US2533182A - Preparation of colored metallo-alpha-oximino ketone complex images - Google Patents

Preparation of colored metallo-alpha-oximino ketone complex images Download PDF

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US2533182A
US2533182A US103758A US10375849A US2533182A US 2533182 A US2533182 A US 2533182A US 103758 A US103758 A US 103758A US 10375849 A US10375849 A US 10375849A US 2533182 A US2533182 A US 2533182A
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oximino
metallo
colored
complex
image
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US103758A
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Donald E Sargent
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GAF Chemicals Corp
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General Aniline and Film Corp
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    • 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
    • G03C5/40—Chemically transforming developed images
    • 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
    • G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
    • G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials

Definitions

  • the present invention relates to photographic materials containing colored metallo-w-oximinoketone complex images, and to a method of preparing such images.
  • One of the most commonly used methods for forming colored photographic images involves developing an exposed silver halide emulsion with a primar aromatic amino developer in the presence of a color former such as a phenol or a compound containing a reactive methylene group.
  • a color former such as a phenol or a compound containing a reactive methylene group.
  • the oxidation products of the developer react with thecolor former to produce-a colored dye image.
  • Such images sufier from the disadvantage that they are not particularly lightfast.
  • chelate compounds usually green, blue-green or blue in coloriand pr'esumably of the following structure loo 1.
  • n is equal to or 3.
  • a-oximino-ketones have found use as reagents for detecting ferrous iron, and the ferrous iron complexes thereof have in certain cases been used as dyestuffs for textiles (see Color Index Nos. 1 to 6).
  • a-OX- imino-ketones are produced which react with soluble metal salts to yield the aforesaid highly colored metallo-a-oximino-ketone complexes.
  • the metal salt employed is a ferrous salt, the complex is a brilliant cyan in color and is soluble in aqueous alkalies.
  • zthioba'r'bituric acid and the 1-'aryl-, 1-alkyl-, 1-ara1kyl-, or l-alkylenederivatives thereof such as 1-phenyl-2thiobarbituric acid, l-(a-naphthyl) -.2 thiobarbituric acid, -1 -(,B- naphthyl') -2-thiobarbituric acid, 1-toluy1-2thiobarbituric acid, 1-methyl- -thiobarbituric acid, 1-ethy1-2-thiobarbituric acid, 1-propyl-2-thiobarbituric acid, 1-butyl-2-thiobarb-ituric acid, 1- octyl-Z-thiobarbituric acid, 1-decyl-2-thiobarbituric acid, 1-dOdecyl-Z-thiobarbituri-c
  • the metal complex is bound imagewise to the silver halide through the medium of the aforesaid isothioamide group.
  • a bath containing a small amount of sodium nitrite dissolved in a weak organic acid such as acetic acid, formic acid, and the like it is preferable to use a bath containing a small amount of sodium nitrite dissolved in a weak organic acid such as acetic acid, formic acid, and the like. Excellent results have been obtained when employing a 1-3% solution of sodium nitrite dissolved in 2-5% of acetic acid.
  • the metal salts which may be employed for producing the metallo-a-oximino-ketone complex are any water soluble ferrous or cobaltous salts, such as ferrous sulfate, ferrous nitrate, ferrous acetate, ferrous chloride, cobaltous sulfate, cobaltous acetate, cobaltous chloride, and the like. Where a cobaltous salt is used for forming the metal complex, the resulting image is orange in color rather than cyan.
  • Example I An alkali soluble cyan colored ferrous iron complex was prepared from l-a-naphthyl-flthiobarbituric acid in the following manner: A solution of 1.35 parts of 1-(a-naphthyD-2-thiobarbituric acid in 20 parts of glacial acetic acid was cooled to 10 C. and heated with stirring with 3.5 parts of a 10% aqueous sodium nitrite solution. During the addition of the nitrite, which took 5 minutes, the temperature was not allowed to rise above 12 C. There resulted a yellowish-brown solution of the 5-oximino compound.
  • a film bearing a silver bromide image was bathed in a 1% solution of this l-(a-naphthyl) 2-thio-5-oximino barbituric acid-ferrous iron complex in 5% sodium carbonate solution. The film was washed to remove unreacted complex. There resulted an insoluble brilliant cyan image, the white areas being unafiected. This is presumably due to the formation of an insoluble silver salt in situ with the silver halide.
  • the cyan image prepared in this way showed no appreciable fading after 50 hours exposure in an accelerated light-aging test (Fade-Ometer).
  • Example II The procedure is the same as in Example I excepting that the l-(a-naphthyl) -2-thiobarbituric acid is replaced by an equivalent amount of 2- thiobarbituric acid.
  • the image formed is cyan in color and possesses a light fastness comparable to the image of Example I.
  • Example III The procedure is the same as in Example I excepting that the l-(a-naphthyl) -2-thiobarbituric acid is replaced by an equivalent amount of 5- thioureido-l-naphthol. An image of a greener shade but of high light fastness is formed.
  • Example IV The procedure is the same as in Example I excepting that the ferrous sulfate is replaced by an equivalent amount of cobaltous acetate. There is produced a bright orange image which is extremely fast to light.
  • a thioamide group capable of isomerizing to an isothioamide group and yielding a-oximino-ketone structures upon nitrosation, and having a structure selected 6 from the class consisting of a-ketd methylene and 1- and 2-hydroxy naphthalene structures, and reacting the resulting nitrosated compound with a soluble metal salt selected from the class consisting of soluble ferrous and cobaltous salts.

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  • General Physics & Mathematics (AREA)

Description

Patented Dec. 19.56
UNITED STATES PATENT OFFICE PREPARATION OF COLORED 'METALIJO-a- OXIMINO KETONE COMPLEX IMAGES Donald @Sarg'e'nt, Easton, 12a,, assignor to General Aniline & Film Corporation, New York, N. Y., a corporation of Delaware No Drawing. Application July 8, 1949,
' Serial No. 103,758
3 Claims. 1
The present invention relates to photographic materials containing colored metallo-w-oximinoketone complex images, and to a method of preparing such images.
One of the most commonly used methods for forming colored photographic images involves developing an exposed silver halide emulsion with a primar aromatic amino developer in the presence of a color former such as a phenol or a compound containing a reactive methylene group. The oxidation products of the developer react with thecolor former to produce-a colored dye image. Such images sufier from the disadvantage that they are not particularly lightfast.
It is known that a-OXlIIliIlO-kBtOllGS having a structure:
are capable of reacting with certain metallic ions such as ferrous ions to yield highly colored products. When an iron salt capable of yielding ferrous ions is used, chelate compounds usually green, blue-green or blue in coloriand pr'esumably of the following structure loo 1.
are formed. (In this formula n is equal to or 3.) a-oximino-ketones have found use as reagents for detecting ferrous iron, and the ferrous iron complexes thereof have in certain cases been used as dyestuffs for textiles (see Color Index Nos. 1 to 6).
I have now discovered that intensely colored metallo-a-oximino-ketone complexes containing a thioamide structure, capable of isomerizing to The metallo-a-oximino ketone complexes utilized in the formation of said coloredimages are produced from a compound containing a thioamide structure capable of 'isomerizing to an iso-thioamide structure and being capable of yielding an a OXlIl'lil'lO-KSEOIIG upon nitrosation. Such compounds contain an u-keto methylene structure Or a structure capable of yielding an a-keto methylene structure upon isomerization. When such compounds are nitrosated, a-OX- imino-ketones are produced which react with soluble metal salts to yield the aforesaid highly colored metallo-a-oximino-ketone complexes. If the metal salt employed is a ferrous salt, the complex is a brilliant cyan in color and is soluble in aqueous alkalies.
Compounds within the above category which I have found to be particularly suitable for such use are zthioba'r'bituric acid and the 1-'aryl-, 1-alkyl-, 1-ara1kyl-, or l-alkylenederivatives thereof, such as 1-phenyl-2thiobarbituric acid, l-(a-naphthyl) -.2 thiobarbituric acid, -1 -(,B- naphthyl') -2-thiobarbituric acid, 1-toluy1-2thiobarbituric acid, 1-methyl- -thiobarbituric acid, 1-ethy1-2-thiobarbituric acid, 1-propyl-2-thiobarbituric acid, 1-butyl-2-thiobarb-ituric acid, 1- octyl-Z-thiobarbituric acid, 1-decyl-2-thiobarbituric acid, 1-dOdecyl-Z-thiobarbituri-c acid, 1- benzyl- Z-thiobarbituric acid, l-(l-methyl-2- naphthyi)-2-thiobarbituric acid, l-allyl-Z-thiobarbituric acid, l-isopropenyl-2-thiobarbituric acid and thiourea-substituted on one nitrogen atom b a hydroxy-naphthyl group such as '5- thioureido-l-naphthol, S-thioureido-l-naphthdl. 7-thi0ureido -2naphthol, S-thioureido-l-naphthol.
The above *thioureido naphthcls are included with the thiobarbituric acids for the reason that, like the thiobarbituric acids, the thioamide grouping therein has the known abilit under salt forming conditions to isoinerize to the isothioamide grouping and for the further reason that the 'aand '18- naphthols have the known ability to yield a-OX- imino-ketone structures upon nitrosation.
By treating a photographic element containing a silver halide image withan aqueous alkaline solution of the aforesaid colored metal complexes, the metal complex is bound imagewise to the silver halide through the medium of the aforesaid isothioamide group. The white areas which-contain no silver halide are unaf- Preparation of iron complex Alkali soluble ferrous iron complex (cyan dye) wherein n=2 or 3.
Deposition of colored complex image -0 I e N o=o" giggle Alkali soluble ferrous iron complex image Insoluble silver salt of cyan ferrous iron complex wherein X=halogen and n=2 or 3.
It is to be understood that these equations are merely indicative of my theory of the reaction and is not to be construed as the exact mechanism by which the complex images are produced.
In the nitrosation step, it is preferable to use a bath containing a small amount of sodium nitrite dissolved in a weak organic acid such as acetic acid, formic acid, and the like. Excellent results have been obtained when employing a 1-3% solution of sodium nitrite dissolved in 2-5% of acetic acid.
The metal salts which may be employed for producing the metallo-a-oximino-ketone complex are any water soluble ferrous or cobaltous salts, such as ferrous sulfate, ferrous nitrate, ferrous acetate, ferrous chloride, cobaltous sulfate, cobaltous acetate, cobaltous chloride, and the like. Where a cobaltous salt is used for forming the metal complex, the resulting image is orange in color rather than cyan.
The invention is further illustrated by the following examples, it being understood that the invention is not restricted thereto.
Example I An alkali soluble cyan colored ferrous iron complex was prepared from l-a-naphthyl-flthiobarbituric acid in the following manner: A solution of 1.35 parts of 1-(a-naphthyD-2-thiobarbituric acid in 20 parts of glacial acetic acid was cooled to 10 C. and heated with stirring with 3.5 parts of a 10% aqueous sodium nitrite solution. During the addition of the nitrite, which took 5 minutes, the temperature was not allowed to rise above 12 C. There resulted a yellowish-brown solution of the 5-oximino compound. This cold solution was then poured with rapid stirring into a solution of 2.78 parts of ferrous sulfate (FeSOeJlHzO) in 100 parts of water. The blue-green product was precipitated immediately as a very fine powder. This was filtered off, washed with Water and dried at C. The yield was practically quantitative.
A film bearing a silver bromide image was bathed in a 1% solution of this l-(a-naphthyl) 2-thio-5-oximino barbituric acid-ferrous iron complex in 5% sodium carbonate solution. The film was washed to remove unreacted complex. There resulted an insoluble brilliant cyan image, the white areas being unafiected. This is presumably due to the formation of an insoluble silver salt in situ with the silver halide.
Alkaline solutions of dyes of this type penetrate gelatin only with difiiculty and the cyan image produced may easily be restricted to the top layer in multilayer photographic materials, if desired.
The cyan image prepared in this way showed no appreciable fading after 50 hours exposure in an accelerated light-aging test (Fade-Ometer).
Example II The procedure is the same as in Example I excepting that the l-(a-naphthyl) -2-thiobarbituric acid is replaced by an equivalent amount of 2- thiobarbituric acid. The image formed is cyan in color and possesses a light fastness comparable to the image of Example I.
Example III The procedure is the same as in Example I excepting that the l-(a-naphthyl) -2-thiobarbituric acid is replaced by an equivalent amount of 5- thioureido-l-naphthol. An image of a greener shade but of high light fastness is formed.
Example IV The procedure is the same as in Example I excepting that the ferrous sulfate is replaced by an equivalent amount of cobaltous acetate. There is produced a bright orange image which is extremely fast to light.
Various modifications of the invention will occur to persons skilled in this art, and I therefore 5 do not intend to be limited in the patent granted except as necessitated by the appended claims.
I claim:
1. The process of depositing a metallo-c-oximino-ketone complex image in situ with a silver halide image contained in a photographic element which comprises treating a silver halide image in such element with an aqueous alkaline solution of a complex metal compound containing a thioamide group capable of isomerizing to an isothioamide group and capabl of forming silver salts less soluble than silver halides, said complex metal compound being obtained by nitrosating a compound containing. a thioamide group capable of isomerizing to an isothioamide group and yielding a-oximino-ketone structures upon nitrosation, and having a structure selected 6 from the class consisting of a-ketd methylene and 1- and 2-hydroxy naphthalene structures, and reacting the resulting nitrosated compound with a soluble metal salt selected from the class consisting of soluble ferrous and cobaltous salts. 2. The process as defined in claim 1 wherein the compound subjected to nitrosation is l-(anaphthyl)-2 thiobarbituric acid and the water solluble metal salt is a ferrous salt.
3. The process as defined in claim 1 wherein the compound subjected to nitrosation is 2-thiobarbituric acid and the water soluble metal salt is a ferrous salt.
DONALD E. SARGENT.
No references cited.

Claims (1)

1. THE PROCESS OF DEPOSITING A METALLO-A-OXIMINO-KETONE COMPLEX IMAGE IN SITU WITH A SILVER HALIDE IMAGE CONTAINED IN A PHOTOGRAPHIC ELEMENT WHICH COMPRISES TREATING A SILVER HALIDE IMAGE IN SUCH ELEMENT WITH AN AQUEOUS ALKALINE SOLUTION OF A COMPLEX METAL COMPOUND CONTAINING A THIOAMIDE GROUP CAPABLE OF ISOMERIZING TO AN ISOTHIOAMIDE GROUP AND CAPABLE OF FORMING SILVER SALTS LESS SOLUBLE THAN SILVER HALIDES, SAID COMPLEX METAL COMPOUND BEING OBTAINED BY NITROSATING A COMPOUND CONTAINING A THIOAMIDE GROUP CAPABLE OF ISOMERIZING TO AN ISOTHIOAMIDE GROUP AND YIELDING A-OXIMINO-KETONE STRUCTURES UPON NITROSATION, AND HAVING A STRUCTURE SELECTED FROM THE CLASS CONSISTING OF A-KETO METHYLENE AND 1- AND 2-HYDROXY NAPHTHALENE STRUCTURES AND REACTING THE RESULTING NITROSATED COMPOUND WITH A SOLUBLE METAL SALT SELECTED FROM THE CLASS CONSISTING OF SOLUBLE FERROUS AND COBALTOUS SALTS.
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Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3660092A (en) * 1966-12-20 1972-05-02 Agfa Gevaert Ag Colorphotographic material
US4555477A (en) * 1985-01-02 1985-11-26 Eastman Kodak Company Photographic element and process utilizing metal complex color masking dyes
US4555478A (en) * 1985-01-02 1985-11-26 Eastman Kodak Company Photographic element and process for providing metal complex color images
US4557998A (en) * 1985-01-02 1985-12-10 Eastman Kodak Company Colorless ligand-releasing monomers and polymers and their use to provide dyes with metal ions
US4568633A (en) * 1985-01-02 1986-02-04 Eastman Kodak Company Photographic elements and processes utilizing imagewise reduction of ferric ions
US4680356A (en) * 1985-01-02 1987-07-14 Eastman Kodak Company Colorless ligand-releasing monomers and polymers and their use to provide dyes with metal ions
US4764454A (en) * 1985-12-20 1988-08-16 Fuji Photo Film Co., Ltd. Color photographic material with color forming ligand compounds and a method of processing

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
None *

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3660092A (en) * 1966-12-20 1972-05-02 Agfa Gevaert Ag Colorphotographic material
US4555477A (en) * 1985-01-02 1985-11-26 Eastman Kodak Company Photographic element and process utilizing metal complex color masking dyes
US4555478A (en) * 1985-01-02 1985-11-26 Eastman Kodak Company Photographic element and process for providing metal complex color images
US4557998A (en) * 1985-01-02 1985-12-10 Eastman Kodak Company Colorless ligand-releasing monomers and polymers and their use to provide dyes with metal ions
US4568633A (en) * 1985-01-02 1986-02-04 Eastman Kodak Company Photographic elements and processes utilizing imagewise reduction of ferric ions
EP0186870A2 (en) * 1985-01-02 1986-07-09 EASTMAN KODAK COMPANY (a New Jersey corporation) Photographic elements and processes utilizing imagewise reduction of ferric ions
US4680356A (en) * 1985-01-02 1987-07-14 Eastman Kodak Company Colorless ligand-releasing monomers and polymers and their use to provide dyes with metal ions
EP0186870A3 (en) * 1985-01-02 1988-09-14 Eastman Kodak Company Photographic elements and processes utilizing imagewise reduction of ferric ions
US4764454A (en) * 1985-12-20 1988-08-16 Fuji Photo Film Co., Ltd. Color photographic material with color forming ligand compounds and a method of processing

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