US3770440A - Spectrally sensitized photographic silver halide emulsion - Google Patents

Spectrally sensitized photographic silver halide emulsion Download PDF

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US3770440A
US3770440A US00149276A US3770440DA US3770440A US 3770440 A US3770440 A US 3770440A US 00149276 A US00149276 A US 00149276A US 3770440D A US3770440D A US 3770440DA US 3770440 A US3770440 A US 3770440A
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silver halide
group
halide emulsion
emulsion
photographic silver
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A Sato
K Shiba
M Hinata
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Fujifilm Holdings Corp
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Fuji Photo Film Co Ltd
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    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B23/00—Methine or polymethine dyes, e.g. cyanine dyes
    • C09B23/16—Methine or polymethine dyes, e.g. cyanine dyes the polymethine chain containing hetero atoms
    • C09B23/162—Methine or polymethine dyes, e.g. cyanine dyes the polymethine chain containing hetero atoms only nitrogen atoms
    • C09B23/164—Methine or polymethine dyes, e.g. cyanine dyes the polymethine chain containing hetero atoms only nitrogen atoms containing one nitrogen atom
    • 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
    • G03C1/00—Photosensitive materials
    • G03C1/005—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
    • G03C1/06—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with non-macromolecular additives
    • G03C1/08—Sensitivity-increasing substances
    • G03C1/10—Organic substances
    • G03C1/12—Methine and polymethine dyes

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  • Z represents an atomic group necessary to complete a benzene ring, the hydrogen atom'of which may be substituted; R and R -each represent a member 6 Claims, 1 Drawing Figure PATENTEDNUV 6 I975 B F F U I 8 E I D /DYE STUFF l0 WAVELENGTH (my) INVENTORS AKIRA SATO KEISUKE SHIBA MASANAO HINATA Q axnq Tiffani? 0m,
  • the above mentioned object of the invention can be accomplished by incorporating a new sensitizing dye represented by the following general formula (I) or (II) in a silver halide emulsion.
  • Z represents an atomic group necessary for forming a benzene ring, the hydrogen atom of which may be substituted for by conventional substituents for benzimidazolo cyanine dyes.
  • substituents in this case are those well known for benzimidazolocarbocyanines, such as halogen atoms, e.g.
  • R and R represent the same or different alkyl groups, such as methyl, ethyl, n-propyl and n-butyl groups, and substituted alkyl groups conventionally used as nitrogen substituents in benzimidazolo cyanine dyes, except a sulfoalkyl group, such as hydroxy alkyl (e.g. B-hydroxyethyl, -y-hydroxypropyl), acetoxyalkyl (e.g. B-acetoxyethyl, 'y-acetoxypropyl) carboxyalkyl (e.g.
  • hydroxy alkyl e.g. B-hydroxyethyl, -y-hydroxypropyl
  • acetoxyalkyl e.g. B-acetoxyethyl, 'y-acetoxypropyl
  • carboxyalkyl e.g.
  • fl-carbamoylethyl 'y-carbamoyl-propyl, B-carbamoylbutyl, fl-N-ethylcarbamoylethyb, y-N-ethylcarbamoylpropyl, B-N-methylcarbarnoylbutyl), sulfamoylalkyl (e.g. 'y-sulfamoylpropyl, 8-sulfamoylbutyl), aminosulfonylalkyl (e.g.
  • A represents aryl groups, such as a phenyl group, a methoxyphenyl, a tolyl or a chlorophenyl group.
  • X represents an acid anion, such as a chloride, bromide, iodide, thiocyanate, perchlorate, benzenesulfonate, p-toluene-sulfonate, niethylsulfate or ethylsulfate ion.
  • the feature of the sensitizing dyes of this invention resides in the fact that they are limited by general formulas (I) or (II) to a tetramethinehemicyanine or tetramethinehemicyanine base having a benzimidazole nucleus which tends to form a .l-aggregate.
  • these dyes are effective for raising the spectral sensitivity in the orthoregion.
  • tetramethinehemicyanines or tetramethinehemicyanine bases having benzothiazole, benzoselenazole or benzoxazole nucleus mentioned in U.S. Pat. Nos. 2,369,509 and 2,369,509 are difficult to form the J-aggregate and have a low spectral sensitivity.
  • the sensitizing dyes represented by general formula (II) are obtainable by treating the sensitizing dye (I) with an aqueous akaline solution and removing the I-IX.
  • the acetanilide intermediate is dissolved in methanol and then mixed with 4N caustic soda and with water to deposit a crystal which is then filtered, washed with water and recrystallized from methanol to obtain 1.5 g of Dye 3melting at 274C.
  • the sensitizing dyes used in this invention are capable of spectrally sensitizing a silver halide photographic emulsion, and in particular, effectively enlarging the light-sensitive region of a gelatino-silver halide photographic emulsion. They can also sensitize other photographic emulsions containing a hydrophilic colloid besides gelatin. Illustrative of these are agar colloidion, cellulose derivatives, polyvinyl alcohol or a natural hydrophilic resin.
  • various silver salts such as mixed silver halides, such a s silver iodobromide, silver chlorobromide, a silver chloroiodobromide, and silver bromide.
  • the sensitizing dye may be added to a photographic emulsion in a conventional manner.
  • the sensitizing dye is dissolved in a suitable solvent, such as methanol and added to an emulsion in the form of a solution.
  • a suitable solvent such as methanol
  • the quantity of the sensitizing dye to be incorporated in the emulsion may be varied within a wide range of 5-200 mg per 1 kg of the emulsion according to the desired effect.
  • sensitizing dyes as well as commonly used additives, such as sensitizers, stabilizers, color tone regulators, hardeners, surfactants, fog inhibitors, plasticizers, development accelerators, color couplers, fluorescent whitening agents and ultraviolet ray absorbers.
  • the photographic emulsion of this invention may be coated in a conventional manner onto a suitable support member, such as glass, a cellulose derivative film, a synthetic resin film, baryta paper, a resin laminated paper or synthetic paper.
  • a suitable support member such as glass, a cellulose derivative film, a synthetic resin film, baryta paper, a resin laminated paper or synthetic paper.
  • a photographic silver halide emulsion was prepared by adding the following sensitizing dye of this invention to a gelatino-silver iodobromide emulsion (AgI AgBr 6 mols 94 mols) or gelatino-silver chlorobromide emulsion (AgBr AgCl 40 mols 60 mols).
  • This emulsion was coated onto a cellulose triacetate film base, dried, exposed to a light source of daylight color of 64 luxes (corresponding to 5,400K) through a Fuji No. 3 Filter (yellow filter) and then developed.
  • the spectral sensitivity is a specific sensitivity when the spectral sensitivity of the sensitizing dye B is 100 when exposed using a Fuji No. 3 Filter (yellow filter).
  • the chemical structural formulas of the sensitizing dyes used for the comparison are as follows:
  • FIG. 1 shows spectrograms of the sensitizing dye 10, a typical example of the new sensitizing dyes according to this invention, (solid line) and the dye B for comparison (broken line) It will be understood from the drawing that the sensitizing dye of this invention forms a J-aggregate. This is a very excellent attribute as disclosed earlier.
  • Z represents an atomic group necessary to complete a benzene ring, which may be substituted or unsubstituted, said substituents being selected from the group consisting of halogen, trifluoromethyl, trifluoromethylsulfonyl, alkylsulfonyl, sulfamoyl, al-
  • R and R each represents a member selected from the group consisting of the same or a different alkyl group and a substituted alkyl group selected from the group consisting of hydroxyalkyl, acetoxyalkyl, carboxyalkyl, cyanoalkyl, carbamoylalkyl, sulfamoylalkyl, aminosulfonylalkyl, allyl and aralkyl;
  • A represents an aryl group, and X represents an acid anion.
  • the photographic silver halide emulsion of claim 1 wherein the sensitizing dye is selected from the group consisting of Dye 1 Calls l CHzCHzCI-Iz UN 5.

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  • Chemical & Material Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Organic Chemistry (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • General Physics & Mathematics (AREA)
  • Silver Salt Photography Or Processing Solution Therefor (AREA)

Abstract

A photographic silver halide emulsion containing at least one sensitizing dye represented by the formula (I) or (II):

wherein Z represents an atomic group necessary to complete a benzene ring, the hydrogen atom of which may be substituted; R and R1 each represent a member selected from the group consisting of the same or different alkyl groups and a substituted alkyl group except a sulfoalkyl group; and A represents an aryl group and X represents an acid anion.

Description

Sato et al.
[ SPECTRALLY SENSITIZED PHOTOGRAPHIC SILVER HALIDE EMULSION [75] Inventors: Akira Sato; Keisuke Shiba; Masanao Hinata, all of Kanagawa, Japan [73] Assignce: Fuji Photo Film Co., Ltd.,
Kanagawa, Japan [22] Filed: June 2, 1971 [21] Appl. No.: 149,276
[30] Foreign Application Priority Data June 2, 1970 Japan 45/47381 [52] U.S. Cl. 96/139, 260/3092 [51] Int. Cl G03c 1/10 [58] Field of Search 96/120, 129, 139
[56] References Cited UNITED STATES PATENTS I 2,298,732 10/1942 Brooker et al .0. 96/139 2,369,509 2/1945 White 96/139 2,553,989 5/1951 Dormael 96/139 3,490,910 l/l970 Rauch et al 96/139 Primary Examiner-J. Travis Brown Attorney-Sughrue, Rothwell, Mion, Zinn and Macpeak 51 Noy, 6 1973 [57] ABSTRACT A photographic silver halide emulsion containing at least one sensitizing dye represented by the formula (l) or (ll):
wherein Z represents an atomic group necessary to complete a benzene ring, the hydrogen atom'of which may be substituted; R and R -each represent a member 6 Claims, 1 Drawing Figure PATENTEDNUV 6 I975 B F F U I 8 E I D /DYE STUFF l0 WAVELENGTH (my) INVENTORS AKIRA SATO KEISUKE SHIBA MASANAO HINATA Q axnq Tiffani? 0m,
2". Murat-l ATTORNEYS SPECTRALLY SENSITIZED PHOTOGRAPHIC SILVER HALIDE EMULSION BACKGROUND OF THE INVENTION 1. Field of the Invention This invention relates to a photographic silver halide emulsion containing a new sensitizing dye and more particularly, it is concerned with a silver halide emulsion having a high spectral sensitivity in the orthoregion.
2. Description of the Prior Art It has been well known in the technique for making a photographic silver halide emulsion that, when a sensitizing dye is added to a silver halide emulsion, it is spectrally sensitized and its light-sensitive wavelength region is enlarged. The spectral sensitivity is often affected by the chemical structure of a sensitizing dye. In particular, a strong sensitivity near the spectral sensitivity maximum due to the J-aggregate of a sensitizing dye adsorbed on surfaces of silver halide grains is liable to be affected because the formation of a J-aggregate depends on the chemical structure of the sensitizing dye; for example, the kind of heterocyclic ring or substituent. Therefore, it is very important in practice to select a sensitizing dye to be used in the case of sensitizing strongly the light-sensitive wavelength region required by a photographic light-sensitive material.
Moreover, when a photographic silver halide material containing a sensitizing dye is subjected to ordinary processings such as developing, fixing, stabilizing and water washing, staining often occurs due to coloring by the sensitizing dye remaining in the emulsion layer.
SUMMARY OF THE INVENTION It is the principal object of this invention to provide a silver halide emulsion which has a high spectral sensitivity in the ortho-region and which does not retain stains after development.
The above mentioned object of the invention can be accomplished by incorporating a new sensitizing dye represented by the following general formula (I) or (II) in a silver halide emulsion.
(I III N In these formulas, Z represents an atomic group necessary for forming a benzene ring, the hydrogen atom of which may be substituted for by conventional substituents for benzimidazolo cyanine dyes. Substituents in this case are those well known for benzimidazolocarbocyanines, such as halogen atoms, e.g. fluorine, chlorine, bromine and iodine, a trifluoromethyl group, a trifluoromethylsulfonyl group, an alkylsulfonyl group, such as methylsulfonyl group, sulfamoyl group, an alkylaminosulfonyl group such as a methylaminosulfonyl or ethylaminosulfonyl group, a dialkylaminosulfonyl group, such as a dimethylaminosulfonyl, diefthylamino'sulfonyl, pipei'idinosulfonylfrnorpholiriosul I fonyl or a pyrrolidinosylfonyl group, a cyano group, a carboxyl group and an alkoxycarbonyl group, such as a methoxycarbonyl or an ethoxycarbonyl group. R and R represent the same or different alkyl groups, such as methyl, ethyl, n-propyl and n-butyl groups, and substituted alkyl groups conventionally used as nitrogen substituents in benzimidazolo cyanine dyes, except a sulfoalkyl group, such as hydroxy alkyl (e.g. B-hydroxyethyl, -y-hydroxypropyl), acetoxyalkyl (e.g. B-acetoxyethyl, 'y-acetoxypropyl) carboxyalkyl (e.g. carboxymethyl, fl-carboxyethyl, y-carboxypropyl, 8-carboxybutyl), cyanoalkyl (e.g. B-cyanoethyl, y-cyanopropyl, 8-cyanobutyl), carbamoylalkyl (e.g. fl-carbamoylethyl, 'y-carbamoyl-propyl, B-carbamoylbutyl, fl-N-ethylcarbamoylethyb, y-N-ethylcarbamoylpropyl, B-N-methylcarbarnoylbutyl), sulfamoylalkyl (e.g. 'y-sulfamoylpropyl, 8-sulfamoylbutyl), aminosulfonylalkyl (e.g. -y-N- ethylaminosulfonylpropyl, 8-N- ethylaminosulfonylbutyl), allyl (e.g. vinylmethyl) and aralkyl (e.g. phenethyl) groups. A represents aryl groups, such as a phenyl group, a methoxyphenyl, a tolyl or a chlorophenyl group. X represents an acid anion, such as a chloride, bromide, iodide, thiocyanate, perchlorate, benzenesulfonate, p-toluene-sulfonate, niethylsulfate or ethylsulfate ion.
DETAILED DESCRIPTION OF THE INVENTION The feature of the sensitizing dyes of this invention, at least with regard to chemical structure resides in the fact that they are limited by general formulas (I) or (II) to a tetramethinehemicyanine or tetramethinehemicyanine base having a benzimidazole nucleus which tends to form a .l-aggregate. In particular, these dyes are effective for raising the spectral sensitivity in the orthoregion. As compared with this, tetramethinehemicyanines or tetramethinehemicyanine bases having benzothiazole, benzoselenazole or benzoxazole nucleus, mentioned in U.S. Pat. Nos. 2,369,509 and 2,369,509 are difficult to form the J-aggregate and have a low spectral sensitivity.
The chemical structural formulas of typical examples 45 ar the .newsensitizing dyes representedby general formulas (I) or (II) are shown below, butare not limited to such:
Dye 1 EE; m
can 7 Dye 4 (31115 CIIgCIlzCHa Dye 5 Cl Br cmcmcmcN (ll Hs Dye 7 Dyo 8 Dye 0 (Z, R, R and X being defined as above), or heating in acetic anhydride to synthesize an acetanilide intermediate followed by hydrolysis. Moreover, the sensitizing dyes represented by general formula (II) are obtainable by treating the sensitizing dye (I) with an aqueous akaline solution and removing the I-IX.
SYNTHESIS EXAMPLE I 3 .8 g of 5 ,6-dichloro-1,3-diethyl-2- methylbenzimidazolium iodide and 2.2 g of B-anilinoacroleinanil are heated at 170C for 6 hours in 50 ml of acetic anhydride on an oil bath. The reaction solution is cooled and mixed with ether in large excess to deposit a product. The ether is removed by decantation and the product is washed with ether. The product is recrystallized from ethanol to obtain 2.2 g of acetanilide intermediate melting at 225-228C. The acetanilide intermediate is dissolved in methanol and then mixed with 4N caustic soda and with water to deposit a crystal which is then filtered, washed with water and recrystallized from methanol to obtain 1.5 g of Dye 3melting at 274C.
SYNTHESIS EXAMPLE 2 l g of Dye 3 is suspended in ml of acetone and mixed with 4N caustic soda to dissolve the crystal. Water is added thereto to deposit a product which is then washed with water and extracted with benzene to obtain 0.3 g of Dye l0 melting at 174C.
Other dyes can be obtained in a similar manner mentioned above.
The sensitizing dyes used in this invention are capable of spectrally sensitizing a silver halide photographic emulsion, and in particular, effectively enlarging the light-sensitive region of a gelatino-silver halide photographic emulsion. They can also sensitize other photographic emulsions containing a hydrophilic colloid besides gelatin. Illustrative of these are agar colloidion, cellulose derivatives, polyvinyl alcohol or a natural hydrophilic resin.
For the emulsion of this invention there are used various silver salts, such as mixed silver halides, such a s silver iodobromide, silver chlorobromide, a silver chloroiodobromide, and silver bromide.
For the preparation of a photographic emulsion sensitized according tothe invention, the sensitizing dye may be added to a photographic emulsion in a conventional manner. Ordinarily the sensitizing dye is dissolved in a suitable solvent, such as methanol and added to an emulsion in the form of a solution. The quantity of the sensitizing dye to be incorporated in the emulsion may be varied within a wide range of 5-200 mg per 1 kg of the emulsion according to the desired effect.
Furthermore, to the photographic emulsion of this invention may be added known sensitizing dyes as well as commonly used additives, such as sensitizers, stabilizers, color tone regulators, hardeners, surfactants, fog inhibitors, plasticizers, development accelerators, color couplers, fluorescent whitening agents and ultraviolet ray absorbers.
The photographic emulsion of this invention may be coated in a conventional manner onto a suitable support member, such as glass, a cellulose derivative film, a synthetic resin film, baryta paper, a resin laminated paper or synthetic paper.
A better understanding of the present invention will be attained from the following examples which are merely illustrative and not limitative of the present invention.
EXAMPLES A photographic silver halide emulsion was prepared by adding the following sensitizing dye of this invention to a gelatino-silver iodobromide emulsion (AgI AgBr 6 mols 94 mols) or gelatino-silver chlorobromide emulsion (AgBr AgCl 40 mols 60 mols).
This emulsion was coated onto a cellulose triacetate film base, dried, exposed to a light source of daylight color of 64 luxes (corresponding to 5,400K) through a Fuji No. 3 Filter (yellow filter) and then developed.
For the'gelatino-silver iodobromide emulsion, there was employed a developer having the-composition shown in Table land for. the gelatino-silver chlorobromide emulsion, there was employed another developer as shown in Table 2. I
TABLE 1 metol 2 g sodium sulfite 100 g hydroquinone 5 g borax 2 g Water to 1000 ml TABLEZ metol 3.1 g sodium sulfite 45 g hydroquinone 12 g anhydrous sodium carbonate 67.5 g
potassium bromide 1.9 g
water to 1000 ml TABLE 3 Amt. of dye Absorption added max. wave- Sensitization Relative 2X10- mol length m wavelength spectral cone. mL/kg. (in maximum sensi- Dye N emulsion methanol) m tivity 1 520 120 2 540 276 3 550 379 4 550 346 5 545 174 6 550 200 7. 540 25b 8... 545 282 9. 545 276 10 550 363 A (compauso 520 30 B (compnrison) 555 100 U (eomparison) 545 110 Amt. of dye added 1X10- Sensitization Relative mol cone. maximum spectral ml./kg. wavelength sensiemulsion m tivity The spectral sensitivity is a specific sensitivity when the spectral sensitivity of the sensitizing dye B is 100 when exposed using a Fuji No. 3 Filter (yellow filter). The chemical structural formulas of the sensitizing dyes used for the comparison are as follows:
AF ikiTiiF -CH=CH-CH=CHN C1 i]: :4-
N+ dunno-3 g I -CH=CH-CH=CHN ii (LE5 I- Hac I -/Se -CH OCH: 32m 1- FIG. 1 shows spectrograms of the sensitizing dye 10, a typical example of the new sensitizing dyes according to this invention, (solid line) and the dye B for comparison (broken line) It will be understood from the drawing that the sensitizing dye of this invention forms a J-aggregate. This is a very excellent attribute as disclosed earlier.
What is claimed is:
l. A photographic silver halide emulsion containing at least one sensitizing dye represented by the formula (I) or (II):
wherein Z represents an atomic group necessary to complete a benzene ring, which may be substituted or unsubstituted, said substituents being selected from the group consisting of halogen, trifluoromethyl, trifluoromethylsulfonyl, alkylsulfonyl, sulfamoyl, al-
kylaminosulfonyl, dialkylaminosulfonyl, cyano, carboxyl, and alkoxycarbonyl; R and R each represents a member selected from the group consisting of the same or a different alkyl group and a substituted alkyl group selected from the group consisting of hydroxyalkyl, acetoxyalkyl, carboxyalkyl, cyanoalkyl, carbamoylalkyl, sulfamoylalkyl, aminosulfonylalkyl, allyl and aralkyl; A represents an aryl group, and X represents an acid anion.
2. The photographic silver halide emulsion of claim 1, wherein the amount of the sensitizing dye present ranges from to 200 mg per 1 kg of the emulsion.
3. The photographic silver halide emulsion of claim 1, wherein the sensitizing dye is selected from the group consisting of Dye 1 Calls l CHzCHzCI-Iz UN 5. The photographic'silver halide emulsion-of claim

Claims (5)

  1. 2. The photographic silver halide emulsion of claim 1, wherein the amount of the sensitizing dye present ranges from 5 to 200 mg per 1 kg of the emulsion.
  2. 3. The photographic silver halide emulsion of claim 1, wherein the sensitizing dye is selected from the group consisting of
  3. 4. A photographic light-sensitive element having at least one layer which comprises the silver halide emulsion of claim 1.
  4. 5. The photographic silver halide emulsion of claim 1, wherein A is phenyl, methoxyphenyl, tolyl, or chlorophenyl.
  5. 6. The photographic silver halide emulsion of claim 1, wherein X is halide, thiocyanate, perchlorate, benzene sulfonate, p-toluene sulfonate, methyl sulfate, or ethyl sulfate.
US00149276A 1970-06-02 1971-06-02 Spectrally sensitized photographic silver halide emulsion Expired - Lifetime US3770440A (en)

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AT2816U3 (en) * 1998-11-19 1999-08-25 Balloonart Veranstaltungs Gmbh ADVERTISING MEDIA WITH AN INFLATABLE COVER AND WITH A COMPRESSED AIR GENERATOR
EP1750173A1 (en) 2005-08-04 2007-02-07 Fuji Photo Film Co., Ltd. Silver halide photosensitive material and packaged body containing the same
WO2025058077A1 (en) 2023-09-15 2025-03-20 富士フイルム株式会社 Compound, composition, functional material, photographic photosensitive silver halide material, and diffusion transfer type photographic photosensitive silver halide material

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2298732A (en) * 1940-12-16 1942-10-13 Eastman Kodak Co Polymethine base
US2369509A (en) * 1940-12-04 1945-02-13 Eastman Kodak Co Polymethine compounds and process for preparing them
US2553989A (en) * 1947-03-14 1951-05-22 Gevaert Photo Prod Nv Hemicyanine dyestuffs
US3490910A (en) * 1968-02-02 1970-01-20 Gaf Corp Silver halide emulsions sensitized with cyanine dyes containing a tetrahydrobenzo-benzoxazole nucleus

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2369509A (en) * 1940-12-04 1945-02-13 Eastman Kodak Co Polymethine compounds and process for preparing them
US2298732A (en) * 1940-12-16 1942-10-13 Eastman Kodak Co Polymethine base
US2553989A (en) * 1947-03-14 1951-05-22 Gevaert Photo Prod Nv Hemicyanine dyestuffs
US3490910A (en) * 1968-02-02 1970-01-20 Gaf Corp Silver halide emulsions sensitized with cyanine dyes containing a tetrahydrobenzo-benzoxazole nucleus

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AT2816U3 (en) * 1998-11-19 1999-08-25 Balloonart Veranstaltungs Gmbh ADVERTISING MEDIA WITH AN INFLATABLE COVER AND WITH A COMPRESSED AIR GENERATOR
EP1750173A1 (en) 2005-08-04 2007-02-07 Fuji Photo Film Co., Ltd. Silver halide photosensitive material and packaged body containing the same
WO2025058077A1 (en) 2023-09-15 2025-03-20 富士フイルム株式会社 Compound, composition, functional material, photographic photosensitive silver halide material, and diffusion transfer type photographic photosensitive silver halide material

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FR2109604A5 (en) 1972-05-26
DE2127347C3 (en) 1974-03-14
JPS4912655B1 (en) 1974-03-26
DE2127347A1 (en) 1971-12-16
DE2127347B2 (en) 1973-08-09

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