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US4330608A Expired / Lapsed US ⏱️ 0.0 years remaining

Benzotriazole stabilized photosensitive device

Assignee: Xerox Corp
•
Filing: 1980-12-11
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Granted: 1982-05-18
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Expires: 2000-12-11
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Abstract

Abstract An imaging member comprising a hole generation layer and a contiguous hole transport layer, said generation layer comprising a photoconductive material exhibiting the capability of photogeneration of holes and injection of said holes, said hole transport layer comprising a di or triarylmethane compound of the general formula: ##STR1## wherein R 1 and R 2 are independently selected from the group consisting of a C 1 -C 8 alkyl, aryl, alkaryl and aralkyl, where said aryl is a phenyl group or a condensed ring group, where the alkyl group of said alkaryl and aralkyl is a C 1 -C 4 group; R 3 is independently selected from the group consisting of hydrogen and CH 3 ; and R 4 is the same as R 1 and R 2 or a disubstituted aminophenyl group wherein the substituents are independently selected from the group consisting of a C 1 -C 8 alkyl, aryl, alkaryl and aralkyl as defined supra, said di or triarylmethane is dissolved in a polycarbonate resinous material, said charge transport layer being substantially nonabsorbing in the spectral region at which the photoconductive material generates and injects said holes, but being capable of supporting the injection of said holes and transporting said holes through said transport layer and dissolved in said transport layer a stabilizing proportion of a substituted or unsubstituted 2-(2'-hydroxyphenyl)-benzotriazole.

Inventors

  • 👤 William W. Limburg
  • 👤 Damodar M. Pai

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-04 17:53
CPC Classifications
G; G03; G03G; G03G5/00; G03G5/02; G03G5/04; G03G5/06; G03G5/0622; G03G5/0624; G03G5/0627; G03G5/0633; G03G5/0601; G03G5/0612; G03G5/0614; G03G5/06142; G03G5/06144

Claims Analysis

Total Claims: 6
Claim 1
Independent Claim 243 words
In an imaging member comprising a hole generation layer and a contiguous hole transport layer, said generation layer comprising a photoconductive material exhibiting the capability of photogeneration of holes and injection of said holes, said hole transport layer comprising a di or triarylmethane compound of the general formula: ##STR4## wherein R 1 and R 2 are independently selected from the group consisting of a C 1 -C 8 alkyl, aryl, alkaryl and aralkyl, where said aryl is a phenyl group or a condensed ring group, the alkyl group of said alkaryl and aralkyl is a C 1 -C 4 group; R 3 is independently selected from the group consisting of hydrogen and CH 3 ; and R 4 is the same as R 1 and R 2 or a disubstituted aminophenyl group wherein the substituents are independently selected from the group consisting of a C 1 -C 8 alkyl, aryl, alkaryl and aralkyl, said di or triarylmethane is dissolved in a polycarbonate resinous material in a proportion of about 25-75% by weight, said charge transport layer being substantially nonabsorbing in the spectral region at which the photoconductive material generates and injects said holes, but being capable of supporting the injection of said holes and transporting said holes through said transport layer, the improvement consisting of stabilizing said triarylmethane compound against the deleterious effects of ultraviolet light by the presence in said transport layer of a stabilizing proportion of a substituted or unsubstituted 2-(2'-hydroxyphenyl)-benzotriazole.
Claim 2
Dependent Claim 243 words
In an imaging member comprising a hole generation layer and a contiguous hole transport layer, said generation layer comprising a photoconductive material exhibiting the capability of photogeneration of holes and injection of said holes, said hole transport layer comprising a di or triarylmethane compound of the general formula: ##STR4## wherein R 1 and R 2 are independently selected from the group consisting of a C 1 -C 8 alkyl, aryl, alkaryl and aralkyl, where said aryl is a phenyl group or a condensed ring group, the alkyl group of said alkaryl and aralkyl is a C 1 -C 4 group; R 3 is independently selected from the group consisting of hydrogen and CH 3 ; and R 4 is the same as R 1 and R 2 or a disubstituted aminophenyl group wherein the substituents are independently selected from the group consisting of a C 1 -C 8 alkyl, aryl, alkaryl and aralkyl, said di or triarylmethane is dissolved in a polycarbonate resinous material in a proportion of about 25-75% by weight, said charge transport layer being substantially nonabsorbing in the spectral region at which the photoconductive material generates and injects said holes, but being capable of supporting the injection of said holes and transporting said holes through said transport layer, the improvement consisting of stabilizing said triarylmethane compound against the deleterious effects of ultraviolet light by the presence in said transport layer of a stabilizing proportion of a substituted or unsubstituted 2-(2'-hydroxyphenyl)-benzotriazole.
Claim 3
Dependent Claim 62 words
The member of claim 1 wherein the benzotriazole has the following general formula: ##STR5## wherein R 1 is hydrogen or a C 1 -C 5 alkyl, an aryl, alkaryl, aralkyl, sulfhydryl, NO 2 or a halogen; and R 2 and R 3 are independently selected from the group consisting of hydrogen, a C 1 -C 5 alkyl, aryl, alkaryl or aralkyl group.
Claim 4
Dependent Claim 24 words
The member of claim 2 wherein said transport layer is stabilized by a member selected from the group consisting of 2-(2'-hydroxy-3'-t-butyl-5'-methylphenyl)-5-chlorobenzotriazole; 2-(2'-hydroxy-5'-methylphenyl)-benzotriazole; and 2-(2'-hydroxy-3',5'-di-t-butylphenyl)-benzotriazole.
Claim 5
Dependent Claim 19 words
The member of claim 3 wherein said photoconductive material is trigonal selenium and said triaryl methane compound is bis(4-diethylamino-2-methylphenyl)phenylmethane.
Claim 6
Dependent Claim 26 words
The member of claim 3 wherein the benzotriazole compound is present in from about 0.1-10 percent by weight based on the weight of the transport molecule.

References Cited (Backward Citations)

US3004896A Cited
US3253921A Cited
US3542547A Cited
US3533794A Cited
US4050935A Cited
US4115116A Cited
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USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1985-05-17 1985-11-16 1986-05-18 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1989-05-17 1989-11-16 1990-05-18 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1993-05-17 1993-11-16 1994-05-18 $7700.00 Window Closed / Lapsed

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