US2295008A - Photographic color forming compound - Google Patents

Description

Patented Sept. 8, 1942 rno'roeaarmccoma FORMING COMPOUND Henry D. Porter and Arnold Weissberger, Rochester, N. Y., assignors to Eastman Kodak Company, Rochester, N. Y., acorporation of New Jersey No Drawing. Application March 11, 1941, Serial No. 382,746. In Great Britain March 12, 1940 11 Claims. (Cl. 95-6) I This invention relates to color photography and more particularly to compounds which form dyes by coupling with the developing compound on photographic development.

The method of forming colored photographic images by depositing a. colored compound in the photographic layer adjacent the silver image on.

development has been described in numerous prior patents. Dyes formed in this way are insoluble in water and in the ordinary photographic developing and fixing baths, although the silver images formed simultaneously with them during photographic development may be removed from the photographic layer to leave pure dye images in the layer. Compounds employed in conjunction with the develop agent for the silver and which couple with the development product of the developer during photographic development i Y are referred to herein as coupling components or couplers. Depending upon their solubility or diffusion characteristics,' these compounds may be incorporated in the emulsion layer prior to ex- 1 posure'or may be dissolved in the developing.

solution. when these coupling components are incorporated in the photographic layer prior to exposure, they do not aiiect the exposure and development of the layer in the usual way, but when the development is carried out with a suitable developing agent, they combine with the oxidation product of the developer to form a colored image in situ with the silver image.

The developing agents used in color forming development of the typecontemplated by our invention comprise aromatic amino developers-including the mono-, diand triaminoaryl compounds and their derivatives formed by substitution in the amino group as well as in the ring,

such as allwlphenylenediamines, alkyltoluene diamines and p-aminophenols. These compounds are ordinarily used in the salt form such as the .hydrochloride or the sulfate which are more stable .than the amines themselves. Suitable.

compoimds are diethyl-p-phenylenediamine hydrochloride, monomethyl p phenylenediamine hydrochloride and dimethyl-p-phenylenediamine sulfate. The p-aminophenols and their substitution products may also be used where the amino group is imsubstituted. All of these com- I 7 pounds have an unsubstituted amino group which enables the oxidation products oi" the developer to couple with the color-forming compoundsto form a dye image.

We have found that certain substituted ain which X is an group, such as methyl,

ethyl, or propyl, and Y is a group which, together with the carbon atom to which it is'attached, forms an oxime, hydrazone, or semicarbazone The following examples illustrate coupler compounds of this general formula:

. 0H (1) CH3 JI=NOH tacetyl-l-naphthol-oxime 2 0 cm p 2-acetyl-l-naphthul phenyl-hydmzone (4) 0H CHs' 1 CB; I z

2-aoetyl-l-naphtho l-a-methyl a-phenylhydrazone These compounds may be prepared by reacting a suitable l-hydroxy-Z-naphthyl ketone with a lat-substituted hydroxylamine, a a-substituted hydrazine or a 2 or 4 substituted semicarbazide. 2-acetyl-1-naphthol' oxime may be prepared in the following manner:

Compounds 1 and 3 are suitable for incorporation in photographic developing solutions and compounds 2 and 4 may be incorporated in emulsion layers and do not diffuse from the layer in which they are incorporated in the case of multilayer coatings. Blue-green dyes are formed on photographic development.

A developingfor'mula which may be used is the following:

The developing agent and the proportions of the ingredients used in the above formula may, of course, be varied. Solvents other than acetone, such as alcohols, may also be used.

The couplers which are used in the emulsion .layer may be incorporated in various ways but we prefer to form a solution of the sodium salt of the coupler in alcohol and add this to the emulsion. For example, 3 grams of coupler may be dissolved or suspended in 50 cc.'of ethyl alcohol and sodium hydroxide added in the amount of 1 equivalent weights of the coupler. The sodium hydroxide may be added as solid or as a concentrated solution. The sodium salt of the coupler is thereby generated in a solution of 50 cc. of alcohol and this solution is added to one liter of a gelatino-silver halide. The pH of the emulsion may be adjusted if desired by adding a suitable acid such as acetic or sulfuric acid to neutralize all 'or part of the sodium hydroxide used to form the sodium salt of the coupler.

The coupling compounds may be incorporated either in gelatin or in other colloidal materials such as collodion, organic esters of cellulose or The examples and compounds set forth in the present specification are illustrative only and it is to be understood that our invention should be taken as limited only by the scope of the appended claims.

We claim:

1. The method of producing a colored photographic image in'a silver halide emulsion layer which comprises simultaneously developing an image therein and coupling the development productof an aromatic amino developing agent containing a primary amino group with a compound having the formula:

in which X is an alkyl .group and Y is a group which, together with the carbon atom to which it is attached, produces a group selected from the class consisting of oxime, hydrazone, and semicarbazone groups.

2. The method f producing a colored photo-' in which X is an alkyl group and Y is a group comprising the atoms necessary to form a hydrazone group.

4. The method of producing a colored photographic image in a silver halide emulsion layer which comprises simultaneously developing an image therein and coupling the development 7 product of an aromatic amino developing agent synthetic resins. In case the coupler is incor- D rated in the emulsion or is used in the developing solution, the emulsion may be carried by a transparent medium such as glass, cellulose ester or synthetic resin or anon-transparent reflecting medium such as paper or an opaque cellulose ester. Theemulsion may be coated as a single layer on the support or superposed layers concontaining a primary amino group with Z-acetyl- 1-naphtholphenyl-hydrazone;

5. The method of producing a colored photographic image in a silver halide emulsion layer which comprises simultaneously developing an image therein and coupling the development product of an aromatic amino developing agent containing a primary amino group with 2-acetyl- 1-naphthol-a-methyl-m-phenylhydrazone.

6. The method of producing a colored photographic image in a silver halide emulsion layer which comprises simultaneously developing an image therein and coupling the development product of an aromatic amino developing agent containing a primary amino group with 2-acetyll-naphtholsemicarbazone.

'7. A color forming photographic developer comprising an aromatic amino developing agent containing a primary amino group and a ecupler compound comprising Z-acetyl-l-naphthol oxime.

comprising an aromatic amino developing agent containing a. primary amino group and a coupler compound comprising 2-acetyl-1-naphtholsemicarbazone.

9. A photographic emulsion for forming colored images comprising a colloidal carrier containing a sensitive silver halide and a coupler compound having the formula:

ored images comprising a gelatino-silver halide emulsion ,containing 2- acetyl 1 naphthol-amethyl-a-phenylhydrazone as a coupler.

HENRY D. PORTER, ARNOLD WEISSBERGER;

in which X is an alkyl group and Y is a group