IP Library Granted Patent US 7,700,248
Granted Patent B2
US 7,700,248 · App. 10/615,089 · Granted Apr 20, 2010

Organic charge transporting polymers including charge transport moieties and silane groups, and silsesquioxane compositions prepared therefrom

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Quick Facts
Patent No.
US 7,700,248
App. No.
10/615,089
Granted
Apr 20, 2010
Kind
B2
Abstract

Disclosed are polymers which include tertiary aryl amine moieties that can function as hole transport agents and which also have reactive silane groups thereon capable of being condensed to a silsesquioxane composition, as well as the silsesquioxane compositions prepared therefrom. The silsesquioxanes can be coated onto substrates to form abrasion-resistant layers having hole transport properties useful in devices that require charge transport properties, such as light-emitting diodes and organic electrophotographic elements such as photoreceptors or photoconductors. Also disclosed are electrophotographic elements which comprise an electrically conducting layer, a charge generating layer overlying the electrically conducting layer, and a charge transport layer overlying the electrically conducting layer. The charge transport layer, which can be an overcoat overlying the charge generating layer, comprises the condensed reaction product of the disclosed polymers.

Claims (108)

1. An electrophotographic element comprising:

an electrically conducting layer;

a charge generating layer overlying said electrically conducting layer; and

a first charge transport layer overlying said electrically conducting layer, said first charge transport layer comprising the condensed reaction product of a charge transport polymer comprising structural units having the formula:

wherein:

A is a tertiary arylamine charge transport moiety;

X is a divalent bridging moiety;

Y is a divalent bridging moiety;

R′ 1 and R′ 2 are independently hydrogen or a C 1-4 alkyl;

G is independently a hydrolyzable group;

R′ 3 is independently a C 1-18 alkyl, a C 1-10 fluoroalkyl, or a C 6-12 substituted or unsubstituted aryl;

c is an integer from 1 to 3;

d is 0 or 1;

a is a mole fraction of from about 0.01 to about 0.99;

b is a mole fraction of from about 0.99 to about 0.01; and

a+b is 1.00 or less,

with optionally at least one additional silane monomer having at least one functional group thereon;

and further comprising a second charge transport layer disposed between said charge generating layer and said first charge transport layer wherein said second charge transport layer comprises the charge transport polymer.

2. An electrophotographic element according to claim 1 , wherein

said first charge transport layer comprises a silsesquioxane of the condensed reaction product of the charge transport polymer

from about 5 to 30 weight percent of basic surface charge colloidal silica based on the weight of the silsesquioxane, wherein the basic surface charge colloidal silica is stabilized with a sodium salt of silanol, and condensation is catalyzed by acetic acid, with optionally at least one additional silane monomer having at least one functional group thereon.

3. The electrophotographic element of claim 2 wherein G is selected from halogen, hydroxyl, or C 1-6 alkoxy groups.

4. The electrophotographic element of claim 2 wherein the tertiary amine charge transport moiety has an oxidation potential of from about 0.6 to about 1.2 volts versus a standard calomel electrode.

5. The electrophotographic element of claim 2 wherein d is 1.

6. The electrophotographic element of claim 5 wherein X is selected from the group consisting of an ester residue —COO— or —OCO—; oxygen; an arylene moiety having up to about 18 carbon atoms; an alkylene moiety having up to about 6 carbon atoms; and combinations thereof.

7. The electrophotographic element of claim 2 wherein Y is selected from the group consisting of an ester residue —COO— or —OCO—; oxygen; an arylene moiety having up to about 18 carbon atoms; an alkylene moiety having up to about 6 carbon atoms; and combinations thereof.

8. The electrophotographic element of claim 2 wherein a is from about 0.1 to about 0.9.

9. The electrophotographic element of claim 2 wherein a is from about 0.15 to about 0.85.

10. The electrophotographic element of claim 2 wherein a is from about 0.25 to about 0.8.

11. The electrophotographic element of claim 2 wherein c is 2.

12. The electrophotographic element of claim 2 wherein c is 3.

13. The electrophotographic element of claim 12 wherein G is methoxy.

14. The electrophotographic element of claim 2 wherein R′ 1 and R′ 2 are independently hydrogen or methyl.

15. The electrophotographic element of claim 2 wherein the optional at least one silane monomer is present.

16. The electrophotographic element of claim 15 wherein the at least one silane monomer is an alkyltrialkoxysilane.

17. The electrophotographic element of claim 15 wherein the at least one silane monomer is at least one alkyltrialkoxysilane corresponding to the formula:

R 1 —Si—(OR 2 ) 3

wherein

R 1 is an aliphatic, cycloaliphatic, or aromatic group containing up to about 18 carbon atoms, and

R 2 is an alkyl group containing 1 to about 6 carbon atoms.

18. The electrophotographic element of claim 17 wherein R 1 is selected from the group consisting of alkyls containing up to about 18 carbon atoms, fluoroalkyl containing up to about 18 carbon atoms, cycloalkyl containing 5 to about 12 carbon atoms, and aryl containing 6 to about 12 carbon atoms.

19. The electrophotographic element of claim 17 wherein R 1 is an alkyl group containing 1 to about 3 carbon atoms.

20. The electrophotographic element of claim 17 wherein R 1 is a methyl group.

21. The electrophotographic element of claim 15 wherein the at least one silane monomer is methyltrimethoxysilane.

22. The electrophotographic element of claim 2 wherein A is selected from the group consisting of:

and mixtures thereof, wherein R 1 , R 2 , R 3 , R 4 and R 5 are independently in each CTM structure selected from hydrogen, an alkyl group having 1 to about 6 carbon atoms, or an alkoxy group having 1 to about 6 carbon atoms.

23. The electrophotographic element of claim 2 wherein the first charge transport layer is an overcoat layer overlying the charge generation layer.

24. The electrophotographic element of claim 23 wherein said first charge transport layer has a thickness of about 0.5 micron to about 10 microns.

25. The electrophotographic element of claim 23 wherein said first charge transport layer has a thickness of about 1 micron to about 3 microns.

26. The electrophotographic element of claim 2 wherein the condensed reaction product is prepared in a polar solvent medium.

27. The electrophotographic element of claim 26 wherein the polar solvent medium comprises water.

28. The electrophotographic element of claim 27 wherein the polar solvent medium further comprises a water-miscible organic solvent.

29. The electrophotographic element of claim 28 wherein said water-miscible organic solvent is selected from the group consisting of methanol, ethanol, isopropyl alcohol, methyl isobutyl ketone, and mixtures thereof.

30. The electrophotographic element of claim 2 further comprising a baffler layer overlying said electrically conducting layer.

31. The electrophotographic element of claim 2 wherein the first charge transport layer has a thickness of up to about 40 microns.

32. An electrophotographic element comprising:

an electrically conducting layer;

a charge generating layer overlying said electrically conducting layer; and

a first charge transport layer overlying said electrically conducting layer, said first charge transport layer comprising the condensed reaction product of a charge transport polymer comprising structural units having the formula:

wherein:

A is a tertiary arylamine charge transport moiety;

X is a divalent bridging moiety;

Y is a divalent bridging moiety;

R′ 1 and R′ 2 are independently hydrogen or a C 1-4 alkyl;

G is independently a hydrolyzable group;

R′ 3 is independently a C 1-18 alkyl, a C 1-10 fluoroalkyl, or a C 6-12 substituted or unsubstituted aryl;

c is an integer from 1 to 3;

d is 0 or 1;

a is a mole fraction of from about 0.01 to about 0.99;

b is a mole fraction of from about 0.99 to about 0.01; and

a+b is 1.00 or less,

with optionally at least one additional silane monomer having at least one functional group thereon;

and further comprising a second charge transport layer disposed between said charge generating layer and said first charge transport layer wherein said second charge transport layer comprises the condensed reaction residue of the charge transport polymer.

33. An electrophotographic element according to claim 32 , wherein said first charge transport layer comprises a silsesquioxane of the condensed reaction product of the charge transport polymer and from about 5 to 30 weight percent of basic surface charge colloidal silica based on the weight of the silsesquioxane, wherein the basic surface charge colloidal silica is stabilized with a sodium salt of silanol, and condensation is catalyzed by acetic acid, with optionally at least one additional silane monomer having at least one functional group thereon.

34. The electrophotographic element of claim 33 wherein G is selected from halogen, hydroxyl, or C 1-6 alkoxy groups.

35. The electrophotographic element of claim 33 wherein the tertiary amine charge transport moiety has an oxidation potential of from about 0.6 to about 1.2 volts versus a standard calomel electrode.

36. The electrophotographic element of claim 33 wherein d is 1.

37. The electrophotographic element of claim 33 wherein X is selected from the group consisting of an ester residue —COO— or —OC—; oxygen; an arylene moiety having up to about 18 carbon atoms; an alkylene moiety having up to about 6 carbon atoms; and combinations thereof.

38. The electrophotographic element of claim 33 wherein Y is selected from the group consisting of an ester residue —COO— or —OCO—; oxygen; an arylene moiety having up to about 18 carbon atoms; an alkylene moiety having up to about 6 carbon atoms; and combinations thereof.

39. The electrophotographic element of claim 33 wherein a is from about 0.1 to about 0.9.

40. The electrophotographic element of claim 33 wherein a is from about 0.15 to about 0.85.

41. The electrophotographic element of claim 33 wherein a is from about 0.25 to about 0.8.

42. The electrophotographic element of claim 33 wherein c is 2.

43. The electrophotographic element of claim 33 wherein c is 3.

44. The electrophotographic element of claim 43 wherein G is methoxy.

45. The electrophotographic element of claim 33 wherein R′ 1 and R′ 2 are independently hydrogen or methyl.

46. The electrophotographic element of claim 33 wherein the optional at least one silane monomer is present.

47. The electrophotographic element of claim 46 wherein the at least one silane monomer is an alkyltrialkoxysilane.

48. The electrophotographic element of claim 46 wherein the at least one silane monomer is at least one alkyltrialkoxysilane corresponding to the formula:

R 1 —Si—(OR 2 ) 3

wherein

R 1 is an aliphatic, cycloaliphatic, or aromatic group containing up to about 18 carbon atoms, and

R 2 is an alkyl group containing 1 to about 6 carbon atoms.

49. The electrophotographic element of claim 48 wherein R 1 is selected from the group consisting of alkyls containing up to about 18 carbon atoms, fluoroalkyl containing up to about 18 carbon atoms, cycloalkyl containing 5 to about 12 carbon atoms, and aryl containing 6 to about 12 carbon atoms.

50. The electrophotographic element of claim 48 wherein R 1 is an alkyl group containing 1 to about 3 carbon atoms.

51. The electrophotographic element of claim 48 wherein R 1 is a methyl group.

52. The electrophotographic element of claim 46 wherein the at least one silane monomer is methyltrimethoxysilane.

53. The electrophotographic element of claim 33 wherein A is selected from the group consisting of:

and mixtures thereof, wherein R 1 , R 2 , R 3 , R 4 and R 5 are independently in each CTM structure selected from hydrogen, an alkyl group having 1 to about 6 carbon atoms, or an alkoxy group having 1 to about 6 carbon atoms.

54. The electrophotographic element of claim 33 wherein the first charge transport layer is an overcoat layer overlying the charge generation layer.

55. The electrophotographic element of claim 54 wherein said first charge transport layer has a thickness of about 0.5 micron to about 10 microns.

56. The electrophotographic element of claim 54 wherein said first charge transport layer has a thickness of about 1 micron to about 3 microns.

57. The electrophotographic element of claim 33 wherein the condensed reaction product is prepared in a polar solvent medium.

58. The electrophotographic element of claim 57 wherein the polar solvent medium comprises water.

59. The electrophotographic element of claim 58 wherein the polar solvent medium further comprises a water-miscible organic solvent.

60. The electrophotographic element of claim 59 wherein said water-miscible organic solvent is selected from the group consisting of methanol, ethanol, isopropyl alcohol, methyl isobutyl ketone, and mixtures thereof.

61. The electrophotographic element of claim 33 further comprising a barrier layer overlying said electrically conducting layer.

62. The electrophotographic element of claim 33 wherein the first charge transport layer has a thickness of up to about 40 microns.

Assignments (3)
SECURITY INTEREST Recorded Feb 21, 2012
From: EASTMAN KODAK COMPANY; PAKON, INC.
To: CITICORP NORTH AMERICA, INC., AS AGENT
Reel/Frame 028201/0420 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 21, 2004
From: NEXPRESS DIGITAL L.L.C. (FORMERLY HEIDELBERG DIGITAL L.L.C.)
To: EASTMAN KODAK COMPANY
Reel/Frame 015637/0985 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 26, 2004
From: JIN, XIN; FERRAR, WAYNE T.; WEISS, DAVID S.; SORRIERO, LOUIS J.
To: HEIDELBERG DIGITAL L.L.C.; NEXPRESS SOLUTIONS LLC
Reel/Frame 014290/0033 →