Claims
- 1. A charge transporting material comprising a 1,3-pentadiene derivative having formula (I):
- A--CH.dbd.CH--CH.dbd.CH--CH.sub.2 --A (I)
- wherein A represents a 9-anthryl group which may have a substituent, a N-substituted carbazolyl group which may have a substituent, a N-substituted phenothiazinyl group or ##STR180## in which Ar represents an arylene group which may have a substituent, R.sup.1 and R.sup.2 each represent an alkyl group which may have a substituent, an aralkyl group which may have a substituent, an aralkyl group which may have a substituent, or an aryl group which may have a substituent.
- 2. The charge transporting material as claimed in claim 1, wherein the substituent of said 9-anthryl group is a halogen.
- 3. The charge transporting material as claimed in claim 1, wherein the substituent of said N-substituted carbazolyl group is selected from the group consisting of an unsubstituted or substituted alkyl group having 1 to 4 carbon atoms, and an unsubstituted or substituted phenyl group.
- 4. The charge transporting material as claimed in claim 1, wherein the substituent of said N-substituted phenothiazinyl group is an alkyl group having 1 to 4 carbon atoms.
- 5. The charge transporting material as claimed in claim 1, wherein the substituent of said arylene group represented by Ar is selected from the group consisting of an alkyl group having 1 to 4 carbon atoms and an alkoxyl group having 1 to 4 carbon atoms.
- 6. The charge transporting material as claimed in claim 1, wherein the alkyl group represented by R.sup.1 or R.sup.2 is an alkyl group having 1 to 4 carbon atoms.
- 7. The charge transporting material as claimed in claim 1, wherein the substituent of the aralkyl group or aryl group represented by R.sup.1 or R.sup.2 is selected from the group consisting of an alkyl group having 1 to 4 carbon atoms, an alkoxyl group having 1 to 4 carbon atoms, a halogen, and a phenyl group.
- 8. An electrophotographic photoconductor comprising an electroconductive support and a photoconductive layer formed thereon comprising at least one 1,3-pentadiene derivative having the formula (I):
- A--CH.dbd.CH--CH.dbd.CH--CH.sub.2 --A (I)
- wherein A represents a 9-anthryl group which may have a substituent, a N-substituted carbazolyl group which may have a substituent, a N-substituted phenothiazinyl group or ##STR181## in which Ar represents an arylene group which may have a substituent, R.sup.1 and R.sup.2 each represent an alkyl group which may have a substituent, an aralkyl group which may have a substituent, an aralkyl group which may have a substituent, or an aryl group which may have a substituent.
- 9. The electrophotographic photoconductor as claimed in claim 8, wherein said photoconductive layer comprises a charge generating material dispersed in a charge transporting medium comprising said 1,3-pentadiene derivative and a binder agent.
- 10. The electrophotographic photoconductor as claimed in claim 8, wherein said photoconductive layer comprises a charge generation layer containing a charge generating material, and a charge transport layer containing said 1,3-pentadiene derivative as a charge transporting material.
- 11. The electrophotographic photoconductor as claimed in claim 8, wherein the amount of said 1,3-pentadiene derivative is in the range of 30 wt. % to 70 wt. % of the entire weight of said photoconductive layer.
- 12. The electrophotographic photoconductor as claimed in claim 9, wherein the amount of said 1,3-pentadiene derivative is in the range of 10 wt. % to 95 wt. % of the entire weight of said photoconductive layer, and the amount of said charge generating material is in the range of 0.1 wt. % to 50 wt. % of the entire weight of said photoconductive layer.
- 13. The electrophotographic photoconductor as claimed in claim 10, wherein the amount of said charge generating material is in the range of 10 wt. % to 95 wt. % of the entire weight of said charge generation layer, and the amount of said 1,3-pentadiene derivative is in the range of 10 wt. % to 95 wt. % of the entire weight of said charge transport layer.
- 14. The electrophotographic photoconductor as claimed in claim 8, wherein said photoconductive layer has a thickness in the range of 3 to 50 .mu.m.
- 15. The electrophotographic photoconductor as claimed in claim 14, wherein said photoconductive layer has a thickness in the range of 5 to 10 .mu.m.
- 16. The electrophotographic photoconductor as claimed in claim 8, wherein said photoconductive layer contains a sensitizer dye in the amount of 0.1 to 5 wt. % of the total weight.
- 17. The electrophotographic photoconductor as claimed in claim 10, wherein said charge generation layer has a thickness of 5 .mu.m or less, and said charge transport layer has a thickness of about 3 to 50 .mu.m.
- 18. The electrophotographic photoconductor as claimed in claim 8, which further comprises an adhesive or barrier layer between said electroconductive layer and said photoconductive layer, said adhesive or barrier layer having a thickness of 1 .mu.m or less.
Priority Claims (1)
Number |
Date |
Country |
Kind |
63-101316 |
Apr 1988 |
JPX |
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Parent Case Info
This is a division of application Ser. No. 07/751,673, now U.S. Pat. No. 5,166,438, filed on Aug. 23, 1991, which is a continuation of application Ser. No. 07/342,970, filed on Apr. 25, 1989, now abandoned.
US Referenced Citations (3)
Number |
Name |
Date |
Kind |
4485160 |
Suzuki et al. |
Nov 1984 |
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4521605 |
Okazaki et al. |
Jun 1985 |
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4981768 |
Monbaliu et al. |
Jan 1991 |
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Divisions (1)
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Number |
Date |
Country |
Parent |
751673 |
Aug 1991 |
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Continuations (1)
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Number |
Date |
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Parent |
342970 |
Apr 1989 |
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