IP Library Granted Patent US 9,783,553
Granted Patent B1
US 9,783,553 · App. 15/362,868 · Granted Oct 10, 2017

Silver ion α-oxy carboxylate-oxime complexes

Inventors: Deepak Shukla (Webster, NY); Thomas Robert Welter (Webster, NY)
Assignee: EASTMAN KODAK COMPANY
C07F1/005
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Quick Facts
Patent No.
US 9,783,553
App. No.
15/362,868
Granted
Oct 10, 2017
Kind
B1
Abstract

A non-hydroxylic-solvent soluble silver complex comprises a reducible silver ion complexed with an α-oxy carboxylate and an oxime compound. The non-hydroxylic-solvent soluble silver complex can be represented by the following formula (I): (Ag + ) a (L) b (P) c    (I) wherein L represents the α-oxy carboxylate; P represents the oxime compound; a is 1 or 2; b is 1 or 2; and c is 1, 2, 3, or 4, provided that when a is 1, b is 1, and when a is 2, b is 2. Such complexes can be incorporated into photosensitive compositions in method to provide thin films or patterns in various articles to provide electrically-conductive silver metal.

Claims (33)

1. A non-hydroxylic-solvent soluble silver complex consisting of a reducible silver ion complexed with an α-oxy carboxylate and an oxime compound,

the non-hydroxylic-solvent soluble silver complex being represented by the following formula (I):

(Ag + ) a (L) b (P) c    (1)

wherein L represents the α-oxy carboxylate; P represents the oxime compound; a is 1 or 2; b is 1 or 2; and c is 1, 2, 3, or 4, provided that when a is 1, b is 1, and when a is 2, b is 2.

2. The non-hydroxylic-solvent soluble silver complex of claim 1 , wherein L is represented by the following formula (II):

wherein R 1 , R 2 , and R 3 are independently hydrogen or branched or linear alkyl groups.

3. The non-hydroxylic-solvent soluble silver complex of claim 2 , wherein R 1 is hydrogen or a branched or linear alkyl group having 1 to 3 carbon atoms, and R 2 and R 3 are independently branched or linear alkyl groups having 1 to 8 carbon atoms, wherein any of the hydrogen atoms in the R 1 , R 2 , and R 3 branched or linear alkyl groups optionally can be replaced with a fluorine atom.

4. The non-hydroxylic-solvent soluble silver complex of claim 1 , wherein the α-oxy carboxylate has a molecular weight of 250 or less.

5. The non-hydroxylic-solvent soluble silver complex of claim 1 , wherein L is represented by the following formula (III):

wherein R 4 is a branched or linear alkyl group having 1 to 8 carbon atoms and optionally, any of the hydrogen atoms in the R 4 branched or linear alkyl group can be substituted with a fluorine atom.

6. The non-hydroxylic-solvent soluble silver complex of claim 1 , wherein the α-oxy carboxylate is selected from:

the group consisting of lactate, 2-hydroxybutyric acid, 2-hydroxy-3-methylbutyric acid, 2-hydroxy-3,3-dimethylbutyric acid, 2-hydroxy-isobutyric acid, 2-hydroxy-2-methylbutyric acid, 2-ethyl-2-hydroxybutyric acid, 2-hydroxy-2,3-dimethylbutyric acid, 2-ethyl-2-methoxybutyric acid, 2-methoxy-2-methylpropanoic acid, 1-hydroxycyclopentane-1-carboxylic acid, 2,3-dihydroxy-2,3-dimethylsuccinic acid, and 2,4-dihydroxy-2,4-dimethylpentanedioic acid; or

the group consisting of pyruvic acid, 3-methylpyruvic acid, 3,3-dimethylpyruvic acid, 3,3-dimethyl-2-oxobutanoic acid, 3,3-dimethyl-2-oxopentanoic acid, and 2,3-dioxosuccinic acid.

7. The non-hydroxylic-solvent soluble silver complex of claim 1 , wherein P is an oxime compound represented by the following formula (IV):

wherein R 5 and R 6 are independently hydrogen or an alkyl group having 1 to 6 carbon atoms, provided that at least one of R 5 and R 6 is the alkyl group, or R 5 and R 6 can together represent the carbon atoms sufficient to provide a 5- or 6-membered carbocyclic ring; and R 7 is hydrogen, an alkyl group having 1 to 6 carbon atoms, an acyl group having 1 to 6 carbon atoms, a —C(═O)R 8 group, or a carbonyloxyalkyl group [—C(═O)OR 8 ], wherein R 8 is hydrogen or an alkyl having 1 to 6 carbon atoms.

8. The non-hydroxylic-solvent soluble silver complex of claim 7 , wherein one of R 5 and R 6 is hydrogen and the other is an alkyl having 1 to 3 carbon atoms, or both R 5 and R 6 are independently alkyl groups each having 1 to 3 carbon atoms.

9. The non-hydroxylic-solvent soluble silver complex of claim 7 , wherein R 7 is hydrogen or an alkyl group having 1 to 3 carbon atoms.

10. The non-hydroxylic-solvent soluble silver complex of claim 1 , wherein the oxime compound is selected from the group consisting of acetoxime, acetaldoxime, Aldicarb, dimethylglyoxime, methylethyl ketone oxime, propionaldehyde oxime, cyclohexanone oxime, cyclopentanone oxime, heptanal oxime, acetone-O-methyl oxime, acetaldehyde-O-methyl oxime, propionaldehyde-O-methyl oxime, butanaldehyde-O-methyl oxime, 2-butanone-O-methyl oxime, cyclopentanone-O-methyl oxime, and 2-butanone-O-ethyl oxime.

11. The non-hydroxylic-solvent soluble silver complex of claim 1 , wherein the oxime compound has an oxidation potential of at least 1.5 V vs. saturated calomel electrode (SCE); the α-oxy carboxylate has a first oxidation potential of at least 1 V vs. SCE; and upon decarboxylation of the α-oxy carboxylate, a second radical is generated that has an oxidation potential of less than 1 V vs. SCE.

12. The non-hydroxylic-solvent soluble silver complex of claim 1 , wherein the oxime compound has an oxidation potential of at least 1.5 V vs. SCE.

13. The non-hydroxylic-solvent soluble silver complex of claim 1 , wherein the oxime compound has a molecular weight of 200 or less.

14. The non-hydroxylic-solvent soluble silver complex of claim 1 , wherein the oxime compound has a boiling point of less than 150° C. at 760 mm atmospheric pressure.

15. The non-hydroxylic-solvent soluble silver complex of claim 1 , wherein the oxime compound has a boiling point of less than 100° C. at 760 mm atmospheric pressure.

16. The non-hydroxylic-solvent soluble silver complex of claim 1 , which meets a silver ion stability test wherein, when the non-hydroxylic-solvent soluble silver complex is held for 24 hours at ambient temperature and under yellow safelight, less than 0.1 mol % of its original silver ion content is reduced to silver metal.

17. The non-hydroxylic-solvent soluble silver complex of claim 1 , wherein:

L has a molecular weight of 250 or less, and L is represented by either the following formula (II) or (III):

wherein R 1 is hydrogen or an alkyl group having 1 or 2 carbon atoms, R 2 and R 3 are independently branched or linear alkyl groups having 1 to 8 carbon atoms, wherein any of the hydrogen atoms in the R 1 , R 2 , and R 3 branched or linear alkyl groups optionally can be replaced with a fluorine atom, and R 4 is a branched or linear alkyl group having 1 to 8 carbon atoms wherein any of the hydrogen atoms optionally can be replaced with a fluorine atom; and

P is represented by the following Structure (IV):

wherein R 5 and R 6 are independently hydrogen or an alkyl group having 1 to 6 carbon atoms, provided that at least one of R 5 and R 6 is the alkyl group, or R 5 and R 6 can together represent the carbon atoms sufficient to provide a 5- or 6-membered carbocyclic ring; and R 7 is hydrogen, an alkyl group, an acyl group, a —C(═O)R 8 group, or a carbonyloxyalkyl group, [—C(═O)OR 8 ], wherein R 8 is hydrogen or an alkyl having 1 to 6 carbon atoms.

18. The non-hydroxylic-solvent soluble silver complex of claim 1 , wherein:

(i) a and b are both 1 and c is 1 or 2;

(ii) a and b are both 2 and c is 2; or

(iii) a and b are both 2 and c is 4.

Assignments (9)
INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded Mar 4, 2021
From: EASTMAN KODAK COMPANY
To: ALTER DOMUS (US) LLC
Reel/Frame 056733/0681 →
NOTICE OF SECURITY INTERESTS Recorded Mar 4, 2021
From: EASTMAN KODAK COMPANY
To: BANK OF AMERICA, N.A., AS AGENT
Reel/Frame 056984/0001 →
INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded Mar 4, 2021
From: EASTMAN KODAK COMPANY
To: ALTER DOMUS (US) LLC
Reel/Frame 056734/0233 →
INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded Mar 4, 2021
From: EASTMAN KODAK COMPANY
To: ALTER DOMUS (US) LLC
Reel/Frame 056734/0001 →
RELEASE OF SECURITY INTEREST Recorded Jul 30, 2019
From: JP MORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT
To: EASTMAN KODAK COMPANY; FAR EAST DEVELOPMENT LTD.; PFC, INC.; KODAK (NEAR EAST), INC.; KODAK AMERICAS, LTD.; KODAK IMAGING NETWORK, INC.; KODAK PORTUGUESA LIMITED; KODAK REALTY, INC.; LASER PACIFIC MEDIA CORPORATION; PAKON, INC.; QUALEX, INC.; KODAK PHILIPPINES, LTD.; NPEC, INC.; CREO MANUFACTURING AMERICA LLC; KODAK AVIATION LEASING LLC
Reel/Frame 049901/0001 →
RELEASE OF SECURITY INTEREST Recorded Jul 22, 2019
From: JP MORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT
To: EASTMAN KODAK COMPANY; FAR EAST DEVELOPMENT LTD.; FPC, INC.; KODAK (NEAR EAST), INC.; KODAK AMERICAS, LTD.; KODAK IMAGING NETWORK, INC.; KODAK PORTUGUESA LIMITED; KODAK REALTY, INC.; LASER PACIFIC MEDIA CORPORATION; PAKON, INC.; QUALEX, INC.; KODAK PHILIPPINES, LTD.; NPEC, INC.; CREO MANUFACTURING AMERICA LLC; KODAK AVIATION LEASING LLC
Reel/Frame 050239/0001 →
SECURITY INTEREST Recorded Mar 23, 2017
From: EASTMAN KODAK COMPANY; FAR EAST DEVELOPMENT LTD.; FPC INC.; KODAK (NEAR EAST), INC.; KODAK AMERICAS, LTD.; KODAK REALTY, INC.; LASER-PACIFIC MEDIA CORPORATION; QUALEX INC.; KODAK PHILIPPINES, LTD.; NPEC INC.
To: BANK OF AMERICA, N.A.
Reel/Frame 041696/0145 →
SECURITY INTEREST Recorded Mar 23, 2017
From: EASTMAN KODAK COMPANY; FAR EAST DEVELOPMENT LTD; FPC INC; KODAK (NEAR EAST), INC.; KODAK AMERICAS, LTD.; KODAK REALTY, INC.; LASER-PACIFIC MEDIA CORPORATION; QUALEX INC.; KODAK PHILIPPINES, LTD.; NPEC INC.
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 041695/0364 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 29, 2016
From: SHUKLA, DEEPAK; WELTER, THOMAS ROBERT
To: EASTMAN KODAK COMPANY
Reel/Frame 040439/0862 →