US3615607A

US3615607A - Method of desensitizing light-sensitive silver halide photographic materials with cycloheptimidazole derivatives

Info

Publication number: US3615607A
Application number: US28084A
Authority: US
Inventors: Nobuo Soma; Mitsuo Watatani
Original assignee: Konica Minolta Inc; Sankyo Co Ltd
Current assignee: Konica Minolta Inc; Sankyo Co Ltd
Priority date: 1967-03-13
Filing date: 1970-04-13
Publication date: 1971-10-26
Anticipated expiration: 1988-10-26

Abstract

Light-sensitive silver halide photographic materials are desensitized by treatment with a compound of the formula

WHEREIN R1 is hydrogen, lower alkyl, halogen, cyano or dialkyl amino and R2 is aryl or pyridinium which may or may not be substituted.

Description

United States Patent Nobuo Soma Tokyo;

Mitsuo Watatani, deceased, late of Tokyo by Takako Watatani, heir; J unichi Nakazawa, Tokyo; Yoshio Sato, Tokyo; Yoshimi Kuwabara, Tokyo; l-lidehiko Ishikawa, Kanagawa, all of Japan 28,084

Apr. 13, 1970 [72] Inventors 211 App]. NO.

7 7 Filed Patented Assignees Oct. 26, 1971 Sankyo Co., Ltd.;

Konishiroku Photo Industry Co. Tokyo, Japan METHOD OF DESENSITIZING LIGHT-SENSITIVE SILVER lIALIDE PHOTOGRAPIIIC MATERIALS WITH CYCLOIIEPTIMIDAZOLE DERIVATIVES 13 Claims, No Drawings s2]'u.s.c| 96/101, 96/109, 96/107, 96/64 51 161.121 G03Cl/36 so FieldofSearch; 96/101, 109,107,64

Division of Ser. No. 622,475, M ar. 13,196?

Primary Examiner- Norman G. Torchin Assistant Examiner-Won H. Louie, Jr.

- An0rneyWaters, Roditi, Schwartz and Nissen ABSTRACT: Light-sensitive silver halide photographic materials are desensitized by treatment with a compound of the formula wherein R, is hydrogen, lower alkyl, halogen, cyano or dialkyl amino and R is aryl or pyridinium which may or may not be substituted.

METHOD OF DESENSITIZING LIGHT-SENSITIVE SILVER HALIDE PHOTOGRAPHIC MATERIALS WITH CYCLOHEP'IIMIDAZOLE DERIVATIVES CROSS-REFERENCE TO RELATED APPLICATION This application is a division of copending application Ser. No. 622,475;filed Mar. 13, 1967 and claiming a priority of Mar. 19, 1966 based on an application filed in Japan.

DETAILED DESCRIPTION OF THE INVENTION This invention relates to the desensitization of light-sensitive silver halide photographic materials. The desensitizer which is used in the method of the invention has the chemical structure represented by the general formula (I) shown below. It is the principal object of the present invention to provide for desensitization without any staining or coloration of photographic pictures and in accordance therewith, there is provided a method in which use is made of desensitizers which exert no adverse influence on the contrast of photographed images.

Heretofore, a number of compounds have been known to be useful as desensitizers for light-sensitive silver halide photographic materials, which compounds include, for example, phenosafranine, malachite green, pinacryptol yellow, pinacryptol green, etc. These known desensitizers suffer from several disadvantages and are not satisfactory in actual use. For instance, some of these desensitizers will stain or color the photographic picture or will impair the photographic properties of the resulting image, because they are themselves inherently colored substances. More specifically, phenosafranine which is a substance having red color usually causes reddish coloration of the photographic materials, sometimes with a decrease in contrast of the photographed images. Malachite green and pinacryptol green, both of which are green compounds, will decrease the whiteness of the background of photographic pictures. Furthermore, pinacryptol green sometimes has an adverse effect on the stability of a fogged emulsion. Pinacryptol yellow, which is generally preferred among the known desensitizers because it causes no problem in the contrast of photographic images, will nevertheless cause yellowish coloration which decreases the whiteness of the surface of photographic materials. Moreover, it has a serious disadvantage which is its instability in developing solutions. Thus, all the known desensitizers are not satisfactory because of their undesirable influence on the photographic properties of the resulting images.

In accordance with the present invention, there is provided a new descnsitizing method which uses a desensitizing com pound having the following chemical structure:

where in R is hydrogen, lower alkyl, halogen, cyano or dimethylamin'o and R is aryl or pyridinium group which may or may not be substituted.

The compounds defined above are available at relatively cheap cost. Almost all of these are colorless substances, and the other few are substances which have very slight color insufficient to cause coloration. The compounds all meet the following photographic requirements:

I. They should have the capability of decreasing photographic sensitivity;

2. They should not cause fogging or decrease in contrast;

3. They should not affect fogged silver halide crystals;

4.They should not contaminate binders (e.g., gelatine) or supports; and

5. They should be soluble in water. It is, of course possible .to use the compounds in a developing solution.

Compounds of the above general formula (I) wherein R is a substituted or unsubstituted aryl group can be prepared according to the method described in Japanese Pat. publication No. 20706/ I965, that is, by the reaction of a 2-halo or 2- methoxytropane of the formula wherein X is halogen or methoxy and R, is defined as above with an amidine of the formula C-R; 97 N wherein R, is defined as above. Compounds of the above-mentioned formula (I) wherein R is a substituted or unsubstituted pyridinium group can be prepared in a known manner by the reaction of a 2-halo-cycloheptimidazole with pyridine which may be optionally substituted with alkyl, halogen, nitro, alkoxy, carbamoyl, alkoxycarbonyl, etc. Typical compounds included in the above formula and operative in the present method are as follows:

2-phenylcycloheptimidazole, M.P. 162 C.

2-phenyl-4-bromocycloheptimidazole, M.P. 153 C.

2-(m-nitrophenyl)cycloheptimidazole, M.P. 267 C.

ecomp.

2-(p-bromophenyl)cyeloheptimidazole, M.P. 204 C.

2-(p-dimethylaminophenyl)cyclohcptimidazolc,

.M.'.Pr...2

2-(p-tolyl)-4-oya.n0cycloheptimidazole, M.P. 217 C.

Z-(p-anisyl) cycloheptimidazole, M.P. 160 C.

1- (2-cycloheptimidazolyl)-pyridinium chloride,

M.P. 230 C. (decomp.)

2-(p-tolyl) cycloheptimidazole, M.P. 180

Z-phenyl-7-isopropylcycloheptimidazole, M.P. 163 C.

CONH;

3-earbamoyl-1-(2-cycloheptimidazOIyD-pyridiniurn chloride, M.P. 240 C. (decomp.)

3-methoxycarbonyl-1-(Z-cycIoheptimidazolyD- pyridinium chloride, M.P. 185 C. (decomp.)

2-phenyl-6-bromoeycloheptimidazole, M.P. 221 C.

2-(p-nitrophenyl)cycloheptimidazole, M.P. 280 C.

These compounds can be used as desensitizers for photographic purposes in the same manner as the known desensitizers for light-sensitive silver halide photographic materials. For example, in accordance with the invention, an exposed high-speed photographic film can be pretreated with an aqueous solution of the desensitizer of the present invention so that the film may be developed under relatively bright conditions which enables one to conduct the development with visual inspection of the progress of development. Alternatively, the desensitizer can be added to the developing solution to be used for photographic development, whereby an exposed photographic film can be treated with said solution under relatively bright conditions because of its decreased sensitivity. Incorporation of the desensitizer into a light-sensitive silver halide photographic emulsion having fogged silver halide crystals can provide one with a direct-positive, light-sensitive material which directly yields a positive image through the Herschel effect or solarization.

' If the desensitizer is used as a pretreating bath for imagewise exposed, light-sensitive silver halide photographic materials, it is conveniently prepared in the form of an aqueous solution at a concentration of 0.0l0.03 percent. After dipping in this solution for several minutes, the photographic material can be treated with a conventional developing solution under relatively bright safelight. If the desensitizer is used in a developing solution, it should be in amount of 0.003 to 0.02 percent. By use of the desensitizer in accordance with the invention, developing procedures can be performed under such bright safelight which allows one to make visual inspection of the result of the developed images. Of course, there is no problem of coloration of thedeveloped images or of any damage to the contrast of the images.

For the preparation of a direct-positive light-sensitive photographic material, the desensitizer is used according to the invention in the amount of 0.005-l g. per g. of silver nitrate, the amount of which is calculated from the silver halide content of the light-sensitive emulsion used. The appropriate amount of the desensitizer is dissolved in water or lower alcohol such as methanol or ethanol or a mixture thereof and the resulting solution is added to the light-sensitive emulsion containing fogged silver halide crystals. Usually it is preferred to combine the desensitizer solution with the fogged emulsion just before the coating of the resulting mixture on a support, but this is not critical. The thus prepared direct-positive light-sensitive material exhibits a much improved Herschel effect, by which an image free of any coloration and with high contrast is obtained.

The following examples describe certain embodiments of the invention, but are not be be construed as limiting the scope thereof.

EXAMPLE 1 Monomethyl-p-aminophcnol sulfate 2.0 g. Sodium sulfite (anhydrous) 80.0 g. Hydroquinonc 4.0 g. Borax 4.0 g. Potassium bromide 0.5 g.

Distilled water to make up I000 ml.

By using the resulting mixture, a commercially available highspeed panchromatic photographic film was treated. The procedures can be effected under relatively bright safelight conditions, without causing any coloration or contamination.

EXAMPLE 2 One kilogram of a pure silver chloride emulsion containing the equivalent of 40 g. of silver nitrate was buffered to a pH of 8.0 by the addition of 30 ml. of aqueous solution of 6 percent sodium metaborate. Then, the emulsion was mixed with 7 ml. of 3 percent formalin and heated at 50 C. for 60 minutes. The thus fogged emulsion was buffered to pH 6.0 by the addition of an aqueous solution of percent citric acid. The emulsion was divided into 10 portions, each of which was mixed with the compound indicated in table 1. The respective portions were coated on photographic papers and then dried. The thus prepared direct-positive, light-sensitiT/e photographic sheets were subjected to stepwise exposure to light through a yellow filter which passes light of a wavelength longer than 450 p. and then treated with a D-72 type developer. The sensitometric results obtained are set forth below:

1) Pinacryptol yellow and phenosafranine were used as control desensitizers.

2) This is expressed as a specific value as compared with the reversal photographic speed of the pinacryptol yellow-loaded photographic sheet, which is rated as 100.

As is apparent from table 1, the sheets in which the desensitizers of this invention were used were excellent in photographic speed and contrast, whereas the control sheets loaded with pinacryptol yellow and phenosafranine suffered respectively from yellowish or reddish coloration.

EXAMPLE 3 One kilogram of a pure silver chloroiodide emulsion containing the equivalent of 40 g. of silver nitrate was buffered to pH 7.5 by the addition of 25 ml. of 5 percent aqueous sodium carbonate solution. Then, the emulsion was mixed with 10 ml. of 3 percent formalin and heated at 55 C. for 40 minutes. The thus fogged emulsion was buffered to pH 6.0 by the addition of an aqueous solution of 10 percent citric acid. The emulsion was divided into 10 portions, each of which was mixed with the compound indicated in table 2. The respective portions were coated on photographic papers and then dried. The thus prepared 10 direct-positive, light-sensitive photographic sheets were subjected to stepwise exposure to white light and then treated with a developing solution. The sensitometric results obtained are set forth below:

As is apparent from table 2, the sheets in which the desensitizers of the invention were used were better in reversal minimum density and contrast, while the control sheets suffered from coloration of their surfaces.

What is claimed is:

1. A method comprising treating light-sensitive silver halide photographic materials with a desensitizing amount of a compound having the chemical formula wherein R, is hydrogen, lower alkyl, halogen, cyano or a 4-, 6- or'7-positioned dimethylamino and R is phenyl, phenyl substituted by nitro, bromo, amino, dimethylamino, methoxy or methyl; or pyridinium or pyridinium substituted by carbamoyl or methoxy carbonyl.

2. A method as claimed in claim 1, wherein R, is hydrogen and R is phenyl.

3. A method as claimed in claim 1, wherein R, is 4-positioned bromine and R is phenyl.

4. A method as claimed in claim 1, wherein R, is hydrogen and R is m-nitrophenyl.

5. A method as claimed in claim 1, wherein R, is hydrogen and R is o-nitrophenyl.

6. A method as claimed in claim 1, wherein R, is hydrogen and R is p-anisyl.

7. A method as claimed in claim 1, wherein R, is hydrogen and R is pyridinium chloride.

8. A method as claimed in claim 1, wherein R, is hydrogen and R is p-tolyl.

9. A method as claimed in claim 1, wherein R, is hydrogen and R is 3-carbamoyl pyridinium chloride.

10. A method as claimed in claim 1, wherein R, is hydrogen and R is 3-methoxycarbonyl pyridinium chloride.

11. A method as claimed in claim 1, wherein R, is 6-positioned dimethylamino and R is phenyl.

12. A method as claimed in claim 1, wherein R, is 6-positioned bromine and R is phenyl.

13. A method as claimed in claim 1, wherein R, is hydrogen and R is p-nitrophenyl.

Claims

2. A method as claimed in claim 1, wherein R1 is hydrogen and R2 is phenyl.
3. A method as claimed in claim 1, wherein R1 is 4-positioned bromine and R2 is phenyl.
4. A method as claimed in claim 1, wherein R1 is hydrogen and R2 is m-nitrophenyl.
5. A method as claimed in claim 1, wherein R1 is hydrogen and R2 is o-nitrophenyl.
6. A method as claimed in claim 1, wherein R1 is hydrogen and R2 is p-anisyl.
7. A method as claimed in claim 1, wherein R1 is hydrogen and R2 is pyridinium chloride.
8. A method as claimed in claim 1, wherein R1 is hydrogen and R2 is p-tolyl.
9. A method as claimed in claim 1, wherein R1 is hydrogen and R2 is 3-carbamoyl pyridinium chloride.
10. A method as claimed in claim 1, wherein R1 is hydrogen and R2 is 3-methoxycarbonyl pyridinium chloride.
11. A method as claimed in claim 1, wherein R1 is 6-positioned dimethylamino and R2 is phenyl.
12. A method as claimed in claim 1, wherein R1 is 6-positioned bromine and R2 is phenyl.
13. A method as claimed in claim 1, wherein R1 is hydrogen and R2 is p-nitrophenyl.