oxidized color developing agent. Alternatively, the COUP moiety can be selected from unstable dyes and dyes that decompose into colorless products. Further, the COUP portion can be selected to provide a dye that is washed away from the photographic recording element during processing.

The COUP moiety may be unballasted or ballasted with an oil-soluble or fatty tail group. The COUP moiety can be a monomer, or can form part of a dimer, oligomer or polymer coupler, where one or more ETA moieties or-(L) _n -ETA moieties is an ETA releasing compound. Can have inside.

Many of the various forms of COUP moieties are known, and most COUP moieties are synthesized to facilitate the formation of image dyes having their primary absorption in the red, green or blue regions of the visible spectrum. .

For example, couplers which form cyan dyes upon reaction with oxidized color developing agents are disclosed in US Pat.
772, 162, 2,895,826, 3,0
02,836, 3,034,892, 2,47
4,293, 2,423,730, 2,36
7,531, 3,041,236, 4,33
3,999, and "Farbkuppler-eine Literat"
ure Ubersicht, published by Agfa Mitteilungen, Chapter III
Vol., Pp. 156-175 (1961). In the following coupler moieties, the unfinished bond indicates a coupling site to which the-(L) _n- ETA moiety can bind.

Preferably, such a cyan dye-forming coupler is a phenol that forms a cyan dye upon reaction with an oxidized color developing agent at the coupling site (ie, the carbon atom at the 4-position of phenol or naphthol). And naphthols. Preferred ETARC COUP moieties of the type found in cyan dye-forming couplers are:

[0130]

Embedded image

Wherein R ⁹ and R ¹⁰ can represent a ballast group or a substituted or unsubstituted alkyl or aryl group, and R ¹¹ is one or more halogens (eg, chloro, fluoro), Represents alkyl having 1 to 4 carbons or alkoxy having 1 to 4 carbons.

Other couplers which form magenta dyes upon reaction with oxidized color developing agents are disclosed in US Pat.
00,788, 2,369,489, 2,34
3,703, 2,311,082, 3,82
4,250, 3,615,502 and 4,07
Nos. 6,533, 3,152,896, 3,51
9,429, 3,062,653, 2,90
8,573, 4,540,654 and "Farbkuppler-eine Literature Ubersicht", Agfa M
It is described in typical patent specifications and publications such as Itteilungen, Vol. III, pp. 126-156 (1961).

Preferably, such magenta dye-forming couplers have a coupling moiety (ie, a pyrazolone 4
Pyrazolones and pyrazolotriazoles which form a magenta dye upon reaction with an oxidized color developing agent. Preferred ETARC COUP moieties of the type found in magenta dye-forming couplers are:

[0134]

Embedded image

In the above formula, R ⁹ and R ¹⁰ are the same as defined above. R ^{10 in the} pyrazolone structure is generally phenyl or substituted phenyl, for example, 2,4,6-trihalophenyl, and in the case of a pyrazolotriazole structure, R ¹⁰
Is typically alkyl or aryl.

Couplers which form yellow dyes upon reaction with oxidized color developing agents are disclosed in US Pat.
5,057, 2,407,210, 2,29
8,443, 3,048,194, 3,44
No. 7,928 and "Farbkuppler-eine Literat"
ure Ubersicht, published by Agfa Mitteilungen, Chapter III
Volume, pp. 112-126 (1961).

Preferably, such yellow dye-forming couplers are acylacetamides, such as benzoylacetanilides and pivalylacetanilides. These couplers react with the oxidized color developing agent at the coupling site (ie, the active methylene carbon atom). Preferred ETARC COUP moieties of the type found in yellow dye-forming couplers are:

[0138]

Embedded image

In the above formula, R ⁹ and R ¹⁰ are the same as defined above, and include hydrogen, alkoxy, alkoxycarbonyl, alkanesulfonyl, arenesulfonyl, aryloxycarbonyl, carbonamido, carbamoyl,
It can also be a sulfonamide, or a sulfamoyl, and R ¹¹ is hydrogen or one or more halogen, lower alkyl (eg, methyl, ethyl), lower alkoxy (eg, methoxy, ethoxy), or ballast (eg, An alkoxy) group having 16 to 20 carbon atoms.

Couplers which form colorless products upon reaction with oxidized color developing agents are described in GB-A 86
No. 1,138, and U.S. Pat. Nos. 3,632,345, 3,928,041, and 3,958,993.
And 3,961,959. Preferably, such couplers are cyclic carbonyl-containing compounds that form a colorless product upon reaction with the oxidized developing agent and have an L group attached to the carbon atom alpha to the carbonyl group.

Preferred ETARC C of the type found in couplers which form colorless compounds upon coupling
The OUP part is:

[0142]

Embedded image (Wherein R ⁹ is as defined above, and r is 1 or 2).

Depending on the particular coupler moiety, the particular color developing agent and the type of processing, the reaction product of the coupler moiety with the oxidized color developing agent is (1) colored and non-diffusible (2) is colored and diffusible (can be removed from the photographic element during processing or moved from the coupling position), or (3) It is colorless and diffuse or non-diffusible (in this case,
(Which does not contribute to the image dye). If it is desired that such reaction products be removable during processing, the radicals R ⁹ and R ¹⁰ of the above structure are further hydrogen when attached to an NH group or to a ring carbon atom. be able to.

Particularly preferred is COUP- (L) _n -ET
The structure of A is as follows:

Embedded image

[0145]

Embedded image

[0146]

Embedded image

[0147]

Embedded image

[0148]

Embedded image

[0149]

Embedded image

[0150]

Embedded image

[0151]

Embedded image

Another specific example of an ETARC coupler is Mich
No. 4,859,578 to Platt.
Et al., U.S. Pat. No. 4,912,025 and Saito
No. 5,605,786 (the contents of which are incorporated herein by reference).

Although ETARC can itself produce image dyes upon coupling, in many cases ETA
The concentration of RC, in the absence of other image dye sources, is lower than can provide the desired dye density level.
It is therefore conceivable to introduce the conventional image dye-forming coupler of the dye image-forming phase unit in addition to the ETARC. Image dye-forming couplers generally form cyan, magenta or yellow dyes upon coupling, and are also suitable COUPs for ETARC additives which form cyan, magenta or yellow dyes upon coupling.
It can take the form of conventional cyan, magenta or yellow image dye-forming couplers, as disclosed in the above cited patent documents showing parts. Conventional image dye-forming couplers and additional forms of this are described in Research Disclosure, Item 38957, X.C. "Dye image forming agents and improving agents", B.I. It is described in "Image dye-forming coupler". Additionally, other conventional dye image improvers, such as Research Disclosure, Item 38957, X.C. C. Those described in "Image Dye Modifiers" are not required, but can be used in combination with ETARC couplers, if necessary.

Element I embodies a photographic element according to the present invention having a construction limited to essential features. [Element I] Emulsion layer unit support

As described above, this emulsion layer unit
Cationic starch peptizer, FED sensitizer, ETAR
C and a single high bromide {111} tabular grain emulsion containing the dye image providing coupler described above. Cationic starch peptizer added at the time of emulsion precipitation,
It forms a very small portion of the total vehicle of the emulsion layer. Additional cationic starch of the type used as a deflocculant can also be added to act as a binder. However, it is preferred to use other conventional hydrophilic colloid binders, especially gelatin and gelatin derivatives, as the binder. U.S. Pat. No. 5,726,008 to Maskasky, which is incorporated herein by reference, contains a gelatin that is cold cured containing at least 45% and at least 20% water dispersible starch. The vehicle is described. In addition to peptizers and binders, the vehicle reacts with the hardener to enhance its physical integrity as a coating and other additives, such as latex, are usually introduced. Research Disclosure, Item 38957, II. "Vehicles, vehicle extenders, vehicle-like additives and vehicle-related additives" and IX. Conventional components that can be included in the vehicle of the emulsion layer summarized in "Film physical property improving additives",
For example, coating aids (such as surfactants), plasticizers and lubricants,
Matting agents, as well as antistatic agents are common ingredients, with the traditional choice being Research Disclosure, Item 3895
7, IX. It is specifically described in “Coating film property improving additive”.

The support can take any of the forms of conventional photographic element supports. Generally, the support is a transparent (eg, a transparent film support) or a white reflective support (eg, a photographic paper support). List of photographic element supports, research disclosures, items
38957, XV. It is described in "Support". In primary applications, higher image speeds are particularly sought for camera speed or "photographic" films with transparent supports. If the film has a transparent support and produces a negative dye image, the image on the processed film is usually mostly used as an exposure master to create a visible image of the print element (eg, color paper). .

When the film has a transparent support and produces a positive dye image, the image is generally viewed directly by a projector. When retrieving by scanning the dye image of the film, the increased sensitivity of the photographic film can be realized by using a reflective support. It is particularly contemplated to use a support that is specular, which enhances imaging sensitivity during imagewise exposure, but is converted to a transparent form during processing to facilitate normal use of the photographic film. US Patent Application No. 0 to Maskasky et al.
No. 9 / 118,172 (filed July 17, 1998, titled "DyeImage Forming Photographic Element an"
d Processing to Produce A Viewable Image discloses the use of a transparent film support having a silver mirror coating that can be removed during photographic processing.

In fact, photographic element structures have additional general features. Elements IIa and IIb illustrate conventional photographic element constructions useful for dye producing black and white imaging single color dye images. [Element IIa] Protective overcoat emulsion layer Unit antihalation layer Support magnetic image forming layer [Element IIb] Protective overcoat emulsion layer unit support pelloid layer magnetic image forming layer

The support can take any of the above-mentioned forms, that is, a usual form. In Element IIa, an antihalation layer is inserted between the support and the emulsion layer unit. If the support is transparent, the antihalation layer can be moved to the back side of the support, as shown in element IIb, and can be a pelloid layer. The antihalation layer and the pelloid layer each contain one or more dyes that can be rendered colorless (ie, decolorized) during photographic processing. Dyes of this type are described in Research Disclosure, Item 38957, VII. "Absorbing and scattering materials", B.A. "Absorbing material" and C.I. It is described in "Color Removal".

A protective overcoat is provided to protect the emulsion layer units. The antihalation layer, the pelloid layer, and the protective overcoat each have a vehicle. The vehicle also contains a selection of binders, hardeners, and the remaining components of the emulsion layers described above. Surface layers, pelloid layers and protective overcoats are the most preferred places for surface modifying additives such as lubricants, matting agents, and antistatic agents. Also, the protective overcoat is
Also preferred for locations where UV stabilizers are included, for an overview, Research Disclosure, Volume 370, February 1995, Item
37038, X.A. It is described in "UV stabilizers".

The magnetic image-forming layer is an optional layer, but is preferred if it has the purpose of storing information about the photographic elements used for exposure or subsequent processing.
The magnetic imaging layer is described in Research Disclosure, Item 38957, XIV. "Easy Scan Configuration" and James
U.S. Patent Nos. 5,254,441 and 5,254,
No. 449.

The emulsion layer unit can consist of a single emulsion layer, but the emulsion layer unit can be a blend of emulsions of the invention or a mixture of one or more emulsions of the invention and one or more conventional emulsions. It is also recognized to have a formulation. It is also common practice to divide the emulsion layer unit into two or three separate emulsion layers with different image forming sensitivities.

By forming an emulsion layer unit consisting of a high-speed emulsion layer and a low-speed emulsion layer (the high-speed emulsion layer is arranged so as to receive the exposure radiation first, that is, far from the support). Higher sensitivity can be realized than when a high-speed emulsion and a low-speed emulsion are combined in a single layer. Arranging the low sensitivity emulsion layer to receive the exposure radiation first provides higher contrast than if the high speed emulsion and the low speed emulsion were combined and coated in a single layer. If three separate emulsion layers are coated, a third layer is inserted between the high and low speed emulsions and is selected to provide an intermediate speed.
The function of the third emulsion layer is to enable a longer exposure latitude. Chang and Friday U.S. Patent Nos. 5,314,793 and 5,360,703, which are incorporated herein by reference.
Describes an emulsion layer unit having three emulsion layers of different sensitivities to provide useful exposure latitudes in excess of 1.0 Log E.

When one or more other emulsions are combined with an emulsion satisfying the grain, peptizer and coupler requirements of the present invention (hereinafter referred to as "the emulsion of the present invention"), Research Disclosure, Item 38957, I. "Emulsion grains and their precipitation", further describing emulsion combinations, paragraph E. It can be selected from the usual negative-working radiation-sensitive silver halide emulsions described in "Formulations, Layers and Performance Categories." When one or more conventional emulsions are used in combination with one or more emulsions of the present invention, it is preferable to select the emulsion of the present invention with high sensitivity.
This is because the emulsion of the present invention exhibits unexpectedly high sensitivity. If a conventional emulsion is present in the emulsion layer unit along with the emulsion of the present invention, it may also be high (50% silver based).
(More than mol%) bromide emulsions and are often tabular grains.

The photographic elements of the present invention can rely on developed silver and image dyes to produce a visible image. It is specifically contemplated to apply the invention to dye producing black and white imaging.

In primary applications, one might consider relying entirely on image dyes to create a visible image. Elements I, IIa and IIb can be used to produce positive dye images. It is preferable to generate a positive dye image by color reversal processing. Color reversal processing is a dye-free development of the imagewise exposed element, followed by a second dye-image development step of developing residual silver halide not developed in the first development step. Possible color reversal processing and element configuration for photographic elements intended for color reversal processing are described in Research Disclosure, Item 38957, XIII. B. “Configuration applicable only to color positive” "Color reversal" and X
VIII. "Chemical development system", B.A. "Color, Specific Processing Systems", summarized in paragraph (1).

In a particularly preferred form, the photographic elements of this invention form negative dye images. Color negative processing and element composition especially considered for photographic elements intended for color reversal processing are described in Research Disclosure, Item 3895.
7, XII. "Configuration applicable only to color negative" and XVIII. "Chemical development system", B.A. "Color, Specific Processing Systems", summarized in paragraphs (3)-(10).

For all forms of processing, development occurs in the presence of a color developing agent. The color developing agent is a reducing agent, which can react with a conventional image dye-forming coupler by oxidation to form a dye. Generally, color developing agents include:
Contains a primary amine group attached to the phenyl ring. Preferred color developing agents are p-phenylenediamines, especially N, N-dialkyl-p-phenylenediamines. Details of the color developing agent are described in Research Disclosure, Item 38957, A.I. "Developers" and James
The Theory of the Photographic Process, Macmillan
Publishing Co. New York, Chapter 12, "Principles and Chemistry of Color Photography", III. It is described in "Color Developer".

The following structure provides sufficient image information to enable reproduction of the image and color of a photographic subject on a full color recording photographic element according to the present invention (ie, on a color recording photographic element itself or on another color recording photographic element). (Recordable element).

[Color Recording Element] Protective overcoat Third color recording layer unit Second intermediate layer Second color recording layer unit First intermediate layer First color recording layer unit Undercoat Transparent film support Peroid magnetic image forming layer

The support and the first, second and third color recording layer units are essential components in all color recording applications. The remaining components are optional or required only for specific applications. The protective overcoat, the transparent film support, the pelloid, and the magnetic imaging layer have already been described and will not require detailed description.

Each recording layer unit is comprised of the above-mentioned components, except for the following, emulsion layer units selected to respond to one of the blue, green and red portions of the visible spectrum. It is. At least one emulsion according to the invention is present in at least one, preferably in each recording layer unit. Any of the following layer unit orders is possible.

SQ-1 | B | G | R | S |, SQ-2 | B | R | G | S |, SQ-3 | G | R | B | S |, SQ-4 | R | G | B | S |, SQ-5 | G | B | R | S | and SQ-6 | R | B | G | S | where B is a blue recording layer unit, G is a green recording layer unit, R Is a red recording layer unit, and S is a transparent film support.

Each of the blue, green and red recording layer units preferably contains a dye image providing compound which produces a dye image of a different hue. If the dye image of the color recording element is intended for direct viewing (e.g., when creating a color slide image or when used as an exposure master for a color print element), the blue, green and red recording layer units may include yellow, It is configured to generate magenta and cyan dye images, respectively. Preferably, the blue recording layer unit contains a yellow dye-forming coupler, the green recording layer unit contains a magenta dye-forming coupler, and the red recording layer unit contains a cyan dye-forming coupler. In addition, conventional image dye improvers can be incorporated into the recording layer unit and such improvers are described in Research Disclosure, Item 38957, X.C. "Dye image forming agents and modifiers", C.I. "Image dye improver" and D.I. "Hue improver /
Stabilizers ".

[0175] The first and second intermediate layers and the undercoat can have the same vehicle as described above. The undercoat can be replaced with an antihalation layer as described above, and the pelloid can be omitted. Preferably, the first and second intermediate layers contain an oxidized developing agent scavenger to prevent oxidized color developing agent from migrating from one layer unit to an adjacent layer unit. Common oxidized developer scavengers include:
Ballasted (ie, immobilized) hydroquinone and aminophenol developing agents are included.

When trying to read image information from a photographic element of the present invention by reflection and / or transmission scanning,
Color reversal films can produce images that are pleasing to the eye, or many color negative films can form a negative image that can be transmitted and exposed to provide a visually pleasing positive image. But no longer important. It is only necessary that the first, second and third layer units have a recoverable record of the subject, including color, when exposed and processed. A false color record is just as useful for this purpose as the original color record, and indeed, to produce three retrievable color records without actually producing three dye images. Is possible. Color negative films intended only for scanning,
No masking coupler is required. Bohan U.S. Pat. No. 5,038,434 discloses a color negative film containing a masking coupler that is equally suitable for image recovery by printing or scanning. Color recording photographic elements specially adapted for scanning and retrieving image information are described in Research Disclosure, Item 38957, XIV. "Easy Scan Configuration", described in paragraph (1). In addition, U.S. Pat. No. 5,300,300 to Sutton et al. Refers to the following detailed disclosure of a recently issued patent specification of a color recording photographic element configuration that is particularly suited for scanned image retrieval: 4
13 and 5,334,469; Sutton U.S. Patents 5,314,794 and 5,389,506;
U.S. Pat. No. 5,389,503 to Evans et al., U.S. Pat. No. 5,391,443 to Simons et al., U.S. Pat. No. 5,418,119 to Simons, and U.S. Pat. No. 5,420,003 to Gasper et al. No. each statement.

[0177] Improvements in the edges of color recording films are provided in the art to provide an information record completely separate from the color image record. For example, an edge soundtrack is often provided on motion picture film. Improving the edge area configuration is described in Research Disclosure, Item 38957, XIV.
"Easy Scan Configuration", described in paragraph (3).

As an alternative to constructing a full-color recording photographic element with separate blue, green and red recording layer units, it is usual to provide two-layer, or even three-layer, units recording in the same region of the spectrum. . The most common reason for taking these configurations is that it allows the fastest emulsion, which records a particular region of the spectrum, to receive the exposing light before passing through the slow emulsion layers of the other layer units. is there. This increases sensitivity and image sharpness. Color-recording photographic elements having various arrangements of layer units, including at least two separate layer units recording exposure to the same region of the spectrum
Is a Research Disclosure, Item 38957, X
I. This is described in "Layers and Layer Arrangement".

The following are just a few examples of the many possible additional layer unit sequences (including at least two separate layer units that record exposure to the same region of the spectrum).

[0180] _{SQ-7 | B | G f} | R f | G s | R s | S |, SQ-8 | B f | G f | R f | B s | G s | R s | S |, SQ _{-9 | B | G f | R} f | G m | R m | G s | R s | S |, SQ-10 | G f | R f | B f | G s | R s | B s | S | _{, SQ-11 | G f |} R f | B f | G m | R m | B m | G s | R s | B s | S | , and _{SQ-12 | R f | B} | G f | R f | G _s | R _s | S | where B, G, R and S have the same definition as above. f is the high or highest sensitivity of the layer unit recording in the same region of the spectrum. m is the medium sensitivity of the layer unit recording in the same region of the spectrum. s is the low or minimum sensitivity of the layer unit recording in the same region of the spectrum.

In SQ-12, two R _f layer units are shown. The _Rf layer unit furthest from the support is:
It has much less silver halide coverage than the remaining _Rf layer units and is sometimes referred to as a skin layer. Its function is to provide a small sensitivity enhancement to the red record in order to correct the undesired sensitivity and sharpness of the absence of that red recording layer unit position when compared to the green recording layer.

More specific examples of full color recording layer units which can be readily improved by including one or more emulsions of the present invention are described in Research Disclosure, Item 37038, XIX. Color negative example 1 XX. Color Negative Example 2 XXI. Color reversal example 1 XXII. It is described in Color Reversal Example 2.

Full color recording photographic elements are commonly used to record exposure over the full range of the visible spectrum. Occasionally, color recording photographic elements are also used to record near ultraviolet and / or near infrared exposures of the spectrum. If this is done, additional layer units can be provided for this purpose.

Any of the conventional and convenient techniques for imagewise exposing a dye image-forming photographic element can be used to expose a photographic element of the present invention. The exposure (E), measured in lux seconds, is the product of the exposure illuminance (I), measured in lux, and the exposure time (ti), measured in seconds: E = (I) (ti)

For ordinary photographic applications, the exposure is between 10 ^{-5 and} 10
^{For 3} seconds, even a relatively inexpensive camera can be 10 ^-3 to 1
It can fit in the range of 0 ² seconds. According to the reciprocity law, different combinations of exposure times and exposure illuminances (i.e., the same exposure) resulting in the same product will produce the same image density.
In practice, the performance of a photographic element exhibits various deviations from reciprocity, usually referred to as reciprocity failure. However, according to, for example, the reciprocity law, if the exposure amount (E) is kept constant, plotting the density and the exposure time (ti) should produce an invariable density curve. (Reciprocity failure). Compared with otherwise similar starch peptized high bromide {111} tabular grain emulsions and gelatino peptized high bromide {111} tabular grain emulsions, the starch peptized emulsion is greatly reduced. Showed reciprocity failure (ie, more closely followed reciprocity)
That was completely unexpected.

Exposure of camera speed color recording photographic elements with limited use cameras and recyclable cameras is specifically contemplated. Limited-use cameras and built-in film configurations are described in Research Disclosure, Item 338957, Section XVI. "Exposure" is a particular subject of paragraph (2).

Research Disclosure, Item 36
Although 544 and 37038 have been used to illustrate conventional photographic element constructions and their exposure and processing, many other references also disclose conventional constructions, including the following:

The Theory of the Photograph by James
ic Process, 4th Edition, Macmillan, New York, I 977; Th
e Kirk-Othmer Encyclopedia of Chemical Technology,
John Wiley and Sons, New York, I993; Neblette's I
maging Processes and Materials, Van Nostrand Reinh
old, NewYork 1988; and Keller, Science and Technol
ogy of Photography, VCH, New York, 1993.

[0189]

The invention can be better appreciated by reference to the following specific embodiments. Example 1 This example was prepared similarly, except that the sensitivity advantage demonstrated by the FED sensitized cationic starch peptized high bromide {111} tabular grain emulsion was prepared using a gelatin peptizer. It has the purpose of explanation compared to emulsions. Emulsion S1 (Inventive Example) 8 L of distilled water and 160 g of oxidized waxy corn starch (starch derivative, STA-LOK® 140: treated to contain quaternary ammonium groups and oxidized with 2% by weight chlorine bleach 100% amylopectin containing 0.31% nitrogen and 0.00% phosphorus
The mixture with Staley Manufacturing Co., Decatur IL.) Was heated at 85 ° C. for 45 minutes to prepare a starch solution. After cooling to 40 ° C., distilled water was added to adjust the mass to 8.0 kg. 26.5m of 2M NaBr solution
L and maintain the pH at 5.0 while adding saturated bromine water (~
(0.9 mmol) 2.0 mL was added dropwise immediately before use.

PH 5.0 at 40 ° C. and through emulsion precipitation.
A 2.5 M AgNO ₃ solution was added to the vigorously stirred reaction vessel of the starch solution maintained at 200 mL /
Minutes and added for 21 seconds. At the same time, a salt solution of 2.5 M NaBr and 0.4 g / L bromine was added initially at 200 mL / min and then at the rate required to maintain pBr at 2.11. Then, the addition of this solution was stopped, and 94 mL of the salt solution was added in 1 minute, and the temperature of the contents in the reaction vessel was increased to 60 ° C. at a rate of 1.67 ° C./minute. 60
After holding at 10 ° C. for 10 minutes, 240 mL of AgNO ₃ solution was added.
Was added at 10 mL / min for 1 minute and the addition rate was increased to 19 mL / min in 12 minutes. Salt solution was added simultaneously at the rate required to maintain pBr at 1.44. The addition was stopped and 40 mL of a buffer consisting of 2.94 M sodium acetate and 1.00 M acetic acid was added. The addition of the AgNO ₃ solution was then accelerated from 19 mL / min to 54 mL / min over 45 minutes, and then maintained at this flow rate until a total of 2.4 L of the AgNO ₃ solution was added. 2.5M NaBr, 0.04M K to maintain pBr at 1.44
A solution of I and 0.45 g / L bromine was added simultaneously.

The tabular grain emulsion thus obtained was treated at 40 ° C. with p
Washed by ultrafiltration to Br 3.26. Then, 27 g of bone gelatin per mole of silver (methionine content ~
55 μmol / g gelatin) was added. This {111}
Tabular grains have an average equivalent circular diameter of 3.8 μm and an average thickness of 0.3 μm.
07 μm and an average aspect ratio of 54. The tabular grain population constituted 99% of the total projected area of the emulsion grains.

[0192]Emulsion G1 (control) Distilled water 7. 10 g of low methionine bone gelatin in L
Onine content <3 μm / g gelatin) and NaBr46
In a mmol solution, at 40 ° C., pH 5.0, add aqueous
10 mL was added. 40 ° C and pH through emulsion precipitation
The gelatin being vigorously stirred, maintaining at 5.0
2.5M AgNO in the reaction vessel of the solution _Three 200 solution
Added at mL / min for 21 seconds. At the same time, 2.5M NaB
r and a 0.4 g / L bromine salt solution, initially 200 m
L / min, then required to maintain pBr at 2.11
Added at the rate you want. Then, the addition of this solution is stopped.
mL of the salt solution is added in 1 minute, and the contents of the reaction vessel are added.
Temperature to 60 ° C at a rate of 1.67 ° C per minute
Was. Then, 1.750 kg of seed emulsion (0.042 mol
All were discarded except for Ag). This seed emulsion was prepared at 60 ° C for a total of 2
After holding for 2 minutes, 100 g of oxidized bone gelatin,
Containing 1 L of distilled water, 15.3 mL of 2 M NaBr, 40
Preheated to 60 ° C pretreated with 2.0 mL of bromine water at
Solution was added. Then, at 60 ° C., AgNO_Three Dissolution
The solution was added at 1.0 mL / min for 1 minute, and the addition rate was 1
Speed up to 25mL / min in 50 minutes, total 2453mL
AgNO_Three Use this flow rate until the solution is added
Was. 240 mL AgNO_Three Salt until solution is added
The solution was added simultaneously and 0.45 g / L of bromine water
2.5M NaBr and 0.04M KI with
Fresh salt solution was added during the remaining precipitation to a pBr of 1.4.
Added to keep at 4. The total emulsion production time is 19
4 minutes. The emulsion was cooled to 40 ° C and pBr
Ultrafiltered to 3.26. Then, 1 mole per silver mole
2.4 g bone gelatin (methionine content ~ 55 μmol
/ G gelatin).

The obtained tabular grains were measured, and the average E
The parameters of CD, thickness, and tabular grain to total grain projected area ratio were the same as for emulsion S1.

[0194] The on each particle of the epitaxy emulsion S1 G1 is deposited epitaxially in the following operation. A vigorously stirred 1.0 mole aliquot of the emulsion was added at 40 ° C. to 0.25 M AgNO ₃
The solution was added to adjust the pAg to 7.59. Then 1
Add 5 mL of M KI, then add 3.77 M NaCl
Was added. The blue spectral sensitizing dye, anhydro-5,5'-dichloro-3,3'-bis (3-sulfopropyl) thiocyanine hydroxide, triethylammonium salt, is added to the surface of the particles in the form of a gelatin dye dispersion. It was added in an amount of 80% of the coating amount. After stirring for 25 minutes, 84 mL of a 0.25 M NaCl solution and 0.25 M
Was added, followed by the addition of 8 mmol AgI fine particle (（0.05 μm) emulsion. To this vigorously stirred mixture was added 0.5 M AgNO ₃ for 76 minutes.
Added at mL / min for 1.1 minutes.

According to electron microscopic analysis of the obtained emulsion,
The tabular grains were found to have an epitaxial deposition located primarily at the corners and edges of the tabular grains. As formulated, these deposits contained 42 mole percent chloride, 42 mole percent bromide and 16 mole percent bromide, based on silver.
It had an apparent halide composition of mole% iodide.

Each of emulsions S1 and G1 having chemically sensitized epitaxy
While stirring at 0 ° C., NaSCN (0.925 mmol), 1,3-dicarboxymethyl-1,3-dimethyl-2-thiourea (the optimal amount is the same for each emulsion;
8 μmol), bis (1,4,5-trimethyl-
1,2,4-triazolium-3-thiolate) gold (I) tetrafluoroborate (optimal amount for each emulsion is the same, 1.5 μmol), 3- {3-[(methylsulfonyl) amino ] -3-oxopropyl @ benzothiazolium tetrafluoroborate (optimal amount for each emulsion is the same, 81 μmol).
Thereafter, these emulsions were heated at 50 ° C. for 10 minutes,
C. and cooled in sequence to 1- (3-acetamidophenyl) -5-mercaptotetrazole (0.489 mmol), FED2 (2.8 .mu.mol), and 4-hydroxy-6-methyl-1,3,3a. , 7-Tetraazaindene (10 mmol) was added.

Performance Comparison Each of the sensitized emulsions S1 and G1 was coated on a transparent acetate support having an antihalation layer on the opposite side. These coatings, silver 1.08 g / m ^2, the yellow dye-forming coupler 1.62 g / m ^2, had a laydown of gelatin and surfactant 3.2 g / m ^2. A solution of gelatin and bis (vinylsulfonylmethyl) ether is
Each was overcoated with 0.9 g / m ^{2 of} gelatin and 72 mg / m ² of a hardener. Each film coating was exposed for 0.01 second to a 5500K color temperature tungsten light source filtered through a Kodak Wratten ^™ 2B filter and a 0-4 density step tablet. KODAK FLEXICOLOR exposed film coating
Treated using ^TM C-41 color negative filtration treatment.

The minimum density (Dmin), gamma and sensitivity were compared in Table III below. Sensitivity is reported as relative log sensitivity. The sensitivity of 1 relative logarithmic sensitivity difference is 0.01 LogE
(E is the exposure amount expressed in lux seconds). The sensitivity was measured on the characteristic curve at the intersection of the extrapolated linear portion of the characteristic curve and the linear extrapolation of the Dmin portion of the characteristic curve. Gamma is the slope of the linear portion of the characteristic curve.

[0199]

[Table 3]

Table III clearly shows that cationic starch peptized high bromide {111} tabular grain emulsion S1 is almost one stop (0.30 Log E) more sensitive than comparative gelatin peptized emulsion G1. . The one stop sensitivity advantage means that the sensitivity is doubled. Specifically, the 24 higher relative logarithmic sensitivity units of Emulsion S1 have a 0.24 Log E sensitivity advantage over Emulsion G1.

Example 2 The large speed advantage of emulsion S1 over emulsion G1 in Example 1 is due in part to the known speed advantage of replacing gelatin with a cationic starch peptizer. Some are unexpected. The purpose of this example was to ascertain the range of sensitivity benefits that would result from replacing gelatin with a cationic starch peptizer in the absence of a FED sensitizer.

Emulsions S1 and G1 were prepared again as emulsions S2 and G2, omitting the FED sensitizer and omitting the bromine oxidizing agent used to suppress the increase in fog caused by the FED sensitizer. The performance comparison of Example 1 was repeated. The following table shows the performance comparison.

[0203]

[Table 4]

The speeds reported in Tables III and IV are all based on Emulsion G2. It is clear from Table IV that replacing gelatin with a cationic starch peptizer resulted in a sensitivity advantage of 0.07 Log E (as already known in the art). Subtracting this expected speed advantage from the 0.24 Log E speed advantage observed for Emulsion S1, FE
An unexpected added sensitivity advantage in the presence of D sensitizer is 0.17 Log E (about 1.5 stops, 0.15 Lo
gE).

Example 3 The purpose of this example is to demonstrate the advantage of minimum density due to the presence of the oxidizing agent during precipitation of emulsion S1. Emulsion S3 satisfying the requirements of the present invention was precipitated in the same manner as Emulsion S1, except that the bromine oxidizing agent added during precipitation was omitted. Example 1 was repeated in all other respects. The reported grain characteristics of emulsions S1 and S3 were the same. Emulsion S1, G1
And the performance of S3 is compared to Table V.

[0206]

[Table 5]

Table V clearly shows that, even without the bromine oxidizer, significant unexpected sensitivity advantages due to cationic starch peptizer and FED sensitizer remain. The disadvantage of omitting the oxidizing agent is Dmin
Is increased by 0.11. This increase in minimum density can be accommodated in some applications, such as color negative imaging, but may not be desirable, for example, in color printing. Thus, the use of an oxidizing agent is preferred, but not required.

Example 4 The purpose of this example is to demonstrate that it is effective to delay the addition of the oxidizing agent until after deposition. Example 1 was repeated as for Emulsion S1, with the difference that bromine was not added to the emulsion at the time of precipitation but was added after precipitation by the following procedure. Example Emulsion S4 was prepared in the same manner as Emulsion S1, except that bromine was not used before or during precipitation. After completion of the precipitation, 28 mL of saturated bromine water (~ 0.013 mol) was added.
At 40 ° C., it was added to the stirring emulsion while maintaining the pH at 5.0 with diluted NaOH. The reaction lasted for 2 minutes after the addition of the aqueous bromine, as indicated by the amount of NaOH required to maintain the pH at 5.0. This emulsion was ultrafiltered.

The measured grain parameters of the example emulsions S1 and S4 were the same. The performance of emulsions S1, S3 and S4 are compared in Table VI.

[0210]

[Table 6]

From Table VI it is clear that the addition of bromine after deposition (pptn) is not as effective as the addition of bromine during precipitation, but is effective in limiting the minimum concentration. Each emulsion S
1, S3 and S4 also showed an unexpected sensitivity advantage of using a cationic starch peptizer in combination with an FED sensitizer.

Example 5 The purpose of this example was to exceed the FED sensitized gelatin peptized high bromide {111} tabular grain emulsion when ETARC was added to the emulsion of the imaging layer unit of the photographic element.
D-sensitized cationic starch peptizer high bromide # 11
It is to demonstrate a further unexpected increase in speed advantage demonstrated by 1｝ tabular grain emulsions.

[0213]Emulsion S5 This emulsion is a re-preparation of emulsion S1.Emulsion G5 Maintained at 40 ° C. and pH 5.0 through emulsion precipitation.
In 7.0 L of distilled water and 46 mmol of NaBr,
10 g of low methionine bone gelatin with vigorous stirring
(Methionine content less than 3 μmol / g gelatin)
2.5M AgNO _Three Solution at 200 mL / min for 21 seconds
added. At the same time, a 2.5 M NaBr salt solution was
At 200 mL / min, then maintain pBr at 2.11
Added at the speed required to do so. And the addition of this solution
Was stopped and 82 mL of the salt solution was added over 1 minute.
60 ° C at a rate of 1.67 ° C per minute
Up. Then, 1.750 kg of seed emulsion (0.0
All but 42 mol Ag) were discarded. 60 ° C
After holding for a total of 22 minutes with 100 g of oxidized bone
Contains 1 L of ratine and distilled water and 15.3 mL of 2M NaBr.
And the solution preheated to 60 ° C. was added. Then 60
AgNO_Three Add solution at 1.0 mL / min for 1 minute
And increase the addition rate to 25 mL / min for 150 minutes.
For a total of 2453 mL AgNO_Three Solution is added
This flow rate was used until 240 mL AgNO_Three solution
Salt solution is added simultaneously until is added, and
New salt solution of 2.5M NaBr and 0.04M KI
The solution is maintained at a pBr of 1.44 during the rest of the precipitation.
Used for

The total emulsion production time was 194 minutes.
Emulsions with longer production times as compared to S5 contribute to greater grain growth and inhibit the action of gelatino-peptizer as compared to cationic starch peptizers. The emulsion was cooled to 40 ° C. and ultrafiltered to pBr 3.26. Thereafter, 12.4 g of bone gelatin per mole of silver (methionine content -55 [mu] mol / g gelatin) was added.

The obtained tabular grains were measured, and the average E
The CD, thickness, and tabular grain ratio to total grain projected area ratio parameters were the same as for emulsion S5.

Epitaxy and Chemical Sensitization These sensitization procedures were performed as described in Example 1.

Performance Comparison Each of the sensitized emulsions S5 and G5 was coated on a transparent acetate support having an antihalation layer on the opposite side. 2
Type coatings were prepared containing each emulsion, one coating containing the ETARC coupler and the other coating containing no ETARC coupler.
A coating containing no ETARC coupler was prepared as follows: this emulsion layer contained 0.81 g / m ² silver,
Cyan dye 0.324 g / m ^2, had a gelatin and surfactant 4.32 g / m ^2. A solution of gelatin and bis (vinylsulfonylmethyl) ether was overcoated with 0.9 g / m ^{2 of} gelatin and 72 mg / m ² of hardener, respectively.

Coatings containing ETARC couplers
The emulsion layer was prepared as follows: this emulsion layer contained 0.81 silver.
g / m^Two 0.27 g / m of cyan dye-forming coupler ^Two ,
0.16 g / m^Two ETARC coupler E-25, lined up
With gelatin and surfactant 4.32 g / m^Two It had.
Gelatin and bis (vinylsulfonylmethyl) ether
The solution was gelatin 0.9 g / m2^Two And a hardener 72 mg /
m^Two To overcoat each.

Each film coating was exposed for 0.01 second to a 5500K color temperature tungsten light source filtered through a Kodak Wratten ^™ 2B filter and a 0-4 density step tablet. The exposed film coating was processed using KODAK FLEXICOLOR ^™ C-41 color negative filtration.

The minimum density (Dmin), gamma and sensitivity were compared in Table VI below. Adjusted sensitivity is reported in relative log sensitivity units. The sensitivity of 1 relative logarithmic sensitivity difference is 0.01 Log
It is equal to the exposure difference of E (E is exposure in lux seconds).
Sensitivity is calculated using the extrapolated straight line portion of the characteristic curve and Dmin
It was measured on the characteristic curve at the intersection with the linear extrapolation of the part. Adjustment sensitivity measures sensitivity adjusted to eliminate differences in measured granularity. It was measured using a 48 μm diameter. As is generally recognized, a sensitivity difference of seven particles is equal to one stop (0.30 Log E or 30 relative log sensitivity units). For example, if two emulsions exhibit the same sensitivity (where one indicates a granularity of more than 7 grain units), re-creating one of the emulsions to reduce the granularity by 7 grain units would result in 30 emulsions. It can be expected that the sensitivity is reduced by the relative logarithmic sensitivity unit. Adjustment speed is commonly used to compare the performance of emulsions that differ in both speed and granularity. Gamma is the slope of the linear portion of the characteristic curve.

[0221]

[Table 7]

From Table VII it can be seen that G5 without ETARC
And S5 emulsions are clearly seen to provide very similar performance in terms of minimum density, gamma and adjusted sensitivity. However, it should be pointed out that the sensitivity of S5 emulsion was disadvantaged by the addition of bromine so that the minimum density could be comparable to that of the control G5 emulsion. If the control G5 emulsion was prepared with the presence of the bromine oxidizer, its sensitivity would have been greatly reduced. On the other hand, if the S5 emulsion was prepared without an oxidizing agent, its minimum density would have increased.

Table VII clearly shows that the addition of ETARC increased the adjusted relative speed of the photographic element containing emulsion G5 by 10 relative logarithmic speed units. S
It was completely unexpected that the addition of ETARC to a 5-containing photographic element would increase the adjusted relative log sensitivity by 26. This is a relative logarithmic speed increase due to the addition of ETARC that is 16 relative logarithmic speed units (0.16 Log E) greater than expected, based on the speed increase seen in the G5 emulsion comparator. Furthermore, this increase in sensitivity
Note that in addition to the above demonstrated unexpectedly large gain in sensitivity from the use of FED sensitizers. Thus, the photographic elements of the present invention have an otherwise equivalent ETARC.
Very large and unexpected speed advantages can be realized when compared to photographic elements containing FED sensitized gelatin peptized high bromide {111} tabular grain emulsions containing couplers.

[0224] Other preferred embodiments of the present invention are described below in connection with the claims. (Embodiment 1) The photographic recording element according to claim 1, wherein the fragmentable electron-donating sensitizer has a portion that facilitates adsorption to the surface of silver halide grains. (Embodiment 2) The radiation-sensitive silver halide grains contain more than 70 mol% of bromide based on the amount of silver and have a total grain projected area of 7%.
A photographic recording element according to claim 1, comprising tabular grains accounting for more than 0%.

(Embodiment 3) The radiation-sensitive silver halide grains according to claim 1, which contain at least 90 mol% of bromide based on silver and include tabular grains occupying at least 90% of the total grain projected area. Photo recording element. (Embodiment 4) The photographic record according to claim 1, wherein the fragmentable electron-donating sensitizer fragments upon oxidation to provide radicals having an oxidation potential equal to or less than -0.7. element.

(Embodiment 5) The photographic recording element according to claim 1, wherein the cationic starch is a water-dispersible oxidized cationic starch. (Aspect 6) The cationic starch according to claim 1, wherein the cationic starch contains α-D-glucopyranose repeating units, and on average at least 1% of the α-D-glucopyranose repeating units have been opened by oxidation. Photo recording element. (Aspect 7) The electron transfer agent releasing coupler can act as an electron transfer agent of the coupler upon release.
A photographic recording element according to claim 1, which contains an -aryl-3-pyrazolidinone moiety.

 ────────────────────────────────────────────────── ─── Continued on front page (72) Inventor Kenneth James Reed United States, New York 14626, Rochester, West Amy Lane 35 (72) Inventor Victor P. Scassia United States, New York 14626, Rochester, Fortune Lane 24 (72) Inventor James Anthony Friday United States, New York 14617, Rochester, Simpson Road 148

Claims (2)

[Claims] 1. a support; and (a) radiation-sensitive silver halide grains, (b) a sensitizer for the silver halide grains, (c) a peptizer for the silver halide grains, A photographic recording element comprising: (d) at least one dye image providing coupler; and (e) at least one dye image forming layer unit having at least one dye image enhancing coupler, wherein said radiation sensitive halogen Silver halide particles are (1) $ 11
Said sensitizer comprising 1｝ major surfaces, (2) tabular grains containing more than 50 mol% bromide based on silver, and (3) more than 50% of total grain projected area. Contains a fragmentable electron-donating sensitizer, the peptizer is a water-dispersible cationic starch, and the dye image-providing coupler reacts with an oxidized primary amine color developing agent. A photographic recording element wherein the coupler is a coupler capable of forming a dye image upon release and wherein the dye image enhancing coupler is a coupler capable of reacting with an oxidized primary amine color developing agent to release an electron transfer agent. 2. A transparent film support, and comprising blue, green and red recording layer units coated on said support for recording the exposure amounts for the blue, green and red regions of the visible spectrum, respectively. A photographic element, wherein at least one recording layer unit contains the emulsion of claim 1.