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US4481268A Expired / Lapsed US ⏱️ 0.0 years remaining

Method of forming a photographic dye image

Assignee: Eastman Kodak Co
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Filing: 1982-09-02
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Granted: 1984-11-06
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Expires: 2002-09-02
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Abstract

Abstract A method of forming a photographic azo or azamethine dye image in an exposed photographic silver halide element, the method of comprising the steps of (a) developing the imagewise exposed material to form an imagewise pattern of oxidized color developing agent, (b) reacting the oxidized color developing agent with a color coupler to produce an image dye, characterized in that at least one of the color developing agent and the color coupler possesses a metal chelating site such that the image dye is capable of forming a bi-, tri- or higher-dentate metallized dye, and (c) contacting the image dye with polyvalent metal ions to form a metallized dye image. Specified color developing agents include heterocyclic substituted hydrazides and specified couplers include benziso-oxazolones and 2H-pyrazolo-[3,4-b]pyridines in addition to more conventional compounds.

Inventors

  • 👤 Joseph Bailey
  • 👤 David Clarke
  • 👤 Michael W. Crawley
  • 👤 Peter D. Marsden
  • 👤 Jasbir Sidhu

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-30 02:52
CPC Classifications
G; G03; G03C; G03C7/00; G03C7/30; G03C7/407; G03C7/413; G03C7/4136; G03C5/00; G03C5/26; G03C5/29; G03C5/30; G03C5/3028; G03C7/3046; G03C7/32; G03C7/3231; G03C7/392; G03C7/39208; Y; Y10; Y10S; Y10S430/00; Y10S430/156

Claims Analysis

Total Claims: 22
Claim 1
Independent Claim 105 words
A method of forming a photographic azo or azomethine dye image in an exposed photographic silver halide element, the method comprising the steps of (a) developing the imagewise exposed material to form an imagewise pattern of oxidized color developing agent, then (b) reacting the oxidized color developing agent with a color coupler to produce an image dye, wherein both the color developing agent and the color coupler possess at least one metal chelating site such that the image dye is capable of forming a tri- or higher-dentate metallized dye, and (c) contacting the image dye with polyvalent metal ions to form a metallized image dye.
Claim 2
Independent Claim 105 words
A method of forming a photographic azo or azomethine dye image in an exposed photographic silver halide element, the method comprising the steps of (a) developing the imagewise exposed material to form an imagewise pattern of oxidized color developing agent, then (b) reacting the oxidized color developing agent with a color coupler to produce an image dye, wherein both the color developing agent and the color coupler possess at least one metal chelating site such that the image dye is capable of forming a tri- or higher-dentate metallized dye, and (c) contacting the image dye with polyvalent metal ions to form a metallized image dye.
Claim 3
Independent Claim 170 words
A method of forming a photographic azo or azomethine dye image in an exposed photographic silver halide element, the method comprising the steps of (a) developing the imagewise exposed material to form an imagewise pattern of oxidized color developing agent, (b) reacting the oxidized color developing agent with a color coupler to produce an image dye, wherein both the color developing agent and the color coupler possess at least one metal chelating site such that the image dye is capable of forming a tri- or higher-dentate metallized dye, and wherein the color developing agent is hydrazide of the formula: ##STR143## wherein R 5 is substituted or unsubstituted alkyl, aryl or heterocyclyl, X 2 is --N═ or ##STR144## X 3 is --CO-- or --SO 2 --, Z 3 represents the atoms necessary to complete an aromatic carbocyclic or heterocyclic nucleus, and G is a metal chelating group, a salt thereof, or a hydrolyzable precursor thereof, and, (c) contacting the image dye with polyvalent metal ions to form a metallized dye image.
Claim 4
Independent Claim 170 words
A method of forming a photographic azo or azomethine dye image in an exposed photographic silver halide element, the method comprising the steps of (a) developing the imagewise exposed material to form an imagewise pattern of oxidized color developing agent, (b) reacting the oxidized color developing agent with a color coupler to produce an image dye, wherein both the color developing agent and the color coupler possess at least one metal chelating site such that the image dye is capable of forming a tri- or higher-dentate metallized dye, and wherein the color developing agent is hydrazide of the formula: ##STR143## wherein R 5 is substituted or unsubstituted alkyl, aryl or heterocyclyl, X 2 is --N═ or ##STR144## X 3 is --CO-- or --SO 2 --, Z 3 represents the atoms necessary to complete an aromatic carbocyclic or heterocyclic nucleus, and G is a metal chelating group, a salt thereof, or a hydrolyzable precursor thereof, and, (c) contacting the image dye with polyvalent metal ions to form a metallized dye image.
Claim 5
Dependent Claim 84 words
A method as in claim 2 wherein the color developing agent has one of the formulas: ##STR145## wherein R 6 is hydrogen, unsubstituted or substituted alkoxy, R 7 is --NO 2 , --SO 2 R 8 or --COR 8 , R 8 is a tertiary amino group, R 9 is hydrogen or --NO 2 , R 10 is alkyl or alkoxy, R 12 is hydrogen, unsubstituted or substituted alkyl, aryl or heterocyclyl, or --CN, and R 2 is unsubstituted or substituted alkyl or aryl.
Claim 6
Dependent Claim 35 words
A method as in claim 1 wherein the color coupler is a phenol, naphthal, pyrazolone, pyrazolotriazole, or open chain ketomethylene dye-forming coupler having a metal chelating group attached to a position adjacent the coupling position.
Claim 7
Independent Claim 212 words
A method of forming a photographic azo or azomethine dye image in an exposed photographic silver halide element, the method comprising the steps of (a) developing the imagewise exposed material to form an imagewise pattern of oxidized color developing agent, (b) reacting the oxidized color developing agent with a color coupler to produce an image dye; wherein both the color developing agent and the color coupler possess at least one metal chelating site such that the image dye is capable of forming a tri- or higher-dentate metallized dye, and wherein the color coupler has the formula: ##STR146## wherein X is --O-- or ═NY in which Y is --COR 1 , --COOR 1 , --SO 2 R 2 , --CONR 2 R 3 or --CSNHR 2 , the residue of X forming a chelating group after coupling, R 1 is alkyl of 1 to 4 carbon atoms, R 2 is an unsubstituted or substituted or substituted alkyl or aryl, R 3 is hydrogen or R 2 , and Z 1 represents the atoms necessary to complete a diffusible or non-diffusible coupler capable of forming a non-diffusible azo or azomethine dye on coupling with oxidized color developing agent; and, (c) contacting the image dye with polyvalent metal ions to form a metallized dye image.
Claim 8
Independent Claim 212 words
A method of forming a photographic azo or azomethine dye image in an exposed photographic silver halide element, the method comprising the steps of (a) developing the imagewise exposed material to form an imagewise pattern of oxidized color developing agent, (b) reacting the oxidized color developing agent with a color coupler to produce an image dye; wherein both the color developing agent and the color coupler possess at least one metal chelating site such that the image dye is capable of forming a tri- or higher-dentate metallized dye, and wherein the color coupler has the formula: ##STR146## wherein X is --O-- or ═NY in which Y is --COR 1 , --COOR 1 , --SO 2 R 2 , --CONR 2 R 3 or --CSNHR 2 , the residue of X forming a chelating group after coupling, R 1 is alkyl of 1 to 4 carbon atoms, R 2 is an unsubstituted or substituted or substituted alkyl or aryl, R 3 is hydrogen or R 2 , and Z 1 represents the atoms necessary to complete a diffusible or non-diffusible coupler capable of forming a non-diffusible azo or azomethine dye on coupling with oxidized color developing agent; and, (c) contacting the image dye with polyvalent metal ions to form a metallized dye image.
Claim 9
Dependent Claim 117 words
A method as in claim 5 wherein the color coupler has the formula: ##STR147## wherein X 1 is --N═ or ##STR148## wherein G is a metal chelating group, a salt thereof or a hydrolyzable precursor thereof, Y is --COR 1 , --COOR 1 , --So 2 R 2 , --CONR 2 R 3 or --CSNHR 2 wherein R 1 is alkyl group of 1 to 4 carbon atoms, R 2 is a substituted or unsubstituted alkyl or aryl, R 3 is hydrogen or R 2 , and Z 2 represents the atoms necessary to complete a diffusible or non-diffusible coupler capable of forming a non-diffusible azo or azomethine dye on coupling with an oxidized color developing agent.
Claim 10
Dependent Claim 20 words
A method as in claim 1 wherein the color coupler is diffusible and is contained in the color developer solution.
Claim 11
Dependent Claim 18 words
A method as in claim 1 wherein the color coupler is non-diffusible and is in the photographic element.
Claim 12
Dependent Claim 25 words
A method as in claim 1 wherein the metal chelating sites are oxygen or nitrogen atoms capable of forming a coordination complex with metal ions.
Claim 13
Dependent Claim 20 words
A method as in claim 1 wherein the metal ions are ions of copper, nickel, chromium, cobalt, manganese or zinc.
Claim 14
Dependent Claim 32 words
A method as in claim 1 wherein the metallization is carried out after dye formation using a metallizing solution containing metal ions at a pH within the range of 5.0 to 12.0.
Claim 15
Dependent Claim 24 words
A method as in claim 1 wherein the dye formation takes place in the presence of an electron transfer agent or a development accelerator.
Claim 16
Dependent Claim 39 words
A method as in claim 1 wherein the photographic silver halide element is a multilayer color element comprising image-forming units sensitive to blue, green and red light, respectively, and capable of forming yellow, magenta and cyan dye images respectively.
Claim 17
Independent Claim 171 words
A method of forming a photographic azo dye image in an exposed photographic silver halide element, the method comprising the steps of (a) developing the imagewise exposed material to form an imagewise pattern of oxidized color developing agent, then (b) reacting the oxidized color developing agent with a color coupler to produce an azo image dye, wherein at least the color developing agent possesses at least one metal chelating site such that the azo image dye is capable of forming a bi-, tri- or higher-dentate metallized dye, and wherein the color developing agent is a hydrazide of the formula: ##STR149## wherein R 5 is substituted or unsubstituted alkyl, aryl or heterocyclyl, X 2 is --N═ or ##STR150## X 3 is --CO-- or --SO 2 --, Z 3 represents the atoms necessary to complete an aromatic carbocyclic or hereocyclic neculeus, and G is a metal chelating group, a salt thereof, or a hydrolyzable precursor thereof, and, (c) contacting the azo image dye with polyvalent metal ions to form a metallized dye image.
Claim 18
Independent Claim 171 words
A method of forming a photographic azo dye image in an exposed photographic silver halide element, the method comprising the steps of (a) developing the imagewise exposed material to form an imagewise pattern of oxidized color developing agent, then (b) reacting the oxidized color developing agent with a color coupler to produce an azo image dye, wherein at least the color developing agent possesses at least one metal chelating site such that the azo image dye is capable of forming a bi-, tri- or higher-dentate metallized dye, and wherein the color developing agent is a hydrazide of the formula: ##STR149## wherein R 5 is substituted or unsubstituted alkyl, aryl or heterocyclyl, X 2 is --N═ or ##STR150## X 3 is --CO-- or --SO 2 --, Z 3 represents the atoms necessary to complete an aromatic carbocyclic or hereocyclic neculeus, and G is a metal chelating group, a salt thereof, or a hydrolyzable precursor thereof, and, (c) contacting the azo image dye with polyvalent metal ions to form a metallized dye image.
Claim 19
Dependent Claim 85 words
A method as in claim 14 in which the color developing agent has one of the formulas: ##STR151## wherein R 6 is hydrogen, unsubstituted or substituted alkoxy, R 7 is --NO 2 , --SO 2 R 8 or --COR 8 , R 8 is a tertiary amino group, R 9 is hydrogen or --NO 2 , R 10 is alkyl or alkoxy, R 12 is hydrogen, unsubstituted or substituted alkyl, aryl or heterocyclyl, or --CN, and R 2 is unsubstituted or substituted alkyl or aryl.
Claim 20
Dependent Claim 126 words
A method as in claim 14 in which the color coupler has the forumla: ##STR152## wherein X is --O-- or ═NY in which Y is --COR 1 , --COOR 1 , --SO 2 R 2 , --CONR 2 R 3 or --CSNHR 2 , the residue of X forming a chelating group after coupling, R 1 is alkyl of 1 to 4 carbon atoms, R 2 is an unsubstituted or substituted alkyl or aryl, R 3 is hydrogen or R 2 , and Z 1 represents the atoms necessary to complete a diffusible or non-diffusible coupler capable of forming a non-diffusible azo dye on coupling with oxidized color developing agent; and, (c) contacting the image dye with polyvalent metal ions to form a metallized dye image.
Claim 21
Dependent Claim 115 words
A method as in claim 14 in which the color coupler has the formula: ##STR153## wherein X 1 is --N═ or ##STR154## wherein G is a metal chelating group, a salt thereof or a hydrolyzable percursor thereof, Y is --COR 1 , --COOR 1 , --SO 2 R 2 , --CONR 2 R 3 or --CSNHR 2 wherein R 1 is alkyl of 1 to 4 carbon atoms, R 2 is a substituted or unsubstituted alkyl or aryl, R 3 is hydrogen or R 2 , and Z 2 represents the atoms necessary to complete a diffusible or non-diffusible coupler capable of forming a non-diffusible azo dye on coupling with an oxidized color developing agent.
Claim 22
Dependent Claim 23 words
A processed phtotographic element containing at least one layer containing a metallized dye formed by color coupling development in accordance with claim 1.

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1987-11-06 1988-05-07 1988-11-06 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1991-11-06 1992-05-07 1992-11-06 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1995-11-06 1996-05-07 1996-11-06 $7700.00 Window Closed / Lapsed

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