US3173906A - Azo dyes - Google Patents

Description

United States Patent 3,173,906 AZD DYES Milton Green, Newton Center, and Howard G. Rogers,

Weston, Mass., assignors to Polaroid Corporation, (1ambridge, Mass., a corporation of Delaware No Drawing. Filed May 8, 1962, Ser. No. 193,293 10 Claims. (2. 26tl-l62) This invention relates to photography and more particulanly to products, compositions and processes for the development of photosensitive silver halide elements.

It is one object of the present invention to provide novel processes and compositions for the development of silver halide emulsions, in which novel colored silver halide developing agents are used.

Another object is to provide novel processes and compositions for the development of silver halide emulsions, in which the novel silver halide developing agent is capable of developing an exposed silver halide emulsion and imparting a reversed or positive colored image of the developed image to a superposed image-receiving material.

Further objects are to provide said novel silver halide developing agents, and novel products, processes and compositions suitable for use in preparing monochromatic and multichromatic photographic images by the employment of said novel silver halide developing agents.

Other objects of the invention will in part be obvious and will in part appear hereinafter.

The invention accordingly comprises the processes involving the several steps and the relation and order of one or more of such steps with respect to each of the others, and the products and compositions possessing the features, properties and the relation of elements which are exemplified in the following detailed disclosure, and the scope of the application of which will be indicated in the claims.

The objects of this invention may be accomplished by the use of certain novel dyes which have the ability to develop an exposed silver halide emulsion; thus these dyes may be referred to as dye developers. These novel dyes or dye developers will be further described hereinafter.

The dye developers and the photographic processes and compositions disclosed herein are particularly useful in the treatment of an exposed silver halide emulsion, whereby a positive dye image may be imparted to another element, herein referred to as an image-carrying or imagereceiving element.

US. Patent No. 2,983,606, issued May 9, 1961, to Howard G. Rogers, discloses diffusion transfer processes wherein a photographic negative material, such as a photographic element comprising an exposed silver halide emulsion, is developed in the presence of a dye developer to impart to an image-receiving layer a reversed or positive dye image of the developed image by permeating into said emulsion a suitable liquid processing composition and bringing said emulsion into superposed relationship with an appropriate image-receiving layer. The inventive concepts herein set forth provide novel dye developers which may be advantageously used in such processes.

In carrying out the process of this invention, a photo sensitive element containing a silver halide emulsion is exposed and wetted with a liquid processing composition,

3,173,906 Patented Mar. 16, 1965 for example by immersing, coating, spraying, flowing, etc., in the dark, and the photosensitive element superposed prior to, during or after wetting, on an imagereceiving element. In a preferred embodiment, the photosensitive element contains a layer of dye developer, and the liquid processing composition is applied to the photosensitive element in a uniform layer as the photosensitive'element is brought into superposed position with an image-receiving element. The liquid processing composition permeates the emulsion to provide a solution of dye de veloper substantially uniformly distributed therein. As the exposed silver halide emulsion is developed, the oxidation product of the dye developer is immobilized or precipitated in situ with the developed silver, thereby providing an imagewise distribution of unoxidized dye developer dissolved in the liquid processing composition. This immobilization is apparently due, at least in part, to a change in the solubility characteristics of the dye developer upon oxidation, and especially as regards its solubility in alkaline solutions. It may also be due, in part, to a tanning efiect on the emulsion by the oxidized developing agent. At least part of this imagewise distribution of unoxidized dye developer is transferred, by imbibition, to a superposed image-receiving layer. The image-receiving layer receives a depthwise diliusion, from the emulsion, of unoxidized dye developer, without ap preciably disturbing the imagewise distribution thereof, to provide a reversed or positive, colored image of the developed or negative image. The image-receiving element may contain agents adapted to mordant or otherwise fix the diiiused, unoxidized dye developer. Imbibition periods of approximately one minute have been found to give good results, but this contact period may be adjusted where necessary to compensate for variations in temperature or other conditions. The desired positive image is revealed by separating the image-receiving layer from the silver halide emulsion at the end of the imbibition period.

The dye developers of this invention may be utilized in the photosensitive element, for example in, on or behind the silver halide emulsion, or they may be utilized in the image-receiving element or in the liquid processing composition. In a preferred embodiment, a coating or layer of the dye developer is placed behind the silver halide emulsion, i.e., on the side of the emulsion adapted to be located most distant from the photographed subject when the emulsion is exposed and preferably also adapted to be most distant from the image-receiving layer when in superposed relationship therewith. Placing the dye developer behind the emulsion layer, as in the preferred embodiment, has the advantage of providing increased contrast in the positive image, and also minimizes any light-filtering action by the colored dye developer. In this preferred embodiment, the layer of dye developer may be applied by using a coating solution containing, e.g., about 0.5 to 8%, by weight, of the dye developer. Similar concentrations may be used if the dye developer is utilized as a component of the liquid processing composition. In an especially useful mode of disposing the dye developers in the photosensitive elements, the dye developer is dissolved in a water-immiscible solvent and then dispersed in a gelatin coating solution.

The liquid processing composition which is used in the processes herein disclosed comprises at least an aqueous solution of an alkaline compound, for example, diethylamine, sodium hydroxide or sodium carbonate, and may contain the dye developer. In some instances, it may contain an additional silver halide developing agent. If the liquid processing composition is to be applied to the emulsion by being spread thereon, preferably in a relatively thin, uniform layer, it may also include a viscosityincreasing compound constituting film-forming material of the type which, when spread over a water-absorbent base, will form a relatively firm and relatively stable film. A preferred film-forming material is a high molecular weight polymer such as a polymeric, water-soluble ether inert to an alkali solution, as, for example, a hydroxyethylcellulose or sodium carboxymethyl cellulose. Other film-forming materials or thickening agents whose ability to increase viscosity is substantially unaffected when left in solution for a long period of time may also be used.

The novel azo dye developers of this invention may be represented by the formula:

Y is a 2,5-dihydroxyphenyl group, which group also may be nuclear substituted by alkyl or halogen (such as chlorine) groups;

Ar is a divalent aryl nucleus, such as a benzene or naphthalene nucleus, aring carbon of said aryl nucleus being 'directly attached to an azo (N N) group;

R is a divalent alkylene group, preferably an alkylene group containing no more than five carbons, and more preferably an ethylene (CH -CH or trimethylene (CH CH CH group, directly attached to a :ring carbon of said aryl nucleus Ar;

Each Z is an alkyl group, preferably a lower alkyl such as methyl or ethyl, an alkoxy group, preferably a lower .alkoxy group such as methoxy or ethoxy, or a halogen such as chlorine;

pis Ger 1;

n isO, 1 or.2;

m is 0 or 1;

X is the radical of an azo coupling component, e.g., a radical selected from the group consisting of benzene radicals and naphthalene radicals;

X is the radical of an azo coupling component or a radical; .and where X is the radical of an azo coupling component .or coupler, X and X may be the same or different, i.e., similar or dissimilar.

In a preferred embodiment, the compounds are monoazo and the aryl nucleus, Ar, is a benzene nucleus. Such compounds may be represented by the formula:

position ortho or para to the hydroxyl or amino group,

e.g., phenol, anilines, naphthols, anthrols, naphthylamines,

-etc.; heterocyclic aromatic compounds containing hydroxyl or amino groups, such as pyrazolones or pyrroles; aliphatic or alicyclic activated methylene couplers, i.c., compounds? having an aliphatic or alicyclic methylene group activated by two adjacent keto, aldehyde, ester or nitrile groups, which may be the same or dilferent, or a keto, aldehyde, ester or nitrile group in combination with an amide group, 7 e.g., 1,3-diketones or ,B-ketonic acid arylamides; etc., and substituted derivatives thereof. Examples of groups which may be present in such substituted derivatives include alkyl, sulfo, alkoxy, aryl, aryloxy, amino, keto, alkylamino, arylamino, hydroxyl, cyano, alkylamido, arylamido, carbalkoxy, carboxamido, sulfonamido, etc.

As used herein With reference to X and X the expression radical of a phenolic coupler is intended to refer to hydroxyphenyl, hydroxynaphthyl, hydroxyanthryl, etc. radicals, and substituted derivatives thereof; the expression radical of an aromatic amino coupler is intended to refer to aminophenyl, aminonaphthyl, etc. radicals, and substituted derivatives thereof; and the expressions radical of a heterocyclic aromatic coupler, radical of an aliphatic activated methylene coupler and radical of an alicyclic activated methylene coupler are to be similarly construed.

The novel compounds within Formulae A and B may be prepared fromstarting materials represented by the formula:

wherein Z, 11, Ar, p and R have the same meaning as above and Y is an 0,0'-bis-acyl derivative of Y. The presence of the acyl radicals in the above starting materials is necessitated by the fact that free hydroquinone groups would effect decomposition of the intermediate diazonium compound required in preparation of the desired dye developers. Once the reactions are completed, the desired dihydroxyphenyl compounds may be readily obtained wherein Z, n, p, R and Y have the same meaning as above.

.The preparation of starting materials within Formula C wherein p is 1 is disclosed in our copending application Serial No, 663,866, fil d June 6, 1957 (now U.S.'-Patent No. 3,009,958, issued November 21, 1961), and in a division thereof, Serial No. 93,303, filed March 6, 1961 (now US. Patent No. 3,081,339, issued March 12, 1963).

The preferred starting materials within the group represented by Formula C are:

p-Aminophenethylthiohydr0quin0ne-O,O'-diacetate su faces p Aminophenylthiohydroquinone-0,0-diacetate As examples of other compounds within Formula C, mention may be made of:

2- (p-aminophenethylthio) --methyl-hydro quinone- 0,0'-diacetate 2- (p-aminophenethylthio) -5-chloro-hydro quinone- 0,0'-diacetate 2- (p-aminophenylthio) -3 ,6-dimethyl-hydroquinone- 0,0'-diacetate 2- (p-aminophenethylthio) -3 ,5 ,G-trirn ethyl-hydroquinone- 0,0-di acetate p-Aminophenylmethylthio-hyd roquinone-0,0'-diacetate 2- ['y- 4'-aminophenyl -p ropylthio] hydroqu inone- 0,0'-diacetate 2- (4'-amino-3 '-methoxy-phenylthio) -hydro quinone- 0,0'-diacetate 2- {4-amino-3 '-methylphenylthio] -hydro quinone- 0,0-diacetate 2- m-4'-aminon aphthylthio) -hyd roquinone-0,0 -diacetate 2- (4'-amino-3 '-chlorophenylthio) -hydro quinone- 0,0-diacetate As noted above, R preferably is a lower alkylene group. It will be understood that the selection of particular alkylene, alkyl and alkoxy groups in the compounds of Formula C may be varied as desired, so long as the resulting dye developer is capable of being dissolved in the alkaline photographic processing solution and of transferring by diffusion within a reasonable imbibition time. The selection of solubilizing groups as substituents of the azo coupler radical, including their exclusion or inclusion, provides a useful means of modifying the solubility and diifusion properties of the resulting dye developer to meet the requirement of any particular application.

By the use of two moles of the diazonium salt to each mole of the coupling component, one may couple twice into certain of the azo coupling components which provide the az-o coupling radical X and which have two available coupling positions, as, for example, phenols and aromatic amines such as 1,6dihydroxy naphthalene and l,5-diamino-naphthalene. In this connection, it should be noted that coupling may be effected in two steps using one mol of each of the desired diazotized developer groups.

Further by coupling the diazotized compounds of Formula C with coupling components which will provide the coupling residue X with a diazotizable amino group, or a nitro group which may be reduced to a diazotizable amino group, the resulting monoazo compounds represented by the formula:

may in turn be diazotized and coupled with a coupling component which will provide the X coupling residue and produce compounds represented by the formula: (F) Y S (R) 1,-A rN=NX N=N-X wherein both X and X are azo coupler radicals.

The preparation of diazo dye developers within the scope of this invention may give rise to a mixture containing both monazo and diazo dye developers. It is to be understood that such mixtures may frequently be used Without separation.

a i As examples of suitable monoazo compounds within Formula E which can be further diazotized and coupled, mention may be made of:

2, idimethoxy-l- [p (2 ,5 -bis-acetoxyphenylthi0ethyl) phenylazo] -aniline and (BCH:

2,5dime thoxy-4- [p- (2' ,5-bis-acetoxyphenylthi0) phenylaz01-uniline Another method for preparing compounds within the scope of Formula A is to prepare a compound represented by the formula:

wherein R, Ar, Z, n, p, X and m have the same meaning as above; X is a residue of a coupling component, a

HO- N l-phenyLB-methyl-4- [p- (2 ,5 -dihydroxyphenylthioethyl pheny1azo1-5-pyrazo10ne on (llH a (XVII) na n-r s-N=N t, (in -CzHr-OH 2 [p- 1-methy12' ,5'-dihydroxyphenylthio) phenylazo 1 -4B hydroxy ethoxy-l-naphthol phenylazo]pheny1azo)-4-methoxy-1-naphth0l (XIX) (RH (1311 in o -s-omcmu=ni) l O H O (XX) H Where the axe coupling component is a phenolic coupler, and particularly an m-naphthol, it has been found that coupling ortho to the hydroxyl group gives a dye developer of superior color properties and reduced pH sensitivity over a fairly wide range on either side of neutral.

As examples of additional coupling components which may be used to provide X and X mention may be made of:

4-benzyl-1-naphthol 4-methyll-naphthol 4rnethoxyl-naphthylamine 4-acetamido-l-naphthylamine S-aminol-naphthol Phenol Aniline 1,5 -napl1thalene diamine p-Cresol 1-hydroxyanthracene 2-hydroxyanthra cene 1-hydroxy-Z-naphthanilide Diketohydrindene Malononitrile Acetoacetanilide 1-phenyl 3-amino-5-pyra20i0ne l-phenyl-3-acetamido-5-pyrazolone B-Naphthol 4-amino-1-naphthol 4-sulfo- 1-n aphthol 4-hexyloxy-1-naphthol 2- u-cyanoacetyl] -coumarone The novel dye developers of this invention are to be distinguished from the compounds disclosed and claimed in the copending application of Myron S. Simon, Serial No. 612,053, filed September 25, 1956 (now abandoned in favor of Serial Nos. 196,523 and 196,524, now US. Patent No. 3,134,765, both filed May 21, 1962), and also the compounds disclosed and claimed in the copending applications of Elkan R. Blout, Milton Green and Howard G. Rogers, Serial No. 612,045, filed September 25, 1956 (now abandoned), and in serial Nos. 144,816 now US. Patent No. 3,134,672, and 145,978, now US. Patent No. 3,134,764, both filed October 18, 1961, as continuationsin-part of said Serial No. 612,045, by the presence of the thio radical. The dye developers of this invention have unexpectedly been found to give diffusion transfer images of higher contrast than those of the above-mentioned copending applications, as well as faster film speeds than similar dye developers wherein the thio linkage is absent.

In general, starting materials within Formula C above, wherein p is 0, may be prepared by reacting the appropriate nitrophenylthiol or nitronaphthylthiol with the appropriate benzoquinone, followed by acylating the hydroxyl groups and reducing the nitro group. Starting materials within Formula C, wherein p is 1, generally may be prepared by reacting the appropriate Z-mercapto-hydroquinone with the appropriate nitrophenylalkyl halide or nitronaphthylakyl halide, preferably the bromide followed by acylation and reduction.

The following examples of the preparation of dye developers within the scope of this invention are given for purposes of illustration only:

Example 1 0.02 mol of 2,5-bis-acetoxyphenylthioethylanilinehydrochloride (prepared by the procedure disclosed in our aforementioned copending application) is dissolved in 150 cc. of water containing 0.05 mol concentrated hydrochloric acid and diazotized at 0 to 5 C. by the addition of 0.02 mol sodium nitrite in 15 cc. of water. After ten minutes the solution is clarified and the pH raised to 5-6 with sodium acetate. The clear diazo solution is then added at room temperature over a period of half an hour to a solution of 0.018 mol of 1-phenyl- 3-methyl-5-pyrazolone in 300 cc. of ethanol, and 300 cc. of 10% sodium bicarbonate is added portionwise. The resulting yellowish slurry is stirred at room temperature for two hours, filtered, and the filter cake washed thoroughly with 10% sodium bicarbonate. The filter cake is reslurried in dilute acetic acid solution, filtered, and washed thoroughly with water. The product is dried in vacuo over sulfuric acid.

The acetoxy radicals are hydrolyzed oil by dissolving the above product in 160 cc. of ethanol, 40 cc. of Water followed by 18 g. potassium hydroxide and the flask immediately evacuated. It is shaken for five minutes with intermittent heating on a steam bath, then cooled and acidified directly with hydrochloric acid, and diluted with water to complete the precipitation. After filtration the solid is washed with water.

To purify, the filter cake is dissolved in a minimum amount of ethanol, under nitrogen, and the hot solution treated with activated charcoal. The material is reprecipitated from the filtrate by a 1% sodium chloride solution containing a trace of hydrogen chloride; the solid filtered and the procedure repeated. The resulting yellow solid is filtered, Washed with Water, and dried to give 1-phenyl-3-methyl-4-[p-(2',S-dihydroxyphenylthioethyl)-phenylazo]-5-pyrazolone, melting at to C. The visible spectrum exhibits a A at 395 m e=25,300 in acetone.

Example 2 0.006 mol of 2,5-bis-acetoxyphenylthioethylanilinehydrochloride, diazotized as in Example 1, is added at well with water. as'oliition of 3 g. of potassium hydroxide in 20 cc.

dissolved in ethanol.

about C. to a solution of 0.008 mol oi 4-methoxy-1- stirred for rear hours, filtered, and the filter cake washed The moist filter cake is dissolved in at water and '40 cc. of ethanol and the flask is immediately evacuated. It is shaken for three minutes with ihtermittent warming on a steam bath, after which the solution iscooled briefly and then filtered rapidly into dilute hydrochloric acid. The resulting precipitate is filtered and washed well with water. The product is purified by recrystallization from aqueous methylcellosolve and dried to give 2-[p-(2,5'-dihydroxyphenylthioethyl)- phenylazo]-4-methoxy 1-naphthol, melting at 165 to 170 C. The visible spectrum exhibits a kmax. at 520 mp, e=22,700 in acetone.

Exampie 3 :2,ibis-acctoxyphenylthioafiiline is prepared by disservin 4.5 g, of p nitro thiophenol in. 250 cc. of ethanol and easing slowly over a period 'of about one-half hour use-t nfoil bf 10 g. of benzoquinone in 200 cc. ethanol. The resulting solution is poured into 2 liters of ice water and the precipitate is filtered and dried and recrystallized from a benzene-hexane solution. The product was refluxed with 150 cc. of acetyl chloride and 1 cc. of concentrated sulfuric acid for two hours, cooled, and

' poured into ice water to yield a gum which soon solidi fies. The solid is triturated with water, filtered and dried over phosphorous pentoxide. The product is dissolved in ethanol and eataly'tically reduced over a palladium barium Sulfate bed;

0.01 mol at the 2,5-biseacetoxyphenylthioaniline,

area above, is dissolved in 20 cc. er water and 1.6 cec'f concentrated hydrochloric and and diazotized by adding 0.7 g. of sodium nitrite dissolved in 10 cc. of wat r at C. I The diazo product is added, dropwise with stirring, to a solution of 0.01 mol of 1-phenyl-3-methyl-5-pyrazolone in 50 cc. of Water, 4.2 g. of sodium bicarbonate and cc. of ethanol, the solution having previously been cooled to 5 C. The resulting yellow precipitate is filtered and then treated, under nitrogen, with 25 cc. of ethanol and 25 cc. of sodium hydroxide solution for five minutes at 90 to 100 C. The product is precipitated by adding dilute hydrochloricacid and is recrystallized from ethanol to yield the desired 1- phenyl 3 methyl 4 [p (2',5' dihydroxyphenyl thio)-phenylazo]-5-pyrazolone, melting at 202 to 204 C. The visible spectrum exhibits a A at 420 m e='24,500 in 95% ethanol.

Example 4 0.005 mol of 2,5-bis-acetoxyphenylthioaniline is diazotized in a manner similar to that described in Example 3.

0.005 mol of 4-methoxy-l-naphthol is added to cc. of acetone and 2.1 g. of sodium bicarbonate in 10 cc. of water and the suspensioncooled to 5 C. The diazo solution is added dropwise and the suspension is stirred for five minutes. A red precipitate is filtered out and The solution is then filtered and the product precipitated with water. The precipitate is filtered and the wet filter cake hydrolyzed by heating, under nitrogen, with 20 cc. of ethanol and 20 cc. of

10% sodium hydroxide for four minutes. Precipitation with dilute hydrochloric acid gives 2-[p-(2,5-dihydroxyphenylthio)-phenylazo]-4-methoxy-1-naphthol, melting at 146-149" C. The visible spectrum exhibits a Amax. at 530 m e=l9,000 in acetone.

It is to be understood that the 0,0'-bis-acyl compounds of Formula C may also be prepared by selective acylation of the hydroxyl groups of the corresponding p-dihydroxyphenyl compound in a manner similar to that 12 described in US. Patent No. 3,019,254, issued January 30, 1962, to Milton Green and Helen P. Husek.

Othercompounds which are also novel and are closely related to the compounds within Formula A may be prepared by oxidizing the dihydroxpyhenyl groups of said compounds within Formula A to the corresponding quinone or dioxophenyl compounds under conditions which do no attack the azo bond. As examples of useful oxidizing agents for carrying out this oxidation, mention may be made of mercuric acetate and p-benzoquinone. These azo quinones may be used in the photographie processes disclosed and claimed in the copendiiig application of Howard G. Rogers, Serial No.

825,359, filed July 6, 1959, as a continuation-in-part of, and replacement for, Serial No. 599,122, filed July 20, 1956 (now abandoned). The preferred compoundscf this liass mhno'ciuinbnes which may be repretested by the formula:

wherein R, Ar, Z, n, p and m have the same meaning as above; X and X are radicals of azo coupling components; and Y is a 2,5-dioxophenyl group which may also be substituted by alkyl and halogen groups. As an example of such compounds, mention may be made oi:

Eli-cm Example 5 0.10 mol of 1=phenyl*3-methyl-4-[p (2',5 -dihydroxy phenylthio)-phenylazo]-5-pyrazolone, as prepared in Ex= ample 3, and 0.12 mol of mercuric acetate are dissolved in dimethylfor-marnide and reacted While open to the air over a steam bath for three to four hours. Upon cooling, the insoluble mercurous acetate, is filtered out and the product is precipitated by adding water. By crys= tallization of the product from a chloroform-methylcellosolve solution l-phenyl-methyll[p-(2',5'-dioxophenylthio)-phenylazo] -5-pyrazolone is obtained.

In the following examples all parts are given by weight except where otherwise noted, and all operations involving light-sensitive materials are carried out in the absence of actinic radiation. These examples are intended to be illustrative only of the photographic use of the dye developers and should notbe construed as limiting the invention in any way.

Example 6 A photosensitive element is prepared by coating a gelatin-coated film base with a solution comprising 3% of 1- phenyl 3 methyl 4 [p (2,5 dihydroxyphcnylthioethyl)-phenylazo]-5-pyrazolone (Formula I, as prepared in Example 1) in a solution of 4% cellulose acetate hydrogen phthalate in a 50:50 mixture, by volume, of tetrahydrofuran and acetone. After this coating has dried, a silver iodobromide emulsion is applied. An imagereceiving element is prepared by coating a cellulose acel3 tate-coated baryta paper with a solution comprising 4% N-methoxymethyl polyhexarnethylene adiparnidc in ethanol. The photosensitive element is exposed and brought into superposed relationship with said image-receiving element as an aqueous liquid composition comprising:

Percent Sodium carboxymethyl cellulose 4.5 Potassium bromide 0.2 Sodium hydroxide 2.0 l-phenyl-3-pyrazolidone 0.2

is spread between said elements. After an imbibition period of approximately one minute, the image-receiving element is separated and contains a yellow positive image.

Example 7 When the procedure of Example 6 is repeated, using as the dye developer 4% of 2-[p-(2,5' dihydroxyphenylthioethyl)-phenylazo]-4-methoxy-lnaphthol (Formula III, as prepared in Example 2) and using as the image-receiving element a cellulose acetate-coated baryta paper, which is coated with an aqueous solution containing 4% of polyvinyl alcohol, a magenta positive image is obtained.

Example 8 A photosensitive element is prepared similar to that described in Example 6 using 4% of 2-[p-(4-methyl-2',5- dihydroxyphenylthioethyl) phenylazo] --4 methoxy 1- naphthol (Formula II). Exposure and processing with a liquid processing composition and image-receiving element similar to those described in Example 6 give a magenta positive image.

Example 9 Use of a photographic element prepared and processed in a manner similar to that described in Example 6 using 3 of 2- {p-(2,5'-dihydroxyphenylthio) -phenylazo] -4- methoxy-l-naphthol (Formula V) gives a magenta positive image.

Example 12 The process described in Example 6 is repeated using a 2.5% of 2-[oz-cyano-u(p-[2,5-dihydroxyphenylthio]- phenylazo)-acetyl]-naphthalene (Formula VI) as the dye developer and an aqueous processing composition comprising:

Percent Sodium carboxymethylcellulose 45 Potassium bromide 0.2 Sodium hydroxide 1.5 1-phenyl-3-pyrazolidone .2

The image-receiving element, prepared as described in Example 6, contains a yellow positive dye image when separated from the photosensitive element after an imbition period of one minute.

Example 12 A photosensitive element was prepared in a manner similar to the above examples, except that the dye developer was 2 [p (2',5 dihydroxyphenylpropylthio)- phenylazo] 4 rnethoxy 1 naphthol. After the coating containing the dye developer dried, a green-sensitive I l silver iodobromide emulsion was applied and allowed to dry. This photosensitive element was exposed, and brought into superposed relationship with an image-receiving element as an aqueous liquid composition comprising:

Water cc NaOH g 5.17 Hydroxyethyl cellulose (high viscosity) [commercially available from Hercules Powder Co., Wilmington 99, Delaware, under the trade name Natrosol 250] g 4.03 Sodium thiosulfate g 1.15 Benzotriazole g 2.3 N-benzyl-d-picoliniinn bromide g 2.3

was spread between said elements. The image-receiving element comprised a 2:1 mixture, by Weight, of polyvinyl alcohol and poly-4-vinylpyridine on a baryta paper sup port. After an imbibition period of approximately one minute, the image-receiving element was separated and contained a magenta positive image.

As will be readily understood by one skilled in the art, the dye developers not specifically described in the above specific examples may be prepared by diazotization and coupling procedures similar to those illustrated by Examples 1 through 4, substituting the desired azo coupler and amino compound Within the aforementioned Formula C.

Although the above examples have employed the dye developer in a layer of cellulose acetate hydrogen phthalate, it will be understood that the dye developer may be dissolved in a Water-immiscible solvent, the resulting solution dispersed in gelatin, and the dispersion coated to provide the dye developer layer.

It should be noted that certain dye developers may be sensitive to pH changes. Since the dye developer is rendered effective by solution in an aqueous alkaline liquid processing composition, it accordingly is necessary to assure that the environment in which the transferred and unreacted dye developer is deposited has, or is capable of attaining, the requisite pH value ailording the desired color to the diffused dye developer. This may be accom plished by use of a volatile basic compound such as diethylamine in the liquid processing composition. If sodium hydroxide is utilized in the processing liquid, it becomes carbonated after processing and by contact with the air and this is effective to provide the desired pH change. Further control of the pH of the transferred and unreacted dye developer may be had by utilizing an image-receiving element which is diiiicuitly penetrable by alkali, for example, an appropriate nylon such as N-methoxymethyl polyhexamethylene adipamide, or by the use of a receiving element in which an acid or an acid-forming compound, e.g., oleic acid, has been incorporated.

The dye developers of this invention are also useful in integral multilayer photosensitive elements for use in multicolor diilusion transfer processes. As an example of such photosensitive elements, mention may be made of the photosensitive elements disclosed and claimed in the copending US. application of Edwin H. Land and Howard G. Rogers, Serial No. 565,135, filed February 13, 1956, wherein at least two selectively sensitized photosensitive strata are superposed on a single support and are processed, simultaneously and Without separation, with a single common image-receiving element. A suitable arrangement of this type comprises a support carrying a red-sensitive silver halide emulsion stratum, a greensensitive silver halide emulsion stratum and a blue-sensitive silver halide emulsion stratum, said emulsions having associated therewith, respectively, a cyan dye developer, 21 magenta dye developer and a yellow dye developer. In one of the preferred embodiments of photosensitive elements of this type, the dye developers are disposed in separate alkali-permeable layers behind the photosensitive attends s is silver halide emulsion stratum with which they are associate'd. I

The photosensitive eler'iientswitliifi are steps of this invention may be used in roll film units wliich contain a plurality of photosensitive frames. The photosensitive elements of this invention are especially useful in composite roll film intended for use in a Pol aroid Land Camera or a similar camera structure such, for example, as the camera forming the subject matter of U.S. Patent No. 2,435,717, issued to Edwin H. Land on February 10, 1948. lngeneral, such composite roll films comprise a photosensitive roll, a roll of image-receiving material and a plurality of pods containing an aqueous alkaline processing solution The rolls and pods are so associated with each other that, upon processing, the photosensitive els rnent may be'superposed on the image-receiving element the pods may be ruptured to spread the aqueous alkaline pfocessing solution between the superposed elements. The nature construction of the pods used in such units are well known to tl'i art; Seeder example, U.S. Patents Nos. 2,543,181 and 2,634,886, issued to Edwin H. Land.

it will be noted that the liquid processing composition may contain one or more auxiliary or accelerating silver halidedeveloping agents, such as p-methylaminophenol (lvietol); 2,4-diaminophenol (Amidol); benzylaminophe ol; hydroquinone; a substituted hydroquinone such as toluhydroduinone, phenylhydroquinone, or 4-rnethylphenylllydr'oiiuiii-onetor a 3 pyrazolidone such as 1phenyl-3- pyrazolidon. These silver halide developing agents are siibsta'ntially colt irle'ss, at e st in their unoxidized form. It is possible that some ofthedye dev'eltipei oxidized in exposed areas may be oxidized by ad rir'g y' transfer fe= action with oxidized auxiliary developing agent.

In addition, development may be eitected in the presence of an oniurn compound, particularly a quaternary ammonium compound, in accordance with the processes disclosed and claimed in the copending application of Milton Green and Howard G. Rogers, Serial No. 50,851, filed August 22, 1966. 4 The dye dev'eloper's of this invention may be used also in conventional photographic processes, such as tray or tank development of conventional photosensitive films, plates or papers to obtain black and white, monochromatic dntoncd prints or negatives. By way of example, a developer composition suitable ft'ii such use may com rise an aqueous solution of approximately 1 2% of the dye developer, 1% sodium hydroxide, 2% sodium sulfite and 0.05% potassium bromide. After development is completed, any unfeacted dye developer is washed out of the photosensitive element, preferably with an alkaline Washi'rig medium or other medium in which the unreacted dye developer is soluble. The expression toned is used to designate photographic images wherein the silver is retained with the precipitated dye, whereas monochromatic is intended to designate dye irrrages'free of silver.

It should be noted that the dye developers of this medium are self-sufficient topnovide the desired color image and do not depend upon coupling reactions to produce the desired color. They thus provide a complete departure from conventional photographic color processes in which the color is produced by a coupling reaction between a color former or coupler and the oxidized developing agent, as well as so-called auto-coupling processes in which color is obtained by a reaction of the oxidized developing agent with unoxidized developing agent.

It will be apparent that, by appropriate selection of the image-receiving element from among suitable known opaque and transparent materials, it is possible to obtain either a colored positive reflection print or a colored posi tive transparency. Likewise, the inventive concepts herein set forth are adaptable for multicolor work by the use of special photographic materials, for example, film materials of the type containing tWo or more photosensitized elements associated with an appropriate number of image-- receiving elements and adapted to be treated with one or more liquid processing compositions, appropriate dye dc velopers suitable to impart the desired subtractive colors being incorporated in the photosensitized elements or in the liquid processing compositions. Examples of such photographic materials are disclosed in U.S. Patent No. 2,647,049 to Edwin H. Land.

As examples of useful image 'receivingmaterials, men tion'may be made of nylon, e'.g., N-ntethoxyrnethylpoly' hexarnethylene adipamide, polyvinyl alcohol, and gelatin, particularly polyvinyl alcohol or gelatin containing a dye niordant such as poly-4-vinylpyridine. The image-receiving element also may contain a development restrainer, e.g., 1-phenyl-5-mercaptotetrazole, as disclosed in the co pending application of- Howard G. Rogers and Harriet W. Lutes, Serial No. 50,849, filed August 22, 1960.

The dye developers herein set forth are also useful in the formation of colored images in accordance with the photographic products and processes described and claimed in U.S. Patent No. 2,968,554, issued to Edwin l i- Land on January 17, 1961.

The nov'elc'ompounds herein disclosed are also suitable for use as dyes for textile fibres, such as nylon.

In the preceding portions of the specification the expression color has been frequently used. This expression is intended to include the use of a plurality of colors to obtain black.

This application is in part a continuation of our copending application Serial No. 663,905, filed June 6, 1957, (now abandoned).

Since certain changes may be made in the above products', compositions and processes without departing from the scope of the invention herein involved, it is intended that all matter contained in the above description shall be interpreted as illustrative and not in a limiting sense.

What is claimed is'.'

1. An azo dye of the formula:

wherein Y is selected from the group consisting. of 2,5- dihydroxyphenyl and methyl and chloro nuclear substituted 2,5-dihydroxyphenyl groups; Ar is a divalent aryl nucleus selected from the group consisting of benzene and naphthalene nuclei, a ring carbon of said aryl nucleus being directly attached to an N:N- group; R is a divalent lower alkylene group directly attached to a ring carbon of said aryl nucleus Ar; each Z is selected from the group consisting of lower alkoxy, lower alkyl and chloro groups; p is O to 1, inclusive; n is O to 2, inclusive; m is 0 to 1, inclusive; X is selected from the group consisting of benzene radicals and naphthalene radicals; and X is selected from the group consisting of the radical of an azo coupling component and a radical, provided that X is the radical of an azo coupling component when m is 0.

2. An azo dye as defined in claim 1, wherein Ar is a benzene nucleus, R is ethylene, n is O, p is 1, m is O, X is the radical of an azo coupling component, and Y is 2,5-dihydroxyphenyl.

3. An azo dye as defined in claim 1, wherein Ar is a benzene nucleus, p is 0, n is O, m is 0, X is the radical of an azo coupling component, and Y is 2,5-dihydroxyphenyl.

4. 2 [p-(2,5'-dihydroxyphenylthioethyl)-phenylazo]- 4-methoxy-l-naphthol. I

5. 1 phenyl 3 methyl 4 [p'(.2',5' dihydroxyphenyhljiio)-phenylazo]-5-pyrazolone.

6. 2 [p (2',5' dihydroxyphenylthia)mhenylazo]-4- methoxy-l-naphthol.

7. 1 phenyl-3-methyl-4-[P-(25'-dihydroxyphenyithioethyD-phenylazo] -5-pyrazo10ne.

8. 2 [a-cyan-o-u-(p-[2',5'-dihydroxyphenylthio]-p11enylazo -acety1] -naphtha1ene.

9. A benzoquinone of an azo dye as defined in claim 1.

10. 1 phenyi-3-methy1-4-[p-(2',5'-dioxophenyithio)- phenylazo] -5 pyrazolone.

18 References Cited in the file of this patent UNITED STATES PATENTS Land Aug. 22, 1961 OTHER REFERENCES

Claims (1)

1. AN AZO DYE OF THE FORMULA: