US2216441A

US2216441A - Photographic emulsion

Info

Publication number: US2216441A
Application number: US146425A
Authority: US
Inventors: Grafton H Keyes
Original assignee: Eastman Kodak Co
Current assignee: Eastman Kodak Co
Priority date: 1937-06-04
Filing date: 1937-06-04
Publication date: 1940-10-01
Anticipated expiration: 1957-10-01

Description

Oct; 1, 1940. G. H. KEYES' 2,216,441

PHOTOGRAPHIC EMULSION Filed June 4, 193': 2 Sheets-Sheet 1 Z-Ernw-E- MOkRHOLYO-ALL Pnommn:

Fig.5.

Z-Ernw. I'PIPERIDYL I w as 'zzomp BY I A: ORNEY.

Patented Oct. 1, 1940 UNITED STATES PATENT OFFICE PHOTOGRAPHIC EMULSION Application June 4, 1937, Serial No: 146,425

2 Claims.

This invention relates to new dyes and to photographic emulsions containing the same.

Certain dyes of the cyanine class and dyes of the merocyanine class are known to alter the 5 sensitivity of photographic emulsions. More recently certain dyes of the hemioxonol class have been found to alter the sensitivity of photographic emulsions. See a copending application of Leslie G. S. Brooker, Serial No. 101,105, filed m September 16, 1936. Now, I have found new and unusual dyes and that these new dyes alter the sensitivity of photographic emulsions, particularly silver halide emulsions, in a new and useful manner.

An object of my invention, therefore, is to provide new dyes and a process for the preparation thereof. A further object is to provide photographic emulsions sensitized with such new dyes. A further object is to provide a photographic elemerit comprising a support coated with such sensitized emulsions. Other more specific objects will become apparent hereinafter.

' The dyes of my invention can, for convenience, be illustrated by the followinggeneral formula:

wherein A represents a divalent non-metallic atom of the oxygen group, such as oxygen or sulfur, L represents a methenyl group, n represents a positive odd integer not greater than five, D and E each represent an organic (carbon-containing) group or D and E together represent the non-metallic atoms necessary to complete a cyclic organic nucleus. P represents hydrogen or an aliphatic group while Q represents an aliphatic group, or P and Q together represent the non-metallic atoms necessary to complete a cyclic basic nucleus other than a pyrrol nucleus. The term "aliphatic group is intended to include saturated as well as unsaturated aliphatic groups and to include also substituted aliphatic groups, e. g., benzyl, B-hydroxyethyl, or the like.

45 A preferred group of my new dyes (among the members of which are very good photographic sensitizers) can be illustrated by the following formula:

wherein A, L, n, P and Q have the values indicated above under Formula I, and Z represents 5l the non-metallic atoms necessary to complete a heterocyclic nucleus, e. g., a five-membered or six-membered heterocycllc nucleus.

More particularly, in Formulas I and II, P and Q can each represent an alkyl group, such as methyl, ethyl, n-butyl, allyl, benzyl, p-hydroxy- 5 ethyl, furylmethyl (furfuryl) or the like and P and Q together can represent the non-metallic atoms necessary to complete an organic cyclic basic nucleus, such as a piperidine, a tetrahydroquinoline, an N-alkylpiperazine, a piperazine, a m morpholine or like basic nucleus. Z can represent the non-metallic atoms necessary to complete a five-membered heterocyclic nucleus, such as a thiazolone nucleus, for example, a 2,4(3,5) thiazoledione nucleus, such as 2,4(3,5.) -thiazolei5 dione, 3-alky1'-2,4(3,5) -thiazoledione, 3-phenyl- 2,4 (3,5) -thiazoledione or 3-naphthyl-2,4 (3 .5) -thiazoledione nuclei, a 2-thio- 2,4(3,5) -thiazoledione (a rhodanine) nucleus, such as 3-alkyl-2-thio- 2,4(3,5)-thiazoledione (3-alkylrhodanine) 3- 2o phenyl-2-thio-2,4 (3,5) -thiazoledione (3-phenylrhodanine) 3-naphthy1-2-thio-2,4(3,5)-thiazoledione (B-naphthylrhodanine) nuclei or 3-(1-benzothiazyl)'-2-thio-2,4(3,5) thiazoledione (3-(1- benzothiazyl-)-rhodanine) nuclei, a 2,4-dithio- 25 2,4(3,5) -thiazoledione (4-thiorhodanine) nucleus, such as 2,4-dithio-2,4(3,5) thiazoledione or its 3- alkyl, 3-phenyl or 3-naphthyl derivatives, a 2- alkylmercapto-4(5)-thiazo1one nucleus, such as 2-ethylmercapto-4(5)-thiazolone, a thiazolidone 3 nucleus, such as 4-thiazolidone or its 3-alkyl 3-phenyl or 3-naphthyl derivatives a 2-alkylphenylamino-4(5)-thiazolone nucleus or a 2-diphenylamino-4(5)-thiazolone nucleus; an oxazolone nucleus, for example, a 2-thio-2,4(3,5)- 35 oxazoledione nucleus, such as a 3-alkyl-2-thio- 2,4(3,5)-oxazoledione nucleus; an 'imidazolone nucleus, for example a 2,4(3,5)-imidazoledione nucleus, such as 2,4(3,5) -imidazoledione '(hydantoin) or its 3-alkyl, 3-phenyl or 3-naphthyl de- 40 rivatives as well as its 1,3-dia1kyl, 1-alky1-3- phenyl, l-alkyl-3 -naphthyl, 1,3-diphenyl, etc., derivatives, 9. 2-thio-2,4(3,5) -imidazoledione nucleus, such as 2-thio-2,4(3,5)rimidazoledione (2-thiohydantoin) or its 3-alkyl, 3-phenyl or 3-naphthyl derivatives as well as its 1,3-dialkyl, l-alkyl-B-phenyl, l-alkyl-3-naphthyl, 1,3-d1- phenyl, etc., derivatives, a 4-thio-2,4(3,5) -imi-. dazoledione nucleus, such as 4-thio-2,4(3,5)- imidazoledione (4-thiohydantoin) or its3-alkyl, 5g 3-phenyl or 3-naphthyl derivatives as well as its 1,3-dialkyl, 1-alkyl-3-phenyl, l-alkyl-B-naphthyl, 1,3-diphenyl etc., derivatives, a 2-alkylmercapto-5(4)-imidazolone, such as Z-propylmercapto-5 (4)-imidazolone; a thionaphthenone nu- 5| cleus, such as 2-(1)-thionaphthenone or 1(2)- thionaphthenone, a pyrazolone nucleus, for example a -thiopyrazoione, such as 1-phenyi-3- methyl-5-thiopyrazolone; an oxindole nucleus, such as 2,3-dihydro-3-ketoindole, and like fivemembered heterocyclic nuclei. The dyes containing a five-membered heterocyclic nuclei containing both a nuclear nitrogen and a nuclear sulfur atom give rise to emulsions of particular utility. The dyes containing a flve-membered heterocyclic nuclei containing a nuclear nitrogen atom and a nuclear thiocarbonyl group, I have found, are also very well adapted to the pro- .duction of useful photographic emulsions. Z can also represent the non-metallic atoms necessary to complete a six-membered heterocyclic nucleus, such as a 2,4,6-triketohexahydropyrimidine nucleus, for example barbituric acid or 2-thiobarbituric acid as well as their l-alkyl or 1,3-dialkyl derivatives; at 3,4-dihydro-2(1)-quinolone nucleus, such as 3,4-dlhydro-2(1)-quinolone (dihydrocarbostyril; a 3,4 dihydro-2(1) equinoxalone nucleus, such as 3,4-dihydro-2(1)-quinoxalone (oxydihydroquinoxaline); S-phenomorpholone (1,4,2-benzoxazine-3 (4) -one or benzo-fi-morpholone) nuclei; 1,4,2-benzothiazine-3(4)-one (ketodihydrobenzoparathiazine) nuclei and the like six-membered heterocyclic nuclei. The dyes containing a six-membered nuclei containing two nuclear nitrogen atoms or a nuclear nitrogen atom and a nuclear sulfur atom are especially well adapted to the manufacture of photographic emulsions, I have found.

The new dyes of my invention characterized by Formula II can be prepared by reacting a basic primary or secondary non-aromatic amine, particularly a monoamine, with a compound of the following formula.

III.

wherein A represents a divalent non-metallic atom, such as oxygen or sulfur, L represents a methenyl group, n represents a positive odd integer not greater than five, R represents an acyl group, such as acetyl, propionyl or benzoyl, R represents an aryl group, such as a phenyl, a diphenyl, a xylyl or a naphthyl group, i. e., an

aryl group of twelve or less nuclear carbonatoms, for example, and Z represents the nonmetallic atoms necessary to complete a heterocyclic nucleus, such as the flve-membered or six-membered heterocyclic nucleus illustrated above in connection with Formula II. Compounds represented by Formula III are described in the copending application of Leslie G. S. Brooker, Serial No. 101,105, filed September 16, 1936. Certain compounds (where n equals one) represented by Formula III have also been described by Dains et al. See for example J. Am. Chem. Soc. 31, 1148 (1909); 35, 959 (1913); 38, 1841 (1916); 40, 562 (1918); 44, 2310 (1922) and Ber. 35, 2496 (1902).

As shown in the above referred to application of Leslie G. S. Brooker compounds of Formula III can be prepared by first reacting a compound of the following formula:

wherein L represents a methenyl group, n represents a positive odd integer not greater than five, and R and R" represent aryl groups, such anilino-a-bromo-acrolein as phenyl, xylyl, diphenyl or naphthyl, with a heterocyclic compound of the following formula:

wherein A represents a divalent non-metallic atom. such asoxygen or sulfur, and Z represents the non-metallic atoms necessary to complete a heterocyclic nucleus, such as the five-membered or six-membered heterocyclic nuclei pointed out above under Formula H. Some of the compounds represented by Formula IV are basic and accordingly form salts with acids such as hydrochloric, sulfuric and the like. These salt forms can be used as well to react with the compounds of Formula V. Examples of compounds of Formula IV and their salts which can be advantageously employed are: diphenyl-formamidine, fl-anilinoacrolein anil and its hydrochloride, anil, p-anilino-achloro-acrolein anil and their hydrochlorldes, glutaconic-aldehyde dianilide hydrochloride, a- (B naphthylimino-e-(p naphthylamino) amethyl-a, 'y-pentadiene hydrochloride (see Konig, Journal fur praktlsche Chemie (2nd Series), Vol. 69, page 136), etc. Compounds such as diphenyl formamidine are advantageously reacted with compounds of Formula V, in the presence of a petroleum fraction, e. g., kerosene, as shown in the examples below. Compounds such as 18- anilinoacrolein anil or glutaconic aldehyde or their hydrochlorides or other salts can be reacted with compounds of Formula V by heating the substances together, advantageously in the presence of a strong tertiary organic base.

The reaction products of-compounds of Formula IV and compounds of Formula V can be advantageously converted into their acylated derivatives, i. e. the compounds of Formula III,

by treatment with organic acid anhydrides, such as acetic, propionic, butyric or benzoic anhydrides. This conversion can be effected during the reaction of compounds of Formula IV with compounds of Formula V, as illustrated below. Other methods of forming the acylated compounds of Formula III, can be employed such as treatment with acid chlorides instead of acid anhydrides. I have found the acetylated com- I pounds of Formula HI very suitable for preparing my new dyes. 7

Basic non-aromatic primary or secondary amines which can be used to react with compounds of Formula III are, for example, allphatic amines for instance, monoalkylamines, such as methylamine, ethylamine, n-butylamine, sec-butylamine, isopropylamine, n-decylamines, allylamine, cyclohexylamine, furylmethylamine, tetrahydro-furylmethyl-amine, benzylamine, phydroxyethylamine, or the like or dialkyl-amines, such as dimethylamine, diethyl-amine, di-nbutylamine, di-p-hydroxyethylamine, diallylamine or the like, or heterocyclic basic secondary amines for instance flve-membered heterocyclic secondary amines, such as pyrrolidenes, or the like, or six-membered heterocyclic basic secondary amines, such as piperidine, piperazine, N-

alkylpiperazines, 1,2;3,4-tetrahydroquinoline, morpholines or the like. Pyrrol cannot be employed in my process.

By the term "non-aromatic amines," I mean an amine in which the amino group is not directly attached to a benzene ring or like aromatic ring system as the amino group is in aniline, methylaniline, aand fl-naphthylamlne. 1- aminoanthraquinone, a-aminopyridine, -amin0- quinoline, etc.

Compounds of Formula V are all characterized by containing a nuclear methylene group adjacent to a nuclear carbonyl group, such as an oxocarbonyl or thiocarbonyl group.

The basic non-aromatic primary or secondary amines are advantageously reacted with the compounds of Formula III in the presence of a diluent, such as a lower aliphatic alcohol, 1. e., one of four carbon atoms or less. However, the diluent is not essential. If used, the diluent is advantageously substantially anhydrous} Other diluents such as ethylidene dichloride, ethylene dichloride or dioxane can be used. The diluent should be inert toward the dyes and is advantageously chosen so that the formed dye will separatetherefrom at least upon cooling the reaction mixture. Heat accelerates the formation of my new dyes. The basic non-aromatic primary or secondary amine is advantageously employed in molecular excess, from 1.5 to 3 molecular proportions (mol.) per molecular proportion of compound of Formula III is suitable. With a molecular ratio of 1:1 the yield of my new dyes is generally lower than when an excessof the non-aromatic amine is employed.

While the process of preparing my new dyes is subject to variation particularly as respects the nature and quantities of reactants, the nature and quantity of diluent employed and the temperatures, the following examples will serve to illustrate the mode of preparation the dyesof Formula II where n represents one. These examples are not intended to limit my invention.

EXAMPLE 1.5- (1 -piperidyl) -methylene- 3-phen1 lrhodanine 0.9 g. (1 mol.) of 5-acetanilidomethylene-3- phenylrhodanine, 0.6 g. (3 mol.) of piperidine and 30 cc. of absolute ethyl alcohol were heated under reflux for about 30 minutes. The dye separated from the cooled reaction-mixture and after two recrystallizations from methyl alcohol formed yellow needles melting at 286-288 C.

The 5 acetanilidomethylene 3 phenylrhodanine used in the above example was prepared by heating under reflux for about 15 minutes 1.55 g. (1 mol.) of 5-anilinomethylene-3-phenylrhodanine, 15 cc. of acetic anhydride and 0.5 g. (1 mol.) of triethylamine. The crude product was recrystallized twice from methyl alcohol and was obtained as minute yellow crystals melting at 194-198" C. with decomposition. The 5-anilinomethylene-3-phenylrhodanine was prepared according to the method of Dains, Kansas ,Univ.

Science Bull. 15, 265 (1924) by heating together equimolecular proportions of 3-phenylrhbdanine and diphenylformamidine in kerosene (about 300 cc. per gram molecular proportion of 3-phenylrhodanine is suitable) at about 120 C. The reaction product separated and was washed'with methyl alcohol. It was recrystallized from glacial acetic acid.

EXAMPLE 2.3-ethyl-5- (1 -piperidyl) methylenerhodanine IH, a!

9.75 g. (1 mol.) of 5-acetanilidomethylene-3- ethylrhodanine, 9.6 g. (3 mol.) of piperdine and 15 cc. of absolute ethyl alcohol were heated under reflux for about 30 minutes. The dye separated from the cooled reaction mixture. It was twice recrystallized from methyl alcohol and was chtained as pale yellow needles melting at 150.5- 7

- ing at 128-130 C. The 5-anilinomethylene-3- ethylrhodanine was prepared by heating together equimolecular proportions of 3-ethylrhodanine and diphenylformamidine according to the method of Dalns (see Ex. 1).

EXAMPLE 3.5- (4-morpholyl) -methylene-3-ethyl- 2-thio2,4(3,5) oxazoledione 9.7 g. (1 mol.) of 5-acetanilidomethylene-3- ethyl-2-thio-2,4(3,5)-oxazoledione, 0.7 g. (3 mol.) morpholine and 10 cc. absolute ethyl alcohol were heated'under reflux for about 30 minutes. The dye separated from the cooled reaction mixture. It was recrystallized from water and was obtained as colorless crystals melting at 164-6" C. with decomposition. It gave a colorless aqueous solution.

The 5 acetanilidomethylene-li-ethyl 2,4(3,5) oxazoledione employed in the above example was prepared by heating 8.7 g. (1 mol.) of 5-anilinomethylene-3-ethyl-2,4(3,5) oxazoledione with 30 cc. of acetic anhydride and 3.7 g. (1 mol.) of triethylamine at 100 C. for about 10 minutes. The crude product separated from the cooled reaction mixture. It was twice recrystallized from methyl alcohol and obtained as nearly colorless crystals, melting at 158-l60 C. The 5-anilinomethylene-3-ethyl-2,4 (3,5) oxazoledione was obtained according to the method of Dains as illustrated in Example 1 by heating equimolecular proportions of diphenylformamidine and 3-ethyl- 2,4(3,5) -oxazoledione together in kerosene.

In the above examples, the piperidine and morpholine can be replaced with other basic primary or secondary non-aromatic amines, such as pointed out above in connection with reaction with compounds of Formula III. Likewise the 3-ethylrhodanine and 3-phenylrhodanine can be replaced by other heterocyclic compounds containing a nuclear methylene group adjacent to a nuclear carbonyl group, such as correspond to the flve-membered and six-membered heterocyclic nuclei pointed out under Formula 11 above, for example.

The following examples will serve to illustrate the formation of the dyes of Formula II, where n represents three. These examples are'not intended to limit my invention.

ExAnrLn 4.3-ethyZ-5- ['7- (1 -piperidgl) allylidene] '-rhodanine 0.8 g. (1 mol.) of 5-('y-acetanilidqallylidene)- S-ethylrhodanine, 0.6 g. (3 mol.) of piperdine and 15 cc. of absolute ethyl alcohol were heated under reflux for about 30 minutes. The dye separated from the cooled reaction mixture. It was twice recrystallized from methyl alcohol and obtained as light brownish crystals having a bluish reflux and melting at 1879 C. with decomposition. Its methyl alcoholic solution was deep yellow.

The 5-(y-acetanilidoa1lylidene) 3 ethylrhodanine employed above was prepared by refluxing 3.2 g. (1 mol.) of 3-ethylrhodanine, 5.2 g. (1 mol.) of fi-anilinoacrolein anil hydrochloride and 30 cc. of acetic anhydride for about one hour. The reaction product separated from the cooled reaction mixture and after two recrystallizations from acetic acid was obtained as pale yellow crystals melting at 2255-2265 C.

Exmpm: 5.3-ethyl-5- ['y- (4-morpholyl) allvlidene] -rhodanine EYE.

0.8 g. (1 mol.) of -(y-acetanilidoallylidenehiiethylrhodanine, 0.7 g. (3 mol.) of morpholine and cc. of absolute ethyl alcohol were heated under reflux for about 30 minutes. The dye separated from the cooled reaction mixture and after two recrystallizations from methyl alcohol was obtained as minute orange red crystals, melting at 225.5227.5 C. with decomposition. Its methyl alcoholic solution was yellow.

Examu: 6.5 -(-y-diethylaminoallylidene) 3- 0.8 g. (1 mol.) of 5-('y -acetanilidoallylidene)- 3-ethylrhodanine, 0.6 g. (3 mol.) of diethylamine and 15 cc. of absolute ethyl alcohol were heated under reflux for about 30 minutes. The dye separated from the cooled reaction mixture and after two recrystallizations from methyl alcohol formed amber needles with a blue reflux, melting at 13- 135 C. with decomposition. Its methyl alcoholic solution was yellow.

EXAMPLE 7.2-diphenylamino-5- ['1- (1 -piperidyl) -allylidene] -4( 5) -thiazol071e 1.0 g. (1 mol.) of 5-('y-acetanilidoallylidene)- 2-diphenylamino-4(5)-thiazolone, 0.6 g. (3 mol.) of piperidine and cc. of absolute ethyl alcohol were heated under reflux for about minutes. The dye separated from the cooled reaction mixture. After two recrystallizations from ethyl alcohol, the dye was obtained as brownish yellow crystals melting at 251-253 C. with decomposition. Its ethyl alcoholic solution was yellow.

The 5- (y-acetanilidoallylidene) -2-diphenylamino-4(5)-thiazolone employed above was made by refluxing 2.7 g. (1 mol.) o1'2-diphenylamino- 4(5)-thiazolone, 2.6 g. (1 mol.) of p-anillnoacrolein anil hydrochloride and 20 cc. of acetic anhydride for about 30 minutes. The crude product separated from the cooled reaction.mix-- A. ll,

1.6 g. (1 mol.) of 5-(-y-acetanilidoallylidene)- 3-ethyl-2-thlo-2,4(3,5)-oxazoledione, 1.2 g. (3

' mol.) of piperidine and 10 cc. absolute ethyl alcohol were heated under reflux for about 30 minutes. The dye separated from the cooled reaction mixture. After two recrystallizations from 70% aqueous ethyl alcohol, the dye was obtained as orange yellow crystals melting at 120.5-123.5 with decomposition. The ethyl alcoholic solution of the dye was yellow.

The 5- ('y-acetanilidoallylidene) -3-ethyl-2-thio- 2,4(3,5)-oxazoledione employed above was prepared by refluxing 2.9 g. (1 mol.) of 3-ethyl-2- thio-2,4(3,5)-oxazoledione, 5.2 g. (1 mol.) of anilinoacrolein anil hydrochloride, 30 cc. of absolute ethyl alcohol and 2.0 g. (2 mol.) of triethylamine for about 30 minutes. The crude product, 5-(r -anilinoallylidene) -3-ethyl- 2 thio 2,4(3,5) oxazoledione, separated from the cooled reaction mixture. 5.8 g. (1 mol.). of this crude product, 30 cc. of acetic anhydride and 2.0 g. (1 mol.) of triethylamine were heated to refluxing for about 5 minutes. The product separated from the cooled reaction mixture and after two recrystallizations from methyl alcohol was obtained as minute greenish yellow crystals melting at 247- 249 C. with decomposition.

Exnum: 9.1 -benzothiazyl-3-methut-4- [-y- (piperidyl) allyliden e] -5-p1/razolone 1.0 g. (1 mol.) of 4-( -acetanilidoallylidene) -1- benzothiazyl-3-methyl-5 pyrazolone, 0.6 g. (3 mol.) of piperidine and 10 cc. absolute ethyl alcohol were refluxed for about 30 minutes. The

5 dye separated from the cooled reaction mixture. After two recrystallizations from methyl alcohol, the dye was obtained as reddish crystals with a greenish reflex melting at 256258 C. with decomposition. Its methyl alcoholic solution was purplish orange.

The 4- (y-acetanilidoallylidene) l-ben'zothiazyl- 3-methyl-5-pyrazolone employed above was prepared by refluxing 4.6 g. (1 mol.) of l-benzothiazyl-3-methyl-5-pyrazolone, 5.2 g. (1 mol.) 01' pl-anilinoacrolein anil hydrochloride and 25 cc. of acetic anhydride for about minutes. The product separated from the cooled reaction mixture and was used without recrystallization.

30 EXAMPLE 10.3 ethyl 1-phenyl-5-[ -(1-piperidyl) allylidene] -2-thiohydantoin ethyl-1-phenyi-2-thiohydantoin, 0.6 g. (3 mol.) of piperidine and 25 cc. of absolute ethyl alcohol were refluxed for about 30 minutes. The dye separated from the cooled reaction mixture. .It was recrystallized. twice from methyl alcohol and obtained as reddish crystals melting at 189-191 C. with decomposition.

The 5-(-, acetanilidoallylidene) 3 ethyl 1 phenyl-2-thiohydantoin, was prepared by refluxing 4.4 g. (1 mol.) of 3-ethyl-1-phenyl-2-thiohydantoin, 5 g. (1 mol. of fl-anilinoacrolein anil hydrochloride, 30 cc. of absolute ethyl alcohol and 2.0 g. (1 mol.) of triethylamine were refluxed for about 30 minutes. rated from the cooled reaction mixture and was used without recrystallization. 1.75 g. (1 mol.) of this crude product, 10 cc. of acetic anhydride and 0.5 g. (1 mol.) of triethylamine were heated no at 100 C. for about minutes. The product aiter two recrystallizations from methyl alcohol formed yellow crystals melting at 184-186" C. with decomposition.

EXAMPLE 11.--3-methyl-1 -phenyl-4- ['7- (1 -pipe1'- idyl) -allylidene] -5-pyrazolone 0.85 g.(1 mol.) of 4-(v-acetanilidoallylidene) -3- methyl-1-phenyl-5-pyrazolone, 0.6 g. (3 mol.) of

The crude product sepaseparated from the cooled reaction mixture andpiperidine and 10 cc. of absolute ethyl alcohol were heated under reflux for about 30 minutes. The dye separated from the cooled reaction mixture. It was twice recrystallized from methyl alcohol and obtained as orange crystals melting at 187-189 C. Its methyl alcoholic solution was yellow.

T h e 4 ('y-acetanilidoallylidene) -3-methyl-1- phenyl-5-pyrazolone employed above was prepared by refluxing 3,5 g. (1 mol.) of 3-methyl-1- phenyl-5-pyrazolone, 5 g. (1 mol.) of p-anilinoacrolein anil hydrochloride, cc. of acetic anhydride and2 g. (1 mol.) of triethylamine for about minutes. The product separated from the cooled reaction mixture and after two recrystallizations from methyl alcohol was obtained as flaky orange crystals melting at 212-214 C. with decomposition.

In the above eight examples, the piperidine morpholine and diethylamine can be replaced by any oithe basic primary or secondary nonaromatic amines pointed out above in connection with. reaction with compounds of Formula III. Likewise the 3-ethyl-2-thio-2,4(3,5) -oxazoledione, l-benzothiazyl- 3 -methyl- 5 -pyrazo,- lone, 3 ethyl 1 -.phenyl 2 -thiohydantoin, 3- methyl- 1 -phenyl- 5 -pyrazolone, 3-ethylrhodanine, 2-diphenylamino-4(5)-thiazolone, 4-thiorhodanine and barbituric acid can be replaced with any heterocyclic compound containing a nuclear methylene group adjacent to a nuclear carbonyl group, such as correspond to the five-. membered and six-membered heterocyclic nuclei pointed out above under Formula II, for example. The dyes derived from piperidine are especially well adapted to the manufacture of photographicemulsions, I have found.

The following examples serve to illustrate the preparation of the dyes of Formula 11 where n equals flve. These examples are not intended to limit my invention.

EXAMPLE 12. 3-ethyl-5- [5-(1-m'peridyl) -A2,4-

pentadienylidene] -rho dam'ne 0.9 g. (1 mol.) of 5-(5-acetanilido-A2,4-pentadienylidene)-3-ethylrhodanine, 0.6g. (3 mol.)

The dye was obtained as dark blue hydrochloride; 40 cc. of absolute ethylalcohol and 2 g. (1 mol.) of triethylamine for about three minutes. The product separated from the cooled reaction mixture and without recrystallization was heated to boiling with cc. of acetic anhydride. The product separated from the cooled reaction mixture and was used without recrystallization.

Exaurns 13.3-ethyl-5-[5-(4-morpholyl)-A2,4- pentadienylidene] rhodanine 0.9 g. (1 mol.) of 5-(5-acetanilido-A2A-pentadienylidene-3-ethylrhodanine, 0.7 g. (3 mol.) of morpholine and 25 cc. of absolute ethyl alcohol were heated under reflux for about 30 minutes.

The dye separated from the cooled reaction mixture. It was recrystallized three. times from ethyl alcohol and obtained as dark blue crystals melting at 179-182 C. with decomposition. Its ethyl alcoholic solution is bluish red.

ExAmrLr: 14. 5- (5-diethylamino-A2,4-pentadienylidene) -3-ethylrhodaninei CsHs 8 .\NC:H|

N-cH=oH-oH=oH-cH=.c =0

CgHs 0.9 g. (1 mol.) of 5-(5-acetanilido-A2,4-pentadienylidene)-3-ethylrhodanine, 0.9 g. (3 mol.)

secondary amines pointed out in the above in connection with reaction with compounds of Formula III above. The 3-ethyl-rhodanine can be replaced by any heterocyclic compound conv taining a nuclear methylene group adjacent to a nuclear carbonyl group, such as correspond to the heterocyclic nuclei pointed out under Formula II above.

To prepare dyes of Formula II where Z represents the non-metallic atoms necessary to complete a 2-alkylmercapto- 4(5) imidazolone nu cleus, dyes of Formula II where Z represents the non-metallic atoms necessary to complete a rhodanine or a hydantoin (free from substituents in the 1-position) nucleus can be treated with alkylating agents. For example, dyes such as 5 (1 piperidyl) -methylenerhodanine, 5-[ -(1- piperidyl) allylidene] rhodanine, 5 'E-y- (4-morpholyl) allylidene] -rhodanine, 5- [5-(1-piperidyl) A2,4 pentadienylidenel rhodanine, 5-(1-piperidyl) -methylenehydantoin, S-diethylaminomethylene-2-thiohydantoin, 5 ['y-(l-piperidyhallylidene] -2-thiohydantoln and 5- [5- (4-morpholyl) A2,4-pentadienylidene]-2-thiol.ydantoln can be' alkylated by suspending one molecular proportion in methyl alcohol, adding about 1.2 mol. of powdered alkali, e. g. potassium hydroxide and then adding about 1.2 mol. of alkylating agent, e. g., dialkyl sulfates, or advantageously alkylp-toluene-sulfonates. The reaction mixture is refluxed for about 30 minutes ordinarily, though longer time may be required in some instances.

The alkylated dye separates from the chilled e- 7l action mixture.

wherein A, L, n, P and Q have the values pointed out under Formulas I and II above and D represents a cyano (CN) group, an acyl group, such as acetyl, propionyl, butyryl, benzoyl or naphthoyl, a carboxyl group or a carbolkoxy group and E represents an aryl group, such as phenyl or naphthyl, an arylamino group, such as phenyiamino or naphthyl amino, or an alkyl group, such as methyl, ethyl or the like.

These new related dyes can be prepared in a manner similar to that illustrated above, 1. e., by reacting a basic non-aromatic primary or secondary amine with a compound of the following formula:

wherein A, n, R and B. have the values pointed out under Formula III above while D and E have the values pointed out under Formula VI above.

VII.

The basic primary or secondary non-aromatic.

amines which can be reacted with compounds of Formula VII are the same as those pointed out above in connection with reaction with compounds of Formula III. The compounds of Formula VII are first obtained by methods similar to those illustrated above for preparing compounds of Formula III. Thus, for example, di phenylformamidine (in kerosene) or p-anilinoacrolein anil hydrochloride (in acetic anhydride) or glutaconic aldehyde dianllide hydrochloride (in acetic anhydride) can be condensed with the following: benzoylacetonitrile, naphthoylacetonitrile, cyanoacetanilide, malonic acid, diethylmalonate, acetoacetic ester, acetylacetone, benzoylacetone, or the like. The resulting compound is then converted to its acylated form if it is not already in that form. The acylation can be effected as illustrated in the above examples.

The following example which is not intended to limit my invention illustrates the preparation of my new dyes of Formula IV:

Exsmru: 15.-a- (1 -piperidul) -allylidenel 0.8 g. (1 mol.) of a-(y-acetanilido-allylidene)- benzoylacetonitrile. 0.6 g. (3 mol.) of piperidine and 15 cc. of absolute ethyl alcohol were heated under reflux for about 30 minutes. The dye separated from the cooled reaction mixture and after two recrystallizations from methyl alcohol was obtained as orange-yellow needles melting at -162" C. with decomposition. Its methyl alcoholic solution was yellow.

The a- ('y-acetanilido-allylidene) -benzoylacetonitrile used in the above example was prepared by first refluxing for about 30 minutes 1.45 g. (1 mol.) of benzoylacetonitrile, 2.5 g. (1 mol.) of

p-anilinoacrolein anil hydrochloride, 20 cc. of

40 cc. of acetic anhydride and 2.0 g. of triethylamine were heated at 100 C. for about 10 minutes. The crude product separated from the cooled reaction mixture and after two recrystallizations from methyl alcohol was obtained as yellow needles melting at 208210 with decomposition.

These new dyes of my invention represented by Formula VI are useful in preparing photographic emulsions, in preparing light filters and in the dyeing of textiles made from cellulose acetate yarn.

Dyessimilar in structure to the preferred group of the dyes of my invention (represented by Formula 11 above) can be prepared from carbocyclic compounds containing a nuclear methylene group adjacent to'a nuclear carbonyl group, e. g., from 1,3-cyclohexadione or from indandione or the like. The method of preparation is similar to that illustrated above, viz., first condensing the indandione or similar carbocyclic compound ,with a compound of Formula III followed by treating the resulting condensation product with a primary or secondary non-aromatic amine as illustrated above. The dyes from these carbocyclic compounds, such as indandione or 1,3-cyclohexadione, are of lesser utility in manufacturing photographic emulsions, but are suited for the preparation of light filters and can be used for dyeing of textiles made from cellulose acetate yarn.

From the breadth of description given throughout these specifications, it is clear that dyes containing simple substituents on the nuclei or methenyl (CH) chains are a part of my invention. Still further examples of the preparation of my new dyes could be given, but the foregoing will be sufilcient toteach those skilled in the art the manner of obtaining my new dyes.

My new dyes can be called hemioxonol dyes. Those containing one methenyl group (where n in Formulas I and II represents one) can be called simple hemioxonol dyes; those containing a chain of three methenyl groups (where n represents three) can be called hemicarboxonol dyes) and those containing a chain of five methenyl groups (where n represents five) can be called hemidicarboxonol dyes.

My new hemioxonol dyes give rise to photographic emulsions possessing novel sensitivity when incorporated therein. My invention is particularly directed to the customarily employed gelatino-silver-halide emulsions. However, my new hemioxonol dyes can be employed in emulsions in which the carrier is other than gelatin,

for example, a resinous substance or cellulosic derivative which has substantially no deleterious effect on the light-sensitive materials. As silver halide emulsions, we include such emulsions as are commonly employed in the art, for example, silver chloride or silver bromide emulsions which can contain other salts which may be lightsensitive. By way of illustration, the hereindescribed sensitized photographic emulsions were prepared employing ordinary gelatino-silverchloride and gelatino-silver-bromide emulsions. My new simple hemioxonol dyes (where n represents one) are advantageously employed with silver chloride emulsions. My new hemicarboxonol dyes are likewise advantageously employed in manufacturing sensitized silver chloride emulsions.

In the preparation of photographic emulsions containing my new hemioxonol dyes, it is only necessary to disperse the dyes in the emulsions.

The methods of incorporating dyes in emulsions are simple and well lmown to those skilled in the art. In practicing-my invention, it is-convenieut to add the dyes to theemulsions from solutionsin appropriate solvents. The solvent must, of course, be compatible with the emulsion, substantially free from any deleterious effect on the light-sensitive materials and capable of dissolving the dyes. Methanol has proven satisfactory as a solvent for my new dyes. Acetone can be employed for those dyes which show low solubility in methanol. The dyes are advantageously incorporated in the finished washed emulsion and should be uniformly distributed throughout to secure best results.

The concentration of my new dyes in the emulsions can vary widely, e. g., from about 2 to about 100 mg. per liter of fiowable emulsion. The concentration of the dye will vary according to the type of light-sensitive material in the emulsion and according to the efiects desired. The suitable and most economical concentration for any given emulsion will be apparent to those skilled in the art, upon making the ordinary tests and observations customarily used in the art of emulsion-making. To prepare a 'gelatino-silverhalide emulsion, the following procedure is satisfactory: A 'quantity of the dye is dissolved in methyl alcohol or acetone and a volume of this solution (which may be diluted with water) containing from 2 to 100 mg. of dye is slowly added to about 1000 cc. of a gelatino-silver halide emulsion with stirring. Stirring is continued until the dye is uniformly and practically homogenously dispersed. With the more powerful of my new sensitizing hemioxonol dyes, 10 to 20 mg. of dye per 1000 cc. of emulsion suffice to produce the maximum sensitizing effect with the ordinary gelatino-silver-halide emulsions. The above statements are only illustrative and not to be understood as limiting my invention in any sense, as it will be apparent that my dyes can be incorporated by other methods in many of the photographic emulsions customarily employed in the art, such for instance as by bathing the plate or film, upon which the emulsion has been coated, in a solution of the dye in an appropriate solvent, although such a method is ordinarily not to be preferred. The claims are intended to cover any combination of these new dyes with a photographic silver halide emulsion whereby the dye exerts a sensitizing effect upon the emulsions as well as a photographic element comprising a support, ordinarily transparent, upon which the light-sensitive emulsion is coated or spread and allowed to dry.

The accompanying drawings are by way of iilustration and depict the sensitivity of emulsions Each figure containing eight of my new dyes. in the drawings is a diagrammatic reproduction of a spectrogram showing the sensitivity of silver chloride or silver bromide emulsions containing one of my new dyes. In Fig. l, the sensitivity of an ordinary gelatino-silver-chloride emulsion containing 3-ethyl 5 -(1-piperidyl) -methylenerhodanine is depicted. In Fig. 2, the sensitivity of an ordinary gelatino-silver-bromide emulsion containing 8-ethyl-5- [-y(4 morpholyl) allylidene] rhodanine is depicted. In Fig. 3, the sensitivity of an ordinary gelatino-silver-chloride emulsion containing 3 ethyl- 5 -['y-(1 piperidyl) allylidene] -2-thio-2,4(3,5) -oxazole,dione is depicted. In Fig. 4, the sensitivity of an ordinary gelatinosilver-chloride emulsion containing 2-diphenylamino-5-[ -(1-piperidyl) allylidene] 4(5) -thiazolone is depicted. In Fig. 5, the sensitivity of an ordinary gelatino-silver-chloride emulsion containing 3-ethyl-1-phenyl-5- [-y-(l-piperidyl) allylidenel-2-thiohydantoin is depicted. In Fig. 6, the sensitivity of an ordinary gelatino-silverbromide emulsion containing l-benzothiazyl-3- methyl-4- [7-(1 piperidyl) -allylidene]- 5 pyrazolone is depicted. In Fig. 7, thesensitivity of an ordinary gelatino-silver-bromide emulsion containing 3 ethyl 5 -[5 (1 piperidyl) -A2,4 pentadienylidenelrhodanine is depicted. In Fig. 8, the sensitivity of an ordinary gelatino-silverbromide emulsion containing 5-(diethylamino- A2,4-pentadienylidene)-31-ethylrhodanine is depicted. As shown, the dyes containing a piperidyl nucleus give rise to emulsions of particular utility.

Still further examples illustrating my invention could be given, but the foregoing will be sumcient to teach those skilled in the art the manner in which my invention is carried outv and the principles of sensitizing photographic emulsions with my new dyes.

What I claim as my invention and desire to be secured by Letters Patent of the United States is:

l. 'A photographic silver halide emulsion sensitized with a sensitizing dye selected from the group of dyes characterized by the following formula:

wherein A represents a divalent non-metallic atom selected from the group consisting of oxygen and sulfur, L represents a methenyl group, n represents a positive odd integer not greater than five, P and Q together represent the nonmetallic atoms necessary to complete a six-membered organic cyclic basic nucleus and Z represents the non-metallic atoms necessary to complete a heterocyclic nucleus selected from the group consisting of five-membered and six-membered heterocyclic nuclei.

2. A photographic gelatino-silver-halide emulsion sensitized with a sensitizing dye selected from the group of dyes characterized by the following formula:

' wherein A represents a divalent non-metallic atom selected from the group consisting of oxy- 3. A photographic gelatino-silver-halide emulsion sensitized with a sensitizing dye selected from the group of dyes characterized by the following formula:

from the group of dyes characterized by the following formula:

wherein n represents a positive odd integer not greater than-five, P and Q together represent the non-metallic atoms necessary to complete a six-membered organic cyclic basic nucleus and Z represents the non-metallic atoms necessary I to complete a rhodanine nucleus.

5. A photographic gelatino-silver-halide emulsion sensitized with a sensitizing dye selected from the group of dyes characterized by the following formula: v

wherein n represents a positive odd integer not greater than flve, P and Q together represent the non-metallic atoms necessary to complete a piperidyl nucleus and Z represents the non-metallic atoms necessary 'to complete a rhodanine nucleus.

6. A photographic gelatino-silver-halide emulsion sensitized with a dye of the following formula:

7. A photographic gelatino-silver-halide emulsion sensitized with a sensitizing dye selected from the group of dyes characterized by the following formula:

wherein n represents a positive odd integer not greater than five, P and Q together represent the non-metallic atoms necessary to complete a six-membered organic cyclic basic nucleus and Z represents the non-metallic atoms necessary to complete a 2-thio-hydantoin nucleus.

8. A photographic gelatino-silver-halide emulsion sensitized with a sensitizing dye selected from the group of dyes characterized by the following formula:

wherein n represents a positive odd integer not greater than five, P and Q together represent the non-metallic atoms necessary to complete a piperidyl nucleus and Z represents the non-metallic atoms necessary to complete a 2-thiohydantoin nucleus.

9. A photographic gelatino-silver-halide emulsion sensitized with a dye of the following formula:

. l0. Aphotographic gelatino-silver halide emulsion sensitized with a sensitizing dye selected from the group or dyes characterized by the following formula:

wherein n represents a positive odd integer not greater than live, P and Q together represent the non-metallic atoms necessary to complete a sixmembered organic cyclic basic nucleus and Z represents the non-metallic atoms necessary to complete a. 3-alkyl-2-thio-2,4-(3,5)oxazoledione nucleus.

11. A photographic gelatino-silver-halide emulsion sensitized with a sensitizing dye selected from the group of dyes characterized by the following formula:

, z. P-N-(cn).='o-d=o wherein P and Q together represent the nonmetallic atoms necessary to complete a piperidyl nucleus and Z represents the non-metallic atoms necessary to complete a 3-ethyl-2-thio-2,4(3,5)

oxazoledione nucleus.

GRAFTON H. KEYES.