JPH02120738A - マゼンタカプラーおよびカルコゲンアゾリウム塩を含んでなる写真記録材料 - Google Patents

マゼンタカプラーおよびカルコゲンアゾリウム塩を含んでなる写真記録材料

Info

Publication number: JPH02120738A
Authority: JP; Japan
Prior art keywords: group; formula; silver halide; chalcogen; salt
Prior art date: 1988-09-14
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Pending

Application number

JP23590089A

Other languages

English (en)

Japanese (ja)

Inventor

George Fu-Liang Wu

ジョージ　フゥーリャン　ウ

Roger Anthony Bryant

ロジャー　アンソニー　ブライアント

Kenneth William Lowe

ケネス　ウィリアム　ロー

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Eastman Kodak Co

Original Assignee

Eastman Kodak Co

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1988-09-14

Filing date

1989-09-13

Publication date

1990-05-08

1989-09-13 Application filed by Eastman Kodak Co filed Critical Eastman Kodak Co

1990-05-08 Publication of JPH02120738A publication Critical patent/JPH02120738A/ja

Status Pending legal-status Critical Current

Links

-1 chalcogen azolium salt Chemical class 0.000 title claims abstract description 59
239000000463 material Substances 0.000 title claims abstract description 27
229910052798 chalcogen Inorganic materials 0.000 title claims abstract description 26
229910052709 silver Inorganic materials 0.000 claims abstract description 42
239000004332 silver Substances 0.000 claims abstract description 42
239000000839 emulsion Substances 0.000 claims abstract description 29
150000003839 salts Chemical class 0.000 claims abstract description 22
125000001424 substituent group Chemical group 0.000 claims abstract description 18
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims abstract description 15
150000001787 chalcogens Chemical group 0.000 claims abstract description 15
125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims abstract description 15
MCSKRVKAXABJLX-UHFFFAOYSA-N pyrazolo[3,4-d]triazole Chemical compound N1=NN=C2N=NC=C21 MCSKRVKAXABJLX-UHFFFAOYSA-N 0.000 claims abstract description 12
238000011161 development Methods 0.000 claims abstract description 9
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 4
125000001183 hydrocarbyl group Chemical group 0.000 claims description 8
125000005647 linker group Chemical group 0.000 claims description 4
239000000126 substance Substances 0.000 claims description 3
KAESVJOAVNADME-UHFFFAOYSA-O hydron;1h-pyrrole Chemical compound [NH2+]1C=CC=C1 KAESVJOAVNADME-UHFFFAOYSA-O 0.000 claims 1
125000000217 alkyl group Chemical group 0.000 abstract description 11
125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract description 4
230000035945 sensitivity Effects 0.000 abstract description 4
150000002500 ions Chemical class 0.000 abstract description 3
239000004215 Carbon black (E152) Substances 0.000 abstract description 2
229910052736 halogen Inorganic materials 0.000 abstract description 2
229930195733 hydrocarbon Natural products 0.000 abstract description 2
150000002430 hydrocarbons Chemical class 0.000 abstract description 2
230000000903 blocking effect Effects 0.000 abstract 2
PUAQLLVFLMYYJJ-UHFFFAOYSA-N 2-aminopropiophenone Chemical compound CC(N)C(=O)C1=CC=CC=C1 PUAQLLVFLMYYJJ-UHFFFAOYSA-N 0.000 abstract 1
150000002367 halogens Chemical class 0.000 abstract 1
125000004432 carbon atom Chemical group C* 0.000 description 15
125000003118 aryl group Chemical group 0.000 description 12
108010010803 Gelatin Proteins 0.000 description 11
150000001875 compounds Chemical class 0.000 description 11
239000008273 gelatin Substances 0.000 description 11
229920000159 gelatin Polymers 0.000 description 11
235000019322 gelatine Nutrition 0.000 description 11
235000011852 gelatine desserts Nutrition 0.000 description 11
229910052717 sulfur Inorganic materials 0.000 description 11
230000009034 developmental inhibition Effects 0.000 description 9
125000003277 amino group Chemical group 0.000 description 8
125000004435 hydrogen atom Chemical group [H]* 0.000 description 7
BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 6
239000010944 silver (metal) Substances 0.000 description 6
125000004434 sulfur atom Chemical group 0.000 description 6
239000002253 acid Substances 0.000 description 5
125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 description 5
238000000576 coating method Methods 0.000 description 5
239000000975 dye Substances 0.000 description 5
125000005843 halogen group Chemical group 0.000 description 5
125000002887 hydroxy group Chemical group [H]O* 0.000 description 5
KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 4
BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 4
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 4
125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 description 4
125000004429 atom Chemical group 0.000 description 4
239000011248 coating agent Substances 0.000 description 4
238000000034 method Methods 0.000 description 4
125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 4
229910052711 selenium Inorganic materials 0.000 description 4
239000011593 sulfur Substances 0.000 description 4
125000001931 aliphatic group Chemical group 0.000 description 3
125000003545 alkoxy group Chemical group 0.000 description 3
125000003368 amide group Chemical group 0.000 description 3
125000005605 benzo group Chemical group 0.000 description 3
125000002837 carbocyclic group Chemical group 0.000 description 3
125000004093 cyano group Chemical group *C#N 0.000 description 3
230000000694 effects Effects 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 3
229910052737 gold Inorganic materials 0.000 description 3
239000010931 gold Substances 0.000 description 3
230000007062 hydrolysis Effects 0.000 description 3
238000006460 hydrolysis reaction Methods 0.000 description 3
125000004430 oxygen atom Chemical group O* 0.000 description 3
238000007142 ring opening reaction Methods 0.000 description 3
239000011669 selenium Substances 0.000 description 3
ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 3
125000000565 sulfonamide group Chemical group 0.000 description 3
229910052714 tellurium Inorganic materials 0.000 description 3
PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical compound [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 description 3
150000007970 thio esters Chemical class 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 2
229910052784 alkaline earth metal Inorganic materials 0.000 description 2
150000001342 alkaline earth metals Chemical class 0.000 description 2
125000004448 alkyl carbonyl group Chemical group 0.000 description 2
125000004414 alkyl thio group Chemical group 0.000 description 2
150000001408 amides Chemical class 0.000 description 2
125000002029 aromatic hydrocarbon group Chemical group 0.000 description 2
125000005129 aryl carbonyl group Chemical group 0.000 description 2
125000003739 carbamimidoyl group Chemical group C(N)(=N)* 0.000 description 2
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 2
150000001721 carbon Chemical group 0.000 description 2
229910052799 carbon Inorganic materials 0.000 description 2
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
229920002678 cellulose Polymers 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 2
KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical group C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 2
150000004820 halides Chemical class 0.000 description 2
230000005764 inhibitory process Effects 0.000 description 2
229910052740 iodine Inorganic materials 0.000 description 2
150000002576 ketones Chemical class 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 2
125000001624 naphthyl group Chemical group 0.000 description 2
229910000510 noble metal Inorganic materials 0.000 description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
238000001556 precipitation Methods 0.000 description 2
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
235000018102 proteins Nutrition 0.000 description 2
108090000623 proteins and genes Proteins 0.000 description 2
102000004169 proteins and genes Human genes 0.000 description 2
230000001235 sensitizing effect Effects 0.000 description 2
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
229910052727 yttrium Inorganic materials 0.000 description 2
QGKMIGUHVLGJBR-UHFFFAOYSA-M (4z)-1-(3-methylbutyl)-4-[[1-(3-methylbutyl)quinolin-1-ium-4-yl]methylidene]quinoline;iodide Chemical compound [I-].C12=CC=CC=C2N(CCC(C)C)C=CC1=CC1=CC=[N+](CCC(C)C)C2=CC=CC=C12 QGKMIGUHVLGJBR-UHFFFAOYSA-M 0.000 description 1
AIGNCQCMONAWOL-UHFFFAOYSA-N 1,3-benzoselenazole Chemical class C1=CC=C2[se]C=NC2=C1 AIGNCQCMONAWOL-UHFFFAOYSA-N 0.000 description 1
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
244000215068 Acacia senegal Species 0.000 description 1
DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical group CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 1
229920001817 Agar Polymers 0.000 description 1
102000009027 Albumins Human genes 0.000 description 1
108010088751 Albumins Proteins 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
241000283690 Bos taurus Species 0.000 description 1
229910000975 Carbon steel Inorganic materials 0.000 description 1
229920002284 Cellulose triacetate Polymers 0.000 description 1
108010035532 Collagen Chemical class 0.000 description 1
102000008186 Collagen Human genes 0.000 description 1
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
229920002307 Dextran Polymers 0.000 description 1
LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 1
MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
229920000084 Gum arabic Polymers 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
244000046146 Pueraria lobata Species 0.000 description 1
235000010575 Pueraria lobata Nutrition 0.000 description 1
206010070834 Sensitisation Diseases 0.000 description 1
229910052770 Uranium Inorganic materials 0.000 description 1
229920002494 Zein Chemical class 0.000 description 1
NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 1
GJEAMHAFPYZYDE-UHFFFAOYSA-N [C].[S] Chemical group [C].[S] GJEAMHAFPYZYDE-UHFFFAOYSA-N 0.000 description 1
239000000205 acacia gum Substances 0.000 description 1
235000010489 acacia gum Nutrition 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
230000002411 adverse Effects 0.000 description 1
239000008272 agar Substances 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
150000001340 alkali metals Chemical class 0.000 description 1
239000012670 alkaline solution Substances 0.000 description 1
125000004453 alkoxycarbonyl group Chemical group 0.000 description 1
125000002877 alkyl aryl group Chemical group 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
239000000908 ammonium hydroxide Substances 0.000 description 1
150000001450 anions Chemical class 0.000 description 1
125000003710 aryl alkyl group Chemical group 0.000 description 1
125000004659 aryl alkyl thio group Chemical group 0.000 description 1
125000005161 aryl oxy carbonyl group Chemical group 0.000 description 1
125000004421 aryl sulphonamide group Chemical group 0.000 description 1
125000005110 aryl thio group Chemical group 0.000 description 1
125000004104 aryloxy group Chemical group 0.000 description 1
239000002585 base Substances 0.000 description 1
IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical group C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 1
229960003237 betaine Drugs 0.000 description 1
229910052797 bismuth Inorganic materials 0.000 description 1
JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 1
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical group C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 1
210000000988 bone and bone Anatomy 0.000 description 1
DNSISZSEWVHGLH-UHFFFAOYSA-N butanamide Chemical group CCCC(N)=O DNSISZSEWVHGLH-UHFFFAOYSA-N 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000010962 carbon steel Substances 0.000 description 1
239000005018 casein Chemical class 0.000 description 1
BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical class NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
235000021240 caseins Nutrition 0.000 description 1
150000001768 cations Chemical class 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000008199 coating composition Substances 0.000 description 1
229920001436 collagen Chemical class 0.000 description 1
239000000084 colloidal system Substances 0.000 description 1
238000004040 coloring Methods 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
239000010946 fine silver Substances 0.000 description 1
150000004676 glycans Chemical class 0.000 description 1
230000026030 halogenation Effects 0.000 description 1
238000005658 halogenation reaction Methods 0.000 description 1
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
230000036571 hydration Effects 0.000 description 1
238000006703 hydration reaction Methods 0.000 description 1
230000003301 hydrolyzing effect Effects 0.000 description 1
238000011065 in-situ storage Methods 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
230000002401 inhibitory effect Effects 0.000 description 1
239000011630 iodine Substances 0.000 description 1
230000001788 irregular Effects 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
239000004816 latex Substances 0.000 description 1
229920000126 latex Polymers 0.000 description 1
DZVCFNFOPIZQKX-LTHRDKTGSA-M merocyanine Chemical compound [Na+].O=C1N(CCCC)C(=O)N(CCCC)C(=O)C1=C\C=C\C=C/1N(CCCS([O-])(=O)=O)C2=CC=CC=C2O\1 DZVCFNFOPIZQKX-LTHRDKTGSA-M 0.000 description 1
238000002156 mixing Methods 0.000 description 1
239000000203 mixture Substances 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
JMANVNJQNLATNU-UHFFFAOYSA-N oxalonitrile Chemical group N#CC#N JMANVNJQNLATNU-UHFFFAOYSA-N 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
239000001814 pectin Chemical class 0.000 description 1
229920001277 pectin Chemical class 0.000 description 1
235000010987 pectin Nutrition 0.000 description 1
230000000737 periodic effect Effects 0.000 description 1
239000000049 pigment Substances 0.000 description 1
239000004848 polyfunctional curative Substances 0.000 description 1
229920001282 polysaccharide Polymers 0.000 description 1
239000005017 polysaccharide Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
238000012545 processing Methods 0.000 description 1
239000000047 product Substances 0.000 description 1
230000008313 sensitization Effects 0.000 description 1
238000000926 separation method Methods 0.000 description 1
VGTPCRGMBIAPIM-UHFFFAOYSA-M sodium thiocyanate Chemical compound [Na+].[S-]C#N VGTPCRGMBIAPIM-UHFFFAOYSA-M 0.000 description 1
AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
235000019345 sodium thiosulphate Nutrition 0.000 description 1
239000002904 solvent Substances 0.000 description 1
230000003595 spectral effect Effects 0.000 description 1
125000005504 styryl group Chemical group 0.000 description 1
125000005156 substituted alkylene group Chemical group 0.000 description 1
125000001174 sulfone group Chemical group 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
150000003512 tertiary amines Chemical group 0.000 description 1
238000012360 testing method Methods 0.000 description 1
229910052716 thallium Inorganic materials 0.000 description 1
BKVIYDNLLOSFOA-UHFFFAOYSA-N thallium Chemical compound [Tl] BKVIYDNLLOSFOA-UHFFFAOYSA-N 0.000 description 1
WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
229910052721 tungsten Inorganic materials 0.000 description 1
239000010937 tungsten Substances 0.000 description 1
238000001429 visible spectrum Methods 0.000 description 1
239000005019 zein Chemical class 0.000 description 1
229940093612 zein Drugs 0.000 description 1

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
- G03C1/005—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
- G03C1/34—Fog-inhibitors; Stabilisers; Agents inhibiting latent image regression
- 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
- 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
- G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
- G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
- G03C7/3003—Materials characterised by the use of combinations of photographic compounds known as such, or by a particular location in the photographic element
- G03C7/3005—Combinations of couplers and photographic additives
- G03C7/3008—Combinations of couplers having the coupling site in rings of cyclic compounds and photographic additives
- G03C7/301—Combinations of couplers having the coupling site in pyrazoloazole rings and photographic additives
- 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
- G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
- G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
- G03C7/392—Additives
- G03C7/39208—Organic compounds
- G03C7/3924—Heterocyclic

Landscapes

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

JP23590089A 1988-09-14 1989-09-13 マゼンタカプラーおよびカルコゲンアゾリウム塩を含んでなる写真記録材料 Pending JPH02120738A (ja)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US24422388A	1988-09-14	1988-09-14
US244223		1988-09-14

Publications (1)

Publication Number	Publication Date
JPH02120738A true JPH02120738A (ja)	1990-05-08

Family

ID=22921883

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP23590089A Pending JPH02120738A (ja)	1988-09-14	1989-09-13	マゼンタカプラーおよびカルコゲンアゾリウム塩を含んでなる写真記録材料

Country Status (3)

Country	Link
EP (1)	EP0359169B1 (fr)
JP (1)	JPH02120738A (fr)
DE (1)	DE68923591T2 (fr)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5164288A (en) *	1990-05-29	1992-11-17	Eastman Kodak Company	Photographic element containing pyrazoloazole coupler and oxidized developer competitor
US5399472A (en) *	1992-04-16	1995-03-21	Eastman Kodak Company	Coupler blends in color photographic materials
US5691124A (en) *	1995-09-15	1997-11-25	Eastman Kodak Company	Color photographic element with improved push processing
EP0763775A1 (fr) *	1995-09-15	1997-03-19	Eastman Kodak Company	Elément photographique couleur contenant des composés benzazolium
DE10031829A1 (de) *	2000-06-30	2002-01-17	Agfa Gevaert Ag	Farbfotografisches Silberhalogenidmaterial
BR0212512A (pt) *	2001-09-14	2004-10-26	Tularik Inc	Composto, composição farmacêutica e métodos para tratar um distúrbio, condição ou doença, elevar os nìveis do colesterol hdl, reduzir os nìveis de triglicerìdeo, tratar diabete, diminuir a resistência à insulina ou diminuir a pressão arterial e modular a ppardelta

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0073636B2 (fr) *	1981-08-25	1992-09-09	EASTMAN KODAK COMPANY (a New Jersey corporation)	Eléments photographiques contenant des coupleurs lestés
US4578348A (en) *	1985-03-18	1986-03-25	Eastman Kodak Company	Hydrolyzed azolium speed enhancing/fog-inhibiting agents for silver halide photography

1989
- 1989-09-11 EP EP19890116757 patent/EP0359169B1/fr not_active Expired - Lifetime
- 1989-09-11 DE DE1989623591 patent/DE68923591T2/de not_active Expired - Fee Related
- 1989-09-13 JP JP23590089A patent/JPH02120738A/ja active Pending

Also Published As

Publication number	Publication date
DE68923591T2 (de)	1996-03-28
EP0359169A3 (en)	1990-12-27
DE68923591D1 (de)	1995-08-31
EP0359169B1 (fr)	1995-07-26
EP0359169A2 (fr)	1990-03-21

Publication	Publication Date	Title
JPH0117565B2 (fr)	1989-03-31
US4604339A (en)	1986-08-05	Method of developing silver halide photographic light-sensitive material
US4555482A (en)	1985-11-26	Silver halide photographic emulsion
EP0476602A1 (fr)	1992-03-25	Matériau photographique couleur à l'halogénure d'argent sensible à la lumière
US5006455A (en)	1991-04-09	Gradation-variable black-and-white paper
JPH02120738A (ja)	1990-05-08	マゼンタカプラーおよびカルコゲンアゾリウム塩を含んでなる写真記録材料
US4040841A (en)	1977-08-09	Silver halide photographic emulsion
EP0304323B1 (fr)	1995-11-08	Matériau photographique couleur pour positif-direct à l'halogénure d'argent sensible à la lumière
EP0195622B1 (fr)	1991-12-18	Agents azolium hydrolysés pour augmenter la sensibilité et inhiber le voile en photographie à l'halogénure d'argent
US3986878A (en)	1976-10-19	Silver halide photographic emulsion
US4097284A (en)	1978-06-27	Method for supersensitizing silver halide photographic emulsions
JPH07199390A (ja)	1995-08-04	写真要素及び写真方法
US3881936A (en)	1975-05-06	Silver halide photographic emulsion containing three sensitizing dyes
US4047964A (en)	1977-09-13	Spectrally sensitized silver halide photographic emulsion
JPS626251A (ja)	1987-01-13	ハロゲン化銀写真感光材料
JPH01253735A (ja)	1989-10-11	ハロゲン化銀写真感光材料
US6503697B2 (en)	2003-01-07	Light-sensitive silver halide photographic material for forming direct-positive images and method for making same
JP3261620B2 (ja)	2002-03-04	ハロゲン化銀写真感光材料及び処理方法
JP2916694B2 (ja)	1999-07-05	ハロゲン化銀写真感光材料及びその製造方法
JPH023037A (ja)	1990-01-08	ハロゲン化銀写真感光材料
EP0608955B2 (fr)	2003-05-14	Emulsions photographiques aux grains tabulaires sensibilisées au vert
US4144070A (en)	1979-03-13	Light-sensitive silver halide photographic materials
JP2847571B2 (ja)	1999-01-20	ハロゲン化銀写真感光材料
JPS6313030A (ja)	1988-01-20	ハロゲン化銀写真感光材料
JP2903450B2 (ja)	1999-06-07	ハロゲン化銀写真感光材料