JPS6329740B2 - - Google Patents

Description

[Detailed description of the invention]

The present invention relates to an electrophotographic photoreceptor, and more particularly to an electrophotographic photoreceptor containing a specific trisazo pigment. Conventionally, as electrophotographic photoreceptors made of inorganic photoconductive materials, those using selenium, cadmium sulfide, zinc oxide, etc. have been widely used. On the other hand, electrophotographic photoreceptors made of organic photoconductive substances include photoconductive polymers typified by poly-N-vinylcarbazole and 2,5-bis(P-
Products using low-molecular organic photoconductive substances such as (diethylaminophenyl) 1,3,4-oxadiazole, and combinations of such organic photoconductive substances with various dyes and pigments are known. Electrophotographic photoreceptors using organic photoconductive substances have strong film-forming properties and can be produced by coating, making it possible to provide extremely highly productive and inexpensive photoreceptors. Further, it has the advantage that color sensitivity can be freely controlled by selecting the sensitizer such as dye-pigment to be used, and a wide range of studies have been made to date. However, there are problems with sensitivity, durability, etc., and so far only a few have been put into practical use. The first object of the present invention is to provide an electrophotographic photoreceptor containing a specific trisazo pigment;
The first object of the present invention is to provide an electrophotographic photoreceptor with high sensitivity, and the third object is to provide an electrophotographic photoreceptor with high durability. This object of the present invention is achieved by an electrophotographic photoreceptor having a layer containing at least one trisazo pigment represented by the following general formula [] as a photosensitive layer. General formula [] In the formula, R ₅ and R ₆ are a hydrogen atom, a halogen atom (e.g., a chlorine atom, a bromine atom, an iodine atom, etc.), an alkyl group (e.g., a methyl group, an ethyl group,
propyl group, butyl group), alkoxy group (e.g. methoxy group, ethoxy group, propoxy group,
(butoxy group, etc.), nitro group, or hydroxyl group. Cp is

【formula】

【formula】 or

[Formula] is shown. X represents an atomic group necessary to complete an aromatic hydrocarbon ring or a heterocycle, and these rings are
Halogen atoms such as chlorine atom, bromine atom, iodine atom, alkyl groups such as methyl group, ethyl group, propyl group, butyl group, amyl group, 2-hydroxyethyl group, 2-methoxyethyl group, 2-ethoxyethyl group, 2-chloroethyl group, 3-hydroxypropyl group, 3-methoxypropyl group, 3-ethoxypropyl group, 4-hydroxybutyl group, 4-
Substituted alkyl groups such as methoxybutyl groups, alkoxy groups such as methoxy, ethoxy, propoxy, and butoxy groups, acyl groups such as acetyl, propionyl, butyryl, penzoyl, and trioyl groups, etc. be able to. Examples of the aromatic hydrocarbon ring include a benzene ring, a naphthalene ring, and examples of the heterocycle include an indole ring, a benzofuran ring, and a carbazole ring. R ₁ represents a hydrogen atom or an alkyl group, and R ₂ represents an alkyl group. As specific alkyl groups, methyl group, ethyl group, n-propyl group, n-butyl group, n-amyl group, n-hexyl group, n-octyl group, etc. are preferable. R ₃ and R ₄ are substituted or unsubstituted alkyl groups (e.g., methyl group, ethyl group, propyl group, butyl group, amyl group, 2-
Chloroethyl group, 2-methoxyethyl group, 2-ethoxyethyl group, 2-hydroxyethyl group, 3-
Chloropropyl group, 3-methoxypropyl group, 3
-ethoxypropyl group, 3-hydroxypropyl group, 4-methoxybutyl group, 4-ethoxybutyl group, 4-hydroxybutyl group), substituted or unsubstituted aralkyl group (e.g. benzyl group,
phenethyl group, chlorobenzyl group, dichlorobenzyl group, trichlorobenzyl group, methoxybenzyl group, acetylbenzyl group, α-naphthylmethyl group, β-naphthylmethyl group) or substituted or unsubstituted aryl group (for example, phenyl group,
Tolyl group, xylyl group, biphenyl group, chlorophenyl group, dichlorophenyl group, hydroxyphenyl group, cyanophenyl group, methoxyphenyl group, dimethoxyphenyl group, α-naphthyl group, β
- naphthyl group, etc.). Representative examples of the trisazo pigment represented by the general formula [] are as follows. The trisazo pigment represented by the general formula [] can be obtained by hexazotizing 4,4',4''-triaminotriphenylamine by a conventional method, and then coupling the corresponding coupler in the presence of an alkali, or
Alternatively, the above-mentioned hexazonium salt of triamine is once isolated in the form of a borofluoride salt or a zinc chloride double salt, and then a coupler is prepared in a suitable solvent such as N,N-dimethylformamide or dimethyl sulfoxide in the presence of an alkali. It can be easily manufactured by coupling with. Next, a method for synthesizing a representative example of the trisazo pigment used in the present invention will be shown. Synthesis example (for the above-mentioned trisazo pigment No. (1)) 4,4',4''-triaminotriphenylamine
7.25g (0.025mol) in 63ml of water and 13.24ml of concentrated hydrochloric acid
(0.15 mol) of sodium nitrite, add 3.54 mol of sodium nitrite to the solution.
A solution prepared by dissolving 1.0 g (0.051 mol) in 10.6 ml of water was added dropwise over 5 minutes while maintaining the liquid temperature at 4.5 to 7°C, and then stirred at the same temperature for 30 minutes. Next, the above hexazotized solution was added to a solution in which 16.08 g (0.080 mol) of 3-hydroxy-naphthalene-2-carboxylic acid methylamide and 22.0 g (0.55 mol) of caustic soda were dissolved in 420 ml of water while keeping the liquid temperature at 4 to 10°C. was added dropwise over 10 minutes, stirred at the same temperature for 2 hours, and then left overnight. After passing through the mouth, washing with water, and drying, the dried pigment was soaked in methyl ethyl ketone for 2.0 hours.
19.7g was obtained. Yield: 85% Elemental analysis: Molecular formula C ₅₄ N ₁₀ H ₄₂ O ₆ Calculated value (%) Analytical value (%) C 69.98 69.88 H 4.54 4.57 N 15.12 15.09 Other trisazo pigments used in the present invention were treated in exactly the same manner. Can be synthesized. An electrophotographic photoreceptor containing an organic pigment on a conductive layer is one in which a layer in which a pigment is dispersed in a binder is provided on a conductive layer as disclosed in Japanese Patent Publication No. 52-1667. Pigments are incorporated into a charge transporting medium consisting of a charge transporting material or the material and an insulating binder (the binder itself may be a charge transporting material) as disclosed in Japanese Patent Publication No. 47-18545 and Japanese Patent Application Laid-open No. 47-30328. A dispersed layer is provided on a conductive layer. A conductive layer as disclosed in JP-A-49-105537,
Consisting of a charge generation layer and a charge transport layer containing organic pigments. There are charge transfer complexes such as those disclosed in JP-A No. 49-91648 in which an organic pigment is added to a charge transfer complex. The electrophotographic photoreceptor of the present invention has the general formula []
It is characterized by containing a trisazo pigment represented by the general formula [], and can be applied to any type of electrophotographic photoreceptor having such characteristics, but charge carriers generated by light absorption of the trisazo pigment represented by the general formula [] In order to increase the transport efficiency of , it is desirable to use it as a type of photoreceptor. Furthermore, a type of photoreceptor in which charge carrier generation and transport functions are separated is most desirable in order to take advantage of the characteristics of the pigment. Therefore, this type of electrophotographic photoreceptor will be explained in detail. The layer structure requires a conductive layer, a charge generation layer, and a charge transport layer, and the charge generation layer can be either above or below the charge transport layer, but in electrophotographic photoreceptors of the type that are used repeatedly, it is mainly An adhesive layer may be provided as necessary for the purpose of improving adhesion with the conductive layer, charge generation layer, and charge transport layer from the viewpoint of physical strength and, in some cases, chargeability. As the conductive layer, a metal plate or foil made of aluminum or the like, a plastic film or aluminum foil laminated with paper on which a metal such as aluminum is vapor-deposited, paper treated with conductivity, etc. are used. Effective materials for the adhesive layer include resins such as casein, polyvinyl alcohol, and water-soluble ethylene-acrylic acid copolymer nitrocellulose. The appropriate thickness of the adhesive layer is 0.1 to 5μ, preferably 0.5 to 3μ. After micronizing the trisazo pigment represented by the general formula [] on the conductive layer or the adhesive layer applied to the conductive layer, it is applied without a binder or, if necessary, dispersed in an appropriate binder solution, and then applied and dried. It can be provided as follows. When dispersing the trisazo pigment, known methods such as ball milling and attritor can be used, and it is desirable that the pigment particles have a size of 5 μm or less, preferably 2 μm or less, and most preferably 0.5 μm or less. The trisazo pigment can also be applied by dissolving it in an amine solvent such as ethylenediamine. Conventional methods such as blade, Mayer bar, spray, and dipping methods are used for application. The thickness of the charge generation layer is 5μ or less, preferably 0.01~
1μ is desirable. When using a binder in the charge generation layer, a large amount of binder will affect sensitivity, so the ratio of binder in the charge generation layer should be 80%.
Below, preferably 40% or less. Binders used include polyvinyl butyral, polyvinyl acetate, polyester, polycarbonate, phenoxy resin, acrylic resin, polyacrylamide, polyamide, polyvinylpyridine resin, cellulose resin, urethane resin,
Various resins such as epoxy resin, casein, and polyvinyl alcohol are used. A charge transport layer can be provided on the charge generation layer provided in this manner. If the charge transport material does not have a film-forming ability, a method may be used in which a solution prepared by dissolving a binder in a suitable solvent is applied and dried by a conventional method to form a charge transport layer. Charge transport substances include electron transport substances and hole transport substances, and electron transport substances include chloranil, bromoanil, tetracyanoethylene, tetracyanoquinodimethane, and 2,4,7-trinitro-9-fluorenone. , 2, 4, 5, 7-
Tetranitro-9-fluorenone, 2,4,7-
trinitro-9-dicyanomethylenefluorenone, 2,4,5,7-tetranitroxanthone,
Examples include electron-withdrawing substances such as 2,4,8-trinitrothioxanthone, and polymerized versions of these electron-withdrawing substances. Examples of hole-transporting substances include pyrene, N-ethylcarbazole, N-isopropylcarbazole,
N-Methyl-N-phenylhydrazino-3-methylidene-9-ethylcarbazole, N,N-diphenylhydrazino-3-methylidene-9-ethylcarbazole, N,N-diphenylhydrazino-
3-methylidene-10-ethylphenothiazine,
N,N-diphenylhydrazino-3-methylidene-10-ethylphenoxazine, P-diethylaminobenzaldehyde-N,N-diphenylhydrazone, P-diethylaminobenzaldehyde-N
-α-naphthyl-N-phenylhydrazone, P-
Pyrrolidinobenzaldehyde-N,N-diphenylhydrazone, 1,3,3-trimethylindolenine-ω-aldehyde-N,N-diphenylhydrazone, P-diethylbenzaldehyde-3-methylbenzthiazolinone-2-hydrazone hydrazones such as 2,5-bis(P-diethylaminophenyl)-1,3,4-oxadiazole, 1
-Phenyl-3-(P-diethylaminostyryl)
-5-(P-diethylaminophenyl)pyrazoline, 1-[quinolyl(2)]-3-(P-diethylaminostyryl)-5-(P-diethylaminophenyl)pyrazoline, 1-[pyridyl(2)]- 3-(P-
diethylaminostyryl)-5-(P-diethylaminophenyl)pyrazoline, 1-[6-methoxy-pyridyl(2)]-3-(P-diethylaminostyryl)-5-(P-diethylaminophenyl)pyrazoline, 1- [pyridyl(3)]-3-(P-diethylaminostyryl-5-(P-diethylaminophenyl)pyrazoline, 1-[lepidyl(2)]-3-(P-
diethylaminostyryl)-5-(P-diethylaminophenyl)pyrazoline, 1-[pyridyl(2)]-
3-(P-diethylaminostyryl)-4-methyl-5-(P-diethylaminophenyl)pyrazoline, 1-[pyridyl(2)]-3-(α-methyl-P-
diethylaminostyryl)-5-(P-diethylaminophenyl)pyrazoline, 1-phenyl-3-
(P-diethylaminostyryl)-4-methyl-5
-(P-diethylaminophenyl)pyrazoline,
1-Phenyl-3-(α-benzyl-P-diethylaminostyryl)-5-(P-diethylaminophenyl)pyrazoline, spiropyrazoline and other pyrazolines, 2-(P-diethylaminostyryl)
-6-diethylaminobenzoxazole, 2-
Oxazole compounds such as (P-diethylaminophenyl)-4-(P-dimethylaminophenyl)-5-(2-chlorophenyl)oxazole,
Thiazole compounds such as 2-(P-diethylaminostyryl)-6-diethylaminobenzothiazole, triarylmethane compounds such as bis(4-diethylamino-2-methylphenyl)-phenylmethane, 1,1-bis(4-N, N-diethylamino-
2-methylphenyl)heptane, 1,1,2,2
-tetrakis(4-N,N-dimethylamino-2
- Polyarylalkane such as methylphenyl)ethane, triphenylamine, poly-N-vinylcarbazole, polyvinylpyrene, polyvinylanthracene, polyvinylacridine, poly-9-vinylphenylanthracene, pyrene-formaldehyde resin, ethylcarbazole formaldehyde resin, etc. There is. The charge transport substance is not limited to those described here, and when used, one type or a mixture of two or more types of charge transport substances can be used. The thickness of the charge transport layer is 5 to 30μ, preferably 8 to 30μ.
It is 20μ. As the binder, acrylic resin, polystyrene, polyester, polycarbonate, etc. can be used. As the binder for the low-molecular hole-transporting substance, a hole-transporting polymer such as the poly-N-vinylcarbazole described above can be used as the binder. On the other hand, as a binder for a low-molecular electron-transporting substance, a polymer of an electron-transporting monomer as described in US Pat. No. 4,122,113 can be used. When using a photoreceptor in which a conductive layer, a charge generation layer, and a charge transport layer are laminated in this order, and the charge transport material is an electron transport material, the surface of the charge transport layer must be positively charged, and exposure after charging is required. Then, in the exposed area, electrons generated in the charge generation layer are injected into the charge transport layer, and then reach the surface and neutralize the positive charge, causing a decrease in surface potential and creating an electrostatic contrast with the unexposed area. . A visible image can be obtained by developing the electrostatic latent image thus formed with a negatively charged toner. This can be directly fixed, or the toner image can be transferred to paper, plastic film, etc. and then developed and fixed. Alternatively, a method may be used in which the electrostatic latent image on the photoreceptor is transferred onto an insulating layer of transfer paper, then developed and fixed. The type of developer, the developing method, and the fixing method may be any known ones or known methods, and are not limited to specific ones. On the other hand, when the charge transport material consists of a hole transport material, the surface of the charge transport layer must be negatively charged.
After charging, when exposed to light, holes generated in the charge generation layer in the exposed area are injected into the charge transport layer, and then reach the surface and neutralize the negative charge, causing a decrease in the surface potential and static electricity between the exposed area and the unexposed area. Electrocontrast occurs. During development, it is necessary to use a positively charged toner, contrary to the case where an electron transport material is used. This type of photoreceptor is made by adding a trisazo pigment represented by the general formula [] to an insulating binder solution such as that used for the charge transport layer of this type of photoreceptor.
After dispersion, it is coated on a conductive support and dried. This type of photoreceptor is prepared by dissolving the charge transport material and the insulating binder used for the charge transport layer in a suitable solvent, adding the trisazo pigment represented by the general formula [], and dispersing it. ,
Obtained by coating and drying on a conductive support. In this type of photoreceptor, a charge transfer complex is formed when the electron transport material and hole transport material described in the type of photoreceptor are combined, so a trisazo pigment represented by the general formula [] is added to the solution of this charge transfer complex. After addition and dispersion, it is obtained by coating and drying on a conductive support. In any of the photoreceptors, the pigment used contains at least one type of pigment selected from the trisazo pigments represented by the general formula [], and if necessary, pigments with different light absorptions are used in combination. For the purpose of increasing the photoreceptor and obtaining a panchromatic photoreceptor, two or more types of trisazo pigments represented by the general formula [] are used in combination, or in combination with a charge-generating material selected from known dyes and pigments. It is also possible. The electrophotographic photoreceptor of the present invention can be used not only for electrophotographic copying machines, but also for laser printers and CRTs.
It can also be widely used in electrophotographic applications such as printers. Next, the present invention will be explained according to examples. Example 1 A polyvinyl alcohol aqueous solution was applied onto an aluminum plate having a thickness of 100 μm and dried to form an adhesive layer with a coating weight of 0.8 g/m ² . Next, polyester resin (Polyester Adhesive 49000 - solid content 20% - manufactured by DuPont, USA)
In a solution of 10g dissolved in 80ml of tetrahydrofuran,
5 g of the trisazo pigment of Pigment No. (1) was dispersed, and this dispersion was applied onto the adhesive layer to form a charge generation layer with a coating weight of 0.20 g/m ² after drying. . Next, 5 g of 1-[pyridyl-(2)]-3-(P-diethylaminostyryl)-5-(P-diethylaminophenyl)pyrazoline and 5 g of polymethyl methacrylate resin (number average molecular weight 100,000) were added to 70% of benzene.
ml and coated on the charge generation layer to form a charge transport layer with a coating weight of 10 g/m ² after drying. The electrophotographic photoreceptor thus prepared was statically charged with corona at 5KV using an electrostatic copying paper tester Model SP-428 manufactured by Kawaguchi Electric Co., Ltd., and after being held in a dark place for 10 seconds, the electrophotographic photoreceptor was charged with an illuminance of 5lux. It was exposed to light and its charging characteristics were investigated. The initial potential is Vo (V), the potential retention rate for 10 seconds in the dark is Rv (%), and the half-decay exposure is E1/2 (lux・
sec), and the charging characteristics of each photoreceptor were investigated, and the results are shown in Table 1. Table 1 Vo: -580 volts Rv: 90% E1/2: 4.3lux・sec Example 2 On the charge generation layer created in Example 1, 2,
A coating solution prepared by dissolving 5 g of 4,7-trinitro-9-fluorenone and 5 g of poly-4,4'-dioxydiphenyl-2,2'-propane carbonate (molecular weight 300,000) in 70 ml of tetrahydrofuran was dried. It was coated at a coating weight of 10 g/m ² and dried. The electrostatic charge of the electrophotographic photoreceptor thus prepared was measured in the same manner as in Example 1. At this time, the charging polarity was as follows. The results are shown in Table 2. Table 2 Vo: +490 volts Rv: 83% E1/2: 11.5lux・sec Examples 3 to 14 Polyvinyl alcohol aqueous solution is applied and dried on the aluminum surface of aluminum vapor-deposited mylar film, coating amount
An adhesive layer of 1.2 g/m ² was formed. Next, 5 g of each trisazo pigment shown in Table 3 below and 2 g of butyral resin (degree of butyralization 63 mol%)
was dispersed with a solution dissolved in 95 ml of ethanol, and then applied to the aluminum surface of an aluminum vapor-deposited mylar film to form a charge generation layer with a coating weight of 0.2 g/m ² after drying. Next, a solution prepared by dissolving 5 g of 1-phenyl-3(P-diethylaminostyryl)-5-(P-diethylaminophenyl)pyrazoline and 5 g of the polycarbonate resin used in Example 2 in 70 ml of tetrahydrofuran was poured onto the charge generation layer. After coating and drying, the coating amount was 11g/
A charge transport layer of m ² was formed. The charging of the photoreceptor thus prepared was measured in the same manner as in Example 1, and the results are shown in Table 3.

[Table] Example 15 An ammonia aqueous solution of casein was applied and dried on an aluminum plate having a thickness of 100 μm to form an adhesive layer with a coating amount of 1.0 g/m ² . Then 2-(P-diethylaminophenyl)-4-
Pigment No. (1) is added to a solution of 5 g of (P-dimethylaminophenyl)-5-(2-chlorophenyl)oxazole and 5 g of poly-N-vinylcarbazole (number average molecular weight 300,000) dissolved in 70 ml of tetrahydrofuran. 1.0
After dispersion, the mixture was coated and dried on the adhesive layer to give a coating weight of 11 g/m ² . The photoreceptor thus prepared was subjected to charge measurement in the same manner as in Example 1, and the measured values were as follows. However, the charging polarity was determined. This result is shown in Table 4.
Shown below. Table 4 Vo: +540 volts Rv: 84% E1/2: 10.3lux・sec

Claims (1)

[Scope of Claims] 1. An electrophotographic photoreceptor comprising a layer containing at least one trisazo pigment represented by the following general formula []. General formula [] (In the formula, R ₅ and R ₆ represent a hydrogen atom, a halogen atom, an alkyl group, an alkoxy group, a nitro group, or a hydroxyl group. Cp represents [Formula] [Formula] or [Formula]. However, X is a substituted or represents an atomic group necessary to complete an unsubstituted aromatic hydrocarbon ring or a substituted or unsubstituted heterocycle. R ₁ represents a hydrogen atom or an alkyl group, and R ₂ represents an alkyl group.
R ₃ and R ₄ represent a substituted or unsubstituted alkyl group, a substituted or unsubstituted aralkyl group, or a substituted or unsubstituted aryl group. )