AU604428B2 - Photosensitive member for electrophotography - Google Patents
Photosensitive member for electrophotography Download PDFInfo
- Publication number
- AU604428B2 AU604428B2 AU47087/89A AU4708789A AU604428B2 AU 604428 B2 AU604428 B2 AU 604428B2 AU 47087/89 A AU47087/89 A AU 47087/89A AU 4708789 A AU4708789 A AU 4708789A AU 604428 B2 AU604428 B2 AU 604428B2
- Authority
- AU
- Australia
- Prior art keywords
- member according
- charge
- layer
- potential
- transport layer
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/153—Charge-receiving layers combined with additional photo- or thermo-sensitive, but not photoconductive, layers, e.g. silver-salt layers
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/02—Charge-receiving layers
- G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
- G03G5/06—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
- G03G5/0601—Acyclic or carbocyclic compounds
- G03G5/0612—Acyclic or carbocyclic compounds containing nitrogen
- G03G5/0614—Amines
- G03G5/06142—Amines arylamine
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Photoreceptors In Electrophotography (AREA)
Description
1 *-YIIII C-L 4 48s F Ref: 116420 FORM COMMONWEALTH OF AUSTRALIA PATENTS ACT 1952 COMPLETE SPECIFICATION
(ORIGINAL)
FOR OFFICE USE: Class Int Class Complete Specification Lodged: Accepted: Published: Priority: Related Art: Name and Address of Applicant: Canon Kabushiki Kaisha 3-30-2 Shimomaruko Ohta-ku Tokyo
JAPAN
Address for Service: Spruson Ferguson, Patent Attorneys Level 33 St Martins Tower, 31 Market Street Sydney, New South Wales, 2000, Australia Complete Specification for the invention entitled: Photosensitive Member for Electrophotography The following statement is a full description of this invention, including the best method of performing it known to me/us rt C Cr 5845/3
II--
ABSTRACT OF THE DISCLOSURE A photosensitive member for electrophotography, including an electroconductive substrate and a photosensitive layer disposed thereon, wherein the photosensitive layer comprises a triarylamine compound represented by the following general formula
R
1 R 2 Ar2 wherein Ari and Ar 2 respectively denote a benzene ring capable of having a substituent; at least one of Ar 1 and Ar 2 has an electron-donating substituent; and R 1 and R 2 respectively denote a hydrogen atom, alkyl or 15 alkoxyl.
0 0 o o 0. o 00
OO
0 00 00o 0 0 0 0 00 0 0 yu017/1074 4.
PHOTOSENSITIVE MEMBER FOR ELECTROPHOTOGRAPHY FIELD OF THE INVENTION AND RELATED ART The present invention relates to a photosensitive member for electrophotography, particularly to a photosensitive member for electrophotography comprising a low-molecular weight organic photoconductor capable of providing improved electrophotographic characteristics.
Hitherto, there have been proposed a large number of organic photoconductive polymers to be used for electrophotographic photosensitive members, such as polyvinyl carbazole. These conventional organic polymers are superior to inorganic photoconductive 15 materials in lightness (in weight), film-forming 0 i4 °O property, etc., but are inferior to the latter in 0a* °0o0 sensitivity, durability, stability to environmental 0 change, mechanical strength, etc.
SOn the other hand, there have been proposed several low-molecular weight organic photoconductive materials such as hydrazone compound Patent 4,150,987), triaryl pyrazoline compound Patent 3,837,851), and 9-styryl anthracene (Japanese Laid-Open SPatent Application (JP-A, KOKAI) Nos. 94828/1976 and S 25 94829/1976).
0004 In a case where the conventional low-molecular 0 ,0 weight organic photoconductors represented by those as rT -2described above are used, the above-mentioned defect in film-forming property, which has conventionally posed a problem in the field of the organic photoconductive polymer, may be obviated by appropriately selecting a binder to be used in combination therewith. However, these conventional organic photoconductors have not provide a sufficient sensitivity.
In such a viewpoint, there has recently been proposed a laminate-type structure wherein the photosensitive layer is function-separated into a charge generation layer and a charge transport layer.
The electrophotographic photosensitive member comprising such a photosensitive layer may be improved in sensitivity to visible light, charge retentivity, 15 surface strength, etc.
90 i As the charge-transporting substance constituting the above-mentioned transport layer, a i large number of organic compounds have heretofore been proposed. Examples thereof include: pyrazoline compounds (Japanese Laid-Open Patent Application No.
72231/1977), hydrazone compounds Patent 842,431 i and Japanese Laid-Open Patent Application No.
52063/1980), triphenylamine compounds (Japanese Laid- Open Patent Application Nos. 195254/1982 and 58445/1979), stilbene compounds (Japanese Laid-Open tc, Patent Application Nos. 151955/1979 and 198043/1983), P' s carbazole compounds (Japanese Laid-Open Patent -3- Application Nos. 150128/1979 and 58451/1988), benzothiophene compounds (Japanese Laid-Open Patent Application No. 110835/1979), etc.
However, in the electrophotographic photosensitive member using the conventional lowmolecular weight organic compound as the chargetransporting substance, the sensitivity and other electrophotographic characteristics are not necessarily sufficient, and the light part potential and dark part potential are liable to show a considerable change, when charging and exposure operations are conducted repetitively.
Accordingly, with respect to such an electrophotographic photosensitive member, there is a is 15 still room for improvement.
S
l SUMMARY OF THE INVENTION An object of the present invention is to provide an electrophotographic photosensitive member which has solved the above-mentioned various problems encountered in the conventional photosensitive member.
Another object of the present invention is to provide an electrophotographic photosensitive member using a novel organic photoconductor which may easily be produced, is relatively inexpensive and is excellent in durability.
According to the present invention, there is -4provided a photosensitive member for electrophotography, comprising an electroconductive substrate and a photosensitive layer disposed thereon, wherein the photosensitive layer comprises a triarylamine compound represented by the following general formula
R
1
R
2 Ar 1 SAr N Ar 2 wherein Ar 1 and Ar 2 respectively denote a benzene ring capable of having a substituent; at least one of Ar, and Ar 2 has an electron-donating substituent; and R 1 and R 2 respectively denote a hydrogen atom, alkyl or alkoxyl.
15 These and other objects, features and 0 09 .o advantages of the present invention will become more 0 0 apparent upon a consideration of the following description of the preferred embodiments of the present invention taken in conjunction with the accompanying drawings.
BRIEF DESCRIPTION OF THE DRAWINGS Figures 1 and 2 show infrared absorption spectra of Compound Example Nos. 10 and 13, respectively, according to the KBr tablet (or pellet) method.
t DETAILED DESCRIPTION OF THE INVENTION In the above general formula Ar 1 and Ar 2 respectively denote a benzene ring capable of having one or more substituent. At least one of Ar 1 and Ar 2 has an electron-donating (or electron donative) group as a substituent. The "electron-donating substituent" used herein refers to a substituent having a greater electron-donating ability than a hydrogen atom.
Specific examples of the electron-donating group may include: alkyl groups (preferably C 1 to C 3 such as methyl, ethyl and propyl; alkoxyl groups (preferably C 1 to C 3 such as methoxy and ethoxy groups; substituted amino group (preferably, disubstituted amino group) such as dimethylamino and 15 diethylamino groups; etc. The substituent of the amino group may preferably be C 1 to C 3 R1 and R 2 respectively denote a hydrogen atom, alkyl groups (preferably C 1 to C 3 such as methyl, ethyl and propyl; alkoxyl groups (preferably CI to C 3 20 such as methoxy and ethoxy.
Incidentally, it has heretofore been known that a triarylamine compound is used as a chargetransporting substance. However, in general, such a conventional triarylamine compound has provided a low sensitivity.
In the present invention, an electron-donating substituent is introduced into at least one of the o 0 0 0n S0 0 o 000 00 0 0 -6benzene rings of ArI and Ar 2 in the above-mentioned formula As a result, according to the present invention, there is provided a charge-transporting substance which is capable of providing high sensitivity and high durability, and may easily be synthesized inexpensively, whereby the problems encountered in the prior art have been solved.
Particularly, a compound of the abovementioned formula having an oxidation potential of 0.9 V or below wherein at least one electron-donating group is introduced into the benzene ring of Ar, and/or Ar 2 may provide an excellent electrophotographic characteristic. Further, such a compound having an oxidation potential of 0.60 V or above and 0.88 V or below may provide an electrophotographic photosensitive member having an extremely high sensitivity.
According to our investigation, it may be considered that the compound having an oxidation potential of above 0.9 V only provides insufficient carrier injection property from a charge-generation layer. On the other hand, the compound having an oxidation potential of below 0.60 V provides relatively large dark decay and relatively high residual potential to deteriorate the electrophotographic characteristic, while the reason for such a phenomenon is not necessarily clear.
Therefore, among the compounds represented by -7the above-mentioned general formula a compound having an oxidation potential of 0.6 0.88 V wherein at least one of the benzene rings of Ar 1 and Ar 2 has an electron-donating substituent is particularly preferred since such a compound may provide an electrophotographic photosensitive member having excellent electrophotographic characteristics.
Representative examples of the compound of the above-mentioned formula are described hereinbelow.
However, the compound represented by the formula (I) usable in the present invention is not restricted to these specific examples.
In the following description, "EOX" denotes an oxidation potential (volt).
_X
-8- <Compound Examples> 1. CH 3 (EOX 0.87) 2.
CH
3 0 oN (EOx 0.88) 3. c~w Q (Eo 0.86) 4. c 3
H
7
Q
(EOX 0. 86) CHO Q (EOX= 0.81) 6. C 2
H
5 0 Q (EOx 0.86) -9- (Eox 0.87)
CM
3
CH
3 Q (Eox 0.85)
C!H-.
CH0
N-Q
(Eox 0.78)
S.
SI;
II
S S S S St
'III
'S
CH
3 0
CM
3 0
CH
3 0<
D
(Eox =0.86) 11.
(Eox =0.86) 4 5 55 S S S St
CH
3 0 0
CH
3 (Eax 0.88)
CH
3 O0Q
CH
3 O 0
CH
3 0
NQNQ
CH
3 0
CH
3
C
2 H 5 0QX (E ox 0.69) (E ox 0.85) 0 000 0 00 00 1 0 00 0000 0000 00 0 1 I 0~ 01 0000 0 II 0 II to I O 14 O 40 104000 O 1
CR
3 0,D (E ox 0.84) (E ox 0.83) 17.
CH
3 O 0 25 CR 3 0-O (Eox 0.77) -11 19.
C
2 oc 5 0N oQ
CH
3 O
Q/
CH
3 0o
CH
3 O0D
CH
3 0 (Eax 0.68) (E ox 0.79) 20.
(Eox 0.98) 1*1
S
It,
CH
3
CH
3 0q
N
CH
3
CH
3 0 Eox 0.82) (Eox 0.83) t I C~ II I S I I I II IjISSI S S -12-
C
2 H 5 0 -c Qo
C
2
H
5 0 Q
C
3
H
7 0 Q
N-
(CH
3 2 CH
QO
(CH
3 2 CH-CQ
C
4
H
9 Ql
C
4 H 9 Q
CH
3 -0 1
Q
CH
3 Q
CH
3
CH
3 (E ox 0. 68) (E ox 0.80) 26.
(Eox 0. 87) (Eox 0. (Ex 0.82) Eox 0.99) II-~ Ilra i -13- 29. CCH 3
CH
3 00
CH
3 iCH
(C
2
H
5 2
N-
0o N (E X 0.61) (E X 0.41) 0 o rot 0 4«f
I
41 *r i 444' c ic 4 44 4 44 t I Measurement of oxidation potential The oxidation potential values referred to in the present invention are based on a measurement using a potential-sweeping method wherein a saturated calomel electrode was used as the reference electrode, and a 0.1 N solution of (n-Bu) 4 N+ClO4 in acetonitrile was used as the electrolytic solution. In this measurement, the potential of the working electrode comprising platinum was swept to obtain a currentpotential curve. The oxidation potential was defined as the potential value corresponding to the peak of the thus obtained current-potential curve.
More specifically, a sample was dissolved, at a concentration of about 5 10 mmol in an electrolytic solution of 0.1 N (n-Bu) 4 N+C104 in acetonitrile. Then, a voltage was externally applied -14to the resultant sample solution, and a change in current was measured while linearly changing the voltage from a low potential value, theareby to obtain a current-potential curve. In this measurement, a counter electrode comprising platinum was used, and the potential (difference) between the working electrode and the counter electrode was measured while the potential (difference) between the reference electrode and the counter electrode was defined as 0 (zero). In the present invention, the oxidation potential was determined by the potential value corresponding to the peak of the current value in the above-mentioned current-potential curve.
The above-mentioend Compound Example may be synthesized in the following manner.
<Synthesis of Compound Example No. r 5.0 g (0.025 mol) of ditolylamine, 14.2 g 0 t la f(0.051 mol) of iodobiphenyl, 13.8 g (0.100 mol) of t anhydrous potassium carbonate, 3.0 g of copper power (0.047 mol) and 50 ml of ortho-dichlorobenzene were charged in a three-necked 200 ml-flask equipped with a thermometer and a condenser, and were heated under A C stirring for 20 hours at a reflux temperature. After the reaction mixture was cooled, the solid content was removed from the reaction mixture by filtration, the filtrate was concentrated under reduced pressure, and then ethanol was added to the resultant product to j r i obtain tan crystals of crude ditolylbiphenylamine.
The crude product was charged to a silica gel column and was developed by using a toluene-hexane solvent to obtain 6.8 g (yield 77.9 of white crystals of purified ditolylbiphenylamine showing a melting point of 126.5 127.7 OC. Figure 1 shows an infrared absorption spectrum chart obtained by measuring the thus obtained compound by a KBr tablet (or pellet) method.
Elemental analysis (C 26
H
23
N)
Theoretical value 89.36 6.63 4.01 Observed value 89.40 6.61 3.99 Further, the above-mentioned Compound Example No. 13 was synthesized in a similar manner as described o° above. Figure 2 shows an infrared absorption spectrum chart obtained by measuring the thus obtained compound 00* in the same manner as described above.
i 0 Since the compound according to the present invention may easily be synthesized in a high yield by using a one-step process as described above, it may 00 provide an inexpensive electrophotographic t photosensitive member.
The other compounds according to the present 25 invention may be synthesized in a similar manner as described in the above Synthesis Example.
In a preferred embodiment of the present -16invention, the photosensitive layer is functionseparated into a charge generation layer and a charge transport layer, and the charge transport layer comprises the triarylamine compound represented by the above-mentioned general formula as a chargetransporting substance.
The charge transport layer according to the present invention may preferably be formed by dissolving the above-mentioned compound of the formula in an appropriate solvent together with a binder, applying the resultant coating liquid such as solution onto a predetermined surface, and drying the resultant coating.
Examples of the binder to be used in the charge transport layer may include: polyarylate 6 resins, polysulfone resins, polyamide resins, acrylic 0. resins, acrylonitrile resins, methacrylic resins, vinyl 44** Schloride resins, vinyl acetate resins, phenol resins, epoxy resins, polyester resins, alkyd resins, 0*#i polycarbonate, polyurethane, or copolymer resins containing two or more of the recurring units of these resins, such as styrene-butadiene copolymers, styreneacrylonitrile copolymers, styrene-maleic acid copolymers, etc. Also, other than such insulating 25 polymers, organic photoconductive polymers such as polyvinylcarbazole, polyvinylanthracene and polyvinylpyrene may be used.
w I -17- In the charge transport layer, the chargetransporting substance may preferably be used in an amount of 10 500 wt. parts, more preferably 50 200 wt. parts, per 100 wt. parts of the binder.
The charge transport layer is electrically connected to the charge generation layer as described hereinafter, and has a function of receiving charge carriers injected from the charge generation layer in the presence of an electric field and of transporting these charge carriers to the surface of the charge transport layer. In such an embodiment, the charge transport layer may be disposed on the charge generation layer, or may be disposed under the charge generation layer. The charge transport layer may preferably be disposed on the charge generation layer.
It is not preferred that the charge transport layer has a too large a thickness, since there is a certain limit to the thickness thereof suitable for the transport of the charge carriers. In general, the charge transport layer may preferably have a thickness of 5 microns, more preferably 10 30 microns.
The organic solvent to be used in the abovementioned formation of the charge transport layer may vary depending on the kind of the binder used therefor, S 25 and may preferably be selected from those which do not substantially dissolve the charge generation layer or a primer (or undercoat) layer as described hereinafter.
Iri- _I -18- Specific examples of such an organic solvent may include: alcohols such as methanol, ethanol, and isopropanol; ketones such as acetone, methyl ethyl ketone, and cyclohexanone; amides such as N,Ndimethylformamide and N,N-dimethylacetamide; sulfoxides such as dimethyl sulfoxide; ethers such as tetrahydrofuran, dioxane, and ethylene glycol monomethyl ether; esters such as methyl acetate and ethyl acetate; aliphatic halogenated hydrocarbons such as chloroform, methylene chloride, dichloroethylene, carbon tetrachloride, and trichloroethylene; aromatic compounds such as benzene, toluene, xylene, monochlorobenzene, and dichlorobenzene; etc.
The coating may be effected by various coating methods such as dip coating, spray coating, wire bar coating, and blade coating. The drying should o 4, preferably be conducted in the sequence of drying at room temperature to a "tack-free" state and then heat drying. In general, the heat drying may preferably be conducted for a time in the range of 5 minutes to 2 hours at a temperature of 30 °C to 200 OC under quiescent condition or under blowing.
The charge transport layer according to the present invention can further contain an additive selected from various species thereof. Examples of such an additive may include: plasticizers such as diphenyl, m-terphenyl and dibutyl phthalates; surface- -19lubricating agents such as silicone oil, graft-type silicone polymers, and various fluorocarbons; potential stabilizing agents such as dicyanovinyl compounds and carbazole derivatives; anti-oxidizing agents such as p-carotene, Ni complexes, and 1,4-diazabicyclo[2,2,2]octane; etc.
The charge generation layer may comprise a charge-generating substance. Specific examples of the charge-generating substance may include: inorganic charge-generating substances such as selenium, selenium-tellurium, and amorphous silicon; and organic charge-generating substances including: cationic dyes such as pyrylium dye, thiapyrylium dye, azulenium dye, thiacyanine dye, and quinocyanine dye; polycyclic quinone pigments such as squarium salt dye, phthalocyanine pigment, anthanthrone pigment, dibenzpyrene-quinone pigment, and pyranthrone pigment; indigo pigment; quinacridone pigment; azo pigment; etc.
These charge-generating substances may be used singly or as a combination of two or more species. The charge generation layer may be formed by using such a chargegenerating substance in the form of a vapor deposition layer or coating layer.
Among the above-mentioned charge-generating substances, the azo pigment particularly includes various types. Representative structures of the azo pigment preferably used in the present invention are described hereinbelow. When the azo pigment is represented by a general formula including the following central skeleton A: AfN=N-Cp)n wherein Cp denotes a coupler portion (or coupler moiety) and n is 2 or 3, specific examples of the central skeleton A include those comprising the following structures: o a 0 I 000 t 4 -21- A-i R R.
O~-CH=C 0 (Rt: Cl, OCH 3
CN)
A- 2 A- 3 R R (0 CICH-o-CH=C 0(R: H, CN) R -NR 0 Q(X: 0, S R: H, CH 3 1 Cl) A- 4 0 00 C I S I.
A-
R
R
0, S R: H, CH 3 1 Cl) A- 6
RR
H, CH 3 Cl, -22- A-7 ©CH 0 A-8 0 9 >CH=CH 0 A- 9 0, S) 0, S) Lit A-il1 N-N1 0 CH=CH- ,LCH=CH
II
N
0 N 7 CH=CH-KO 0, S) H, CH 3 A- 12
X
00-O CH 2 0, S, so 2 A-i13 (C1 C C C C 0 -23- A-i 4 0, S) A-i 0) A- 16 N-N N-N 0)J x c CX: 0, S) A-i 7 A-i 8 =N-N=CH-K0~ 0 A- 19 1 .1 -24- R j A-21 H, CH 3 A-22 -00 Specific examples of the coupler portion Cp include those having the following structures: Cp-1 HO CONH-)-- H OQ R H, halogen atom, alkoxy, alkyl, nitro group, etc.
n 1 or 2) Cp-2 HO CONHR -0Q Cp-3
CH
3
C
2
H
5
C
3
H
7 alkyl or -(R R' H, halogen atom, alkoxy, alkyl, nitro group, etc.) H CONHN=CH-R -0 0Q 2 Cp- 4
H
0 HN-Q0
R
H, halogen atom, alkoxyl, alkyl, niitro group, etc.) N-R or alkyl, aryl, etc.) £9 I I
III
2p::6
C
HO
0 0
HO
n 0
H
N 0 0 2
HO
N
or 0 0 0 00 (Rif R: H, halogen atom, 2alkoxy, alkyl, nitro group, etc.
n =1 or 2) -26- The above-mentioned central structures A and coupler Cp may appropriately be combined to form a pigment as a charge-generating substance.
The charge generation layer may be formed by vapor-depositing such a charge-generating substance by means of a vacuum vapor deposition device, or by applying a dispersion containing such a chargegenerating substanr dispersed therein, together with an appropriate binder as desired.
The binder to d for forming the charge generation layer may be selected from a wide variety of insulating resins or alternatively from organic photoconductive polymers such as polyvinylcarbazole, polyvinylanthracene, and polyvinylpyrene. There may preferably be used the insulating resin such as polyvinyl butyral, polyarylates polycondensation product between bisphenol A and phthalic acid), polycarbonate, polyester, phenoxy resin, acrylic resin, polyacrylamide resin, polyamido, polyvinyl pyridine, cellulose resin, urethane resin, epoxy resin, casein, polyvinyl alcohol, and polyvinyl pyrrolidone.
The resin may preferably be contained in the charge generation layer in an amount of 5 80 wt. more preferably 10 40 wt. Specific examples of the organic solvent usable in the coating of the charge generation layer may include: alcohols such as methanol, ethanol, and -27isopropanol; ketones such as acetone, methyl ethyl ketone, and cyclohexanone; amides such as N,Ndimethylformamide and N,N-dimethylacetamide; sulfoxides such as dimethyl sulfoxide; ethers such as tetrahydrofuran, dioxane, and ethylene glycol monomethyl ether; esters such as methyl acetate and ethyl acetate; aliphatic halogenated hydrocarbons such as chloroform, methylene chloride, dichloroethylene, carbon tetrachloride, and trichloroethylene; aromatic compounds such as benzene, toluene, xylene, monochlorobenzene, and dichlorobenzene; etc.
The charge generation layer may preferably contain the above-mentioned charge-generation substance o in an amount as large as possible, so that it may 0o 15 provide a sufficient absorbance. Further, the charge 9 t 4 generation layer may preferably be a thin layer having a thickness of 5 microns or below, more preferably 0.01 1 micron so that it may inject charge carriers generated therein into the charge transport layer S 20 within the lifetime of the charge carriers. This may t A be attributable to facts such that most of the incident light quantity may preferably be absorbed into the charge generation layer to generate a large number of charge carriers, and that the thus generated charge 25 carriers may preferably be injected into the charge t 0i transport layer without deactivation due to recombination or trapping thereof.
-28- The above-mentioned photosensitive layer having a laminate structure comprising a charge generation layer and a charge transport layer may be disposed on an electroconductive substrate.
The electroconductive substrate may be a Ssubstrate which per se has an electroconductivity such as those of aluminum, aluminum alloy, copper, zinc, and stainless steel; alternatively, the above-mentioned i metal substrate or a substrate of a plastic coated i 10 with, a vacuum vapor-deposited layer of aluminum, i aluminum alloy, indium oxide, tin oxide or indium i oxide-tin oxide alloy, or a mixture of an electroconductive powder (such as aluminum powder, titanium oxide, tin oxide, zinc oxide, carbon black and silver particles) and an appropriate binder; a j substrate of paper or plastic impregnated.with electroconductive particles, or a plastic substrate i coated with an electroconductive polymer layer. The electroconductive substrate may be in any form such as sheet, drum, etc.
Between the electroconductive substrate and i the photosensitive layer, there can be formed a primer or undercoat layer having a barrier function and an adhesive function. The primer layer may comprise e.g., 25 casein, polyvinyl alcohol, nitrocellulose, ethylene- 0: acrylic acid copolymer, polyamide nylon 6, nylon 66, nylon 610, copolymer nylon, alkoxymethylated nylon, -29etc.), polyurethane, gelatin, or aluminum oxide. The thickness of the primer layer should preferably be 0.1 5 microns, particularly 0.5 to 3 microns.
In the electrophotographic photosensitive member according to the present invention, a protective layer can further be disposed on the photosensitive layer. Such a protective layer may comprise a resin, or a resin and an electroconductive material dispersed therein.
In another embodiment of the present invention, a pigment or dye having a photoconductivity may be used as a sensitizer. Examples of such a dye or pigment include: the above-mentioned disazo pigment, S.pyrylium dye, thiapyrylium dye, selenapyrylium dye, benzopyrylium dye, benzothiapyrylium dye, naphthopyrylium dye, and naphthothiapyrylium dye, as described in U.S. Patent 3,554,745; 3,567,438; and 3,586,500.
In a still another embodiment of the present invention, an euteclic (crystal) complex comprising a pyrylium dye (as disclosed in U.S. Patent 3,684,502) and an electrically insulating polymer comprising an alkylidene-diarylene portion may be used as a sensitizer. Such an eutectic complex may be formed by 25 dissolving 4-[4-bis(2-chloroethyl)aminophenyl]-2,6- ,U diphenylthiapyrylium perchlorate and poly(4,4'isopropylidene diphenylene carbonate) in a halogenated i i 1 i i 3
I
I
i i i I j i I ~it~ hydrocarbon-type solvent dichloromethane, chloroform, carbon tetrachloride, 1,1-dichloroethane, 1,2-dichloroethane, 1,1,2-trichloroethane, chlorobenzene, bromobenzene, 1,2-dichlorobenzene, etc.), and then adding a non-polar solvent hexane, octane, decane, 2,2,4-trimethylbenzene, ligroin, etc.) to the resultant mixture so as to produce a particulate eutectic complex. In such an embodiment, the electrophotographic photosensitive member may include a binder such as styrene-butadiene copolymer, silicone resin, vinyl resin, vinylidene chloride-acrylonitrile copolymer, styrene-acrylonitrile copolymer, vinyl acetate-vinyl chloride copolymer, o .o polyvinyl butyral, polymethyl methacrylate, poly-N- 0 0 0 o* 15 butyl methacrylate, polyester, cellulose ester, etc.
0 0 9 The electrophotographic photosensitive member @0 00 0oa according to the present invention may be used not only oa00 for ordinary copying machines but also in the fields related to electrophotography such as laser printers, 20 CRT printers and electrophotographic plate-making.
6 0 t, The present invention will be described in more detail with reference to Examples.
to Example 1 g of a disazo pigment represented by the 1 25 following formula: I t -i i L- UY llrr^-r)1 -31- Cl Cl -HNOC OH CH 3 HO ONHQ 0 0 and a solution obtained by dissolving 2 g of a butyral resin (butyral degree: 63 mol. in 100 ml of cyclohexanone were dispersed for 24 hours by means of a sand mill to prepare a coating liquid. The thus prepared coating liquid was applied onto an aluminum sheet by means of a wire bar to form a charge generation layer having a thickness (after drying) of 0.2 micron.
Then, 10 g of the above-mentioned Compound I II St 15 Example No. 3 and 10 g of a polycarbonate resin (weight-average molecular weight 20,000) were I dissolved in 70 g of monochlorobenzene to prepare a E coating liquid. The coating liquid was applied onto the above-mentioned charge generation layer by means of a wire bar to form a charge transport layer having a Sthickness (after drying) of 20 microns, whereby an !i electrophotographic photosensitive member having a Slaminate structure was prepared.
The thus prepared photosensitive member was charged by using corona KV) according to a static method by means of an electrostatic copying paper tester (Model: SP-428, mfd. by Kawaguchi Denki K,K,) Ir4u ii -32j and retained in a dark place for 1 sec. Thereafter, I the photosensitive member was exposed to light at an Silluminance of 20 lux, to evaluate the charging characteristic. In order to evaluate the charging characteristic, the surface potential (V 0 the ij potential (V 1 obtained after a dark decay of 1 sec, i and the exposure quantity (E 1 required for ii decreasing the potential V 1 to 1/2 thereof were ii measured.
i 10 Further, in order to measure the variations in light part potential and dark part potential in repetitive use, the photosensitive member prepared in this instance was bonded to the cylinder for a photosensitive drum to be used for a plain paper copying (PPC) machine (NP-3525, mfd. by Canon and i !i "subjected to a copying test of 5000 sheets, and thereafter, the variations in the light part potential (VL) and dark part potential (VD) in the initial stage and after the copying of 5000 sheets were determined.
ji |20 The initial VD and VL were set to -700 V and -200 V, |i jrespectively.
sThe results are shown in the following Tab-.e 1.
-L C~gCr"lgL~masro~ssarr_~Parrr~ac Table 1 E1/2 Initial potential Potential after copying of 5000 (lux.sec) sheets (V) VD -700 -680 1.3 VL -200 -207
V
L
U
-34- Examples 2 10, Comparative Examples 1 3 Nine species of photosensitive members were prepared in the same manner as in Example 1 except that the above-mentioned Compound Examples (28) and (30) were respectively used as the charge-transporting substance instead of the Compound Example and that a pigment having the following formula was used as the charge-generating substance (Examples 2 Cl Cl o HNOCHNOC OH N-N HO CONHCONH Q S N=N N=N SThe electrophotographic characteristics of the thus obtained photosensitive members were measured in the same manner as in Example 1.
Further, for the purpose of comparison, three species of photosensitive members were prepared in the same manner as in Example 1 except that the following i comparative compounds were respectively used as the charge-transporting substance (Comparative Examples 1 3).
The electrophotographic characteristics of the thus obtained photosensitive members were measured in the same manner as in Example 1.
F"-
-A.
The results are shown in the following Tables 2 and 3.
Comparative Compounds (1) EOX 0.91
[V]
(disclosed in Japanese Laid-Open Patent Application No. 195254/1982) Cl_ ClQ I -Cl_ EOX 0.98 [V] (disclosed in Japanese Laid-Open Patent Application No. 79450/1980) Q N
C
2
H
S Y/"C 2
H
EOX 0.40 [V] (disclosed in Japanese Laid-Open Patent Application No. 195254/1982) 25 Table 2 Example Compound V 0 v E 12 Initial potential Potential after copying of 5000 sheets Eape (lux.sec) VD (V LI V VD Lj V 2 -702 -690 1.2 -700 -200 -690 -225 E =0.87 3 -685 -680 1 .3 -700 -200 -675 -205 E X=0.81 4 (10) -693 -690 0.8 -700 -200 -690 -205 F X=0.86 (13) -700 -695 0.9 -700 -200 -685 -215 6 (15) -703 -695 0.8 -700 -200 -690 -207 7 (20) -695 -673 2.1 -700 -200 -680 -205
E
0 X=0.98 cont.
Table 2 (cont.) 8 (22) -697 -692 1.2 -700 -200 -670 -215 F X=0.83 9 (28) -680 -650 2.3 -700 -200 -660 -215 E X=0.99 (30) -695 -630 2.9 -700 -200 -540 -235 E X=0.41 4O 00 0 0 0 0 a 4 4 o a I o 000 0 o000 4 0 09 4 60* 0 0 0 0 0 9 0 0 0 0 00 Table 3 Cop. Comp. 0 V1 E1/2 Initial potential Potential after copying of 5000 sheets Example Copounds lux.sec) VD V L
V
D V L
(V)
1 1 -715 -690 3.4 -700 -200 -650 -300 2 2 -650 -600 6.2 -700 -200 -620 -325 3 3 -690 -632 5.4 -700 -200 -570 -375 _1 A1 -39- As apparent from the above-mentioned results obtained in Examples and Comparative Examples, considerably high sensitivity and potential stability in successive copying may be realized by introducing a electron-donating substituent into Ar 1 and/or Ar 2 in the following formula:
R
1
R
2 Ar 1
(I)
Ar 2 Particularly, when the results of Examples 2, 3 and 4 are compared with those of Comparative Example 1, the compounds used in the Examples have a structure similar to that used in Comparative Example 1, but the oxidation potentials of the Examples were decreased to 0.9 V or below due to the introduction of the electrondonating group. The compounds having an oxidation potential of 0.9 V or below clearly provided a high sensitivity, and excellent potential stability in successive copying.
Further, when a group having a considerably strong electron-donating property was introduced into Ar 1 and/or Ar 2 in the formula there was observed a tendency that such a compound provided a somewhat lower sensitivity as compared with that provided by the compound having an oxidation potential of 0.60 0.88
V.
Among the compounds used in the abovementioned Examples, the arylamine compounds represented by the following formulas (III) and (IV) provided a particularly high sensitivity and an excellent potential stability in successive copying.
CH3-
N(IT)
CH
3
-Q
C
2
H
C
2
H
5
Q
(III)
fl 44 e cr a a 4 4 4 I44 044 o o 9 Os *t 44*4 4S 400a0
CH
3 0
CH
3 Example 1 Example 11
(IV)
4 4 0 4o 4 S 0 90 i 4
G
0 0 000000 o 0 0 0 00 A coating liquid obtained by dissolving 5 g of 20 a methoxymethylated nylon resin (number-average molecular weight 32,000) and 10 g of an alcoholsoluble copolymer nylon resin (number-average molecular weight 29,000) in 95 g of methanol was applied onto an aluminum substrate by means of a wire bar to form a 25 primer layer having a thickness of 1 micron (after drying).
Then, 10 g of a charge-generating substance -41represented by the following formula:
C
2
H
HO CONH- Cl Cl a solution obtained by dissolving 5 g of a butyral resin (butyral degree: 63 mol. and 200 g of dioxane were dispersed for 48 hours by means of a ball mill disperser to prepare a coating liquid. The thus prepared coating liquid was applied onto the abovementioned primer layer by a blade coating method to form a charge generation layer having a thickness (after drying) of 0.15 micron.
Then, 10 g of the above-mentioned Compound Example No. 10 and 10 g of a polymethyl methacrylate resin (weight-average molecular weight 50,000) were dissolved in 70 g of monochlorobenzene to prepare a coating liquid. The coating liquid was applied onto the above-mentioned charge generation layer by a blade coating method to form a charge transport layer having tt Itt a thickness (after drying) of 19 microns, whereby an electrophotographic photosensitive member was prepared.
The thus prepared photosensitive member was -42charged by using corona discharge KV) so as to have an initial potential of V 0 left standing in a dark place for 1 sec, and thereafter the surface potential thereof was measured. In order to evaluate the sensitivity, the exposure quantity (El/2, pJ/cm 2 required for decreasing the potential V 1 after the dark decay to 1/2 thereof was measured. The light source used herein was laser light (output: 5 mW, emission wavelength: 780 nm) emitted from a ternary semiconductor comprising gallium/aluminum/arsenic.
The results were as follows:
V
0 -700 V V1: -695 V E1/2: 0.53 pJ/cm 2 The above-mentioned photosensitive member was assembled in a laser beam printer (trade name: LBP-CX, mfd. by Canon as an electrophotographic printer equipped with the above-mentioned semiconductor laser using a reversal development system, and subjected to 20 actual image formation.
The image formation conditions used herein were as follows: Ssurface potential after primary charging: -700 V surface potential after image exposure: -150 V (exposure quantity: 2.0 pJ/cm 2 transfer potential: +700 V polarity of developer: negative i _1; -43process speed: 50 mm/sec developing condition (developing bias): -450 V image exposure scanning system: image scan exposure prior to the primary charging: 50 lux.sec (whole surface exposure using red light) The image formation was effected by linescanning the laser beam corresponding to character and image signals. As a result, good prints were obtained with respect to the characters and images.
Further, when successive image formation of 3,000 sheets was conducted, good prints were stably obtained from the initial stage to 3,000 sheets.
oo Example 12 ooo Exapl 10 g of oxytitanium phthalocyanine was added 15 to a solution obtained by dissolving 5 g of a phenoxy I resin in 485 g of dioxane and dispersed for 2 hours by means of a ball mill. The thus prepared dispersion was applied onto an aluminum sheet by means of a wire bar and then dried at 80 °C for 2 hours to form a charge generation layer having a thickness of 0.5 micron.
Then, 10 g of the above-mentioned Compound Example No. 15 and 10 g of a bisphenol Z-type polycarbonate resin (weight-average molecular weight 50,000) were dissolved in 70 g of monochlorobenzene to prepare a coating liquid. The coating liquid was applied onto the above-mentioned charge generation layer by means of a wire bar and then dried at 110 OC -44for one hour to form a charge transport layer having a thickness of 19 microns, whereby an electrophotographic photosensitive member was prepared.
The thus obtained photosensitive member was evaluated in the same manner as in Example 11. The results were as follows:
V
0 -695 V
V
1 -687 V E1/2: -0.69 pJ/cm 2 Example 13 3 g of 4-(4-dimethylaminophenyl)-2,6diphenylthiapyrilium perchlorate, 5 g of Compound Example No. 10 as a charge-transporting substance, and g of a polyester resin (weight-average molecular weight 49,000) were mixed with 50 g of a solvent comprising toluene and dioxane and dispersed for 6 hours by means of a ball mill. The thus prepared dispersion was applied onto an aluminum sheet by means of a wire bar and then dried at 100 °C for 2 hours to form a photosensitive layer having a thickness of microns, whereby an electrophotographic photosensitive member was prepared.
The thus obtained photosensitive member was evaluated in the same manner as in Example 1. The results were as follows:
V
0 -695 V -680 V E1/2: 1.9 lux.sec (Initial stage) VD: -700 V VL: -200 V (After copying of 5,000 sheets) VD: -680 V VL: -225 V Example 14 An aqueous ammonia solution of casein (comprising 11.2 g of casein, 1 g of 28 ammonia water, and 222 ml of water) was applied onto an aluminum plate by means of a wire bar to form a primer layer having a thickness of 1 micron (after drying).
On the primer layer, a charge transport layer and a charge generation layer were successively formed in the same manner as in Example 9, whereby an electrophotographic photosensitive member was prepared in the same manner as in Example 1 except that the laminate structure was different.
The charging characteristics of the thus obtained photosensitive member were evaluated in the same manner as in Example 1 except that the charging polarity was positive. The results were as follows:
V
0 695 V
V
1 670 V E1/2: 2.0 lux.sec -46- Example A 5 methanol solution of a soluble nylon (6- 66-610-12 quaternary copolymer nylon) was applied onto an aluminum substrate to form a primer layer having a thickness of 0.5 micron (after drying).
Then, 5 of a pigment represented by the following formula: 0-HNOC OH HO CONH-q
CH
3 0 N=N- -CH=C- N=N CH 3 0 CN was dispersed in 95 ml of tetrahydrofuran for 20 hours by means of a sand mill to prepare a dispersion.
Separately, 5 g of the above-mentioned Compound Example No. 28 and 10 g of a bisphenol Z-type polycarbonate resin (weight-average molecular weight 50,000) were dissolved in 30 ml of monochlorobenzene to prepare a solution. The solution was then added to the above-mentioned dispersion, and further dispersed by means of a sand mill for 2 hours, thereby to prepare a coating liquid. The thus prepared coating liquid was applied onto the above-mentioned primer layer by means of a wire bar to form a photosensitive layer having a thickness of 20 microns (after drying), whereby an electrophotographic photosensitive member was prepared.
The electrophotographic characteristics of the -47thus obtained photosensitive member were evaluated in the same manner as in Example 1. The results were as follows: Vg: -690 V
V
1 -675 V E1/2: 3.1 lux.sec
Claims (14)
1. A photosensitive member for electrophoto- graphy, comprising an electroconductive substrate and a photosensitive layer disposed thereon, wherein the photosensitive layer comprises a triarylamine compound represented by the following general formula R 1 R 2 Ar2 4N Ar, Ar 2 wherein Ar 1 and Ar 2 respectively denote a benzene ring capable of having a substituent; at least one of Arl and Ar 2 has an electron-donating substituent; and R 1 and R 2 respectively denote a hydrogen atom, alkyl or alkoxyl.
2. A member according to Claim 1, wherein the triarylamine compound represented by the formula (I) has an oxidation potential of 0.90 V or lower.
3. A member according to Claim 1, wherein the triarylamine compound represented by the formula (I) has an oxidation potential of not lower than 0.60 V and not higher than 0.88 V.
4. A member according to Claim 1, wherein at least one of Ar I and Ar 2 of the formula has an -49- electron-donating substituent selected from the group consisting of an alkyl, an alkoxyl and a substituted amino group.
5. A member according to Claim 1, wherein the triarylamine compound represented by the formula is a compound selected from the group consisting of the following compounds (III) and (IV): CH 3 Q N (II), CH 3 C 2 H 5 -Q N (III), and C 2 H C3 N(IV) CH 3 O
6. A member according to Claim 1 or 5, wherein the photosensitive layer has a laminate structure comprising a charge generation layer and a charge S 25 transport layer. f
7. A member according to Claim 6, which comprises the electroconductive substrate, and the charge generation layer and the charge transport layer in this order on the substrate.
8. A member according to Claim 6, which comprises the electroconductive substrate, and the charge transport layer and the charge generation layer in this order on the substrate. i 10
9. A member according to Claim 6, wherein the charge transport layer comprises a compound selected from the group consisting of those represented by the o formulas (III) and and an insulating ,polymer or organic photoconductive polymer.
A member according to Claim 6, wherein the Scharge transport layer comprises a compound selected from the group consisting of those represented by the formulas (III) and an insulating polymer or organic photoconductive polymer; and at least one species selected from the group consisting of a plasticizer, a surface lubricating agent, a potential stabilizing agent, and an anti-oxidizing agent.
11. A member according to Claim 6, wherein the charge generation layer comprises an organic charge- generating substance and an insulating resin. -51-
12. A member according to Claim 11, wherein the organic charge-generating substance comprises an azo pigment.
13. A member according to Claim 1 or 5, which further comprises a primer layer disposed between the electroconductive substrate and photosensitive layer.
14. A member according to Claim 1 or 5, which further comprises a protective layer disposed on the photosensitive layer. DATED this TWENTIETH day of DECEMBER 1989 Canon Kabushiki Kaisha Patent Attorneys for the Applicant SPRUSON FERGUSON
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63330997A JPH02178668A (en) | 1988-12-29 | 1988-12-29 | Electrophotographic sensitive body |
JP63-330997 | 1988-12-29 |
Publications (2)
Publication Number | Publication Date |
---|---|
AU4708789A AU4708789A (en) | 1990-07-19 |
AU604428B2 true AU604428B2 (en) | 1990-12-13 |
Family
ID=18238678
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU47087/89A Ceased AU604428B2 (en) | 1988-12-29 | 1989-12-21 | Photosensitive member for electrophotography |
Country Status (9)
Country | Link |
---|---|
EP (1) | EP0376313B1 (en) |
JP (1) | JPH02178668A (en) |
KR (1) | KR940003105B1 (en) |
CN (1) | CN1078714C (en) |
AU (1) | AU604428B2 (en) |
CA (1) | CA2006857C (en) |
DE (1) | DE68925955D1 (en) |
FR (1) | FR2641384B1 (en) |
GB (1) | GB2226653B (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5393629A (en) * | 1991-04-26 | 1995-02-28 | Fuji Xerox Co., Ltd. | Electrophotographic photoreceptor |
US5495049A (en) * | 1993-03-22 | 1996-02-27 | Fuji Xerox Co., Ltd. | Triarylamine compounds useful in electrophotographic photoreceptors |
TW382076B (en) * | 1993-06-30 | 2000-02-11 | Canon Kk | Electrophotographic photosensitive member and electrophotographic apparatus using same |
JPH07233106A (en) * | 1994-02-23 | 1995-09-05 | Fuji Xerox Co Ltd | Production of monoiodinated aromatic compound |
US5529868A (en) * | 1994-03-23 | 1996-06-25 | Fuji Xerox Co., Ltd. | Electrophotographic photoreceptor |
US7138555B2 (en) | 2004-04-20 | 2006-11-21 | Xerox Corporation | Process for preparing iodoaromatic compounds and using the same |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0063528A2 (en) * | 1981-04-22 | 1982-10-27 | EASTMAN KODAK COMPANY (a New Jersey corporation) | Condensation polymeric photoconductors containing pendant arylamines, photoconductive compositions and electrophotographic elements containing these photoconductors |
EP0295127A2 (en) * | 1987-06-10 | 1988-12-14 | Xerox Corporation | Arylamine polymers |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4725518A (en) * | 1984-05-15 | 1988-02-16 | Xerox Corporation | Electrophotographic imaging system comprising charge transporting aromatic amine compound and protonic acid or Lewis acid |
JPH0823699B2 (en) * | 1986-02-28 | 1996-03-06 | 三田工業株式会社 | Electrophotographic photoreceptor |
JPH0715583B2 (en) * | 1987-04-30 | 1995-02-22 | 富士ゼロックス株式会社 | Electrophotographic photoreceptor |
JP2753582B2 (en) * | 1987-10-20 | 1998-05-20 | 株式会社リコー | Electrophotographic photoreceptor |
JP2742546B2 (en) * | 1988-02-19 | 1998-04-22 | 株式会社リコー | Aminobiphenyl compound |
-
1988
- 1988-12-29 JP JP63330997A patent/JPH02178668A/en active Granted
-
1989
- 1989-12-21 AU AU47087/89A patent/AU604428B2/en not_active Ceased
- 1989-12-27 GB GB8929200A patent/GB2226653B/en not_active Expired - Lifetime
- 1989-12-28 FR FR8917356A patent/FR2641384B1/en not_active Expired - Fee Related
- 1989-12-28 DE DE68925955T patent/DE68925955D1/en not_active Expired - Lifetime
- 1989-12-28 CA CA002006857A patent/CA2006857C/en not_active Expired - Fee Related
- 1989-12-28 CN CN89109833A patent/CN1078714C/en not_active Expired - Fee Related
- 1989-12-28 EP EP89124081A patent/EP0376313B1/en not_active Expired - Lifetime
- 1989-12-29 KR KR1019890020123A patent/KR940003105B1/en not_active IP Right Cessation
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0063528A2 (en) * | 1981-04-22 | 1982-10-27 | EASTMAN KODAK COMPANY (a New Jersey corporation) | Condensation polymeric photoconductors containing pendant arylamines, photoconductive compositions and electrophotographic elements containing these photoconductors |
EP0295127A2 (en) * | 1987-06-10 | 1988-12-14 | Xerox Corporation | Arylamine polymers |
Also Published As
Publication number | Publication date |
---|---|
FR2641384A1 (en) | 1990-07-06 |
JPH0516019B2 (en) | 1993-03-03 |
AU4708789A (en) | 1990-07-19 |
KR900010481A (en) | 1990-07-07 |
FR2641384B1 (en) | 1993-12-31 |
JPH02178668A (en) | 1990-07-11 |
EP0376313A3 (en) | 1990-08-29 |
GB8929200D0 (en) | 1990-02-28 |
EP0376313B1 (en) | 1996-03-13 |
CN1044172A (en) | 1990-07-25 |
DE68925955D1 (en) | 1996-04-18 |
CA2006857C (en) | 1995-10-24 |
EP0376313A2 (en) | 1990-07-04 |
KR940003105B1 (en) | 1994-04-13 |
GB2226653A (en) | 1990-07-04 |
CA2006857A1 (en) | 1990-06-29 |
CN1078714C (en) | 2002-01-30 |
GB2226653B (en) | 1992-07-01 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US5049464A (en) | Photosensitive member for electrophotography | |
EP0760492B1 (en) | Electrophotographic photosensitive member | |
US5079118A (en) | Photosensitive member for electrophotography with substituted pyrene | |
JP2578502B2 (en) | Electrophotographic photoreceptor | |
JPH02190862A (en) | Electrophotographic sensitive body | |
JP2805376B2 (en) | Organic electronic materials | |
JP2610503B2 (en) | Electrophotographic photoreceptor | |
US5262261A (en) | Photosensitive member for electrophotography | |
AU604428B2 (en) | Photosensitive member for electrophotography | |
AU604429B2 (en) | Photosensitive member for electrophotography | |
JP2692925B2 (en) | Electrophotographic photoreceptor | |
JP2610502B2 (en) | Electrophotographic photoreceptor | |
JP2556572B2 (en) | Electrophotographic photoreceptor | |
JPH0516018B2 (en) | ||
JPH02178667A (en) | Electrophotographic sensitive body | |
JP2610501B2 (en) | Electrophotographic photoreceptor | |
JP3280578B2 (en) | Electrophotographic photoreceptor | |
JP2567089B2 (en) | Electrophotographic photoreceptor | |
JPH0544023B2 (en) | ||
JP2767455B2 (en) | Electrophotographic photoreceptor | |
JPH01136160A (en) | Electrophotographic sensitive body | |
JPH01140162A (en) | Electrophotographic sensitive body | |
JPH0253067A (en) | Electrophotographic sensitive body | |
JPH04312558A (en) | Triarylamine compound and electorophotographic photoreceptor containing the compound | |
JPH04224572A (en) | Tetraphenylfuran derivative and electrophotographic sensitive body containing the same derivative |