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US3369905A - Photographic silver halide emulsions containing polyamine sensitizing agents - Google Patents

Photographic silver halide emulsions containing polyamine sensitizing agents
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US3369905A
US3369905AUS266192AUS26619263AUS3369905AUS 3369905 AUS3369905 AUS 3369905AUS 266192 AUS266192 AUS 266192AUS 26619263 AUS26619263 AUS 26619263AUS 3369905 AUS3369905 AUS 3369905A
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carbon atoms
silver halide
alkyl
emulsion
polyamine
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US266192A
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Jean E Jones
Charles V Wilson
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Eastman Kodak Co
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Eastman Kodak Co
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3,369,905 PHGTOGRAPHIC SILVER HALIDE EMUL- SIONS CONTAINING POLYAMINE SEN- SITIZING AGENTS Jean E. Jones and Charles V. Wilson, Rochester, N.Y., assignors to Eastman Kodak Company, Rochester, N.Y., a corporation of New Jersey No Drawing. Filed Mar. 19, 1963, Ser. No. 266,192 11 Claims. (Cl. 96-107) This invention relates to photography and particularly to sensitizers for photosensitive colloid-silver halide emulsion layers.
Polyalkyleneimino compounds (polyamines) having primary amino end groups are described for use as chemical sensitizers for photographic silver halide emulsions in US. Patents No. 2,743,182, patented Apr. 24, 1956, and No. 2,518,698, patented Aug. 15, 1950. Many of these a chemical sensitizers increase speed of photographic emulsions but have the disadvantage of substantially increasing fog in the emulsions, especially in emulsions sensitized with sulfur and gold.
An object of the present invention is to provide novel photographic colloid-silver halide emulsions containing a polyamine sensitizing agent which will increase the speed of the emulsion with only very slight or no increase in fog, even in emulsions sensitized with sulfur and gold.
This and other objects of the invention are obtained by incorporating into a photographic colloid-silver halide emulsion a polyalkyleneimino compound having at least one secondary or tertiary amino end group. Even better results are obtained when all of the nitrogen atoms in the polyamine chain are fully substituted. Effective amounts of sensitizer in the emulsion are usually in the range from 0.03 to 5.0 grams sensitizer per mole silver.
Polyalkyleneimino compounds that are useful as sensitizers according to the present invention have the formula:
wherein each of R and R represents a member selected from the group consistihg of hydrogen, alkyl containing 1-4 carbon atoms, hydroxyalkyl, aryl, aralkyl, alkyl substituted aryl and alkoxy substituted aryl; R represents a member selected from the group consisting of alkyl containing 1-4 carbon atoms, hydroxyalkyl, aryl, aralkyl, alkyl substituted aryl and alkoxy substituted aryl; each R is an alkylene chain having from 2-3 carbon atoms in the chain with each of said carbon atoms having attached thereto members selected from the group consisting of hydrogen, alkyl containing 1-4 carbon atoms, aryl of 6- carbon atoms and aralkyl, the alkyl group in each said aralkyl being of 1-2 carbon atoms; n is a positive whole integer from 1-3 and the radical I ls] is a unit in the linear chain of the polyamine.
Specific examples of compounds having the above formula are:
( 1 N,N'-di-beta-hydroxyethylethylenediamine (2) 8-amino-3,6-diazaoctanol (3) 3,6,9-triaza-1,1l-undecanediol (4) 3,6,9-trimethyltriaza-1,1l-undecanediol (5) 4,15-diazaoctadecane-1,18-bisdimethylamine Compounds 1 and 3 in the above list may be represented by the formula:
wherein R and R are members selected from the group consisting of alkyl containing 1-4 carbon atoms, hydroxy United States Patent 0 "ice alkyl, aryl, aralkyl, alkyl substituted aryl and alkoxy substituted aryl, R is an alkylene chain having from 2-3 carbon atoms in the chain with each of said carbon atoms having attached thereto members selected from the group consisting of hydrogen, alkyl containing 14 carbon atoms, aryl of 610 atoms and aralkyl, the alkyl group in said aralkyl being of 1-2 carbon atoms, and n is a positive whole integer from 1-3 and the radical NHR is a unit in the linear chain of the polyamine.
Additional specific examples of compounds having the last formula above are:
(6) N,N"'-dimethyltriethylenetetramine (7) N,N"-dimethyldiethylenetriamine (8) N,N'-dimethylethylenediamine (9) N,N'-dibenzylethylenediamine (10) N,N'-di-n-butylethylenediamine l1 N,N'-dimethyltrimethylenediamine 12) N,N-dimethyl-1,2-propanediamine (l3 N,N'-diphenylethylenediamine The invention may be better understood by reference to the following examples which describe in detail some preferred embodiments of the invention.
Example I Conventional fast silver bromoiodide-gelatin emulsions, chemically sensitized with sulfur and gold compounds and spectrally sensitized with cyanine dyes were prepared by conventional procedures and each of the compounds numbered 1-5 above was added respectively to a separate sample of emulsion in the concentrations shown in Table 1. Control samples of each emulsion were also kept. The sensitized and control emulsion samples were coated by conventional melt coating procedures on cellulose acetate film, then chill-set and dried. Respective samples of the film were exposed on an Eastman sensitometer Type IB to light of daylight quality for 1. second and were developed for 5 minutes in Kodak Developer DK-50 at 68 F., then fixed and dried. Relative speed was determined at the exposure necessary to produce density of 0.2 above fog. Results of the tests in terms of relative speed, gamma and fog are tabulated in Table 1.
Emulsion number as above) and Con- Relative Gam- Fog centration in Grams Per Speed ma Density Mole Silver Data in Table 1 show results obtained using different sensitizers of the class described at concentrations from 0.03 to 3.0 grams per mole silver in the emulsion. Optimum results were obtained at concentrations in the magnitude of 0.3 gram per mole, however, the sensitizing effect was appreciable at other concentrations.
Variations from the colloid-silver halide emulsion compositions described in the examples herein may be made within the scope of the present invention. The class of sensitizers defined above are effective to increase speed in a wide variety of photosensitive silver halide emulsions familiar to those skilled in the art. The invention includes photographic emulsions made from suitable colloids other than gelatin and containing other functional addenda as will be familiar to emulsion makers.
The invention has been described with reference to cer- Q a tain preferred embodiments but it will be understood that variations and modifications of the invention as described can be made within the scope of the invention as defined in the following claims.
We claim: 1 1. A colloid-silver halide photographic emulsion containing at least one linear polyamine sensitizing agent having the formula:
U n Rt N-Ra "NR2 wherein each of R and R represents a member selected from the group consisting of hydrogen, alkyl containing 14 carbon atoms, hydroxyalkyl, aryl, aralkyl, alkyl substituted aryl and alkoxy substituted aryl; R represents a member selected from the group consisting of alkyl containing 1-4 carbon atoms, hydroxyalkyl, aryl, aralkyl, alkyl substituted aryl and alkoxy substituted aryl; each R is an alkylene chain having from 23 carbon atoms in the chain with each of said carbon atoms having attached thereto members selected from the group consisting of hydrogen, alkyl containing 1-4 carbon atoms, aryl of 6- 10 carbon atoms and aralkyl, the alkyl group in each said aralkyl being of 1-2 carbon atoms; n is a positive whole integer from 13 and the radical is a unit in the linear chain of the polyamine.
2. A colloidsilver halide photographic emulsion containing at least one linear polyamine sensitizing agent having the general formula:
wherein R and R are selected from the group consisting of alkyl of 1 to 4 carbon atoms, aryl, aralkyl, hydroxy substituted alkyl and'alkyl substituted aryl and alkoxy substituted aryl; R is an alkylene chain having from 2 to 3 carbon atoms in the chain with each of said carbon atoms having attached thereto members selected from the group consisting of hydrogen, alkyl of 1 to 4 carbon atoms, aryl of 6 to 10 carbon atoms and aralkyl, the alkyl group in said aralkyl being of 1 to 2 carbon atoms; and n is a positive whole number from 1 to 3 and the radical, NHR is a unit in the linear chain of the polyamine.
3. An emulsion as set forth in claim 2 wherein said \colloid is gelatin.
4. A colloid-silver halide photographic emulsion containing a linear amine sensitizing agent having the formula:
wherein R is selected from the group consisting of an alkyl radical of 1 to 4 carbon atoms and hydroxy substituted alkyl and R is an alkylene chain having 2 to 3 carbon atoms in the chain with each of said carbon atoms having attached thereto members selected from the group consisting of hydrogen and an alkyl of 1 to 4 carbon atoms.
5. A colloid-silver halide photographic emulsion containing at least one linear polyamine sensitizing agent having the formula:
wherein R and R are hydroxy substituted alkyl, R is an alkylene chain having 2 carbon atoms, n is a positive whole integer from 1 to 2, and the radical NHR is a unit of the linear chain of the polyamine.
6. An emulsion as defined in claim 5 wherein said colloid is gelatin.
7. An emulsion as defined in claim 2 wherein said sensitizing agent is N,N-di-beta-hydroxyethylethylenediamine.
8. An emulsion as defined in claim 1 wherein said sensitizing agent is 8-amino-3,6-diazaoctanol.
9. An emulsion as defined in claim 2 wherein said sensitizing agent is 3,6,9-triaza-1,11-undecanediol.
10. An emulsion as defined in claim 1 wherein said sensitizing agent is 3,6,9-trimethyltriaza-1,1l-undecanediol.
11. A colloid-silver halide photographic emulsion containing 4,15-diazaoctadecane 1,18 bisdimethylamine as a linear polyamine sensitizing agent.
References Cited UNITED STATES PATENTS 3,026,203 3/1962 Chamber et al. 96-107 2,016,471 10/1935 Wilmanns et al 96-107 2,518,698 8/1950 Lowe et al. 96107 NORMAN G. TORCHIN, Primary Examiner.
J. T. BROWN, Assistant Examiner.

Claims (1)

1. A COLLOID-SILVER HALIDE PHOTOGRAPHIC EMULSION CONTAINING AT LEAST ONE LINEAR POLYAMINE SENSITIZING AGENT HAVING THE FORMULA:
US266192A1963-03-191963-03-19Photographic silver halide emulsions containing polyamine sensitizing agentsExpired - LifetimeUS3369905A (en)

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Cited By (8)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
US5488168A (en)*1989-08-251996-01-30Kao CorporationTertiary amino alcohol and method of producing the same
US5674908A (en)*1993-12-201997-10-07Life Technologies, Inc.Highly packed polycationic ammonium, sulfonium and phosphonium lipids
US5677352A (en)*1986-12-021997-10-14University Of Florida Research Foundation, Inc.Polyamines and anti-diarrheal and gastrointestinal anti-spasmodic pharmaceutical compositions and methods of treatment
US5679682A (en)*1986-12-021997-10-21University Of Florida Research Foundation, Inc.Anti-neoplastic, anti-viral or anti-retroviral spermine derivatives
US5753714A (en)*1987-02-031998-05-19Merrell Pharmaceuticals Inc.Polyamine derivatives
US6114394A (en)*1993-02-232000-09-05Merrell Pharmaceuticals Inc.Polyamine derivatives as radioprotective agents
US20050164971A1 (en)*1998-11-122005-07-28Yongliang ChuNew transfection reagents
US10195280B2 (en)2014-07-152019-02-05Life Technologies CorporationCompositions and methods for efficient delivery of molecules to cells

Citations (3)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
US2016471A (en)*1935-10-08Stabilizing silver halide emulsions
US2518698A (en)*1948-11-181950-08-15Eastman Kodak CoChemical sensitization of photographic emulsions
US3026203A (en)*1959-08-171962-03-20Du PontSilver halide photographic emulsions containing linear polyamine sensitizing agents

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
US2016471A (en)*1935-10-08Stabilizing silver halide emulsions
US2518698A (en)*1948-11-181950-08-15Eastman Kodak CoChemical sensitization of photographic emulsions
US3026203A (en)*1959-08-171962-03-20Du PontSilver halide photographic emulsions containing linear polyamine sensitizing agents

Cited By (36)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
US5677352A (en)*1986-12-021997-10-14University Of Florida Research Foundation, Inc.Polyamines and anti-diarrheal and gastrointestinal anti-spasmodic pharmaceutical compositions and methods of treatment
US5679682A (en)*1986-12-021997-10-21University Of Florida Research Foundation, Inc.Anti-neoplastic, anti-viral or anti-retroviral spermine derivatives
US5681837A (en)*1986-12-021997-10-28University Of Florida Research Foundation, Inc.Anti-neoplastic, anti-viral or anti-retroviral spermine derivatives
US5827894A (en)*1986-12-021998-10-27University Of Florida Research Foundation, Inc.Anti-neoplastic, anti-viral or anti-retroviral spermine derivatives
US6455591B1 (en)*1986-12-022002-09-24University Of FloridaPolyamines and anti-diarrheal and gastrointestinal anti-spasmodic pharmaceutical compositions and methods of treatment
US5866613A (en)*1986-12-021999-02-02University Of Florida Research Foundation, Inc.Anti-neoplastic, anti-viral or anti-retroviral spermine derivatives
US6034139A (en)*1986-12-022000-03-07University Of Florida Research Foundation, Inc.Anti-neoplastic, anti-viral or anti-retroviral spermine derivatives
US5753714A (en)*1987-02-031998-05-19Merrell Pharmaceuticals Inc.Polyamine derivatives
US5488168A (en)*1989-08-251996-01-30Kao CorporationTertiary amino alcohol and method of producing the same
US6114394A (en)*1993-02-232000-09-05Merrell Pharmaceuticals Inc.Polyamine derivatives as radioprotective agents
US20090317908A1 (en)*1993-12-202009-12-24Life Technologies CorporationHighly packed polycationic ammonium, sulfonium and phosphonium lipids
US6110916A (en)*1993-12-202000-08-29Life Technologies, Inc.Highly packed polycationic ammonium, sulfonium and phosphonium lipids
US6399663B1 (en)1993-12-202002-06-04Invitrogen CorporationHighly packed polycationic ammonium, sulfonium and phosphonium lipids
US5834439A (en)*1993-12-201998-11-10Life Technologies, Inc.Highly packed polycationic ammonium, sulfonium and phosphonium lipids
US6716882B2 (en)1993-12-202004-04-06Invitrogen CorporationHighly packed polycationic ammonium, sulfonium and phosphonium lipids
US5674908A (en)*1993-12-201997-10-07Life Technologies, Inc.Highly packed polycationic ammonium, sulfonium and phosphonium lipids
US7501542B2 (en)1993-12-202009-03-10Invitrogen CorporationHighly-packed polycationic ammonium, sulfonium and phosphonium lipids
US7479573B2 (en)1998-11-122009-01-20Invitrogen CorporationTransfection reagents
US7601872B2 (en)1998-11-122009-10-13Life Technologies CorporationTransfection reagents
US7173154B2 (en)1998-11-122007-02-06Invitrogen Corp.Transfection reagents
US20070202598A1 (en)*1998-11-122007-08-30Invitrogen CorporationNew transfection reagents
US7323594B2 (en)1998-11-122008-01-29Invitrogen CorporationTransfection reagents
US7470817B2 (en)1998-11-122008-12-30Invitrogen CorporationTransfection reagents
US7145039B2 (en)1998-11-122006-12-05Invitrogen Corp.Transfection reagents
US20050164972A1 (en)*1998-11-122005-07-28Yongliang ChuTransfection reagents
US20090143583A1 (en)*1998-11-122009-06-04Life Technologies CorporationTransfection reagents
US7166745B1 (en)1998-11-122007-01-23Invitrogen CorporationTransfection reagents
US20050164971A1 (en)*1998-11-122005-07-28Yongliang ChuNew transfection reagents
US20100159593A1 (en)*1998-11-122010-06-24Life Technologies CorporationTransfection reagents
US7915450B2 (en)1998-11-122011-03-29Life Technologies CorporationTransfection reagents
US8158827B2 (en)1998-11-122012-04-17Life Technologies CorporationTransfection reagents
US8785200B2 (en)1998-11-122014-07-22Life Technologies CorporationTransfection reagents
US9358300B2 (en)1998-11-122016-06-07Life Technologies CorporationTransfection reagents
US10195280B2 (en)2014-07-152019-02-05Life Technologies CorporationCompositions and methods for efficient delivery of molecules to cells
US10792362B2 (en)2014-07-152020-10-06Life Technologies CorporationCompositions and methods for efficient delivery of molecules to cells
US11872285B2 (en)2014-07-152024-01-16Life Technologies CorporationCompositions and methods for efficient delivery of molecules to cells

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