[0001] This invention relates to photographic elements containing ballasted couplers.
[0002] Images are commonly obtained in the photographic art by a coupling reaction between
the development product of a silver halide developing agent (i.e., oxidized aromatic
primary amino developing agent) and a color forming compound commonly referred to
as a coupler. The dyes produced by coupling are indoaniline, azomethine, indamine
or indophenol dyes, depending upon the chemical composition of the coupler and the
developing agent. The subtractive process of color formation is ordinarily employed
in multicolor photographic elements and the resulting image dyes are usually cyan,
magenta and yellow dyes which are formed in or adjacent silver halide layers sensitive
to radiation complementary to the radiation absorbed by the image dye; i.e., silver
halide emulsions sensitive to red, green and blue radiation.
[0003] Since this is a mature art, the patent and technical literature is replete with references
to compounds which can be used as couplers for the formation of photographic images.
Preferred couplers which form cyan dyes upon reaction with oxidized color developing
agents are phenols and naphthols. Representative couplers are described in the following
patents and publications: U.S. Patents 2,772,162; 2,895,826; 3,002,836; 3,034,892;
2,474,293; 2,423,730; 2,367,531; 3,041,236 and "Farbkuppler-ein Literaturubersicht",
published in Agfa Mitteilungen, Band II, pp. 156-175 (1961).
[0004] US patent application serial no. 85 140 (filed 15 October 1979), priority document
of EP-A-0 028 099 (published on 6 May 1981) describes photographic couplers which
form cyan dyes having particularly desirable hues of narrow bandwidth. inter alia
the document discloses couplers having the general formula:
wherein
R2 is a hydroxyphenylsulphonyl group;
X is hydrogen or a coupling-off group;
Y is oxygen or sulphur,
R1 is a branched alkylene group of 2 to 20 carbon atoms; and
n is 1 to 3.
There is no disclosure on the subject of the reactivity of the couplers of this document.
[0005] Preferred couplers which form magenta dyes upon reaction with oxidized color developing
agent are pyrazolones, pyrazolotriazoles, pyrazolobenzimidazoles and indazolones.
Representative couplers are described in such patents and publications as U.S. Patents
2,600,788; 2,369,489; 2,343,703; 2,311,082; 2,673,801; 3,152,896; 3,519,429; 3,061,432;
3,062,653; 3,725,067; 2,908,573 and "Farbkuppler-eine Literaturubersicht", published
in Agfa Mitteilungen, Band II, pp. 126-156 (1961).
[0006] Couplers which form yellow dyes upon reaction with oxidized color developing agent
are acylacetanilides such as benzoylacetanilides and pivalylacetanilides. Representative
couplers are described in the following patents and publications: U.S. Patents 2,875,057;
2,407,210; 3,265,506; 2,298,443; 3,048,194; 3,447,928 and "Farbkuppler-eine Literaturubersicht",
published in Agfa Mitteilungen, Band II, pp. 112-126 (1961).
[0007] Also known are couplers which form black or neutral dyes upon reaction with oxidized
color developing agent. Representative couplers are resorcinols and m-aminophenols
such as are described in U.S. Patents 1,939,231; 2,181,944; 2,333,106; 4,126,461;
German OLS 2,644,194 and German OLS 2,650,764.
[0008] Also known are compounds which react with oxidized color developing agent in the
same way as couplers but which do not yield a dye. Such compounds are employed to
modify the photographic image by competing with dye-forming coupler for oxidized color
developing agent or by releasing a photographic reagent, such as a development inhibitor,
as a result of the coupling reaction. While many such compounds are not commonly referred
to as couplers, it is convenient to consider them as such in view of the similarities
in the ways they and couplers react during photographic processing. For the purposes
of the present invention, they are considered couplers. Representative couplers are
described in such patents and published patent applications as U.S. Patents 3,632,345;
3,928,041; 3,938,996; 3.958,993; 3,961,959; 4,010,035; 4,029,503; 4,046,574; 4,049,455;
4,052,213; 4,063,950; 4,075,021; 4,121,934; 4,157,916; 4,171,223; 4,186,012 and 4,187,110;
U.K. Patent Specifications 1,445,797; 1,504,094; 1,536,341 and 2,032,914A; Germany
OLS's 2,448,063; 2,552,505; 2,610,546 and 2,617,310; and Belgian Patent 839,083.
[0009] When intended for incorporation in photographic elements, couplers are commonly dispersed
therein with the aid of a high boiling organic solvent, referred to as a coupler solvent.
Couplers are rendered nondiffusible in photographic elements, and compatible with
coupler solvents, by including in the coupler molecule a group referred to as a ballast
group. This group is located on the coupler in a position other than the coupling
position and imparts to the coupler sufficient bulk to render the coupler nondiffusible
in the element as coated and during processing. It will be appreciated that the size
and nature of the ballast group will depend upon the bulk of the unballasted coupler
and the presence of other substituents on the coupler.
[0010] Although numerous couplers are known in the art, there is a continuing problem to
improve, or optimize for particular applications, many properties of the coupler and
the resultant dye.
[0011] It is an object of this invention to provide novel photographic elements that contain
couplers that have improved stability, reactivity and compatibility with other components
in the photographic element, the dyes derived from such couplers having efficient
light absorption and good stability and hue.
[0012] Such can be accomplished by a photographic element comprising a support, a photographic
silver halide emulsion and associated therewith a non-diffusible photographic coupler
which reacts with oxidized colour developing agent to give a compound which may or
may not be an image dye, characterized in that the coupler contains a coupling group
COUP-bonded at a position other than the coupling position to a ballast which is substituted
with a hydroxyphenylsulfonyl or hydroxyphenylsulfinyl group.
[0013] Although substituents of formula
have been suggested for inclusion in photographic dye-forming couplers at other than
the coupling position - see for example U.K. Patent Appliation 2,029,977A - they have
not been suggested as constituents of ballast groups.
[0014] The coupling group COUP- of the couplers used in the photographic elements of the
invention can be any coupling group known or used in the art to form a colored or
colorless reaction product with oxidized color developing agent. The ballast group
of the couplers used in the invention can be any ballast, or portion thereof, which
is substituted with a hydroxyphenylsulfonyl group or hydroxyphenylsulfinyl group with
the exception of couplers of the formula:
wherein
R2 is a hydroxyphenylsulphonyl group;
X is hydrogen or a coupling-off group;
Y is oxygen or sulphur,
R1 is a branched alkylene group of 2 to 20 carbon atoms; and
n is 1 to 3.
[0015] Preferred ballast groups used in the invention am substituted with a group of the
structural formula:
where
p is 1 or 2; and
q is 1 to 3.
[0016] The substituted group can be joined to the coupling group COUP- at any position,
other than the coupling position, where ballast groups commonly are joined. The coupling
position of the coupling group can be unsubstituted, or substituted with a coupling
off group which can modify the equivalency of the coupler, its reactivity, its dispersibility
or which, upon release from the coupler, interacts with other components of the element.
The coupling group can include substituents in other positions.
[0017] Particularly preferred ballast groups used in the invention have the structural formula:
where
I, m and n are each individually 0 or 1, at least one of I, m and n being 1;
L1 represents a bivalent group selected from
L2 represents a bivalent group selected from
L3 represents a bivalent group selected from
wherein the combination of L1, L2 and/or L3 forms a ballast group;
R1 and R3 are each individually hydrogen, alkyl of 1 to 20 carbon atoms or aryl of 6 to 20
carbon atoms
R2 is hydrogen or one or more halogen, alkyl or alkoxy substituents;
X is -O- or -S-;
r is 0 or 1; and
s is 0 or 10.
[0018] The bivalent linking group represented by L L
2 and L
3 can be any of the groups found in ballast groups, such as alkylene of up to 10 carbon
atoms, arylene of 6 to 10 carbon atoms, heterocyclene of 5 to 10 carbon atoms, may
include oxygen, sulfur, amino, amido, sulfonamido, carbamoyl, sulfamoyl, and combinations
of such linking groups, e.g. alkarylene, aralkylene, aminoarylene, aminoalkylene,
amidoarylene, amidoalkylene, ureido, alkarylamido, amidoarylsulfamoyl, aminoarylamido
and aminoarylsulfamoylalkyl.
[0019] Particularly preferred couplers used in the invention have the structural formula:
where:
L4 represents a bivalent group selected from
[0020] COUP, R
1, R
2, R
3, r and s are as defined above.
[0021] In an especially preferred embodiment, the hydroxy group in structural formulae II
and III is in the para position.
[0022] In the above structural formulae the alkyl, alkylene, aryl, arylene and heterocyclene
groups can be unsubstituted or substituted with one or more groups such as halogen,
nitro, amino, carboxy, alkyl, alkoxy, aryl, aryloxy, heterocyclyl, carbamoyl, amido,
sulfamoyl and sulfonamido.
[0023] As indicated above, common yellow dye-forming couplers are acylacetanilides such
as pivalylacetanilides and benzoylacetanilides. Common magenta dye-forming couplers
are pyrazolones, pyrazolotriazoles, pyrazolobenzimidazoles and indazolones. Common
cyan dye-forming couplers are phenols and naphthols, common neutral dye-forming couplers
are resorcinols and m-aminophenols. Common non-dye-forming couplers are acyclic and
cyclic compounds in which the active position, corresponding to the coupling position,
is adjacent to or in conjugation with a carbon group or an imino group, such as a-
or y-substituted ketones or imines, e.g. cyclopentanones, cyclohexanones, indanones,
indanoimines, oxyindoles and oxazolinones. These couplers can form the coupling group
COUP in the above formulae. Structures of representative coupling groups are shown
below. In these structures Z represents hydrogen or coupling-off group and the unsatisfied
bond, or bonds, indicates the preferred position, or positions, at which there can
be attached the remainder of the molecule shown in the above structures; it being
recognized that the coupling group can contain other substituents. Typical suitable
coupling groups that can be used in the photographic elements of the invention are
set out below.
[0024] Cyan dye-forming coupling groups:
[0025] Magenta dye-forming coupling groups:
[0026] (B represents a blocking group capable of being removed during processing, e.g.,
by alkaline cleavage or coupling)
[0027] Yellow dye-forming coupling groups:
[0028] Non-dye-forming coupling groups:
[0029] Neutral dye-forming coupling groups:
[0030] Specific couplers used in the invention, which are shown below, contain ballasts
of general structures B
1 through B
6, where Y is -OH.
[0031] Cyan dye-forming couplers used in the invention including the following; the group
Y in B
2, B
3 and B
4 being -OH:
[0033] Yellow dye-forming couplers used in the invention include the following, the group
Y in B
1, B
2 or B
6 being -OH:
[0034] Noncolor forming couplers used in the invention include the following:
[0035] Couplers used in the invention can be prepared by attaching a blocked hydroxyphenylsulfonyl
or blocked hydroxyphenylsulfinyl group directly to the coupling group or by attaching
such a group to the remainder of the ballast group after which the ballast group is
attached to the coupling group. Thereafter the blocking group is removed. Conventional
condensation reactions can be employed in joining the various groups which ultimately
form the coupler. For many of the couplers used in the invention it is convenient
to provide the hydroxyphenylsulfonyl group using a 4,4'-sulfonyldiphenol mono ether
(e.g. benzyl ether) or mono ester (e.g. acetyl ester.) Conventional reaction techniques
can be employed to attach such a compound to the remainder of the ballast group and
the thus formed ballast group to the coupling group. Thereafter, the blocking group
can be removed by hydrogenation (in the case of the ether) or alkaline hydrolysis
(in the case of an ester). When the coupler, or the remainder of the ballast group,
has an amino group available for reaction, it is convenient to react that amino group
with a blocked hydroxybenzenesulfonyl chloride after which the blocking group is removed.
[0036] The couplers used in the invention can be used in the ways and for the purposes that
nondiffusible couplers are used in the photographic art.
[0037] Typically, the couplers are incorporated in silver halide emulsions and the emulsions
coated on a support to form the photographic elements of the invention. Alternatively,
the couplers can be incorporated in photographic layers adjacent a silver halide emulsion
layer where, during development, the coupler will be in reactive association with
development products such as oxidized color developing agent. Thus, as used herein,
the term "associated therewith" signifies that the coupler is in the silver halide
emulsion or in an adjacent location where, during processing, it will come into reactive
association with silver halide development products.
[0038] The photographic elements of the invention can be single color elements or multicolor
elements. Multicolor elements contain dye image-forming units sensitive to each of
the three primary regions of the spectrum. Each unit can be comprised of a single
emulsion layer or of multiple emulsion layers sensitive to a given region of the spectrum.
The layers of the photographic element, including the layers of the image-forming
units, can be arranged in various orders as known in the art. In an alternative format,
the emulsions sensitive to each of the three primary regions of the spectrum can be
disposed as a single segmented layer, e.g., as by the use of microvessels as described
in Belgian Patent 881,513.
[0039] A typical multicolor photographic element of the invention comprises a support bearing
a cyan dye image-forming unit comprised of at least one red-sensitive silver halide
emulsion layer having associated therewith at least one cyan dye-forming coupler,
a magenta dye image-forming unit comprising at least one green-sensitive silver halide
emulsion layer having associated therewith at least one magenta dye-forming coupler
and a yellow dye image-forming unit comprising at least one blue-sensitive silver
halide emulsion layer having associated therewith at least one yellow dye-forming
coupler, at least one of the couplers in the element being a coupler as described
above. The element can contain additional layers, such as filter layers, interlayers,
overcoat layers, subbing layers, and the like.
[0040] In the following discussion of suitable materials for use in the emulsions used in
the invention, reference will be made to Research Disclosure, December 1978, Item
17643. This publication will be identified hereafter by the term "Research Disclosure".
[0041] The silver halide emulsions employed in the photographic elements of this invention
can be either negative-working or positive-working. Suitable emulsions and their preparation
are described in 'Research Disclosure' Sections I and II and the publications cited
therein. Suitable vehicles for the emulsion layers and other layers of elements of
this invention are described in Research Disclosure Section IX and the publications
cited therein.
[0042] In addition to the couplers used in the invention, additional couplers as described
in Research Disclosure Section VII, paragraphs D, E, F and G and the publications
cited therein can be used. These couplers can be incorporated in the elements and
emulsions as described in Research Disclosure Section VII, paragraph C and the publications
cited therein.
[0043] The photographic elements of this invention or individual layers thereof, can contain
brighteners (see Research Disclosure Section V), antifoggants and stabilizers (see
Research Disclosure Section VI), antistian agents and image dye stabilizer (see Research
Disclosure Section VII, paragraphs I and J), light absorbing and scattering materials
(see Research Disclosure Section VIII), hardeners (see Research Disclosure Section
XI), plasticizers and lubricants (see Research Disclosure Section XII), antistatic
agents (see Research Disclosure Section XIII), matting agents (see Research Disclosure
Section XVI) and development modifiers (see Research Disclosure Section XXI).
[0044] The photographic elements of the invention can be coated on a variety of supports
as described in Research Disclosure Section XVII and the references described therein.
[0045] Photographic elements of the invention can be exposed to actinic radiation, typically
in the visible region of the spectrum, to form a latent image as described in Research
Disclosure Section XVIII and then processed to form a visible dye image as described
in Research Disclosure Section XIX. Processing to form a visible dye image includes
the step of contacting the element with a color developing agent to reduce deveopable
silver halide and oxidize the color developing agent. Oxidized color developing agent
in turn reacts with the coupler to yield a dye.
[0046] Preferred color developing agents are p-phenylene diamines. Especially preferred
are 4-amino-N,N-diethyl-aniline hydrochloride, 4-amino-3-methyl-N,N-diethylniline
hydrochloride, 4-amino-3-methyl-N(ethyl-N-(3-(methanesulfonamido) ethylaniline sulfate
hydrate, 4-amino-3-methyl-N-ethyl-N-(3-hydroxyethylaniline sulfate, 4-amino-3-(3-(methanesulfonamido)ethyl-N,N-diethyl-aniline
hydrochloride and 4-amino-N-ethyl-N-(2-methoxy ethyl)-m-toluidine di-p-toluene sulfonic
acid.
[0047] With negative working silver halide this processing step leads to a negative image.
To obtain a positive (or reversal) image, this step can be preceded by developing
exposed silver halide with a non-chromogenic developing agent without forming a dye,
and then uniformly fogging the element to render unexposed silver halide developable.
Alternatively, a direct positive emulsion can be employed to obtain a positive image.
[0048] Development is followed by the conventional steps of bleaching and fixing, or bleach-fixing,
to remove silver and silver halide, washing and drying.
[0049] The following examples are included for a further understanding of this invention.
Preparative Example 1
Preparation of ballast Group Intermediate B2CI, where Y = OBz (Bz is benzyl)
[0050] To a solution of 90 g (0.31 mol) methyl 2-bromododecanoate and 104.4 g (0.31 mol)
4,4'-sulfonyl-diphenol monobenzyl ether in 0.35 I dry acetone were added 1 g sodium
iodide and 214.2 g (1.55 mol) potassium carbonate. After refluxing the mixture 20
h, solids were removed by filtration and the filtrate concentrated to a waxy solid.
Recrystallization from methanol gave a white solid (B
20CH
3, Y = OBz), mp 73-75°C, with the correct elemental analysis and expected NMR spectrum.
A solution of 120 g (0.21 mol) of this product in 0.8 I dimethylformamide was added
with stirring to 0.5 I of 2.3 mol aqueous potassium hydroxide solution, water was
added and the cloudy solution stirred 0.5 h before pouring into acidic ice-water.
The resulting solid was collected, dissolved in dichloromethane, and the solution
washed, dried over magnesium sulfate, and concentrated. Recrystallization from acetonitrile
yielded 67 g white solid (B
20H, Y = OBz), mp 119-121 °C, with the expected NMR spectrum and elemental analysis.
This acid was converted to the acid chloride by dissolving 67 g (0.12 mol) in 0.4
I thionyl chloride and stirring 5 h. Excess thionyl chloride was removed under vacuum
and the product recrystallized from dry acetonitrile to give a white solid (B
2CI, Y = OBz), mp 84-85°C, with the expected NMR spectrum and elemental analysis.
Preparative Example 2
Preparation of ballast Group Intermediate B2CI, where Y = OAc
[0051] A solution of 455 g (0.82 mol), B
20CH
3, Y = OBz in 1.6 I tetrahydrofuran and 0.4 I acetic acid was hydrogenated 12 h at
50 psi and 50°C over 45 g 5% palladium on charcoal catalyst. The catalyst was removed
by filtration and the concentrated filtrate drowned in water. An ethyl acetate solution
of resulting white solid was washed, dried, concentrated, and the product recrystallized
from acetonitrile to give 340 g (0.74 mol) white solid (B
20CH
3, Y = OH), 63-65°C with the expected elemental analysis. Hydrolysis of this ester
was accomplished by slowly adding an aqueous solution containing 40 g (1 mol) sodium
hydroxide to a stirred solution of the ester in 1 I dimethylformamide, stirring 2
h then pouring into acidified ice-water. The resulting gummy solid dissolved in ethyl
acetate was washed with dilute hydrochloric acid, dried, and concentrated. Recrystallization
from acetonitrile yielded a white solid (B
20H, Y = OH), mp 116-117°C. This phenolic acid was acetylated by dissolving in 70 ml
acetic anhydride and 7 ml concentrated surfuric acid, stirring 30 minutes at 20°C.,
then on a steam bath for 30 minutes, cooling, and pouring into 81 water. The product
was recrystallized from methanol to give a white solid (B
20H, Y = OAc), mp 73-75°C. Refluxing 35 g (0.07 mol) of this acid in excess thionyl
chloride for 5 h and concentrating yielded a colorless oil, which on trituration in
ligroin gave 22 g white solid (B
2CI, Y = OAc), mp 66-69°C.
Preparative Example 3
Preparation of ballast Group Intermediates B3CI, where Y = OBz
[0052] The procedural steps were similar to those for preparation of B
3CI in Preparative Example 1, except that ethyl 2-bromotetradecanoate was the starting
material. Intermediates included white solids B
30CH
2CH
3, Y = OBz (mp 55-61 °C); B
30H, Y = OBz (mp 117-118°C); and B
3CI, Y = OBz (mp 81-84°C).
Preparative Example 4
Preparation of ballast Group intermediate B1Cl where Y = OBz
[0053] The procedural steps were similar to those for preparation of B
3CI in Preparative Example 1, except that ethyl 2-bromohexanoate was the starting material.
Intermediates included white solids B'OCH
2CH
3, Y = OBz (mp 102-105°C); B
1OH, Y = OBz (mp 147.5-148.5°C); and B
lCI, Y = OBz (mp40°C).
Preparative Example 5
Preparation of ballast Intermediate B4CI where Y = OBz
[0054] A solution of 10.2 g (0.029 mol) methyl 2-p-nitrophenoxy)dodecanoate in 100 ml tetrahydrofuran
was shaken 6 h under 40 psi hydrogen in the presence of 0.7 g 10% palladium on charcoal
catalyst to reduce the nitro group. Then 6.3 ml (0.04 mol) N,N-dimethylaniline and
8.2 g (0.029 mol) p-benzyloxybenzenesulfonyl chloride were added and the mixture stirred
15 hours at 20°C. The catalyst was removed by filtration and the filtrate poured into
cold dilute hydrochloric acid. Ethyl acetate extraction, washing, drying, concentration,
and purification through silica gel yielded 14 g colorless oil (B
40CH
3, Y = OBz). This was dissolved in 60 ml tetrahydrofuran and 40 ml methanol, stirred
0.5 h with 20 ml aqueous sodium hydroxide solution and poured into cold dilute hydrochloric
acid. Ethyl acetate extraction, washing, drying, concentration, ligroin trituration
yielded 12 g white crystals (B
40H, Y = OBz), mp 100-101°C, with the correct elemental analysis. To a stirred solution
of 10 g (0.018 mol) of this acid in 50 ml tetrahydrofuran was added 1.8 ml (0.022
mol) oxalyl chloride and 5 drops dimethyl formamide. After 1.5 h concentration gave
0.018 mol of brown oil B
4CI, Y = OBz.
Preparative Example 6
Preparation of ballast Intermediate B5 H·HCl where Y = OH
[0055] To a solution of 24 g (0.043 mol) acid chloride B
2CI, Y = OBz in 400 ml tetrahydrofuran was a 40% aqueous solution containing 10 g (0.125
mol) methylamine. After 0.5 h stirring, the mixture was poured over acidified ice-water,
extracted with diethyl ether, and the organic layer washed, dried and concentrated
to yield, after further purification on a 50:50 silica gel/Fluorisil (trade mark)
column, a clear colorless oil (B
2NHCH
3, Y = OBz). Reduction was accomplished by refluxing 16 g (0.029 mol) of this amide
product and 16 mi 2 M borane-methyl sulfide complex in 400 ml tetrahydrofuran for
3 h. The cooled reaction mixture was slowly acidified with 50% hydrochloric acid solution,
then extracted with diethyl ether. Acidification and concentration of the washed and
dried organic layer gave 14 g of white solid (B
5H.HCI, Y = OH).
[0056] Final steps in the synthetis of couplers used in this invention generally involved
the attachment of the ballast group and the removal of the ballast blocking group,
if any. For example, in Scheme I an amino-substituted coupling group, COUP-NH
2, is allowed to react with an acid chloride ballast group and the resulting intermediate
is converted to the desired coupler by hydrogenation to remove the benzyl group.
[0057] Where the blocking group is acetyl, as in Scheme II, it is removed by alkaline hydrolysis:
[0058] Alternatively, if the coupler is substituted with an acidic function, a ballast group
containing an amine function may be attached according to Scheme III:
Preparative Example 7
Preparation of Coupler C-8 by Scheme I
[0059] A suspension of 5.4 g (0.018 mol) 2-(p-cyanophenylureido)-5-nitrophenol in 200 ml
tetrahydrofuran was shaken overnight under 40 psi hydrogen with 1.6 10% palladium
on charcoal catalyst and 0.3 ml acetic acid. Then 0.018 mol of the acid chloride B
4CI prepared in Preparative Example 5 and 6.8 ml dimethylaniline were added under nitrogen
and the mixture stirred 0.5 h before removing the catalyst by filtration and pouring
the filtrate into cold dilute hydrochloric acid. Ethyl acetate extraction, washing,
drying, concentration, and crystallization from acetonitrile yielded 10.2 g of the
pale white solid benzyl ether of the desired coupler. A solution of this product in
100 ml tetrahydrofuran was shaken for 15 hours under 40 psi hydrogen with 2.5 g 10%
palladium on charcoal catalyst and 0.5 ml acetic acid. The catalyst was removed by
filtration and the reduction product concentrated and crystallized from acetonitrile
to give 6.1 g white solid coupler C-8, mp 103-106°C, with an infrared spectrum and
elemental analysis consistent with the desired structure.
Preparative Example 8
Preparation of Coupler M-28 by Scheme II
[0060] A solution of 50 g (0.115 mol) 3-(2-chloro-5-nitroanilino)-1-(2,4,6-trichlorophenyl)-2-pyrazolin-5-one
in dimethylformamide and tetrahydrofuran was reduced with 35 psi hydrogen and Raney
nickel catalyst. Removal of the catalyst by filtration and concentration of the filtrate
gave 21 g (0.052 mol) light yellow solid 3-(2-chloro-5-aminoaniiino-1-(2,4,6-trichiorophenyi)-2-pyrazoiin-5-one.
To an acetic acid solution containing 6.9 g (0.017 mol) of this amine and 9.5 g potassium
acetate was added, in small portions, 9.5 g (0.019 mol) of the acid chloride B
2CI prepared in Example 2. After stirring 15 hours, the mixture was concentrated to
a third of its volume, poured into a large volume of water and extracted with diethyl
ether. The organic layers were washed, dried, concentrated, and crystallized from
methanol to give 14 g (0.016 mol) buff-colored solid acetate ester of the desired
coupler, mp 115-116°C. To a solution of this product in dimethylformamide stirred
under nitrogen was added an aqueous solution containing 2 g potassium hydroxide. After
15 minutes the mixture was acidified with hydrochloric acid, poured into dilute hydrochloric
acid, extracted with diethyl ether, washed, dried, concentrated, and crystallized
from methanol to give 9.2 g white crystalline coupler M-28, mp 127-130°C.
Preparative Example 9
Preparation of Coupler M-8 by Scheme I
[0061] A suspension of 10 g (0.035 mol) 6-methyl-3-[3-(p-nitrophenyl)-propyl]-1 H-pyrazole[3,2-c]-5-triazole
in 300 ml tetrahydrofuran was shaken about 2 h at 25°C with 35 psi hydrogen and a
palladium on charcoal catalyst. Removal of the catalyst, concentration of the filtrate,
and recrystallization from acetonitrile gave a buff-colored solid amine, mp 194-6°C.
To a stirred acetic acid solution of 7.6 g (0.03 mol) of this amine product and 2
g potassium acetate was added, in small portions, 16.7 g (0.03 mol) of the acid chloride
B
2CI prepared in Preparative Example 1. After stirring 15 h, the mixture was poured
into a large volume of water, extracted with diethyl ether, and the combined extracts
then washed, dried, and concentrated to give the white solid benzyl ether of the desired
coupler, mp 122-124°C. A concentrated solution of 7 g (0.009 mol) of the product in
tetrahydrofuran was shaken 2 h under 40 psi hydrogen with a mixture of palladium on
charcoal catalyst in ethanol. Removal of the catalyst by filtration, concentration,
and recrystallization from acetonitrile gave 5.5 g cream-colored solid coupler M-8,
mp 170-172°C, with an infrared spectrum and elemental analysis consistent with the
desired compound.
Preparative Example 10
Preparation of Coupler M-32 by Scheme III
[0062] A mixture of 8 g (0.015 mol) 3-(2-chloro-4-fluorosulfonylanilino)-1-(2,6-dichloro-4-dimethylsulfamoyl
phenyl)-2-pyrazolin-5-one and 5.5 g aluminum chloride in 175 ml 1,2-dichloroethane
was refluxed 15 minutes. After cooling to 20°C, 7.25 g (0.015 mol) of the amine salt
B
5H.HCI prepared in Example 6 in 25 ml pyridine was added and the mixture refluxed 2
h. Then a mixture of hydrochloric acid, ice, and diethyl ether was added and the organic
layer washed, dried, concentrated, and triturated with hexane to give 14.2 g light
tan solid coupler M-32 with the correct elemental analysis.
Preparative Example 11
Preparation of Coupler Y-1 by Scheme I
[0063] To a solution of 57.8 g (0.095 mol) α-pivalyl-α-[4-(p-benzyloxyphenylsulfonyl)-phenoxy]-2-chloro-5-amino
acetanilide and 13 g quinoline, cooled to 0°C, was added in one portion 45 g (0.095
mol) of the acid chloride B
1 CI prepared in Preparative Example 4. After stirring 1 h the reaction mixture was
poured into 3 I cold water to produce 98 g (after oven drying) crude product. Recrystallization
from toluene yielded 84.5 g (0.018 mol) white crystalline dibenzyl ether of the desired
coupler. A suspension of 10.4 g (0.01 mol) of this product in 200 ml ethanol and 200
ml tetrahydrofuran was shaken 3 h under 35 psi hydrogen with palladium on charcoal
catalyst. Removal of catalyst by filtration concentration of the filtrate and trituration
in hot cyclohexane gave a good yield of coupler Y-1 with the correct elemental analysis.
Examples 1-14
[0064] Photographic elements of this invention and control elements were prepared and tested
according to the procedures described below.
[0065] All photographic elements were prepared by coating a cellulose acetate butyrate film
support with a photosensitive layer containing a silver bromo-iodide emulsion at 0.91
g Ag/m
2 (when the coupler is 4-equivalent) or 0.46 g Ag/m
2 (when the coupler is 2-equivalent), gelatin at 3.78 g/m
2, and one of the couplers identified in Table I dispersed in one-half its weight of
the coupler solvent described and coated at 1.62 x 10-
3 moles/m
2. The photosensitive layer was overcoated with a layer containing gelatin at 1.08
g/m
2 and bis-vinyl-sulfonylmethyl ether at 1.75 weight percent based on total gelatin.
[0066] Samples of each element were imagewise exposed through a graduated-density test object
and processed at 40°C employing one of three color developing solutions identified
below then stopped, bleached, fixed and washed.
[0067] In each element, well-defined, magenta dye images were produced which were evaluated
by plotting dye density vs. log exposure sensitometric curves and recording the maximum
dye density (D
max) and gamma (y) i.e., the contrast determined by the slope of the straight line portion
of the curve. Additionally, dye hues were evaluated from spectrophotometric curves
by measuring the maximum absorption peak (λ
max) normalized to a density of 1.0 and the half band width (HBW). Halfband width is
the width, in nanometers, of the spectrophotometric curve at one-half the difference
between maximum density and stain. Similarly, the top- band width (TBW) and bottom-band
width (BBW) of the curve were measured at three-fourths and one-fourth, respectively,
of the normalized density. Curve shape factor (CSF) equals 100 x TbW/HBW and provides
a ratio of the width near the top and bottom of the absorption curve. The greater
this ratio, the steeper are the sides of the absorption peak, and the more efficient
is the dye's absorption of light in its spectral region.
[0068] All results are recorded in Table I.
[0069] These results show that couplers of this invention have enhanced activity, which
results in increased maximum dye density and gamma. In addition many of the dyes formed
from couplers of this invention have absorption maxima at desirably longer wavelengths
and have broader half band widths and larger curve shape factors, resulting in more
efficient spectral absorption.
[0070]
[0072] (2) Coupler Solvents:
CS-1 - 1,4-Cyclohexylenedimethylene bis(2-ethyl-hexanoate)
CS-2 - Tri-cresyl phosphate
CS-3 - Dibutyl phthalate
CS-4 - 2,4-Di-t-pentylphenol
[0073] (3) Developer Formulations:
Example 15
[0074] Photographic elements containing additional couplers were prepared, processed and
evaluated as described above in connection with Examples 1-14. The results are reported
in Table II below.
Example 16
[0075] For each of the couplers identified below, photographic elements were prepared as
described above in connection with Examples 1-14. Four samples from each element were
exposed as described above. One pair of the exposed elements was developed in developer
D-2, described above, and the other pair was developed in this developer to which
had been added 1.5 g/i of the soluble competing coupler citrazinic acid. The remaining
processing for one element from each pair was stopping, bleaching, fixing and washing
while for the second element from each pair the bleaching step was omitted so that
the developed silver remained in the element. For those elements in which the silver
remained, the amount of developed silver, in g/m
2 , was determined by x-ray fluorescence analysis and plotted against exposure. For
those elements from which the developed silver had been removed, dye density vs exposure
curves were generated. From the plots for pairs of elements developed with the same
developer composition there was plotted, for each exposure step, dye density vs developed
silver. The slope of the line for the elements developed in the absence of a competing
coupler (Y
o in Table III, below) is a measure of the efficiency with which the coupler forms
dye; the greater the slope the more efficient the coupler. The slope of the line for
the elements developed in the presence of the competing coupler (Y
c in Table III, below) is a measure of the reactivity of the coupler, the greater the
slope, the more reactive the coupler.
[0077] It is apparent from the values for Y
o and Y
c in Table III that the couplers used in the invention react more efficiently with
oxidized developer to form image dye, in the presence or absence of a competing coupler,
than do those couplers with ballasts not used in this invention.