Classifications

• • 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
  • G03C1/76—Photosensitive materials characterised by the base or auxiliary layers
  • G03C1/825—Photosensitive materials characterised by the base or auxiliary layers characterised by antireflection means or visible-light filtering means, e.g. antihalation
  • G03C1/83—Organic dyestuffs therefor
  • G03C1/832—Methine or polymethine dyes
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
  • C07D209/56—Ring systems containing three or more rings
  • C07D209/58—[b]- or [c]-condensed
  • C07D209/60—Naphtho [b] pyrroles; Hydrogenated naphtho [b] pyrroles
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
  • C07D241/36—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems
  • C07D241/38—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems with only hydrogen or carbon atoms directly attached to the ring nitrogen atoms
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
  • C07D241/36—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems
  • C07D241/38—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems with only hydrogen or carbon atoms directly attached to the ring nitrogen atoms
  • C07D241/40—Benzopyrazines
  • C07D241/44—Benzopyrazines with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the hetero ring
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
  • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
  • C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
  • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
  • C07D471/06—Peri-condensed systems
• • 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
  • C09B23/02—Methine or polymethine dyes, e.g. cyanine dyes the polymethine chain containing an odd number of >CH- or >C[alkyl]- groups
• • 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
  • C09B23/02—Methine or polymethine dyes, e.g. cyanine dyes the polymethine chain containing an odd number of >CH- or >C[alkyl]- groups
  • C09B23/04—Methine or polymethine dyes, e.g. cyanine dyes the polymethine chain containing an odd number of >CH- or >C[alkyl]- groups one >CH- group, e.g. cyanines, isocyanines, pseudocyanines
• • 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
  • C09B23/02—Methine or polymethine dyes, e.g. cyanine dyes the polymethine chain containing an odd number of >CH- or >C[alkyl]- groups
  • C09B23/06—Methine or polymethine dyes, e.g. cyanine dyes the polymethine chain containing an odd number of >CH- or >C[alkyl]- groups three >CH- groups, e.g. carbocyanines
• • 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
  • C09B23/02—Methine or polymethine dyes, e.g. cyanine dyes the polymethine chain containing an odd number of >CH- or >C[alkyl]- groups
  • C09B23/08—Methine or polymethine dyes, e.g. cyanine dyes the polymethine chain containing an odd number of >CH- or >C[alkyl]- groups more than three >CH- groups, e.g. polycarbocyanines
  • C09B23/083—Methine or polymethine dyes, e.g. cyanine dyes the polymethine chain containing an odd number of >CH- or >C[alkyl]- groups more than three >CH- groups, e.g. polycarbocyanines five >CH- groups
• • 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
  • C09B23/02—Methine or polymethine dyes, e.g. cyanine dyes the polymethine chain containing an odd number of >CH- or >C[alkyl]- groups
  • C09B23/08—Methine or polymethine dyes, e.g. cyanine dyes the polymethine chain containing an odd number of >CH- or >C[alkyl]- groups more than three >CH- groups, e.g. polycarbocyanines
  • C09B23/086—Methine or polymethine dyes, e.g. cyanine dyes the polymethine chain containing an odd number of >CH- or >C[alkyl]- groups more than three >CH- groups, e.g. polycarbocyanines more than five >CH- groups
• • 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
  • C09B23/10—The polymethine chain containing an even number of >CH- groups
• • 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
  • C09B23/10—The polymethine chain containing an even number of >CH- groups
  • C09B23/105—The polymethine chain containing an even number of >CH- groups two >CH- groups
• • 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
  • C09B23/10—The polymethine chain containing an even number of >CH- groups
  • C09B23/107—The polymethine chain containing an even number of >CH- groups four >CH- groups
• • 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
  • C09B23/14—Styryl dyes
  • C09B23/145—Styryl dyes the ethylene chain carrying an heterocyclic residue, e.g. heterocycle-CH=CH-C6H5
• • 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
• • 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
  • G03C1/14—Methine and polymethine dyes with an odd number of CH groups
  • G03C1/18—Methine and polymethine dyes with an odd number of CH groups with three CH groups
• • 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
  • G03C1/485—Direct positive emulsions
  • G03C1/48515—Direct positive emulsions prefogged
  • G03C1/48523—Direct positive emulsions prefogged characterised by the desensitiser
  • G03C1/4853—Direct positive emulsions prefogged characterised by the desensitiser polymethine dyes
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10S430/00—Radiation imagery chemistry: process, composition, or product thereof
  • Y10S430/001—Electric or magnetic imagery, e.g., xerography, electrography, magnetography, etc. Process, composition, or product
  • Y10S430/102—Electrically charging radiation-conductive surface

Definitions

• This invention relates to photographic materials, and more particularly to improved direct positive photographic materials.
• Direct positive materials have been prepared by adding to a silver halide emulsion reducing agent, a compound of a metal more electropositive than silver, and an electron acceptor.
• a silver halide emulsion reducing agent a compound of a metal more electropositive than silver
• an electron acceptor an electron acceptor.
• One of the principal advantages of such direct positive emulsions is that the high-light areas of the images obtained with these materials are substantially free from fog.
• known materials of this type have required blue light exposure. In other words, they have been substantially insensitive to longer wave length radiation, such as green and red radiation.
• Another object of our invention is to provide improved direct positive photographic materials.
• Another object of our invention is to provide novel, spectrally sensitized photographic emulsions fogged with reducing agent and a compound of a metal more electropositive than silver.
• a further object of our invention is to provide novel improvements in such emulsions which feature use of a compound which functions both as an electron acceptor and as a spectral sensitizer.
• direct positive photographic silver halide emulsions which are fogged with a reducing agent and a compound of a metal more electropositive than silver, are improved by adding to the emulsion a compound which, (1) functions as an electron acceptor and (2) spectrally sensitizes the emulsion to radiation having wave length longer than about 480 me.
• the preferred compounds of this invention are those organic compounds which, (1) have an anodic polarographic potential and a cathodic polarographic potential which, when added together give a positive sum, and (2) which spectrally sensitize photographic emulsions to radiation having a wave length longer than 480 m
• these compounds provide spectral sensitivity such that the ratio of minus blue relative speed to blue relative speed is greater than 7 and preferably greater than 10.
• Organic compounds useful herein may be termed spectral sensitizing electron acceptors.
• An especially useful class of spectral sensitizing electron acceptors are trimethine cyanine dyes containing a 2-aromatically substituted indole nucleus attached by the 3-carbon atom thereice of to the methine chain. Dyes of this type are described by Coenen et al. in U.S. Patent 2,930,694, issued Mar. 29, 1960, and British Patent 970,601 (and corresponding Belgian Patent 630,911).
• a preferred class of spectrally sensitizing electron acceptors are dyes containing an imidazo[4,5-b]quinoxalinium salt moiety, such as the dyes disclosed in Brooker and Van Lare Belgian Patent 660,253, issued Mar. 15, 1965.
• the imidazo [4,5-b]quinoxaline nucleus is attached, through the 2- carbon atom thereof, to the methine chain.
• Another class of highly useful dyes are those having the following formula.
• R R and R each represents an alkyl group, such as methyl, ethyl, propyl or butyl, or an aryl group such as phenyl;
• X represents an anion, such as chloride, iodide, bromide, p-toluenesulfonate, methyl sulfate, perchlorate, thiocyanate, sulfonate, bromide, etc.
• Q represents the atoms necessary to complete a nucleus to form a trimethine cyanine dye, such as a 6-nitrobenzothiazole nucleus, an imidazo [4,5-b]quinoxaline nucleus or a pyrrolo[2,3-b]pyridene nucleus, e.g.,
• R5 /R ⁇ N N wherein R R and R each represents a value selected from those given for R R and R
• a typical specific useful dye of this class is 1,1',3,3,3,3'-hexamethylpyrrolo [2,3-b1pyridocarbocyanine salt (e.g., perchlorate).
• trimethine cyanine dyes having Z-aromatically substituted indole nuclei have the following general formula:
• A represents an aryl substituent, such as phenyl
• R and R each represents an ancohol radical, e.g., an alkyl substituent (including substituted alkyl) and preferably containing from about 1 to 8 carbon atoms, such as methyl, ethyl, propyl, butyl or octyl, or sulfoalkyl such as sulfopropyl or sulfobutyl, sulfatoalkyl such as sulfatopropyl or sulfatobutyl, or carboxyalkyl such as carboxyethyl or carboxybutyl
• Y represents a substituent selected from the group consisting of a hydrogen atom, an aryl group, such as phenyl, and alkyl (e.g., methyl, ethyl, propyl or butyl) or alkoxy (e.g., methoxy,
• Symmetrical imidazo[4,5-b]qninoxaline trimethine cyanine dyes wherein each nucleus is attached through the 2-carbon atom thereof to the methine chain, are useful 3 in the practice of this invention.
• Typical of such dyes are those having the following general formula:
• R R R and R each represents a substituent such as alkyl, e.g., methyl, ethyl, propyl or butyl, and X has the meaning given above.
• alkyl e.g., methyl, ethyl, propyl or butyl
• X has the meaning given above.
• the dyes described above are to be regarded as representative of the spectrally sensitizing electron acceptors useful herein. Any dye which has the polarographic halfwave potential and which imparts the spectral sensitivity specified herein can be used in this invention.
• Examples 1-5 demonstrate the superior results obtained when spectral sensitizing electron acceptors in accordance with the invention are incorporated in direct positive emulsions fogged with reducing agent and a compound of a metal more electropositive than silver.
• Examples A, B, C and D are comparative examples and illustrate the poor results obtained with dyes suggested by the prior art for these emulsions. These poor results are characterized by slow speed and ineffective spectral sensitization.
• a gelatin silver bromiodide emulsion (2.5 mole percent of the halide being iodide) and having an average grain size of about 0.2 micron is prepared by adding an aqueous solution of potassium bromide and potassium iodide, and an aqueous solution of silver nitrate, simultaneously to a rapidly agitated aqueous gelatin solution at a temperature of 70 C., over a period of about 35 minutes.
• the emulsion is chill-set, shredded and washed by leaching with cold water in the conventional manner.
• the emulsion is reduction-gold fogged by first adding 0.75 mg. of thiourea dioxide per mole of silver and heating for 60 minutes at 65 C. and then adding 7.5 mg.
• the fogged emulsion is divided into several portions and 0.87 millimole per mole of silver halide of each of the dyes listed in the following table is added to -a portion of the emulsion.
• Each portion is coated on a cellulose acetate support at a laydown of 100 mg. of silver and.400 mg. of gelatin per square foot.
• Each coating is exposed to a tungsten source on an Eastman Ib sensitometer.
• the emulsions are given a blue exposure through Wratten 35 and 38A filters and a minus blue exposure through a Wratten 16 filter.
• the exposed coatings are processed for 6 minutes at room temperature in Kodak D-19 developer, fixed, washed and dried with the following results.
• the most useful concentration of spectral sensitizing electron acceptors in the fogged emulsions of the invention is from 50 to 2,000, and preferably 400 to 800 mg. per mole of silver. However, these concentrations are given solely by way of instruction; best concentrations vary widely depending on the particular compound used.
• the electron acceptors employed herein, as noted above spectrally sensitize the emulsions of the invention to radiation having a wave length longer than about 480 me. That is, the spectral sensitivity impart-ed to emulsions is at least equal to and usually greater than the sensitivity of the emulsion to blue radiation (i.e., 400 to about 480 mu).
• silver halide emulsion may be used in this invention.
• silver halide emulsions such as silver chloride or silver bromide, and mixed silver halides such as silver bromoiodide, silver chlorobromide or silver chlorobromoiodide are operable.
• Particularly useful are silver bromo halide emulsions comprising more than 50 mole percent bromide. These emulsions are fogged with the combination of a reducing agent and a compound of a metal more electropositive than silver.
• Typical useful reducing agents include stannous salts, e.g., stannous chloride, hydrazine, sulfur compounds, such as thiourea dioxide, phosphonium salts such as tetra (hydroxy methyl) phosphonium chloride, and the like.
• Compounds of metals such as gold, rhodium, platinum, palladium and iridium are used preferably in the form of soluble salts such as auric chloride and (NHQ PdCI
• the spectrally sensitizing electron acceptors which give particularly good results in the practice of this invention can be characterized in terms of their polarographic halfwave potentials, i.e., their oxidation reduction potentials determined by polarography.
• Cathodic measurements can be made with a l l0 molar solution of the electron acceptor in a solvent, for example, methanol which is 0.05 molar in lithium chloride using a dropping mercury elec trode with the polarographic halfwave potential for the most positive cathodic wave being designated E
• Anodic measurements can be made with 1X10- molar aqueous solvent solution, for example methanolic solutions of the electron acceptor which are 0.05 molar in sodium acetate and 0.005 molar in acetic acid using a carbon paste of pyrolytic graphite electrode, with the voltametric half peak potential for the most negative anodic response being designated E,,.
• the reference electrode can be an aqueous silversilver chloride (saturated potassium chloride) electrode at 20 C.
• Electrochemical measurements of this type are known in the art and are described in New Instrumental Methods in Electrochemistry, by Delahay, Interscience Publishers, New York, N.Y., 1954; Polarography, by Kolthoff and Lingane, 2nd edition, Interscience Publishers, New York, -N.Y., 1952; Analytical Chemistry, 36, 2426 (1964) by Elving; and Analytical Chemistry 30, 1576 (1958) by Adams.
• Compounds Which can be employed as spectrally sensitizing electron acceptors in the practice of this invention include organic compounds having an anodic polarographic halfwave potential (E,,) and a cathodic polarographic potential (E which when added together give a positive sum.
• novel emulsions of this invention may be coated on any suitable photographic supports, such as glass, film base such as cellulose acetate, cellulose acetate butyrate, polyester such as polyethylene terephthalate, paper, baryta coated paper, polyolefin coated paper, e.g., polyethylene or polypropylene coated paper, which may be electron bombarded to promote emulsion adhesion.
• film base such as cellulose acetate, cellulose acetate butyrate
• polyester such as polyethylene terephthalate
• paper baryta coated paper
• polyolefin coated paper e.g., polyethylene or polypropylene coated paper, which may be electron bombarded to promote emulsion adhesion.
• the emulsions of this invention may be dispersed in any photographic hydrophilic colloid, such as any of those referred to in US. Patent 3,039,873, column 13, and may contain any of the hardeners or plasticizers referred to in columns 12 and 13 of that patent.
• fogged refers to emulsions containing silver halide grains which produce a density of at least 0.5 when developed, without exposure, for minutes at 68 F. in developer D-K50 when the emulsion is coated at a silver coverage of 50 mg. to 500 mg. per square foot.
• a direct positive photographic silver halide emulsion the halide of which comprises more than 50 mole percent bromide, which emulsion is fogged with the combination of reducing agent and a compound of a metal selected from the group consisting of gold, rhodium, platinum, palladium and iridium: the improvement which comprises adding to said emulsion an organic compound which (1) is an electron acceptor having an anodic polarographic potential and a cathodic polarographic potential which, when added together, give a positive sum and (2) spectrally sensitizes the emulsion to radiation having a wavelength longer than about 480 me so that the ratio of relative minus blue speed to relative blue speed of the emulsion is greater than 7.
• a direct positive photographic silver halide emulsion the halide of which comprises more than 50 mole percent bromide, which emulsion is fogged with the combination of reducing agent and a gold compound: the improvement which comprises adding to said emulsion an organic compound which (1) is an electron acceptor having an anodic polarographic potential and a cathodic polarographic potential which, when added together, give a positive sum and (2) spectrally sensitizes the emulsion to radiation having a wavelength longer than about 480 m so that the ratio of relative minus blue speed to relative blue speed of the emulsion is greater than 3.
• a direct positive photographic silver halide emulsion the halide of which comprises more than 50 mole percent bromide, which emulsion is fogged with the combination of reducing agent and a compound of a metal selected from the group consisting of gold, rhodium, platinum, palladium and iridium: the improvement which comprises adding to said emulsion a dye which (1) is an electron acceptor having an anodic polarographic potential and a cathodic polarographic potential which,
• the dye when added together, give a positive sum and (2) spectrally sensitizes the emulsion to radiation having a wavelength longer than about 480 m so that the ratio of relative minus blue speed to relative blue speed of the emulsion is greater than 7, said dye being a cyanine dye containing an irnidazo[4,5-b]quinoxaline nucleus attached, through the 2-carbon atom thereof, to the methine chain.
• a direct positive photographic silver halide emulsion the halide of which comprises more than 50 mole percent bromide, which emulsion is fogged with the combination of reducing agent and a gold compound: the improvement which comprises adding to said emulsion a dye which l) is an electron acceptor having an anodic polarographic potential and a cathodic polarographic potential which, when added together, give a positive sum and (2) spectrally sensitizes the emulsion to radiation having a wavelength longer than about 480 III/1.
• said dye being a cyanine dye containing an imidazo [4,5-b] quinoxaline nucleus attached, through the 2-carbon atom thereof, to the methine chain.
• a direct positive photographic silver halide emulsion the halide of which comprises more than 50 mole percent bromide, which emulsion is fogged with the combination of reducing agent and a gold compound: the improvement which comprises adding to said emulsion a dye which 1) is an electron acceptor having an anodic polarographic potential and a cathodic polarographic potential which, when added together, give a positive sum and (2) spectrally sensitizes the emulsion to radiation having a wavelength longer than about 480 m so that the ratio of relative minus blue speed to relative blue speed of the emulsion is greater than 10, said dye having the following wherein R7, R R and R each represents an alkyl radical; and, X represents an anion.
• a direct positive photographic silver halide emulsion the halide of which comprises more than 50 mole percent bromide, which emulsion is fogged with the combination of reducing agent and a gold compound: the improvement which comprises adding to said emulsion a dye which (1) is an electron acceptor having an anodic polarographic potential and a cathodic polarographic potential which, when added together, give a positive sum and (2) spectrally sensitizes the emulsion to radiation having a wavelength longer than about 480 m so that the ratio of relative minus blue speed to relative blue speed of the emulsion is greater than 10, said dye being a l,1',4,4-tetraethylimidazo[4, S b] quinoxalinocarbocyanine salt.
• a direct positive photographic silver halide emulsion the halide of which comprises more than 50 mole percent bromide, which emulsion is fogged with the combination of reducing agent and a gold compound: the improvement which comprises adding to said emulsion a dye which (1) is an electron acceptor having an anodic olarographic potential and a cathodic polarographic potential which, when added together, give a positive sum and (2) spectrally sensitizes the emulsion to radiation having a wavelength longer than about 480 m so that the ratio of relative minus blue speed to relative blue speed of the emulsion is greater than 10, said dye being a 1,1',3,3,3',3-hexamethylpyrrolo[2,3-b]pyridocarbocyanine salt.
• a direct positive photographic silver halide emulsion the halide of which comprises more than 50 mole percent bromide, which emulsion is fogged with the combination of reducing agent and a gold compound: the improvement which comprises adding to said emulsion a dye which (1) is an electron acceptor having an anodic polarographic potential and a cathodic polarographic potential which, when added together, give a positive sum and (2) spectrally sensitizes the emulsion to radiation having a wavelength longer than about 480 m so that the ratio of relative minus blue speed to relative blue speed of the emulsion is greater than 10, said dye having the following formula:
• R R and R each represents a substituent selected from the group consisting of alkyl and aryl; X represents an anion; and, Q represents the atoms necessary to complete a nucleus to form a trimethine cyanine dye.
• a direct positive photographic silver halide emulsion the halide of which comprises more than 50 mole percent bromide, which emulsion is fogged with the combination of reducing agent and a compound of a metal selected from the group consisting of gold, rhodium, platinum, palladium and iridium: the improvement which comprises adding to said emulsion a dye which l) is an electron acceptor having an anodic polarograp-hic potential and a cathodic polarographic potential which, when added together, give a positive sum and (2) spectrally sensitizes the emulsion to radiation having a wavelength longer than about 480 mg so that the ratio of relative minus blue speed to relative blue speed of the emulsion is greater than 7, said dye being selected from the group consisting of the dimethine and trimethine cyanine dyes containing a 2- aromatically substituted indole nucleus attached, by the 3-carbon atom thereof, to the methine chain.
• the halide of which comprises more than 50 mole percent bromide, which emulsion is fogged with the combination of reducing agent and a gold compound the improvernent which comprises adding to said emulsion a dye which (1) is an electron acceptor having an anodic polarographic potential and a cathodic polarographi-c potential which, when added together, give a positive sum and (2) spectrally sensitizes the emulsion to radiation having a wavelength longer than about 480 m so that the ratio of relative minus blue speed to relative blue speed of the emulsion is greater than 10, said dye being selected from the group consisting of the dimethine and trimethine cyanine dyes containing a Z-aromatically substituted indole nucleus attached, by the B-carbon atom thereof, to the methine chain.
• a direct positive photographic silver halide emulsion the halide of which comprises more than 50 mole percent bromide, Which emulsion is fogged with the combination of reducing agent and a gold compound: the improvement which comprises adding to said emulsion a dye which (1 is an electron acceptor having an anodic polarographic potential and a cathodic polarographic potential which, when added together, give a positive sum and 2) spectrally sensitizes the emulsion to radiation having a wavelength longer than about 480 m so that the ratio of relative minus blue speed to relative blue speed of the emulsion is greater than 10, said dye having the following formula:

Landscapes

• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Physics & Mathematics (AREA)
• Engineering & Computer Science (AREA)
• Materials Engineering (AREA)
• General Physics & Mathematics (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Spectroscopy & Molecular Physics (AREA)
• Silver Salt Photography Or Processing Solution Therefor (AREA)
• Plural Heterocyclic Compounds (AREA)
• Indole Compounds (AREA)
• Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Applications Claiming Priority (7)

Publications (1)

Family

ID=27569830

Family Applications (2)

Family Applications After (1)

Country Status (11)

Cited By (6)

Families Citing this family (6)

Citations (2)

Family Cites Families (2)

• 1967
  • 1967-01-17 US US609761A patent/US3501310A/en not_active Expired - Lifetime
  • 1967-01-17 US US609740A patent/US3492123A/en not_active Expired - Lifetime
  • 1967-03-09 SE SE3251/67A patent/SE345170B/xx unknown
  • 1967-03-09 FR FR98017A patent/FR1513840A/fr not_active Expired
  • 1967-03-10 BE BE695360D patent/BE695360A/xx not_active IP Right Cessation
  • 1967-03-10 GB GB01294/67A patent/GB1186714A/en not_active Expired
  • 1967-03-10 BR BR187702/67A patent/BR6787702D0/pt unknown
  • 1967-03-10 BE BE695364D patent/BE695364A/xx not_active IP Right Cessation
  • 1967-03-10 BE BE695367D patent/BE695367A/xx not_active IP Right Cessation
  • 1967-03-10 ES ES337856A patent/ES337856A1/es not_active Expired
  • 1967-03-10 CH CH351667A patent/CH474086A/fr not_active IP Right Cessation
  • 1967-03-10 DE DE19671547793 patent/DE1547793A1/de active Pending
  • 1967-03-10 NO NO00167226A patent/NO129424B/no unknown
  • 1967-05-05 GB GB20919/67A patent/GB1190031A/en not_active Expired
  • 1967-05-05 GB GB20914/67A patent/GB1186720A/en not_active Expired
  • 1967-07-06 DE DE1967E0034323 patent/DE1597528B2/de active Granted
  • 1967-08-09 JP JP42050902A patent/JPS521300B1/ja active Pending

Patent Citations (2)

Also Published As

Similar Documents