GB1001067A - Improvements in or relating to sensitized photographic silver halide emulsions and to new sensitizing dyes - Google Patents
Improvements in or relating to sensitized photographic silver halide emulsions and to new sensitizing dyesInfo
- Publication number
- GB1001067A GB1001067A GB14381/62A GB1438162A GB1001067A GB 1001067 A GB1001067 A GB 1001067A GB 14381/62 A GB14381/62 A GB 14381/62A GB 1438162 A GB1438162 A GB 1438162A GB 1001067 A GB1001067 A GB 1001067A
- Authority
- GB
- United Kingdom
- Prior art keywords
- ethyl
- methyl
- iodide
- prepared
- alkyl
- Prior art date
- 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.)
- Expired
Links
- 239000000975 dye Substances 0.000 title abstract 10
- -1 silver halide Chemical class 0.000 title abstract 8
- 239000000839 emulsion Substances 0.000 title 1
- 230000001235 sensitizing effect Effects 0.000 title 1
- 229910052709 silver Inorganic materials 0.000 title 1
- 239000004332 silver Substances 0.000 title 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 abstract 6
- 150000003839 salts Chemical class 0.000 abstract 6
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 abstract 5
- 229920002554 vinyl polymer Polymers 0.000 abstract 5
- 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 abstract 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 abstract 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- 125000004429 atom Chemical group 0.000 abstract 3
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 abstract 3
- 229910021653 sulphate ion Inorganic materials 0.000 abstract 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 abstract 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 abstract 2
- 239000007868 Raney catalyst Substances 0.000 abstract 2
- NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical compound [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 abstract 2
- 229910000564 Raney nickel Inorganic materials 0.000 abstract 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- FHHZTIXPIXHMLC-UHFFFAOYSA-N 2-chloro-6-methylquinoline Chemical compound N1=C(Cl)C=CC2=CC(C)=CC=C21 FHHZTIXPIXHMLC-UHFFFAOYSA-N 0.000 abstract 1
- VHLFWAWGJAWINR-UHFFFAOYSA-M 3-methyl-2-methylsulfanyl-1,3-benzothiazol-3-ium;methyl sulfate Chemical compound COS([O-])(=O)=O.C1=CC=C2[N+](C)=C(SC)SC2=C1 VHLFWAWGJAWINR-UHFFFAOYSA-M 0.000 abstract 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 abstract 1
- IOVCWXUNBOPUCH-UHFFFAOYSA-N Nitrous acid Chemical compound ON=O IOVCWXUNBOPUCH-UHFFFAOYSA-N 0.000 abstract 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 abstract 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 abstract 1
- XQNBGEFLLHOGTQ-UHFFFAOYSA-N [I-].[NH+]1=CC=CC2=CC=CC=C12.C(C)N1N=NCN1 Chemical compound [I-].[NH+]1=CC=CC2=CC=CC=C12.C(C)N1N=NCN1 XQNBGEFLLHOGTQ-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000004467 aryl imino group Chemical group 0.000 abstract 1
- 150000001555 benzenes Chemical group 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- KIWBPDUYBMNFTB-UHFFFAOYSA-M ethyl sulfate Chemical compound CCOS([O-])(=O)=O KIWBPDUYBMNFTB-UHFFFAOYSA-M 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 150000002391 heterocyclic compounds Chemical class 0.000 abstract 1
- 150000004694 iodide salts Chemical group 0.000 abstract 1
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 abstract 1
- 229910052698 phosphorus Inorganic materials 0.000 abstract 1
- 239000011574 phosphorus Substances 0.000 abstract 1
- 238000010992 reflux Methods 0.000 abstract 1
- 125000000547 substituted alkyl group Chemical group 0.000 abstract 1
- 125000003107 substituted aryl group Chemical group 0.000 abstract 1
- 150000003536 tetrazoles Chemical class 0.000 abstract 1
- 125000003831 tetrazolyl group Chemical group 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom 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 ring carbon atoms
- C07D215/38—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom 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 ring carbon atoms
- C07D215/18—Halogen atoms or nitro radicals
-
- 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
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-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
- C09B23/10—The polymethine chain containing an even number of >CH- groups
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/02—Charge-receiving layers
- G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
- G03G5/06—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
- G03G5/0622—Heterocyclic compounds
- G03G5/0624—Heterocyclic compounds containing one hetero ring
- G03G5/0635—Heterocyclic compounds containing one hetero ring being six-membered
- G03G5/0637—Heterocyclic compounds containing one hetero ring being six-membered containing one hetero atom
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/02—Charge-receiving layers
- G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
- G03G5/06—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
- G03G5/0664—Dyes
- G03G5/0666—Dyes containing a methine or polymethine group
- G03G5/0668—Dyes containing a methine or polymethine group containing only one methine or polymethine group
- G03G5/067—Dyes containing a methine or polymethine group containing only one methine or polymethine group containing hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Plural Heterocyclic Compounds (AREA)
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BE630906D BE630906A (en, 2012) | 1962-04-13 | ||
| GB14381/62A GB1001067A (en) | 1962-04-13 | 1962-04-13 | Improvements in or relating to sensitized photographic silver halide emulsions and to new sensitizing dyes |
| US271883A US3337540A (en) | 1962-04-13 | 1963-04-10 | Methine dyes |
| FR931310A FR1467011A (fr) | 1962-04-13 | 1963-04-11 | Colorants méthiniques |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB14381/62A GB1001067A (en) | 1962-04-13 | 1962-04-13 | Improvements in or relating to sensitized photographic silver halide emulsions and to new sensitizing dyes |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1001067A true GB1001067A (en) | 1965-08-11 |
Family
ID=10040173
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB14381/62A Expired GB1001067A (en) | 1962-04-13 | 1962-04-13 | Improvements in or relating to sensitized photographic silver halide emulsions and to new sensitizing dyes |
Country Status (3)
| Country | Link |
|---|---|
| US (1) | US3337540A (en, 2012) |
| BE (1) | BE630906A (en, 2012) |
| GB (1) | GB1001067A (en, 2012) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3979387A (en) | 1975-06-10 | 1976-09-07 | Eli Lilly And Company | 4,5-Dihydrotetrazolo(1,5-A)quinoxalines |
| WO2005015215A1 (en) * | 2003-07-30 | 2005-02-17 | Roche Diagnostics Gmbh | Novel chemiluminescent compounds and their use |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3931156A (en) * | 1961-05-29 | 1976-01-06 | Agfa-Gevaert N.V. | Methine dyes |
| DE1447570A1 (de) * | 1963-07-22 | 1969-05-29 | Agfa Ag | Cyaninfarbstoffe |
| US3417083A (en) * | 1965-09-27 | 1968-12-17 | Eastman Kodak Co | Polymethine pyrylium compounds and process for their preparation |
| US4568679A (en) * | 1980-12-23 | 1986-02-04 | Merck & Co., Inc. | Aralkylaminoethanol heterocyclic compounds |
| JPS60213937A (ja) * | 1984-04-09 | 1985-10-26 | Fuji Photo Film Co Ltd | 感光性写真要素 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2304981A (en) * | 1939-02-08 | 1942-12-15 | Gen Aniline & Film Corp | Sensitizing of photographic silver chloride, chloro-bromide, and chloro-bromo-iodideemulsions |
| BE522654A (en, 2012) * | 1952-09-10 | |||
| BE539643A (en, 2012) * | 1954-07-08 | |||
| US2865749A (en) * | 1956-11-06 | 1958-12-23 | Eastman Kodak Co | Stabilized photographic emulsions |
| US2870014A (en) * | 1957-01-09 | 1959-01-20 | Eastman Kodak Co | Cyanines from triazolo bases |
| GB870633A (en) * | 1958-05-14 | 1961-06-14 | Ilford Ltd | Pentamethincyanines |
| NL241413A (en, 2012) * | 1957-06-05 |
-
0
- BE BE630906D patent/BE630906A/xx unknown
-
1962
- 1962-04-13 GB GB14381/62A patent/GB1001067A/en not_active Expired
-
1963
- 1963-04-10 US US271883A patent/US3337540A/en not_active Expired - Lifetime
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3979387A (en) | 1975-06-10 | 1976-09-07 | Eli Lilly And Company | 4,5-Dihydrotetrazolo(1,5-A)quinoxalines |
| WO2005015215A1 (en) * | 2003-07-30 | 2005-02-17 | Roche Diagnostics Gmbh | Novel chemiluminescent compounds and their use |
| US7563902B2 (en) | 2003-07-30 | 2009-07-21 | Roche Diagnostics Operations, Inc. | Chemiluminescent compounds and their use |
Also Published As
| Publication number | Publication date |
|---|---|
| US3337540A (en) | 1967-08-22 |
| BE630906A (en, 2012) |
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