[go: up one dir, main page]

US3053656A - Photographic silver halide developers containing triazine rings - Google Patents

Photographic silver halide developers containing triazine rings Download PDF

Info

Publication number
US3053656A
US3053656A US780964A US78096458A US3053656A US 3053656 A US3053656 A US 3053656A US 780964 A US780964 A US 780964A US 78096458 A US78096458 A US 78096458A US 3053656 A US3053656 A US 3053656A
Authority
US
United States
Prior art keywords
silver halide
developing
triazine
compound
amino
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US780964A
Inventor
Richard S Corley
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Polaroid Corp
Original Assignee
Polaroid Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Polaroid Corp filed Critical Polaroid Corp
Priority to US780964A priority Critical patent/US3053656A/en
Application granted granted Critical
Publication of US3053656A publication Critical patent/US3053656A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C5/00—Photographic processes or agents therefor; Regeneration of such processing agents
    • G03C5/26—Processes using silver-salt-containing photosensitive materials or agents therefor
    • G03C5/29—Development processes or agents therefor
    • G03C5/30—Developers
    • G03C5/3021—Developers with oxydisable hydroxyl or amine groups linked to an aromatic ring

Definitions

  • One object of the present invention is to provide novel processes and compositions for the development of latent images present in photosensitive silver halide emulsions.
  • a further object of the present invention is to provide novel compounds which are capable of developing exposed silver halide emulsions.
  • the invention accordingly comprises the several steps and the relation and order of one or more such steps with respect to each of the others, and the products and compositions possessing the features, properties and 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.
  • X is selected from the group consisting of R l Y z chloro, hydroxyl, alkyl, amino, aminoalkyl, aryloxy, and alkoxy radicals;
  • R is hydrogen or an alkyl group;
  • Y is a divalent radical or a covalent bond; and
  • Z is an aryl nucleus selected from the group consisting of benzene and naphthalene nuclei substituted by at least two members of the group consisting of hydroxyl and amino groups so as to be capable of developing a silver halide latent image.
  • divalent radicals signified by the term Y in Formula A and suitable for use in the practice of the present invention, mention may be made of: divalent organic radicals such as alkylene radicals, preferably lower alkylene radicals such as ethylene, isopropylene, etc.; arylene radicals such as phenylene, etc.; aralkylene radicals such as phenethyl, etc.; acyl radicals such as t alkyleneetc.
  • silver halide developing agents which contain an aryl nucleus selected from the group consisting of benzene and naphthalene nuclei so substituted by at least two groups selected from the group consisting of hydroxyl and amino groups as to be capable of developing an exposed silver halide emulsion.
  • a preferred silver halide developing group comprises a hydroquinonyl group.
  • Other suitable developing groups include ortho-dihydroxyphenyl, triaminophenyl, orthoand para-amino substituted hydroxyphenyl groups, and the corresponding naphthalene developing groups.
  • the developing group comprises a benzenoid developing configuration, that is, an aromatic developing group which forms quinonoid or quinone products upon oxidation.
  • Z may be substituted by halogen, alkoxy, alkyl, etc., radicals.
  • amino as used herein is intended to include amino groups so substituted as not to impair their respective silver halide developing functions, for example, suitably substituted alkylamino and arylamino groups.
  • Examples of specific triazine photographic developing agents within the scope of the above formula include hydroquinoneamino-dihydroxy s triazine, Z-hydroquinoneamino-4-chloro-6-hydroxy-s-triazine, and 2,4-bis-(hydroquinoneamino) -6-hydroxy-s-triazine.
  • the developing agents of this invention maybe prepared by reacting a triazine compound of the formula:
  • Y is selected from the group consisting of chloro, hydroxyl, alkyl, amino, aminoalkyl, aryloxy, and alkoxy radicals; with a compound of the formula: 1?
  • R, Y and Z have the same significance as in Formula (A); such as Amino-phenethyl-hydroquinone, the preparation of which is disclosed in the copending US. application of Elkan R. Blout, Milton Green, Howard G. Rogers, Myron S. Simon and Robert B. Woodward, Serial No. 612,051, filed September 25, 1956;
  • Amino-propyl-amino-hydroquinone the preparation of which is disclosed in the copending US. application of Milton Green and Myron S. Simon, Serial No. 711,812, filed Ianuary 29, 1958, now Patent No. 3,002,997 issued October 3, 1961; and 1 Amino-hydroquinone, amino-ethyl-hydroquinone, aminophenyl-hydroquinone, and amino-phenyl-sulfonyl-hydroquinone, etc., which may be prepared by known chemical reactions; in an inert organic reaction medium, such as acetone or pyridine. The amine is employed in the ratio of approximately one mole, per mole of triazine compound, for each group to be introduced.
  • Reaction with the triazine compound proceeds roughly stepwise; for example, with cyanuric chloride, the first chlorine reacts at temperatures of about 10 C. to about C., the second chlorine at about 40 to 50 C. and the third chlorine at about 90 to 100 C.
  • the crude product may be hydrolyzed by heating, under nitrogen, for about 15 minutes at 100 C. in excess 5% alkali.
  • the hydrolyzed product may be precipitated in acid, yielding a tan powder.
  • a pink tan powder is obtained which melts at about 310 C., is soluble in alkali, sparingly soluble in methanol, and insoluble in water and acetone.
  • the bis-substituted triazine compound may be prepared by dispersing monobenzoyl hydroquinone-amino cyanuryl dichloride, for example the unfiltered reaction mixture of Example 1 having a pH of 5-6, in water at 40-50 C. A solution of 20 g. of Z-amino-hydroquinonean that this Provides an effective means of controlling 4-benzoate in boiling acetone is then added A solution the degree and nature of substitution of the triazine ring, of 7 of anhydrous ,sodmm carbonate m 5 of thereby enabling him to obtain developing agents of varyi 1s addedgver a penod of one 1 and the mlxture ing developing potential within the scope of this invention.
  • the crude It is generally desirable to protect the hydroxyl and/or action i i may be worked up the same i t amino groups of the developing function, during reaction, 20 as desctlbed
  • Example h Crude Product 13 3' to avoid undesirable side reactions, for example, to emsciluble m acetone i hot organ: solvents $116.11 as ploy a protected derivative of Z, that is, a compound withethanol and mtrobenziene
  • the q blsfprodugt in the formula: may be hydrolyzed by heatmg under nitrogen, 111 warm (D) R alkali for about 10 minutes to g ve an alkali-soluble by- H 1 Y Z drtolysrs product, 2,4-bis-(hydroquinoneamino)-6-hydroxysriazrne.
  • novel triazine developing agents of this invention 8 j may be used in conventional multistage and multibath photographic processing procedures in either black-andwhite or color photography. They are also useful as developing agents in diffusion transfer reversal processes, both dye and silver, and are especially useful in such photographic processes wherein it is desired to eliminate or minimize the need for washing or stabilizing operations in liquid baths subsequent to the formation of the silver print. Example of such processes are disclosed in U.S. Patent 2,647,056 to Edwin H. Land.
  • the herein disclosed novel triazine developing agents are useful in transfer processes of the type disclosed in the said patent to Edwin H. Land, and in other processes in which the problem of a residual stain cannot be readily met by washing operations.
  • the novel developer compositions of this invention have incorporated therein as a further ingredient a silver halide solvent, such as sodium thiosulfate.
  • a silver halide solvent such as sodium thiosulfate.
  • the composition may also include a film-forming thickening agent such, for example, as the high molecular weight polymer, sodium carboxymethyl cellulose.
  • concentrations of about 3%, by weight, of these novel triazine developing agents for example hydroquinoneamino-dihydroxy-s-triazine, will .give good results in the above described transfer processes.
  • the developing agent may be disposed prior to exposure in a photosensitive element comprising the photographic emulsion, and the developer composition containing the agent formed by permeating the emulsion with an aqueous alkaline liquid capable of solubilizing the agent.
  • the developing agent may be dissolved in an aqueous alkaline solution prior to application thereof to an exposed silver halide emulsion.
  • Particularly useful developer compositions may also contain an auxiliary or accelerating developer such as metol, henzylaminophenol or a 3-pyrazolidone such as l-phenyl-3-pyrazolidone.
  • an auxiliary or accelerating developer such as metol, henzylaminophenol or a 3-pyrazolidone such as l-phenyl-3-pyrazolidone.
  • triazine developing agents of this invention may also be used in conventional blackand-white tank and tray development.
  • the triazine developers of this invention are very stable to heat and light.
  • the novel triazine derivatives of aminohydroquinone of this invention are much more stable than aminohydroquinone itself, and this is an important advantage in the use of these triazine compounds.
  • a photographic developer composition comprising an aqueous alkaline solution containing a silver halide solvent and at least one compound of the formula:
  • each X is selected from the group consisting of chloro, hydroxyl and radicals, and Z is a dihydroxyphenyl silver halide developing radical.
  • a novel photographic developer composition as defined in claim 1, wherein said compound is 2-hydroquinoneamino-4-chloro-6-hydroxy-s-triazine.
  • each X is selected from the group consisting of chloro, hydroxyl and radicals, and Z is a dihydroxyphenyl silver halide developing radical.
  • a process as defined in claim 5 wherein said silver halide developing agent is hydroquinoneamino-dihydroxys-triazine.
  • each X is selected from the group consisting of chloro, hydroxyl and radicals, R is a hydrogen atom and Z is a dihydroxyphenyl silver halide developing radical; contacting unexposed and undeveloped silver halide therein with said silver halide solvent and forming thereby an irnagewise distribution of a soluble silver complex in the undeveloped areas of said emulsion; and transferring by imbibition, at least in part, said imagewise distribution of soluble silver complex to a superposed image-receiving layer to provide a silver transfer image.
  • I TZ comprises a hydroquinonealkyleneamino group.

Landscapes

  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Plural Heterocyclic Compounds (AREA)

Description

United States Patent O 3,053,656 PHOTOGRAPHIC SILVER HALIDE DEVELOPERS CONTADIEIG TRIAZINE RINGS Richard S. Corley, Wellesley Hills, Mass., assignor to Polaroid Corporation, Cambridge, Mass., a corporation of Delaware No Drawing. Filed Dec. 17, 1958, Ser. No. 780,964 13 Claims. (Cl. 96--29) This invention relates to photography and more particularly to compositions and processes for development of photosensitive silver halide elements.
One object of the present invention is to provide novel processes and compositions for the development of latent images present in photosensitive silver halide emulsions.
A further object of the present invention is to provide novel compounds which are capable of developing exposed silver halide emulsions.
Other objects of the invention will in part be obvious and will in part appear hereinafter.
The invention accordingly comprises the several steps and the relation and order of one or more such steps with respect to each of the others, and the products and compositions possessing the features, properties and 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.
A novel class of photographic developing agents has been discovered, these compound corresponding to the formula:
wherein X is selected from the group consisting of R l Y z chloro, hydroxyl, alkyl, amino, aminoalkyl, aryloxy, and alkoxy radicals; R is hydrogen or an alkyl group; Y is a divalent radical or a covalent bond; and Z is an aryl nucleus selected from the group consisting of benzene and naphthalene nuclei substituted by at least two members of the group consisting of hydroxyl and amino groups so as to be capable of developing a silver halide latent image.
As examples of divalent radicals, signified by the term Y in Formula A and suitable for use in the practice of the present invention, mention may be made of: divalent organic radicals such as alkylene radicals, preferably lower alkylene radicals such as ethylene, isopropylene, etc.; arylene radicals such as phenylene, etc.; aralkylene radicals such as phenethyl, etc.; acyl radicals such as t alkyleneetc.
and organic radicals which contain both hetero and carbon atoms as constituent components, as for example,
The novel compounds of this invention, as noted above,
are silver halide developing agents which contain an aryl nucleus selected from the group consisting of benzene and naphthalene nuclei so substituted by at least two groups selected from the group consisting of hydroxyl and amino groups as to be capable of developing an exposed silver halide emulsion. A preferred silver halide developing group comprises a hydroquinonyl group. Other suitable developing groups include ortho-dihydroxyphenyl, triaminophenyl, orthoand para-amino substituted hydroxyphenyl groups, and the corresponding naphthalene developing groups. In general, the developing group comprises a benzenoid developing configuration, that is, an aromatic developing group which forms quinonoid or quinone products upon oxidation.
In addition to the substituents which provide the silver halide developing function, Z may be substituted by halogen, alkoxy, alkyl, etc., radicals. The term amino as used herein is intended to include amino groups so substituted as not to impair their respective silver halide developing functions, for example, suitably substituted alkylamino and arylamino groups.
Examples of specific triazine photographic developing agents within the scope of the above formula include hydroquinoneamino-dihydroxy s triazine, Z-hydroquinoneamino-4-chloro-6-hydroxy-s-triazine, and 2,4-bis-(hydroquinoneamino) -6-hydroxy-s-triazine.
The developing agents of this invention maybe prepared by reacting a triazine compound of the formula:
wherein Y is selected from the group consisting of chloro, hydroxyl, alkyl, amino, aminoalkyl, aryloxy, and alkoxy radicals; with a compound of the formula: 1?
HN"Y-Z wherein R, Y and Z have the same significance as in Formula (A); such as Amino-phenethyl-hydroquinone, the preparation of which is disclosed in the copending US. application of Elkan R. Blout, Milton Green, Howard G. Rogers, Myron S. Simon and Robert B. Woodward, Serial No. 612,051, filed September 25, 1956;
Amino-phenethyl-thio-hydroquinone, the preparation of which is disclosed in the copending US. application of Milton Green and Howard G. Rogers, Serial No. 663,876, filed .Tune 6, 1957, now U.S. Patent No. 3,009,958, issued November 21, 1961;
Amino-phenoxy-hydroquinone, the preparation of which is disclosed in the copending US. application of Milton Green and Warren E. Solodar, Serial No. 680,406, filed August 26, 1957;
Amino-propyl-amino-hydroquinone, the preparation of which is disclosed in the copending US. application of Milton Green and Myron S. Simon, Serial No. 711,812, filed Ianuary 29, 1958, now Patent No. 3,002,997 issued October 3, 1961; and 1 Amino-hydroquinone, amino-ethyl-hydroquinone, aminophenyl-hydroquinone, and amino-phenyl-sulfonyl-hydroquinone, etc., which may be prepared by known chemical reactions; in an inert organic reaction medium, such as acetone or pyridine. The amine is employed in the ratio of approximately one mole, per mole of triazine compound, for each group to be introduced. Reaction with the triazine compound proceeds roughly stepwise; for example, with cyanuric chloride, the first chlorine reacts at temperatures of about 10 C. to about C., the second chlorine at about 40 to 50 C. and the third chlorine at about 90 to 100 C. Thus, it will be apparent to one skilled in the The crude product may be hydrolyzed by heating, under nitrogen, for about 15 minutes at 100 C. in excess 5% alkali. The hydrolyzed product may be precipitated in acid, yielding a tan powder. On recrystallization from 5 methanol, a pink tan powder is obtained which melts at about 310 C., is soluble in alkali, sparingly soluble in methanol, and insoluble in water and acetone.
Example 2 The bis-substituted triazine compound may be prepared by dispersing monobenzoyl hydroquinone-amino cyanuryl dichloride, for example the unfiltered reaction mixture of Example 1 having a pH of 5-6, in water at 40-50 C. A solution of 20 g. of Z-amino-hydroquinonean that this Provides an effective means of controlling 4-benzoate in boiling acetone is then added A solution the degree and nature of substitution of the triazine ring, of 7 of anhydrous ,sodmm carbonate m 5 of thereby enabling him to obtain developing agents of varyi 1s addedgver a penod of one 1 and the mlxture ing developing potential within the scope of this invention. surfed an addltlonal hour at 45-50. The crude It is generally desirable to protect the hydroxyl and/or action i i may be worked up the same i t amino groups of the developing function, during reaction, 20 as desctlbed Example h Crude Product 13 3' to avoid undesirable side reactions, for example, to emsciluble m acetone i hot organ: solvents $116.11 as ploy a protected derivative of Z, that is, a compound withethanol and mtrobenziene The q blsfprodugt in the formula: may be hydrolyzed by heatmg under nitrogen, 111 warm (D) R alkali for about 10 minutes to g ve an alkali-soluble by- H 1 Y Z drtolysrs product, 2,4-bis-(hydroquinoneamino)-6-hydroxysriazrne.
wherein R and Y a the same sigflificance Pfsvious' In certain instances, as where these novel triazine com- 3! stated t Z1 l'epfessllts the Pfotected deflvatlves of 3 pounds are used as intermediates, as for example, for beIlZeIlOld sllvfishallde developmg g p selected 'P other photographic compounds, it may be desirable to the group consisting of benzene and naphthalene nuclei so h one or both hydroxyl groups in the developing fnnc substitlfted y at least tWO S QP selectfid from the e P tion esterified to avoid or reduce side reactions. After conslstlng 9 y y and fl'mlflo Q P as to capable reaction the free hydroxyl groups are regenerated by hy- Of l pil f s ti ih i emulsloll, as drolysis of the product. Amino groups in the developing eXaIIlP t 6 es erlva Ves efeo function ma be similarl rotected. An exam le of uch Thelcorlpifi t g iu f th y be p g fiF a protected t riazine comgd und is: P s examp e, y e es err ca 10H 0 e compoun s 0 ormula C. Example 3 After reaction and prior to use as a photographic de- Ten grams of Omonobenzwl hydmqninoneannno di velonmg agent, the ester groups y Ive/removed by cbloro-s-triazine is suspended in 35-50 cc. of acetic anesterrfication, as for example, by hydrolysismthe presence 40 hydride and warmed on a Steam bath Concentrated 0f alkallsulfuric acid is added drop by drop until solution is ob- An eXamp1e of e p p p p the novel tained (s to 10 drops), following which the desired prod- Y p g agents P th1s 111VeI 1t111 and Set out by Way of uct crystallizes out as fine needles. The reaction mixlllustfatlon y 18 e fgllowmlg: l ture is chilled and filtered. The solid material recovered xamp e is washed with cold Water and then with a little 1:1 ace- A solution of 16.2 g. of cyanuric chloride in 35-40 cc. tolls and Watef- The crude Product g, 88% yield, of boiling acetone is poured slowly, with vigorous meis Iecl'ystauized from acetone- TWO chanical stirring, into 400 cc. of water kept at 0 C. in a crops of crystals give a 96% recovery of Qo-asstyl flask submerged in an ice-bath, and 20 g. of 2-aminohybeIlZoyl hydroqllillofleamiflo-dichloro-s-tfialifle 0f the droquinone-4-benzoate in concentrated solution in 35-40 structure: cc. of boiling acetone is poured in. A solution of 7.5 g. 0 of sodium bicarbonate in 50 cc. of water is then added l5 over a period of about 10-15 minutes. The mixture is N stirred for about 15-30 minutes, at which point the pH should be about 5-6. The mixture is then filtered, the filter cake is pressed dry and then washed with water. N N The washed filter cake is dried in a vacuum desiccator 0 over concentrated sulphuric acid. The dry product is ll I J washed by trituration three times with 25-35 cc. portions Q a 1 of boiling ether, filtered and dried.
Average yields of 90 to 95% were obtained in several havmg meltmg pomt of 210: The product is runs performed as described The crude Omonobem soluble 1n water and cold alkali, very slightly soluble in zoyl hydroquinoneamino dichloro s triazine product melts ether and cold acetone and moderately soluble in hot with decomposition, at about 220-223 C. and at 225 C. acetone Analysls of the Product shows: when pure. It is soluble in acetone and aqueous alkali, insoluble in water, and very slightly soluble in ether. Calculated Found nalysis of the product shows:
Calculated for 88 9 CmHmO3N4C1: Found 0 1 -g The novel triazine developing agents of this invention 8 j may be used in conventional multistage and multibath photographic processing procedures in either black-andwhite or color photography. They are also useful as developing agents in diffusion transfer reversal processes, both dye and silver, and are especially useful in such photographic processes wherein it is desired to eliminate or minimize the need for washing or stabilizing operations in liquid baths subsequent to the formation of the silver print. Example of such processes are disclosed in U.S. Patent 2,647,056 to Edwin H. Land.
As noted above, the herein disclosed novel triazine developing agents are useful in transfer processes of the type disclosed in the said patent to Edwin H. Land, and in other processes in which the problem of a residual stain cannot be readily met by washing operations. When used for transfer purposes, the novel developer compositions of this invention have incorporated therein as a further ingredient a silver halide solvent, such as sodium thiosulfate. If the composition is to be applied to the emulsion by being spread thereon in a thin layer, it may also include a film-forming thickening agent such, for example, as the high molecular weight polymer, sodium carboxymethyl cellulose. Experience has shown that concentrations of about 3%, by weight, of these novel triazine developing agents, for example hydroquinoneamino-dihydroxy-s-triazine, will .give good results in the above described transfer processes.
It will be apparent that the relative proportions of the developer set forth above may be varied to suit the requirements of the operator. Thus, it is within the scope of this invention to combine the aforementioned developing agent with suitable preservatives, alkalies, silver halide solvents, etc., other than those specifically mentioned. When desirable, it is also contemplated to include in the developing composition common components such as restrainers, accelerators, etc.
The developing agent may be disposed prior to exposure in a photosensitive element comprising the photographic emulsion, and the developer composition containing the agent formed by permeating the emulsion with an aqueous alkaline liquid capable of solubilizing the agent. Where desired, the developing agent may be dissolved in an aqueous alkaline solution prior to application thereof to an exposed silver halide emulsion.
Particularly useful developer compositions may also contain an auxiliary or accelerating developer such as metol, henzylaminophenol or a 3-pyrazolidone such as l-phenyl-3-pyrazolidone.
It will be apparent that the triazine developing agents of this invention may also be used in conventional blackand-white tank and tray development.
The triazine developers of this invention are very stable to heat and light. For example, the novel triazine derivatives of aminohydroquinone of this invention are much more stable than aminohydroquinone itself, and this is an important advantage in the use of these triazine compounds.
One further and very important advantage in the use of the novel triazine compounds of this invention must be noted. Aminohydroquinone is a non-discriminatory developing agent and is therefore of little photographic value. On the other hand, thelnovel triazine derivatives of aminohydroquinone disclosed herein are very discriminatory in their developing action and they are therefore highly useful as photographic developing agents.
The present application is a continuation-in-part of my copending application Serial No. 440,855, filed July 1, 1954, now abandoned.
Since certain changes may be made in the above product and process 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. A photographic developer composition comprising an aqueous alkaline solution containing a silver halide solvent and at least one compound of the formula:
wherein each X is selected from the group consisting of chloro, hydroxyl and radicals, and Z is a dihydroxyphenyl silver halide developing radical.
2. A photographic developer composition as defined in claim 1, wherein said compound is hydroquinoneaminodihydroxy-s-triazine.
3. A novel photographic developer composition as defined in claim 1, wherein said compound is 2-hydroquinoneamino-4-chloro-6-hydroxy-s-triazine.
4. A novel photographic developer composition as defined in claim 1, wherein said compound is 2,4-bis-(hydroquinoneamino) 6-hydroxy-stfiazine.
5. The process of developing a silver halide emulsion which comprises treating an exposed silver halide emulsion with an aqueous alkaline solution of a silver halide developing agent of the formula:
wherein each X is selected from the group consisting of chloro, hydroxyl and radicals, and Z is a dihydroxyphenyl silver halide developing radical.
6. A process as defined in claim 5 wherein said silver halide developing agent is hydroquinoneamino-dihydroxys-triazine.
7. The process as defined in claim 5, wherein said compound is Z-hydroquinoneamino 4 chloro 6 hydroxys-triazine.
8. The process as defined in claim 5, wherein said compound is 2,4 his (hydroquinoneamino) 6 hydroxy-striazine.
9. A process as defined in claim 5 wherein said compound is disposed, prior to exposure, in a photosensitive element comprising said photographic emulsion and the solution containing said compound is formed by permeating said emulsion with an aqueous alkaline liquid capable of solubilizing said compound.
10. A process as defined in claim 5 wherein said compound is dissolved in an aqueous alkaline solution prior to application thereof to said exposed emulsion.
11. The process which comprises developing an exposed silver halide emulsion with an aqueous alkaline solution containing a silver halide solvent and at least one compound of the formula:
wherein each X is selected from the group consisting of chloro, hydroxyl and radicals, R is a hydrogen atom and Z is a dihydroxyphenyl silver halide developing radical; contacting unexposed and undeveloped silver halide therein with said silver halide solvent and forming thereby an irnagewise distribution of a soluble silver complex in the undeveloped areas of said emulsion; and transferring by imbibition, at least in part, said imagewise distribution of soluble silver complex to a superposed image-receiving layer to provide a silver transfer image.
12. A process as defined in claim 1'1 wherein said com- 10 pound is hydroquinoneamino-dihydroxy-satriazine.
13. The process as defined in claim 11 wherein I TZ comprises a hydroquinonealkyleneamino group.
References Cited in the file of this patent UNITED STATES PATENTS Dearing et a1 Mar. 20, 1945 Friedheim Oct. 9, 1945 DAlelio Jan. 29, 1946 Mackey Nov. 8, 1949 Land Mar. 14, 1950 Knott Nov. 18, 1952 Rogers May 9, 1961 FOREIGN PATENTS France Aug. 25, 1958

Claims (1)

11. THE PROCESS WHICH COMPRISES DEVELOPING AN EXPOSED SILVER HALIDE EMULSION WITH AN AQUEOUS ALKALINE SOLUTION CONTAINNG A SILVER HALIDE SOLVENT AND AT LEAST ONE COMPOUND OF THE FORMULA:
US780964A 1954-07-01 1958-12-17 Photographic silver halide developers containing triazine rings Expired - Lifetime US3053656A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US780964A US3053656A (en) 1954-07-01 1958-12-17 Photographic silver halide developers containing triazine rings

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US44085554A 1954-07-01 1954-07-01
US780964A US3053656A (en) 1954-07-01 1958-12-17 Photographic silver halide developers containing triazine rings

Publications (1)

Publication Number Publication Date
US3053656A true US3053656A (en) 1962-09-11

Family

ID=27032579

Family Applications (1)

Application Number Title Priority Date Filing Date
US780964A Expired - Lifetime US3053656A (en) 1954-07-01 1958-12-17 Photographic silver halide developers containing triazine rings

Country Status (1)

Country Link
US (1) US3053656A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3419393A (en) * 1965-02-24 1968-12-31 Ilford Ltd Cyclic thioether silver halide development accelerators
US4256826A (en) * 1978-08-14 1981-03-17 Eastman Kodak Company Bleach-fix sheets
US5320929A (en) * 1992-12-22 1994-06-14 Polaroid Corporation Image-recording materials

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2371740A (en) * 1942-03-20 1945-03-20 Eastman Kodak Co Developers containing silver halide solvents
US2386204A (en) * 1940-12-10 1945-10-09 Ernst A H Friedheim Substituted 1,3,5-triazinyl-(6)-aminophenyl-arsenic compounds
US2393755A (en) * 1942-08-05 1946-01-29 Gen Electric Method of preparing hydroxyarylamino triazines
US2487569A (en) * 1948-07-21 1949-11-08 Gen Aniline & Film Corp Antistain baths for color photographic materials
US2500421A (en) * 1944-11-03 1950-03-14 Polaroid Corp Photographic silver halide transfer process
US2618557A (en) * 1947-08-26 1952-11-18 Eastman Kodak Co Method of developing sensitive photographic materials
FR1168292A (en) * 1954-03-09 1958-12-05 Polaroid Corp Improvements in photography
US2983606A (en) * 1958-07-14 1961-05-09 Polaroid Corp Processes and products for forming photographic images in color

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2386204A (en) * 1940-12-10 1945-10-09 Ernst A H Friedheim Substituted 1,3,5-triazinyl-(6)-aminophenyl-arsenic compounds
US2371740A (en) * 1942-03-20 1945-03-20 Eastman Kodak Co Developers containing silver halide solvents
US2393755A (en) * 1942-08-05 1946-01-29 Gen Electric Method of preparing hydroxyarylamino triazines
US2500421A (en) * 1944-11-03 1950-03-14 Polaroid Corp Photographic silver halide transfer process
US2618557A (en) * 1947-08-26 1952-11-18 Eastman Kodak Co Method of developing sensitive photographic materials
US2487569A (en) * 1948-07-21 1949-11-08 Gen Aniline & Film Corp Antistain baths for color photographic materials
FR1168292A (en) * 1954-03-09 1958-12-05 Polaroid Corp Improvements in photography
US2983606A (en) * 1958-07-14 1961-05-09 Polaroid Corp Processes and products for forming photographic images in color

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3419393A (en) * 1965-02-24 1968-12-31 Ilford Ltd Cyclic thioether silver halide development accelerators
US4256826A (en) * 1978-08-14 1981-03-17 Eastman Kodak Company Bleach-fix sheets
US5320929A (en) * 1992-12-22 1994-06-14 Polaroid Corporation Image-recording materials
US5424427A (en) * 1992-12-22 1995-06-13 Polaroid Corporation Triazine including substituted color-providing moiety

Similar Documents

Publication Publication Date Title
US3287125A (en) Aminoalkyl hydroxylamines as photographic developers
US3293034A (en) Alkoxy hydroxylamines as photographic developers
US3134672A (en) Photographic products, compositions and processes employing azo dye developers
US2619419A (en) Production of color photographic images
US3455916A (en) Certain n,n-disubstituted hydroxylamines
US3241967A (en) Photographic developer composition containing 2-hydroxymethyl-3-pyrazolidones
US3482971A (en) Scavengers for oxidized developing agent
US3549377A (en) Method of hardening photographic gelatin-containing layers with non-ionic dichlorotriazinyl amino compounds
US3242186A (en) 2, 5-dihydroxytriptycyl compounds and processes for their syntheses
US3053656A (en) Photographic silver halide developers containing triazine rings
US3134764A (en) Azo dyes containing a dihydroxyphenyl silver halide developing radical
US3076808A (en) Anthrapyridone dye developers
US3932480A (en) Benzylthiosulfuric acid salts
US2592363A (en) P-phenylenediamine developer containing nu-alkylacetamido ethyl substituent
US3255231A (en) (dicathyloxyphenylalkyleneamido) arylamines
US3705184A (en) 1:1 chrome-complexed azomethine dye developers
US2552240A (en) N-beta-methylsulfonamidoethyl-p-phenylenediamines
US3309199A (en) Photographic products, compositions and processes utilizing 3-cyano-4-azo-5-pyrazolone dye developers
US3551159A (en) Process for hardening gelatine
US3311474A (en) Photographic material
US3169992A (en) Amine thiosulfate anhydrides
US2657136A (en) Photographic antiplumming agents and compositions containing them
US3142564A (en) Photographic products, processes and compositins utilizing acyl hydroquinones
US3065075A (en) Photographic products and processes utilizing triptycene diol silver halide developers
US2448939A (en) Thioglycolic amide couplers