CH630732A5 - Photographisches lichtempfindliches silberhalogenidmaterial mit mindestens einer farbstoffhaltigen rueckschicht. - Google Patents

Photographisches lichtempfindliches silberhalogenidmaterial mit mindestens einer farbstoffhaltigen rueckschicht. Download PDF

Info

Publication number: CH630732A5
Authority: CH; Switzerland
Prior art keywords: layers; silver halide; photographic; layer; groups
Prior art date: 1977-12-23

Application number

CH1595677A

Other languages

German (de)

English (en)

Inventor

Paul Tschopp

Original Assignee

Ciba Geigy Ag

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.)

1977-12-23

Filing date

1977-12-23

Publication date

1982-06-30

1977-12-23 Application filed by Ciba Geigy Ag filed Critical Ciba Geigy Ag

1977-12-23 Priority to CH1595677A priority Critical patent/CH630732A5/de

1978-12-19 Priority to FR7835626A priority patent/FR2412871A1/fr

1978-12-20 Priority to GB7849224A priority patent/GB2011636B/en

1978-12-21 Priority to DE19782855428 priority patent/DE2855428A1/de

1978-12-21 Priority to IT52410/78A priority patent/IT1109345B/it

1978-12-22 Priority to BE192490A priority patent/BE872993A/fr

1978-12-23 Priority to JP15818478A priority patent/JPS5497016A/ja

1982-06-30 Publication of CH630732A5 publication Critical patent/CH630732A5/de

Links

239000000463 material Substances 0.000 title claims description 37
229910052709 silver Inorganic materials 0.000 title claims description 28
239000004332 silver Substances 0.000 title claims description 28
BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 title claims description 3
-1 silver halide Chemical class 0.000 claims description 64
239000000975 dye Substances 0.000 claims description 44
125000004432 carbon atom Chemical group C* 0.000 claims description 35
108010010803 Gelatin Proteins 0.000 claims description 25
229920000159 gelatin Polymers 0.000 claims description 25
235000019322 gelatine Nutrition 0.000 claims description 25
235000011852 gelatine desserts Nutrition 0.000 claims description 25
239000011230 binding agent Substances 0.000 claims description 21
239000008273 gelatin Substances 0.000 claims description 21
125000000217 alkyl group Chemical group 0.000 claims description 20
229920000642 polymer Polymers 0.000 claims description 19
239000003795 chemical substances by application Substances 0.000 claims description 16
229920000126 latex Polymers 0.000 claims description 14
238000000034 method Methods 0.000 claims description 13
239000000839 emulsion Substances 0.000 claims description 12
230000002378 acidificating effect Effects 0.000 claims description 11
238000005266 casting Methods 0.000 claims description 11
239000004816 latex Substances 0.000 claims description 11
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
229920003176 water-insoluble polymer Polymers 0.000 claims description 11
125000003118 aryl group Chemical group 0.000 claims description 10
239000000203 mixture Substances 0.000 claims description 10
125000003545 alkoxy group Chemical group 0.000 claims description 7
150000001875 compounds Chemical class 0.000 claims description 7
238000004519 manufacturing process Methods 0.000 claims description 7
239000000178 monomer Substances 0.000 claims description 7
238000005554 pickling Methods 0.000 claims description 7
125000001302 tertiary amino group Chemical group 0.000 claims description 7
125000004442 acylamino group Chemical group 0.000 claims description 6
125000004093 cyano group Chemical group *C#N 0.000 claims description 6
125000004663 dialkyl amino group Chemical group 0.000 claims description 6
229910052757 nitrogen Inorganic materials 0.000 claims description 6
AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 claims description 5
125000004433 nitrogen atom Chemical group N* 0.000 claims description 5
125000002947 alkylene group Chemical group 0.000 claims description 4
229910052799 carbon Inorganic materials 0.000 claims description 4
125000003700 epoxy group Chemical group 0.000 claims description 4
229910052736 halogen Inorganic materials 0.000 claims description 4
150000002367 halogens Chemical class 0.000 claims description 4
239000001257 hydrogen Substances 0.000 claims description 4
229910052739 hydrogen Inorganic materials 0.000 claims description 4
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
230000035945 sensitivity Effects 0.000 claims description 4
125000005504 styryl group Chemical group 0.000 claims description 4
125000006296 sulfonyl amino group Chemical group [H]N(*)S(*)(=O)=O 0.000 claims description 4
DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 claims description 3
125000004104 aryloxy group Chemical group 0.000 claims description 3
125000004069 aziridinyl group Chemical group 0.000 claims description 3
239000012876 carrier material Substances 0.000 claims description 3
125000000753 cycloalkyl group Chemical group 0.000 claims description 3
238000009792 diffusion process Methods 0.000 claims description 3
125000005842 heteroatom Chemical group 0.000 claims description 3
UXGLSABDGQOSET-UHFFFAOYSA-N n-carbamoylprop-2-enamide Chemical compound NC(=O)NC(=O)C=C UXGLSABDGQOSET-UHFFFAOYSA-N 0.000 claims description 3
239000002245 particle Substances 0.000 claims description 3
AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 claims description 3
229920002134 Carboxymethyl cellulose Polymers 0.000 claims description 2
239000004354 Hydroxyethyl cellulose Substances 0.000 claims description 2
229920000663 Hydroxyethyl cellulose Polymers 0.000 claims description 2
125000000129 anionic group Chemical group 0.000 claims description 2
230000015572 biosynthetic process Effects 0.000 claims description 2
239000004202 carbamide Substances 0.000 claims description 2
239000001768 carboxy methyl cellulose Substances 0.000 claims description 2
235000010948 carboxy methyl cellulose Nutrition 0.000 claims description 2
239000008112 carboxymethyl-cellulose Substances 0.000 claims description 2
239000003431 cross linking reagent Substances 0.000 claims description 2
125000001475 halogen functional group Chemical group 0.000 claims description 2
235000019447 hydroxyethyl cellulose Nutrition 0.000 claims description 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 2
239000000834 fixative Substances 0.000 claims 2
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 claims 1
125000004429 atom Chemical group 0.000 claims 1
150000001721 carbon Chemical group 0.000 claims 1
125000002091 cationic group Chemical group 0.000 claims 1
125000004122 cyclic group Chemical group 0.000 claims 1
125000002795 guanidino group Chemical group C(N)(=N)N* 0.000 claims 1
125000004356 hydroxy functional group Chemical group O* 0.000 claims 1
230000003993 interaction Effects 0.000 claims 1
230000005923 long-lasting effect Effects 0.000 claims 1
229940098779 methanesulfonic acid Drugs 0.000 claims 1
125000005496 phosphonium group Chemical group 0.000 claims 1
230000002265 prevention Effects 0.000 claims 1
125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 claims 1
238000003860 storage Methods 0.000 claims 1
239000000126 substance Substances 0.000 claims 1
229920003169 water-soluble polymer Polymers 0.000 claims 1
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 14
239000004848 polyfunctional curative Substances 0.000 description 13
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 8
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 7
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 6
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 6
239000002253 acid Substances 0.000 description 6
229920001577 copolymer Polymers 0.000 description 6
230000007423 decrease Effects 0.000 description 6
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 5
125000003172 aldehyde group Chemical group 0.000 description 5
230000000694 effects Effects 0.000 description 5
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 5
150000007513 acids Chemical class 0.000 description 4
125000002252 acyl group Chemical group 0.000 description 4
150000002148 esters Chemical class 0.000 description 4
125000000623 heterocyclic group Chemical group 0.000 description 4
125000001424 substituent group Chemical group 0.000 description 4
229920002554 vinyl polymer Polymers 0.000 description 4
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 3
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 3
RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 3
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 3
125000005907 alkyl ester group Chemical group 0.000 description 3
150000001408 amides Chemical class 0.000 description 3
230000015556 catabolic process Effects 0.000 description 3
239000000084 colloidal system Substances 0.000 description 3
230000000052 comparative effect Effects 0.000 description 3
238000006731 degradation reaction Methods 0.000 description 3
239000011521 glass Substances 0.000 description 3
125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
125000002768 hydroxyalkyl group Chemical group 0.000 description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
150000003440 styrenes Chemical class 0.000 description 3
229940117958 vinyl acetate Drugs 0.000 description 3
229920001567 vinyl ester resin Polymers 0.000 description 3
MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 2
GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 2
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
VFMNIJOKAXPZLE-UHFFFAOYSA-N 4-(5-methyl-3-oxo-1h-pyrazol-2-yl)benzenesulfonic acid Chemical compound N1C(C)=CC(=O)N1C1=CC=C(S(O)(=O)=O)C=C1 VFMNIJOKAXPZLE-UHFFFAOYSA-N 0.000 description 2
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
239000004793 Polystyrene Substances 0.000 description 2
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
229910006074 SO2NH2 Inorganic materials 0.000 description 2
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
238000010521 absorption reaction Methods 0.000 description 2
150000001241 acetals Chemical class 0.000 description 2
239000000654 additive Substances 0.000 description 2
230000002411 adverse Effects 0.000 description 2
229910052784 alkaline earth metal Inorganic materials 0.000 description 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 2
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
229920002301 cellulose acetate Polymers 0.000 description 2
238000004042 decolorization Methods 0.000 description 2
239000008367 deionised water Substances 0.000 description 2
229910021641 deionized water Inorganic materials 0.000 description 2
238000007720 emulsion polymerization reaction Methods 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
HRYUUBFCDGPNLW-UHFFFAOYSA-N n-carbamoyl-3-chloropropanamide Chemical compound NC(=O)NC(=O)CCCl HRYUUBFCDGPNLW-UHFFFAOYSA-N 0.000 description 2
229910052760 oxygen Inorganic materials 0.000 description 2
239000001301 oxygen Substances 0.000 description 2
239000011591 potassium Substances 0.000 description 2
229910052700 potassium Inorganic materials 0.000 description 2
IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 2
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
239000001397 quillaja saponaria molina bark Substances 0.000 description 2
229930182490 saponin Natural products 0.000 description 2
150000007949 saponins Chemical class 0.000 description 2
GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
239000007787 solid Substances 0.000 description 2
229910052717 sulfur Inorganic materials 0.000 description 2
239000011593 sulfur Substances 0.000 description 2
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 2
239000000080 wetting agent Substances 0.000 description 2
239000001124 (E)-prop-1-ene-1,2,3-tricarboxylic acid Substances 0.000 description 1
BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 1
XBYRMPXUBGMOJC-UHFFFAOYSA-N 1,2-dihydropyrazol-3-one Chemical compound OC=1C=CNN=1 XBYRMPXUBGMOJC-UHFFFAOYSA-N 0.000 description 1
IZMZREOTRMMCCB-UHFFFAOYSA-N 1,4-dichloro-2-ethenylbenzene Chemical compound ClC1=CC=C(Cl)C(C=C)=C1 IZMZREOTRMMCCB-UHFFFAOYSA-N 0.000 description 1
OMNYXCUDBQKCMU-UHFFFAOYSA-N 2,4-dichloro-1-ethenylbenzene Chemical compound ClC1=CC=C(C=C)C(Cl)=C1 OMNYXCUDBQKCMU-UHFFFAOYSA-N 0.000 description 1
SBYMUDUGTIKLCR-UHFFFAOYSA-N 2-chloroethenylbenzene Chemical compound ClC=CC1=CC=CC=C1 SBYMUDUGTIKLCR-UHFFFAOYSA-N 0.000 description 1
125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
BTOVVHWKPVSLBI-UHFFFAOYSA-N 2-methylprop-1-enylbenzene Chemical compound CC(C)=CC1=CC=CC=C1 BTOVVHWKPVSLBI-UHFFFAOYSA-N 0.000 description 1
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
RVBUGGBMJDPOST-UHFFFAOYSA-N 2-thiobarbituric acid Chemical group O=C1CC(=O)NC(=S)N1 RVBUGGBMJDPOST-UHFFFAOYSA-N 0.000 description 1
RANPNKFNOWAPSO-UHFFFAOYSA-N 4-(3-oxo-1h-pyrazol-2-yl)benzenesulfonic acid Chemical compound C1=CC(S(=O)(=O)O)=CC=C1N1C(=O)C=CN1 RANPNKFNOWAPSO-UHFFFAOYSA-N 0.000 description 1
JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 1
ZVNPWFOVUDMGRP-UHFFFAOYSA-N 4-methylaminophenol sulfate Chemical compound OS(O)(=O)=O.CNC1=CC=C(O)C=C1.CNC1=CC=C(O)C=C1 ZVNPWFOVUDMGRP-UHFFFAOYSA-N 0.000 description 1
125000002373 5 membered heterocyclic group Chemical group 0.000 description 1
125000004070 6 membered heterocyclic group Chemical group 0.000 description 1
HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
102000008186 Collagen Human genes 0.000 description 1
108010035532 Collagen Proteins 0.000 description 1
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
239000000020 Nitrocellulose Substances 0.000 description 1
229930040373 Paraformaldehyde Natural products 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
239000004372 Polyvinyl alcohol Substances 0.000 description 1
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
241000589614 Pseudomonas stutzeri Species 0.000 description 1
229910021607 Silver chloride Inorganic materials 0.000 description 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
FJWGYAHXMCUOOM-QHOUIDNNSA-N [(2s,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6s)-4,5-dinitrooxy-2-(nitrooxymethyl)-6-[(2r,3r,4s,5r,6s)-4,5,6-trinitrooxy-2-(nitrooxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-3,5-dinitrooxy-6-(nitrooxymethyl)oxan-4-yl] nitrate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O)O[C@H]1[C@@H]([C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@@H](CO[N+]([O-])=O)O1)O[N+]([O-])=O)CO[N+](=O)[O-])[C@@H]1[C@@H](CO[N+]([O-])=O)O[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O FJWGYAHXMCUOOM-QHOUIDNNSA-N 0.000 description 1
125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 description 1
JJHPQGFGFRPCCH-UHFFFAOYSA-N acetic acid;butane Chemical compound CCCC.CC(O)=O JJHPQGFGFRPCCH-UHFFFAOYSA-N 0.000 description 1
150000008065 acid anhydrides Chemical class 0.000 description 1
RZUBARUFLYGOGC-MTHOTQAESA-L acid fuchsin Chemical compound [Na+].[Na+].[O-]S(=O)(=O)C1=C(N)C(C)=CC(C(=C\2C=C(C(=[NH2+])C=C/2)S([O-])(=O)=O)\C=2C=C(C(N)=CC=2)S([O-])(=O)=O)=C1 RZUBARUFLYGOGC-MTHOTQAESA-L 0.000 description 1
DGOBMKYRQHEFGQ-UHFFFAOYSA-L acid green 5 Chemical compound [Na+].[Na+].C=1C=C(C(=C2C=CC(C=C2)=[N+](CC)CC=2C=C(C=CC=2)S([O-])(=O)=O)C=2C=CC(=CC=2)S([O-])(=O)=O)C=CC=1N(CC)CC1=CC=CC(S([O-])(=O)=O)=C1 DGOBMKYRQHEFGQ-UHFFFAOYSA-L 0.000 description 1
229940091181 aconitic acid Drugs 0.000 description 1
150000003926 acrylamides Chemical class 0.000 description 1
150000001252 acrylic acid derivatives Chemical class 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
150000001299 aldehydes Chemical class 0.000 description 1
239000003513 alkali Substances 0.000 description 1
125000004183 alkoxy alkyl group Chemical group 0.000 description 1
XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
125000003277 amino group Chemical group 0.000 description 1
HNYOPLTXPVRDBG-UHFFFAOYSA-N barbituric acid Chemical compound O=C1CC(=O)NC(=O)N1 HNYOPLTXPVRDBG-UHFFFAOYSA-N 0.000 description 1
229910052614 beryl Inorganic materials 0.000 description 1
230000008033 biological extinction Effects 0.000 description 1
210000000988 bone and bone Anatomy 0.000 description 1
KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
239000004327 boric acid Substances 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
OIPQUBBCOVJSNS-UHFFFAOYSA-L bromo(iodo)silver Chemical compound Br[Ag]I OIPQUBBCOVJSNS-UHFFFAOYSA-L 0.000 description 1
MPMBRWOOISTHJV-UHFFFAOYSA-N but-1-enylbenzene Chemical compound CCC=CC1=CC=CC=C1 MPMBRWOOISTHJV-UHFFFAOYSA-N 0.000 description 1
125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
239000011575 calcium Substances 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
125000002843 carboxylic acid group Chemical group 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
150000001805 chlorine compounds Chemical class 0.000 description 1
YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 1
GTZCVFVGUGFEME-IWQZZHSRSA-N cis-aconitic acid Chemical compound OC(=O)C\C(C(O)=O)=C\C(O)=O GTZCVFVGUGFEME-IWQZZHSRSA-N 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
229920001436 collagen Polymers 0.000 description 1
239000003086 colorant Substances 0.000 description 1
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
238000000586 desensitisation Methods 0.000 description 1
125000004915 dibutylamino group Chemical group C(CCC)N(CCCC)* 0.000 description 1
150000001993 dienes Chemical class 0.000 description 1
125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
125000004914 dipropylamino group Chemical group C(CC)N(CCC)* 0.000 description 1
AFOSIXZFDONLBT-UHFFFAOYSA-N divinyl sulfone Chemical class C=CS(=O)(=O)C=C AFOSIXZFDONLBT-UHFFFAOYSA-N 0.000 description 1
MEGHWIAOTJPCHQ-UHFFFAOYSA-N ethenyl butanoate Chemical compound CCCC(=O)OC=C MEGHWIAOTJPCHQ-UHFFFAOYSA-N 0.000 description 1
GLVVKKSPKXTQRB-UHFFFAOYSA-N ethenyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OC=C GLVVKKSPKXTQRB-UHFFFAOYSA-N 0.000 description 1
UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
XUCNUKMRBVNAPB-UHFFFAOYSA-N fluoroethene Chemical compound FC=C XUCNUKMRBVNAPB-UHFFFAOYSA-N 0.000 description 1
239000011888 foil Substances 0.000 description 1
239000001046 green dye Substances 0.000 description 1
230000009931 harmful effect Effects 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
229920001519 homopolymer Polymers 0.000 description 1
BICAGYDGRXJYGD-UHFFFAOYSA-N hydrobromide;hydrochloride Chemical compound Cl.Br BICAGYDGRXJYGD-UHFFFAOYSA-N 0.000 description 1
125000001041 indolyl group Chemical group 0.000 description 1
239000012948 isocyanate Substances 0.000 description 1
150000002513 isocyanates Chemical class 0.000 description 1
125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
239000006224 matting agent Substances 0.000 description 1
FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
235000010981 methylcellulose Nutrition 0.000 description 1
125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
229920001220 nitrocellulos Polymers 0.000 description 1
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
229920002866 paraformaldehyde Polymers 0.000 description 1
125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
235000021110 pickles Nutrition 0.000 description 1
239000000049 pigment Substances 0.000 description 1
229920000233 poly(alkylene oxides) Polymers 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
229920000515 polycarbonate Polymers 0.000 description 1
239000004417 polycarbonate Substances 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
239000002685 polymerization catalyst Substances 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
229920002223 polystyrene Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
235000019422 polyvinyl alcohol Nutrition 0.000 description 1
229920000915 polyvinyl chloride Polymers 0.000 description 1
239000004800 polyvinyl chloride Substances 0.000 description 1
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
RWPGFSMJFRPDDP-UHFFFAOYSA-L potassium metabisulfite Chemical compound [K+].[K+].[O-]S(=O)S([O-])(=O)=O RWPGFSMJFRPDDP-UHFFFAOYSA-L 0.000 description 1
229940043349 potassium metabisulfite Drugs 0.000 description 1
235000010263 potassium metabisulphite Nutrition 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
238000003672 processing method Methods 0.000 description 1
108090000623 proteins and genes Proteins 0.000 description 1
JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical compound O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 1
CYMJPJKHCSDSRG-UHFFFAOYSA-N pyrazolidine-3,4-dione Chemical compound O=C1CNNC1=O CYMJPJKHCSDSRG-UHFFFAOYSA-N 0.000 description 1
GGOZGYRTNQBSSA-UHFFFAOYSA-N pyridine-2,3-diol Chemical compound OC1=CC=CN=C1O GGOZGYRTNQBSSA-UHFFFAOYSA-N 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 1
HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
235000010265 sodium sulphite Nutrition 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
238000007711 solidification Methods 0.000 description 1
230000008023 solidification Effects 0.000 description 1
230000003595 spectral effect Effects 0.000 description 1
238000010186 staining Methods 0.000 description 1
159000000008 strontium salts Chemical class 0.000 description 1
125000000542 sulfonic acid group Chemical group 0.000 description 1
230000008961 swelling Effects 0.000 description 1
BRNULMACUQOKMR-UHFFFAOYSA-N thiomorpholine Chemical compound C1CSCCN1 BRNULMACUQOKMR-UHFFFAOYSA-N 0.000 description 1
GTZCVFVGUGFEME-UHFFFAOYSA-N trans-aconitic acid Natural products OC(=O)CC(C(O)=O)=CC(O)=O GTZCVFVGUGFEME-UHFFFAOYSA-N 0.000 description 1
XOSXWYQMOYSSKB-LDKJGXKFSA-L water blue Chemical compound CC1=CC(/C(\C(C=C2)=CC=C2NC(C=C2)=CC=C2S([O-])(=O)=O)=C(\C=C2)/C=C/C\2=N\C(C=C2)=CC=C2S([O-])(=O)=O)=CC(S(O)(=O)=O)=C1N.[Na+].[Na+] XOSXWYQMOYSSKB-LDKJGXKFSA-L 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
- G03C1/76—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
- G03C1/835—Macromolecular substances therefor, e.g. mordants

Landscapes

Physics & Mathematics (AREA)
Spectroscopy & Molecular Physics (AREA)
Chemical & Material Sciences (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
General Physics & Mathematics (AREA)
Silver Salt Photography Or Processing Solution Therefor (AREA)
Compositions Of Macromolecular Compounds (AREA)

CH1595677A 1977-12-23 1977-12-23 Photographisches lichtempfindliches silberhalogenidmaterial mit mindestens einer farbstoffhaltigen rueckschicht. CH630732A5 (de)

Priority Applications (7)

Application Number	Priority Date	Filing Date	Title
CH1595677A CH630732A5 (de)	1977-12-23	1977-12-23	Photographisches lichtempfindliches silberhalogenidmaterial mit mindestens einer farbstoffhaltigen rueckschicht.
FR7835626A FR2412871A1 (fr)	1977-12-23	1978-12-19	Matiere photographique a base d'halogenure d'argent comportant au moins une couche exempte d'halogenure d'argent contenant un colorant
GB7849224A GB2011636B (en)	1977-12-23	1978-12-20	Photographic silver halide material with at least one dye containing layer free from silver halide
DE19782855428 DE2855428A1 (de)	1977-12-23	1978-12-21	Photographisches silberhalogenidmaterial mit mindestens einer farbstoffhaltigen silberhalogenidfreien schicht
IT52410/78A IT1109345B (it)	1977-12-23	1978-12-21	Materiale fotografico all'alogenuro d'argento e procedimento per produrlo
BE192490A BE872993A (fr)	1977-12-23	1978-12-22	Matiere photographique a base d'halogenure d'argent comportant au moins une couche exempte d'halogenure d'argent contenant un colorant
JP15818478A JPS5497016A (en)	1977-12-23	1978-12-23	Photographic silver halide material having at least one layer containing dye and not silver halide

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH1595677A CH630732A5 (de)	1977-12-23	1977-12-23	Photographisches lichtempfindliches silberhalogenidmaterial mit mindestens einer farbstoffhaltigen rueckschicht.

Publications (1)

Publication Number	Publication Date
CH630732A5 true CH630732A5 (de)	1982-06-30

Family

ID=4413332

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH1595677A CH630732A5 (de)	1977-12-23	1977-12-23	Photographisches lichtempfindliches silberhalogenidmaterial mit mindestens einer farbstoffhaltigen rueckschicht.

Country Status (6)

Country	Link
JP (1)	JPS5497016A (fr)
BE (1)	BE872993A (fr)
CH (1)	CH630732A5 (fr)
DE (1)	DE2855428A1 (fr)
FR (1)	FR2412871A1 (fr)
GB (1)	GB2011636B (fr)

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS53781B2 (fr) *	1973-03-28	1978-01-12
JPS5612854B2 (fr) *	1973-10-08	1981-03-25
CH592700A5 (fr) *	1974-01-31	1977-11-15	Ciba Geigy Ag
JPS52134425A (en) *	1976-05-06	1977-11-10	Fuji Photo Film Co Ltd	Photographic light sensitive material having layer dyed

1977
- 1977-12-23 CH CH1595677A patent/CH630732A5/de not_active IP Right Cessation
1978
- 1978-12-19 FR FR7835626A patent/FR2412871A1/fr active Granted
- 1978-12-20 GB GB7849224A patent/GB2011636B/en not_active Expired
- 1978-12-21 DE DE19782855428 patent/DE2855428A1/de not_active Ceased
- 1978-12-22 BE BE192490A patent/BE872993A/fr not_active IP Right Cessation
- 1978-12-23 JP JP15818478A patent/JPS5497016A/ja active Granted

Also Published As

Publication number	Publication date
FR2412871B1 (fr)	1982-06-25
JPS5497016A (en)	1979-07-31
JPS62491B2 (fr)	1987-01-08
FR2412871A1 (fr)	1979-07-20
GB2011636A (en)	1979-07-11
GB2011636B (en)	1982-04-07
BE872993A (fr)	1979-06-22
DE2855428A1 (de)	1979-07-05

Legal Events

Date	Code	Title	Description
1988-08-31	PL	Patent ceased
2024-10-31	PL	Patent ceased

Publication	Publication Date	Title
DE2934028C2 (fr)	1989-06-15
DE2541274C3 (de)	1980-05-29	Verfahren zur Herstellung eines wäßrigen Latex
DE69013708T2 (de)	1995-06-14	Filterfarbstoffe für photographische Elemente.
DE69301779T2 (de)	1996-11-14	Photographisches Element mit einverleibten polymeren U.V.-Absorbern
DE1286900B (de)	1969-01-09	Gruenempfindliche supersensibilisierte Silberhalogenidemulsion
DE2409689A1 (de)	1974-09-05	Photographisch empfindliche materialien
DE69426059T2 (de)	2001-05-10	Photographische Elemente die Ultraviolett absorbierendes beladenes Polymerlatex enthalten
DE3010057A1 (de)	1980-12-11	Fotografische materialien mit lichthofschutzschicht auf basis von halogensilberemulsionen
DE3217200C2 (fr)	1988-11-10
DE2453217C2 (de)	1982-05-27	Photographisches Aufzeichnungsmaterial
DE3446962A1 (de)	1985-07-04	Photographisches silberhalogenid-druckpapier und verwendung des papiers im schwarz-weiss-entwicklungsverfahren
DE1472848A1 (de)	1969-03-06	Verwendung von Butadienylfarbstoffen als Lichtfilter- und Antilichthoffarbstoffe
DE851724C (de)	1952-10-06	Verfahren zur Herstellung fotografischer Farbbilder in fotografischen Mehrfarbenemulsionen
DE2516967A1 (de)	1975-10-30	Photographisch empfindliches silberhalogenidmaterial
DE2717604A1 (de)	1977-11-03	Farbstoff enthaltende, lichtempfindliche silberhalogenidmaterialien
DE2218218C2 (de)	1986-02-20	Photographisches Aufzeichnungsmaterial und Verfahren zu dessen Herstellung
DE2419582A1 (de)	1974-11-21	Verfahren zur herstellung photographischer bilder
DE2459927A1 (de)	1975-10-30	Farbenphotographisches lichtempfindliches material
DE1547724A1 (de)	1970-02-19	Verwendung von heterocyclischen organischen Verbindungen als Beizmittel in photographischen Schichten
DE2113381A1 (de)	1971-12-09	Polymere mit Guanidylketimin-Struktureinheiten
CH630732A5 (de)	1982-06-30	Photographisches lichtempfindliches silberhalogenidmaterial mit mindestens einer farbstoffhaltigen rueckschicht.
DE849511C (de)	1952-09-15	Sensibilisierte photographische Silberhalogenid-Emulsion und Verfahren zur Herstellung derselben
DE2453654A1 (de)	1975-05-15	Farbphotographisches lichtempfindliches material
DE902220C (de)	1954-01-21	Farbbleichbad fuer die Farbenphotographie
DE932343C (de)	1955-08-29	Verfahren zur Herstellung von Lichthofschutz- und Filterschichten