GB942931A - Photographic silver halide emulsions of increased sensitivity - Google Patents

Photographic silver halide emulsions of increased sensitivity

Info

Publication number
GB942931A
GB942931A GB42124/59A GB4212459A GB942931A GB 942931 A GB942931 A GB 942931A GB 42124/59 A GB42124/59 A GB 42124/59A GB 4212459 A GB4212459 A GB 4212459A GB 942931 A GB942931 A GB 942931A
Authority
GB
United Kingdom
Prior art keywords
groups
alkylmercapto
ethylmercapto
acid
bis
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
GB42124/59A
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 GB942931A publication Critical patent/GB942931A/en
Expired legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03CPHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00Photosensitive materials
    • G03C1/005Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
    • G03C1/04Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with macromolecular additives; with layer-forming substances
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/68Polyesters containing atoms other than carbon, hydrogen and oxygen
    • C08G63/688Polyesters containing atoms other than carbon, hydrogen and oxygen containing sulfur
    • C08G63/6884Polyesters containing atoms other than carbon, hydrogen and oxygen containing sulfur derived from polycarboxylic acids and polyhydroxy compounds
    • C08G63/6886Dicarboxylic acids and dihydroxy compounds
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03CPHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00Photosensitive materials
    • G03C1/005Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
    • G03C1/04Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with macromolecular additives; with layer-forming substances
    • G03C1/043Polyalkylene oxides; Polyalkylene sulfides; Polyalkylene selenides; Polyalkylene tellurides

Landscapes

  • Chemical & Material Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • General Physics & Mathematics (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Polyesters Or Polycarbonates (AREA)

Abstract

Linear polyesters containing alkylmercapto groups as substituents attached to the linear chain and having a molecular weight of at least 350 are derived from glycols and dicarboxylic acids, anhydrides, esters or acid halides, at least one of the reactants containing an alkymercapto substituent. The polyesters may comprise units of either formula I or II: <FORM:0942931/C2/1> wherein R is an alkyl group, R1, R2 and R3 ar alkylene groups or alkylene groups interrupted by single sulphur or oxygen atoms, m is 0 or 1 and p is 1, 2 or 3, at least one of R2 and R3 in formula II containing an alkylmercapto substituent. Examples are given of the reaction of ethylene glycol with methylmercapto-succinic acid, a , a 1-bis (ethylmercapto) apidic acid or a , a 1-bis(ethylmercapto) sebacic acid, and of succinic anhydride with 1, 2-dihydroxy-3-ethylmercapto-propane or the corresponding 3-butylmercapto or 3-hexylmercapto compound, or with 1,10-dihydroxy-2, 9-bis(ethylmercapto) decane. These reactions are carried out by fusing the reactants together and passing dry nitrogen through the melt. Reference also is made to the use of ethylene glycol, propylene glycol, 1, 2-propylene glycol, butylene glycol or hexamethylene glycol with dicarboxylic acids containing one or more alkylmercapto groups, such as those referred to above, and of the use of oxalic, succinic, glutaric, 2; 2-dimethyl-glutaric, adipic, pimelic or sebacic acids or their anhydrides, esters or acid halides, with glycols containing one or more alkylmercapto groups, such as those referred to above. The polyesters may have some or all of their thioether groups converted to ternary sulphonium salt groups by reaction with dimethyl sulphate, diethyl sulphate, methyl benzene sulphonate, or methyl p-toluene sulphonate. Specifications 235,211, 541,589, 636,140, 719,920, 791,219, 942,932, 942,935 and U.S.A. Specification 2,948,614 are referred to.ALSO:Linear polyesters containing alkylmercapto groups as substituents attached to the linear chain and having a molecular weight of at least 350 are derived from glycols and dicarboxylic acids, anhydrides, esters or acid halides, at least one of the reactants containing an alkylmercapto substituent. The polyesters may comprise units of either formula I or II: <FORM:0942931/C3/1> <FORM:0942931/C3/2> wherein R is an alkyl group, R1, R2 and R3 are alkylene groups or alkylene groups interrupted by single sulphur or oxygen atoms, m is 0 or 1 and p is 1, 2, or 3, at least one of R2 and R3 in formula II containing an alkylmercapto substituent. Examples are given of the reaction of ethylene glycol with methylmercapto -succinic acid, a , a 1- bis (ethylmercapto) adipic acid or a , a 1- bis (ethylmercapto) sebacic acid, and of succinic anhydride with 1, 2-dihydroxy-3-ethylmercaptopropane or the corresponding 3-butylmercapto or 3-hexylmercapto compound, or with 1,10-dihydroxy -2,9-bis (ethylmercapto) decane. These reactions are carried out by fusing the reactants together and passing dry nitrogen through the melt. Reference also is made to the use of ethylene glycol, propylene glycol, 1,2-propylene glycol, butylene glycol or hexamethylene glycol with dicarboxylic acids containing one or more alkylmercapto groups, such as those referred to above, and of the use of oxalic, succinic, glutaric, 2;2-dimethyl-glutaric, adipic, pimetic or sebacic acids or their anhydrides, esters or acid halides, with glycols containing one or more alkylmercapto groups, such as those referred to above. The polyesters may have some or all of their thioether groups converted to ternary sulphonium salt groups by reaction with dimethyl sulphate, diethyl sulphate, methyl benzene sulphonate, or methyl p-toluene sulphonate. Specifications 235,211, 541,589, 636,140, 719,920, 791,219, 942,932, 942,935 and U.S.A. Specification 2,948,614 are referred to.
GB42124/59A 1958-12-12 1959-12-11 Photographic silver halide emulsions of increased sensitivity Expired GB942931A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US779852A US3046133A (en) 1958-12-12 1958-12-12 Sensitization of photographic silver halide emulsions with polyester compounds containing thioether-sulfur atoms in the side chain

Publications (1)

Publication Number Publication Date
GB942931A true GB942931A (en) 1963-11-27

Family

ID=25117774

Family Applications (1)

Application Number Title Priority Date Filing Date
GB42124/59A Expired GB942931A (en) 1958-12-12 1959-12-11 Photographic silver halide emulsions of increased sensitivity

Country Status (2)

Country Link
US (1) US3046133A (en)
GB (1) GB942931A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0005200A2 (en) * 1978-04-27 1979-11-14 Agfa-Gevaert AG Silver halide photographic material and method of preparation

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3536677A (en) * 1968-01-29 1970-10-27 Eastman Kodak Co Polythiaalkyl acrylates and acrylamides and copolymers containing same
GB1455413A (en) * 1972-12-07 1976-11-10 Agfa Gevaert Development of photographic silver halide elements
DE2748430A1 (en) * 1977-10-28 1979-05-03 Agfa Gevaert Ag PHOTOGRAPHIC BLEACHING COMPOSITIONS WITH BLADE ACCELERATING COMPOUNDS
JPS59188641A (en) 1983-04-11 1984-10-26 Fuji Photo Film Co Ltd Silver halide photographic emulsion
FR2682498A1 (en) * 1991-10-15 1993-04-16 Kodak Pathe Colouring agents containing thioether macrocycles
US5468588A (en) 1994-10-18 1995-11-21 Minnesota Mining And Manufacturing Company Process for manufacturing diffusion transfer printing plates
JPH08190199A (en) 1994-10-18 1996-07-23 Minnesota Mining & Mfg Co <3M> Photosensitive element
GB9423266D0 (en) * 1994-11-18 1995-01-11 Minnesota Mining & Mfg Chemical sensitisation of silver halide emulsions
US5691130A (en) * 1995-11-28 1997-11-25 Eastman Kodak Company Color recording photographic elements exhibiting an increased density range, sensitivity and contrast

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE347196A (en) * 1927-01-07
US2176074A (en) * 1936-08-12 1939-10-17 Du Pont Polyamides
NL55385C (en) * 1940-06-14 1900-01-01
US2813086A (en) * 1954-05-04 1957-11-12 Hooker Electrochemical Co Sulfur-containing crosslinked polyester elastomers
DE1048476B (en) * 1955-12-01

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0005200A2 (en) * 1978-04-27 1979-11-14 Agfa-Gevaert AG Silver halide photographic material and method of preparation
EP0005200A3 (en) * 1978-04-27 1979-12-12 Agfa-Gevaert Aktiengesellschaft Silver halide photographic material and method of preparation

Also Published As

Publication number Publication date
US3046133A (en) 1962-07-24

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