GB1344993A - Photographic materials - Google Patents

Photographic materials

Info

Publication number
GB1344993A
GB1344993A GB1344993DA GB1344993A GB 1344993 A GB1344993 A GB 1344993A GB 1344993D A GB1344993D A GB 1344993DA GB 1344993 A GB1344993 A GB 1344993A
Authority
GB
United Kingdom
Prior art keywords
reacting
thiazolo
thiazole
bis
azide
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
Application number
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.)
Kodak Ltd
Original Assignee
Kodak Ltd
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.)
Filing date
Publication date
Application filed by Kodak Ltd filed Critical Kodak Ltd
Publication of GB1344993A publication Critical patent/GB1344993A/en
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/48—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups having nitrogen atoms of sulfonamide groups further bound to another hetero atom
    • 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
    • C09B26/00—Hydrazone dyes; Triazene dyes
    • C09B26/02—Hydrazone dyes
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
    • D06P1/38—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using reactive dyes
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00—Photosensitive materials
    • G03C1/76—Photosensitive materials characterised by the base or auxiliary layers
    • G03C1/775—Photosensitive materials characterised by the base or auxiliary layers the base being of paper
    • G03C1/79—Macromolecular coatings or impregnations therefor, e.g. varnishes
    • 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
    • G03C1/815—Photosensitive materials characterised by the base or auxiliary layers characterised by means for filtering or absorbing ultraviolet light, e.g. optical bleaching
    • 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
    • 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
    • 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
    • G03C1/85—Photosensitive materials characterised by the base or auxiliary layers characterised by antistatic additives or coatings
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/004—Photosensitive materials
    • G03F7/008—Azides
    • G03F7/012—Macromolecular azides; Macromolecular additives, e.g. binders
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/004—Photosensitive materials
    • G03F7/038—Macromolecular compounds which are rendered insoluble or differentially wettable
    • 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
    • G03G5/07—Polymeric photoconductive materials

Landscapes

  • Chemical & Material Sciences (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Textile Engineering (AREA)
  • Coloring (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Treatments Of Macromolecular Shaped Articles (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Abstract

1344993 Azidosulphonyl compounds and intermediates therefor KODAK Ltd 29 April 1971 [4 May 1970] 21281/70 Heading C2C [Also in Divisions C3 C4 and G2] Compounds of the formulµ are made by reacting sodium azide with 2 : 5- bis - (x - chlorosulphonyl - 2 - methylphenyl)- thiazolo(5,4-d)thiazole and 2: 5 - bis - (xchlorosulphonyl - 3 - methozyphenyl)thiazolo- (5,4-d)thiazole respectively. The latter are obtained by chlorosulphonation respectively of 2: 5 - bis - (2 - methylphenyl)thiazolo(5,4-d)- thiazole and 2: 5 - bis - (3 - methoxyphenyl)- thiazolo(5,4-d)thiazole which are obtained by reacting o-tolualdehyde or m-methoxybenzaldehyde with dithiooxamide in dimethylformamide. 4 - Azidosulphonylphenylaminopropane- 3<SP>1</SP>-sulphonic acid, potassium salt, of the formula is made by reacting aniline-4-sulphonyl azide and 1: 3-propane sultone and then treating with KOH. Thiophene - 2 : 5 - di(benzoxazol - 2 - yl - xsulphonyl azide) of the formula is made by chlorosulphonating 2: 5-di(benzoxazol - 2 - yl)thiophene and reacting the product with sodium azide. 7(2 - Chloro - 4 - diethylamino - s - triazinyl)- aminocoumarin - 3 - ylbenzene - x - - sulphonyl azide of the formula is made by chlorosulphonating 7-(2-chloro-4- diethylamino - s - triazin - 6 - yl)amino - 3- phenylcoumarin and reacting with sodium azide.
GB1344993D 1970-03-31 1971-04-29 Photographic materials Expired GB1344993A (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
GB1516970 1970-03-31
GB1551470 1970-04-01
GB1756870 1970-04-14
GB2128170 1970-05-04

Publications (1)

Publication Number Publication Date
GB1344993A true GB1344993A (en) 1974-01-23

Family

ID=27448301

Family Applications (3)

Application Number Title Priority Date Filing Date
GB1344991D Expired GB1344991A (en) 1970-03-31 1970-03-31 Dyeing or treating films and fibres
GB1344992D Expired GB1344992A (en) 1970-03-31 1971-04-19 Dyes pigments fluorescent brightening agents and uv-absorbing agents
GB1344993D Expired GB1344993A (en) 1970-03-31 1971-04-29 Photographic materials

Family Applications Before (2)

Application Number Title Priority Date Filing Date
GB1344991D Expired GB1344991A (en) 1970-03-31 1970-03-31 Dyeing or treating films and fibres
GB1344992D Expired GB1344992A (en) 1970-03-31 1971-04-19 Dyes pigments fluorescent brightening agents and uv-absorbing agents

Country Status (4)

Country Link
BE (3) BE765112A (en)
DE (2) DE2115756A1 (en)
FR (3) FR2083686B1 (en)
GB (3) GB1344991A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6699527B1 (en) 1998-11-03 2004-03-02 Isis Innovation Limited Process for surface functionalization of polymeric substrates using diaryl carbenes as reactive intermediates
US8038734B2 (en) 2004-10-12 2011-10-18 Luminex Corporation Methods for forming dyed microspheres and populations of dyed microspheres
US9193678B2 (en) 2009-03-02 2015-11-24 Oxford Advanced Surfaces Ltd Chemical agents capable of forming covalent 3-D networks

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4189429A (en) * 1978-05-08 1980-02-19 Minnesota Mining And Manufacturing Company Hydrolyzable silyl-substituted dyestuffs for transfer printing
DE3736728A1 (en) * 1987-10-29 1989-05-11 Siemens Ag PRINTER INK
US5938793A (en) * 1995-02-13 1999-08-17 Ciba Specialty Chemicals Corporation Process for increasing the sun protection factor of cellulosic fibre materials
TW290606B (en) * 1995-03-17 1996-11-11 Ciba Geigy Ag
CN105189625A (en) * 2013-01-18 2015-12-23 赛尔格有限责任公司 Surface modifying agents, modified materials and methods

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE611823A (en) * 1960-12-24 1962-04-16 Bayer Ag Coloring matters, process for their preparation and application
US3211713A (en) * 1962-10-15 1965-10-12 Hercules Powder Co Ltd Process for modifying hydrocarbon polymers with lower aliphatic monoazidoformates
FR1419946A (en) * 1964-10-23 1965-12-03 Ici Ltd New dyes
FR1500512A (en) * 1965-10-23 1967-11-03 Archer Daniels Midland Co Process for the modification by a carbene of surfaces into an organic substance

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6699527B1 (en) 1998-11-03 2004-03-02 Isis Innovation Limited Process for surface functionalization of polymeric substrates using diaryl carbenes as reactive intermediates
US7034129B2 (en) 1998-11-03 2006-04-25 Isis Innovation Limited Process for surface functionalsation of polymeric substrates using diaryl carbenes as reactive intermediates
US8038734B2 (en) 2004-10-12 2011-10-18 Luminex Corporation Methods for forming dyed microspheres and populations of dyed microspheres
US8361169B2 (en) 2004-10-12 2013-01-29 Luminex Corporation Methods for forming dyed microspheres and populations of dyed microspheres
EP2559738A1 (en) 2004-10-12 2013-02-20 Luminex Corporation Methods for forming dyed microspheres and populations of dyed microspheres
US9193678B2 (en) 2009-03-02 2015-11-24 Oxford Advanced Surfaces Ltd Chemical agents capable of forming covalent 3-D networks

Also Published As

Publication number Publication date
BE766716A (en) 1971-10-01
GB1344992A (en) 1974-01-23
BE765112A (en) 1971-09-30
BE765113A (en) 1971-09-30
GB1344991A (en) 1974-01-23
FR2083686A1 (en) 1971-12-17
DE2115756A1 (en) 1971-11-11
FR2095502A5 (en) 1972-02-11
FR2083686B1 (en) 1976-03-19
FR2091142A5 (en) 1972-01-14
DE2122060A1 (en) 1971-11-18

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Legal Events

Date Code Title Description
PS Patent sealed
PCNP Patent ceased through non-payment of renewal fee