JP2000066425A - Electrophotographic photoreceptor, process cartridge, electrophotographic device and production of electrophotographic photoreceptor - Google Patents

Abstract

PROBLEM TO BE SOLVED: To obtain an electrophotographic photoreceptor excellent in deposition, wear and scuffing resistances, having very good electrophotographic characteristics such as sensitivity and residual potential and capable of exhibiting stable performance even in repetitive use and to obtain a process cartridge with the photoreceptor and an electrophotographic device. SOLUTION: The electrophotographic photoreceptor has a photosensitive layer on the substrate and the photosensitive layer contains at least one of a positive hole transferring compd. having two or more chain polymerizable functional groups in the same molecule and a compd. obtd. by hardening the positive hole transferring compd. by polymn. or crosslinking.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0001]

The present invention relates to an electrophotographic photosensitive member, a process cartridge having the electrophotographic photosensitive member, an electrophotographic apparatus, and a method of manufacturing the electrophotographic photosensitive member.
More specifically, the present invention relates to an electrophotographic photosensitive member having a photosensitive layer containing a specific compound, a process cartridge and an electrophotographic apparatus having the electrophotographic photosensitive member, and a method for manufacturing the electrophotographic photosensitive member.

[0002]

2. Description of the Related Art Conventionally, inorganic materials such as selenium, cadmium sulfide and zinc oxide have been known as photoconductive materials used for electrophotographic photosensitive members. On the other hand, organic materials such as polyvinyl carbazole, phthalocyanine, and azo pigments are noted for their advantages such as high productivity and no pollution, and they tend to be inferior in terms of photoconductive properties and durability as compared with inorganic materials. , Has become widely used.

These electrophotographic photoconductors are often used as function-separated photoconductors in which a charge generation layer and a charge transport layer are laminated in order to satisfy both electrical and mechanical properties. On the other hand, as a matter of course, the electrophotographic photoreceptor is required to have sensitivity, electrical characteristics, and even optical characteristics according to the electrophotographic process applied.
In particular, since various electrical and mechanical external forces such as charging, image exposure, toner development, transfer to paper, and cleaning are directly applied to the surface of the photoreceptor that is used repeatedly, durability is required for them.

[0004] More specifically, durability against the occurrence of surface abrasion and scratches due to rubbing, surface deterioration due to charging, for example, reduction in transfer efficiency and slipperiness, and further deterioration in electrical characteristics such as sensitivity reduction and potential reduction. Durability is also required.

Generally, the surface layer of an electrophotographic photosensitive member using an organic photoconductive material is a thin resin layer, and the characteristics of the resin are very important. In recent years, acrylic resins, polycarbonate resins, and the like have been put to practical use as resins that satisfy the above conditions to some extent. However, not all of the properties described above are satisfied with these resins.
It is difficult to say that the hardness of the resin is sufficiently high for further increasing the durability. Even when these resins are used as a resin for the surface layer, the surface layer is worn with repeated use,
Scratches sometimes occurred.

[0006] Also, due to the recent demand for higher sensitivity,
In many cases, low-molecular-weight compounds such as charge-transporting substances are added in a relatively large amount.In this case, the strength of the film is remarkably reduced due to the action of these low-molecular-weight substances as a plasticizer. And scratches are a more pronounced problem. In addition, a problem that a low molecular weight compound is precipitated while the electrophotographic photosensitive member is stored is likely to occur.

As means for solving these problems, use of a curable resin as a resin for the charge transport layer is disclosed in, for example, Japanese Patent Application Laid-Open No. 2-127652. In this case, a curable resin is used as a resin for the charge transport layer, and the charge transport layer is cured and cross-linked, thereby greatly improving the abrasion resistance and the scratch resistance during repeated use.

However, even if a curable resin is used, the low molecular weight compound acts as a plasticizer in the binder resin to the last, so that the above-mentioned problem of precipitation has not been fundamentally solved. Further, in the charge transporting layer composed of an organic charge transporting substance and a binder resin, the charge transporting ability largely depends on the resin, for example, in a curable resin having sufficiently high hardness, the charge transporting ability is not easily low, Both of the hardness and the electrophotographic properties have not been sufficiently satisfied, for example, the residual potential tends to increase upon repeated use.

In Japanese Patent Application Laid-Open Nos. 5-216249 and 7-72640, a charge transporting layer contains a monomer having a carbon-carbon double bond, and the charge-transporting substance has a carbon-carbon double bond. An electrophotographic photoreceptor having a charge transport layer formed by reacting the bond with heat or light energy is disclosed. However, the charge transporting substance is merely fixed in a pendant manner to the main skeleton of the polymer, and the mechanical action is not sufficient because the plastic action cannot be sufficiently eliminated. In addition, when the concentration of the charge transporting substance is increased to improve the charge transporting ability, the crosslink density decreases and sufficient mechanical strength cannot be secured. Furthermore, there is a concern that the initiators required for polymerization may affect the electrophotographic properties.

As another solution, for example, JP-A-8-248649 discloses an electrophotographic photosensitive member having a charge transporting layer containing a thermoplastic polymer having a group having a charge transporting ability introduced into a main chain. Is disclosed, is effective for precipitation compared to the conventional molecular dispersion type charge transport layer, and also improves the mechanical strength, but is a thermoplastic resin to the last, its mechanical strength There is a limit, and it is hard to say that handling and productivity including the solubility of the resin are sufficient.

As described above, it has been studied to achieve a higher level of both mechanical strength and charge transport ability.

[0012]

SUMMARY OF THE INVENTION An object of the present invention is to solve the problems of the conventional electrophotographic photoreceptor, to improve the wear resistance and scratch resistance by increasing the film strength, and An object of the present invention is to provide an electrophotographic photosensitive member having good precipitation resistance.

Another object of the present invention is to provide an electrophotographic photoreceptor which exhibits very little change or deterioration in photoreceptor characteristics such as a rise in residual potential during repeated use, and exhibits stable performance even after repeated use. Is to provide.

Still another object of the present invention is to provide a process cartridge and an electrophotographic apparatus having the above electrophotographic photosensitive member.

Still another object of the present invention is to provide a method for producing the above electrophotographic photosensitive member.

[0016]

That is, the present invention relates to an electrophotographic photoreceptor having a photosensitive layer on a support, wherein the photosensitive layer has two or more chain-polymerizable functional groups in the same molecule. An electrophotographic photoreceptor comprising at least one of a hole transport compound and a compound cured by polymerizing or crosslinking the hole transport compound.

Further, the present invention is a process cartridge and an electrophotographic apparatus having the above electrophotographic photosensitive member.

Further, according to the present invention, there is provided a method for producing an electrophotographic photosensitive member in which a photosensitive layer is formed on a support, wherein a hole transporting compound having two or more chain polymerizable functional groups in the same molecule is polymerized or A method for producing an electrophotographic photosensitive member, comprising a step of curing by crosslinking.

[0019]

DESCRIPTION OF THE PREFERRED EMBODIMENTS The details of the present invention will be described below.

The term "chain polymerization" in the present invention refers to the former type of polymerization reaction when the reaction for producing a polymer is largely divided into chain polymerization and sequential polymerization.
Tadahiro Miwa, "Chemistry of Basic Synthetic Resins (New Edition)", 1995
July 25 (1st edition, 8th press) As described in 24, the form mainly refers to unsaturated polymerization, ring-opening polymerization, isomerization polymerization, and the like in which the reaction proceeds mainly through intermediates such as radicals or ions.

The term "chain-polymerizable functional group" means a functional group capable of performing the above-mentioned reaction mode. Here, specific examples of unsaturated polymerizable or ring-opening polymerizable functional groups which occupy the majority and have a wide range of application are shown. .

Unsaturated polymerization refers to an unsaturated group such as C ＝ C, C≡C, C ＝ O, C ＝
This is a reaction in which N, C≡N and the like are polymerized, and mainly CＣC. Specific examples of the unsaturated polymerizable functional group are shown below, but are not limited thereto.

[0023]

[Outside 17]

In the above, R represents an alkyl group such as a methyl group, an ethyl group or a propyl group which may have a substituent, an aralkyl group or a substituent such as a benzyl group or a phenethyl group which may have a substituent. An aryl group such as a phenyl group, a naphthyl group and an anthryl group, a hydrogen atom and the like which may be present.

[0025] Ring-opening polymerization is a process in which an unstable cyclic structure having a strain, such as a carbon ring, an oxo ring, or a nitrogen heterocycle, is activated by the action of a catalyst to open the ring, and at the same time, repeats the polymerization to form a chain polymer. Is generated, but in this case, most of the ions basically act as active species.
Specific examples of the ring-opening polymerization functional group are shown below, but are not limited thereto.

[0026]

[Outside 18]

In the above, R 'represents an alkyl group such as a methyl group, an ethyl group and a propyl group which may have a substituent, an aralkyl group such as a benzyl group and a phenethyl group which may have a substituent, and a substituent. And an aryl group such as a phenyl group, a naphthyl group and an anthryl group, or a hydrogen atom which may have a hydrogen atom.

Among the chain polymerizable functional groups according to the present invention as described above, those represented by the following general formulas (5) to (7) are preferable.

[0029]

[Outside 19]

In the formula, E is a hydrogen atom, a halogen atom such as fluorine, chlorine and bromine, a methyl group which may have a substituent,
Alkyl group such as ethyl group, propyl group and butyl group, benzyl group which may have a substituent, aralkyl group such as phenethyl group, naphthylmethyl group, furfuryl group and thienyl group, and phenyl which may have a substituent; Group, naphthyl group,
Aryl groups such as anthryl group, pyrenyl group, thiophenyl group and furyl group, alkoxy groups such as CN group, nitro group, methoxy group, ethoxy group and propoxy group, -COO
R ⁷ and CONR ⁸ R ⁹ are shown.

W is an arylene group such as divalent phenylene, naphthylene and anthracenylene which may have a substituent, a divalent alkylene group such as methylene, ethylene and butylene which may have a substituent, --COO-- , -CH ₂
-, - O -, - OO -, - represented by - S- or CONR ^10.

R ⁷ , R ⁸ , R ⁹ and R ¹⁰ are a hydrogen atom, a halogen atom such as fluorine, chlorine and bromine, an alkyl group such as a methyl group, an ethyl group and a propyl group which may have a substituent, An aralkyl group such as a benzyl group and a phenethyl group which may have a group; and an aryl group such as a phenyl group, a naphthyl group and an anthryl group which may have a substituent, wherein R ⁸ and R ⁹ are the same as each other. Or different.

F represents 0 or 1.

The substituents that E and W may have include:
Halogen atoms such as fluorine, chlorine, bromine and iodine, nitro groups, cyano groups, hydroxyl groups, alkyl groups such as methyl groups, ethyl groups, propyl groups and butyl groups, alkoxy groups such as methoxy groups, ethoxy groups and propoxy groups, phenoxy groups Aryloxy group such as group and naphthoxy group, benzyl group,
Phenethyl group, naphthylmethyl group, aralkyl group such as furfuryl group and thienyl group, phenyl group, naphthyl group,
And aryl groups such as anthryl group and pyrenyl group.

[0035]

[Outside 20]

In the formula, R ¹¹ and R ^{12 each} represent a hydrogen atom, an alkyl group such as a methyl group, an ethyl group, a propyl group or an butyl group which may have a substituent; a benzyl group which may have a substituent; It represents an aralkyl group such as a phenethyl group and an aryl group such as a phenyl group and a naphthyl group which may have a substituent, and g represents an integer of 1 to 10.

[0037]

[Outside 21]

In the formula, R ¹³ and R ¹⁴ represent a hydrogen atom, an alkyl group such as a methyl group, an ethyl group, a propyl group and a butyl group which may have a substituent; a benzyl group which may have a substituent; It represents an aralkyl group such as a phenethyl group and an aryl group such as a phenyl group and a naphthyl group which may have a substituent, and h represents an integer of 0 to 10.

R ¹¹ and R in the above formulas (6) and (7)
^12, the R ¹³ and R ¹⁴ substituents which may be a fluorine, chlorine, bromine and halogen atoms iodine, alkyl group such as a methyl group, an ethyl group, a propyl group and a butyl group, a methoxy group, an ethoxy Groups and aryloxy groups such as phenoxy and naphthoxy groups, benzyl groups, phenethyl groups, aralkyl groups such as naphthylmethyl groups, furfuryl groups and thienyl groups and phenyl groups, naphthyl groups, anthryl groups and pyrenyl groups. And an aryl group such as a group.

Further, among the above general formulas (5) to (7), more particularly preferred chain polymerizable functional groups include those represented by the following general formulas (8) to (14).

[0041]

[Outside 22]

Further, among the above formulas (8) to (14),
The acryloyloxy group (8) and the methacryloyloxy group (9) are particularly preferred from the viewpoint of polymerization characteristics and the like.

The “hole transporting compound having two or more chain polymerizable functional groups in the same molecule” in the present invention means that the above-described chain polymerizable group has at least one functional group in the hole transporting compound. A compound in which two or more are chemically bonded. The two or more chain polymerizable functional groups may all be the same or different.

The hole transporting compound having two or more chain polymerizable functional groups is preferably represented by the following general formula (1).

[0045]

[Outside 23]

P ¹ and P ² represent a chain polymerizable functional group,
P ¹ and P ² may be the same or different. Z represents an organic residue which may have a substituent, and Y represents a hydrogen atom. a,
b and d each represent 0 or an integer of 1 or more. Where a =
If 0, b + d is an integer of 3 or more; if b or d is 0, a is an integer of 2 or more; otherwise, a + b + d is 3
The following integers are shown. When a is 2 or more, P ¹ may be the same or different. When d is 2 or more, P ² may be the same or different. When b is 2 or more, Z may be the same or different. .

Here, "when a is 2 or more, P ¹ may be the same or different" means that n kinds of chain-polymerizable functional groups different from each other are P ¹¹ , P ¹² , P ¹³ , P ¹⁴ , P ^{14 15} ... ^Pln , for example, when a = 3, the chain polymerizable functional groups P ¹ directly bonded to the hole transporting compound A are the same, but two are the same and one is different ( For example, P ¹¹ and P ¹¹
P ¹² Toka) But three different from even respectively (e.g., P ¹² and P ¹⁵ and P ¹⁷ Toka) is intended to mean that may be ( "when d is 2 or more P ² are be the same or different and "May also be the same or different when b is 2 or more" means the same.)

[0048] The A in the above general formula (1) shows the hole-transporting group, as long as it exhibits a hole transporting property may be any, hydrogenated compounds obtained by replacing the P ¹ and Z a hydrogen atom ( As a hole transporting compound), for example, oxazole derivatives, oxadiazole derivatives, imidazole derivatives, triarylamine derivatives such as triphenylamine, 9- (p-diethylaminostyryl) anthracene, 1,1-bis- (4 -Dibenzylaminophenyl)
Propane, styryl anthracene, styryl pyrazoline, phenylhydrazones, thiazole derivatives, triazole derivatives, phenazine derivatives, acridine derivatives,
Examples include a benzofuran derivative, a benzimidazole derivative, a thiophene derivative, and an N-phenylcarbazole derivative.

Further, among the above-mentioned hole transporting compounds, those represented by the following general formula (4) are preferable.

[0050]

[Outside 24]

In the formula, R ⁴ , R ⁵ and R ⁶ each have a C ₁ -C ₁₀ alkyl group such as a methyl group, an ethyl group, a propyl group and a butyl group which may have a substituent, and a substituent. Benzyl group, phenethyl group, naphthylmethyl group, furfuryl group and arenyl group such as thienyl group and optionally substituted phenyl group, naphthyl group, anthryl group, phenanthryl group, pyrenyl group, thiophenyl group, furyl And aryl groups such as a pyridyl group, a quinolyl group, a benzoquinolyl group, a galvazolyl group, a phenothiazinyl group, a benzofuryl group, a benzothiophenyl group, a dibenzofuryl group and a dibenzothiophenyl group.

[0052] provided that at least two of R ^4, R ⁵ and R ⁶ represents an aryl group, R ^4, R ⁵ and R ⁶ may each be the same or different. Further, among them, those in which all of R ⁴ , R ⁵ and R ⁶ are aryl groups are particularly preferred. Further, R ⁴ and R in the above general formula (4)
Any two of ⁵ and R ⁶ may be bonded directly or via a bonding group, and the bonding group may be an alkylene group such as a methyl group, an ethyl group and a propylene group, an oxygen atom and a sulfur atom. And heteroatoms such as CH ＝ C
H group and the like.

Z in the general formula (1) is an alkylene group which may have a substituent, an arylene group which may have a substituent, CR ¹ ＝ CR ² (R ¹ and R ² are An alkyl group, an aryl group, and a hydrogen atom, and R ¹ and R ² may be the same or different), CＯO, S ＝ O, SO ₂ , one selected from an oxygen atom and a sulfur atom, or an arbitrary one thereof The organic residues combined are shown. Among them, those represented by the following general formula (2) are preferable, and those represented by the following general formula (3)
Are particularly preferred.

[0054]

[Outside 25]

In the above general formula (2), X ^{1 to} X ³ are a C _{1 to} C ₂₀ alkylene group such as a methylene group, an ethylene group and a propylene group which may have a substituent, and (CR ¹ ＣＲCR ² )
m, C ＝ O, S ＝ O, SO ₂ , an oxygen atom and a sulfur atom, and Ar ¹ and Ar ² are a divalent arylene group which may have a substituent (phenylene, naphthalene, anthracene, phenanthrene, pyrene Benzothiophene, pyridine, quinoline, benzoquinoline, carbazole, phenothiazine, benzofuran, benzothiophene, dibenzofuran, dibenzofuran, dibenzothiophene, and the like, and two hydrogen atoms).

R ¹ and R ² are an alkyl group such as a methyl group, an ethyl group and a propyl group which may have a substituent, an aryl group such as a phenyl group, a naphthyl group and a thiophenyl group which may have a substituent. And R ¹ and R 2
² may be the same or different.

M represents an integer of 1 to 5, and pt represents an integer of 0 to 10 (however, pt is not simultaneously 0).

In the above general formula (3), X ⁴ and X ⁵ represent (C
_{H 2) m ', (CH} = CR 3) n', C = O and an oxygen atom, Ar ³ is a divalent which may have a substituent arylene group (phenylene, naphthalene, anthracene, phenanthrene, pyrene Benzothiophene, pyridine, quinoline, benzoquinoline, carbazole, phenothiazine, benzofuran, benzothiophene, dibenzofuran, dibenzofuran, dibenzothiophene, and the like, and two hydrogen atoms).

R ³ represents an alkyl group such as a methyl group, an ethyl group and a propyl group which may have a substituent, an aryl group such as a phenyl group, a naphthyl group and a thiophenyl group which may have a substituent, and a hydrogen atom. Is shown. m 'is an integer of 1 to 10, n' is an integer of 1 to 5, and u to w is an integer of 0 to 10 (u to w are particularly preferably 0 to 5).
However, u to w are not simultaneously 0).

R ^{1 to} R ⁶ in the above general formulas (1) to (4),
Examples of the substituent which Ar ^{1 to} Ar ³ , X ^{1 to} X ⁵ and Z may have each include a halogen atom such as fluorine, chlorine, bromine and iodine, a nitro group, a cyano group, a hydroxyl group, a methyl group and an ethyl group. , An alkyl group such as propyl group and butyl group, an alkoxy group such as methoxy group, ethoxy group and propoxy group, an aryloxy group such as phenoxy group and naphthoxy group, a benzyl group, a phenethyl group, a naphthylmethyl group, a furfuryl group and a thienyl group. Aralkyl groups such as, phenyl group, naphthyl group, aryl groups such as anthryl group and pyrenyl group, dimethylamino group, diethylamino group,
Dibenzylamino group, diphenylamino group and di (p-
And a substituted amino group such as a (tolyl) amino group and an arylvinyl group such as a styryl group and a naphthylvinyl group.

The hole-transporting compound having two or more chain-polymerizable functional groups in the same molecule according to the present invention preferably has an oxidation potential of 1.2 (V) or less, and particularly preferably has an oxidation potential of 0.1 (V) or less.
It is preferably from 4 to 1.2 (V).

When the oxidation potential exceeds 1.2 (V), injection of charges (holes) from the charge generating material is unlikely to occur, the residual potential increases, the sensitivity deteriorates, and the potential fluctuation during repeated use increases. Problem easily occurs. When the oxidation potential is less than 0.4 (V), in addition to problems such as a decrease in charging ability,
Since the compound itself is easily oxidized, the compound is liable to be deteriorated, resulting in problems such as deterioration of sensitivity, blurring of an image, and potential fluctuation upon repeated use. The oxidation potential is measured by the following method.

(Measurement Method of Oxidation Potential) A saturated calomel electrode was used as a reference electrode, and 0.1 N (n-Bu) ₄ N ⁺ C
lO ₄ ^- with acetonitrile solution, sweeping the potential applied to the working electrode (platinum) by the potential sweeper, resulting current - potential curve has an oxidation potential the potential when a peak.

More specifically, the sample was set to 0.1N (n-B
_{^{u) 4 N + ClO 4 -}} 5~10m in acetonitrile solution
Dissolve to a concentration of about mol%. Then, a voltage is applied to this sample solution by a working electrode, and a current change when the voltage is linearly changed from a low potential (0 V) to a high potential (+1.5 V) is measured to obtain a current-potential curve. In this current-potential curve, the potential when the current value showed a peak (the first peak when there were a plurality of peaks) was defined as the oxidation potential.

Preferred examples of the hole transporting compound having two or more chain polymerizable functional groups are shown below, but it should not be construed that the invention is limited thereto.

[0066]

[Table 1]

[0067]

[Table 2]

[0068]

[Table 3]

[0069]

[Table 4]

[0070]

[Table 5]

[0071]

[Table 6]

[0072]

[Table 7]

[0073]

[Table 8]

[0074]

[Table 9]

[0075]

[Table 10]

[0076]

[Table 11]

[0077]

[Table 12]

[0078]

[Table 13]

[0079]

[Table 14]

[0080]

[Table 15]

[0081]

[Table 16]

[0082]

[Table 17]

[0083]

[Table 18]

[0084]

[Table 19]

Typical examples of the synthesis of the hole transporting compound having a chain polymerizable functional group used in the present invention are shown below.

(Synthesis Example 1: Synthesis of Compound No. 6) The compound was synthesized according to the following route.

[0087]

[Outside 26]

1 (50 g: 0.47 mol), 2 (40
6 g: 1.4 mol), anhydrous potassium carbonate (193 g)
And copper powder (445 g) in 1,2-dichlorobenzene.
The mixture was heated and stirred at 180 to 190 ° C. for 15 hours together with 2 kg. After filtering the reaction solution, the solvent was removed under reduced pressure, and the residue was subjected to column purification using a silica gel column to obtain 132 g of 3
I got

3 (120 g: 0.28 mol) was added to 1.5 kg of methylcellosolve, and sodium methylate (150 g) was slowly added with stirring at room temperature. After completion of the addition, the mixture is stirred at room temperature for 1 hour, and then at 70 to 80 ° C.
For 10 hours. The reaction solution was poured into water, neutralized with dilute hydrochloric acid, extracted with ethyl acetate, the organic layer was dried over anhydrous sodium sulfate, and the solvent was removed under reduced pressure. The residue was purified by a silica gel column to give 78 g of 4 .

4 (70 g: 0.2 mol) and triethylamine (40 g: 0.4 mol) were added to 400 ml of dry tetrahydrofuran (THF), cooled to 0 to 5 ° C., and acryloyl chloride (55 g: 0.6 mol) was slowly added dropwise. did. After completion of the dropwise addition, the temperature was slowly returned to room temperature, and the mixture was stirred at room temperature for 4 hours. The reaction solution was poured into water, neutralized, extracted with ethyl acetate, the organic layer was dried over anhydrous sodium sulfate, and the solvent was removed. The residue was subjected to column purification using a silica gel column, and 42 g of 5 (Compound No. 6) was obtained.
(Oxidation potential: 0.83 V).

(Synthesis Example 2: Synthesis of Compound No. 71) 4 (10 g: 29 mmol) obtained in Synthesis Example 1 was added to 50 ml of dry THF, cooled to 0 to 5 ° C., and then oily sodium hydride (about 60% ) 3.5 g were added slowly.
After completion of the addition, the mixture was returned to room temperature and stirred for 1 hour, cooled again to 0 to 5 ° C., and allyl bromide (17.5 g: 145 mmol)
l) was slowly added dropwise. After completion of the dropwise addition, the mixture was stirred for 1 hour as it was, then returned to room temperature and further stirred for 5 hours. The reaction solution was poured into water, neutralized, extracted with toluene, the organic layer was dried over anhydrous sodium sulfate, and the solvent was removed. The residue was subjected to column purification using a silica gel column, and the target compound (compound N
o. 5.6 g of (71) was obtained (oxidation potential: 0.81 V).

(Synthesis Example 3: Synthesis of Compound No. 55) Compound No. 55 obtained in the above Synthesis Example 2 was synthesized. 71 g was dissolved in 20 ml of dichloromethane, and then cooled to 0 to 5 ° C.
5.2 g of chloroperbenzoic acid (-70%) was slowly added, and the mixture was stirred for 1 hour, then returned to room temperature and stirred for 12 hours. The reaction solution was poured into water and extracted with dichloromethane. After the organic layer was dried over anhydrous sodium sulfate, the solvent was removed, and the residue was subjected to column purification using a silica gel column to obtain 2.1 g of the target compound (Compound No. 55) (oxidation potential: 0.81 V).

(Synthesis Example 4: Synthesis of Compound No. 31) The compound was synthesized according to the following route.

[0094]

[Outside 27]

6 (40 g: 0.24 mol), 7 (77
g: 0.35 mol), anhydrous potassium carbonate (48.8)
g) and copper powder (75 g) in 1,2-dichlorobenzene 2
It heated and stirred at 180-190 degreeC with 50 g for 10 hours. After filtering the reaction solution, the solvent was removed under reduced pressure, and the residue was subjected to column purification using a silica gel column to obtain 49 g of 8 .

Dimethylformamide (DMF) 242.
After cooling 3 g to 0 to 5 ° C., 84.8 g of phosphorus oxychloride was slowly added dropwise so as not to exceed 10 ° C. After stirring for 15 minutes after the addition, 8 (24 g: 0.093 mol)
l) / DMF (135 g) solution was slowly added dropwise. After the completion of the dropwise addition, the mixture was stirred for 30 minutes, returned to room temperature, stirred for 2 hours, and further heated to 80 to 85 ° C and stirred for 6 hours. The reaction solution was poured into 2 kg of about 15% aqueous sodium acetate solution.
Stirring was performed for 2 hours. After neutralizing it, extraction was performed using toluene, the organic layer was dried over anhydrous sodium sulfate, the solvent was removed, and the residue was subjected to column purification using a silica gel column.
16 g of 9 were obtained.

1.85 g of lithium aluminum hydride was added to 100 ml of dry THF, and the mixture was stirred at room temperature. 9 (15 g: 0.48 mol) / dry THF (10
0 ml) solution was slowly added dropwise. After dropping, add 4 at room temperature.
After stirring for 400 hours, 400 ml of a 5% hydrochloric acid aqueous solution was slowly dropped. After completion of the dropwise addition, the mixture was extracted with toluene, the organic layer was dried over anhydrous sodium sulfate, the solvent was removed, and the residue was purified by a silica gel column to give 13 g of 10 .

10 (10 g: 0.03 mol) and triethylamine (12 g: 0.12 mol) were added to dry TH
After adding to 150 ml of F and cooling to 0 to 5 ° C., acryloyl chloride (8.5 g: 0.09 mol) was slowly added dropwise.
After completion of the dropwise addition, the temperature was slowly returned to room temperature, and the mixture was stirred at room temperature for 4 hours. The reaction solution was poured into water, neutralized, extracted with ethyl acetate, the organic layer was dried over anhydrous sodium sulfate, and the solvent was removed. The residue was purified with a silica gel column to give 5.6 g of 11 (Compound No. 31) (oxidation potential: 0.93 V).

In the present invention, the compound having a hole transporting property in the photosensitive layer is obtained by polymerizing and crosslinking a hole transporting compound having two or more chain polymerizable functional groups in the same molecule. Is incorporated into the three-dimensional crosslinked structure via at least two crosslink points via a covalent bond. The hole transporting compound can be polymerized or cross-linked by itself, or can be mixed with a compound having another chain polymerizable group, and the type / ratio thereof is all arbitrary. Here, the compound having another chain polymerizable group includes any of monomers, oligomers and polymers having a chain polymerizable group.

When the functional group of the hole transporting compound and the functional group of the other chain polymerizable compound are the same group or a group which can be polymerized with each other, the two groups are copolymerized three-dimensionally crosslinked via a covalent bond. It is possible to take a structure. When both functional groups are functional groups that do not polymerize with each other, the photosensitive layer may be a mixture of at least two or more three-dimensional cured products or a three-dimensional cured product of the main component, other chain polymerizable compound monomers,
Or it is configured as containing the cured product,
By properly controlling the compounding ratio / film forming method, IPN (Inter Penetrating N
It is also possible to form an interworking network.

A photosensitive layer is formed from the above-mentioned hole transporting compound and monomers, oligomers and polymers having no chain-polymerizable group or monomers, oligomers and polymers having a polymerizable group other than the chain-polymerizable group. May be. Further, in some cases, they are not chemically bonded to the three-dimensional crosslinked structure. That is, it is possible to contain a hole transporting compound having no chain polymerizable functional group. Further, other various additives, for example, a lubricant such as fine particles of fluorine atom-containing resin may be contained.

The photoreceptor of the present invention has a structure in which a charge generating layer containing a charge generating substance and a charge transporting layer containing a charge transporting substance are laminated as a photosensitive layer on a support in this order or in reverse order. In addition, any structure of a single layer in which a charge generation material and a charge transport material are dispersed in the same layer can be adopted. In the former laminated type, the charge transport layer may have two or more layers, and in the latter single layer type, a charge transport layer may be further formed on the photosensitive layer containing the same charge generating substance and charge transporting substance. It is also possible to form a protective layer on the charge generation layer or the charge transport layer.

In any of these cases, it is sufficient that the photosensitive layer contains a polymerized and cross-linked material of the above-described hole transporting compound having a chain polymerizable group and / or a pre-hole transporting compound. However, in view of the characteristics of the electrophotographic photoreceptor, particularly, electrical characteristics such as residual potential and durability, a function-separated type photoreceptor in which a charge generation layer and a charge transport layer are laminated in this order is preferable, and the advantages of the present invention are provided. Another point is that the surface layer can be made highly durable without lowering the charge transporting ability.

The support of the electrophotographic photosensitive member may be any as long as it has conductivity. For example, aluminum, copper,
A metal or alloy such as chromium, nickel, zinc, and stainless steel formed into a drum or sheet, a metal layer such as aluminum and copper laminated on a plastic film, aluminum, indium oxide, tin oxide, etc., into a plastic film Metals, plastic films, paper, and the like, which are provided with a conductive layer by applying a conductive substance alone or together with a binder resin to form a conductive layer, may be used.

In the present invention, an undercoat layer having a barrier function and an adhesive function can be provided between the support and the photosensitive layer. The undercoat layer improves the adhesion and coating properties of the photosensitive layer,
It is formed for protecting the support, covering defects of the support, improving the charge injection property from the support, and protecting the photosensitive layer against electrical breakdown.

Examples of the material of the undercoat layer include polyvinyl alcohol, poly-N-vinylimidazole, polyethylene oxide, ethyl cellulose, ethylene-acrylic acid copolymer, casein, polyamide, N-methoxymethylated 6 nylon, copolymer nylon, Examples include glue and gelatin. The undercoat layer is formed by applying a solution in which each of these materials is dissolved in a suitable solvent to a support and drying the solution. The thickness is preferably from 0.1 to 2 μm.

As described above, the laminated photosensitive layer has a charge generation layer and a charge transport layer.

As the charge generating substance, selenium-tellurium,
Pyrylium, thiapyrylium dyes, various central metals and crystal systems, specifically, for example, phthalocyanine compounds having crystal forms such as α, β, γ, ε and X type, anthantrone pigments, dibenzpyrene quinone pigments, Pyranthrone pigments, trisazo pigments, disazo pigments, monoazo pigments, indigo pigments, quinacridone pigments, asymmetric quinocyanine pigments, quinocyanines and JP-A-54-143645
And the like.

The charge generation layer contains 0.3% of the charge generation material.
Homogenizer, ultrasonic dispersion, ball mill, vibrating ball mill, sand mill, with up to 4 times the amount of binder resin and solvent,
It is well dispersed by a method such as an admirer and a roll mill, and is formed by applying and drying the obtained dispersion, or as a film of a single composition such as a vapor deposition film of the charge generating substance. The film thickness is preferably 5 μm or less, and particularly preferably 0.1 to 2 μm.

Examples of the binder resin include polymers and copolymers of vinyl compounds such as styrene, vinyl acetate, vinyl chloride, acrylate, methacrylate, vinylidene fluoride, trifluoroethylene, polyvinyl alcohol, polyvinyl acetal, and the like. Polycarbonate, polyester, polysulfone, polyphenylene oxide,
Examples include polyurethane, cellulose resin, phenol resin, melamine resin, silicon resin, epoxy resin and the like.

The hole transporting compound having a chain polymerizable functional group according to the present invention may be used as a charge transporting layer comprising a charge transporting substance and a binder resin on the charge generating layer or on the charge generating layer. Can be used as a surface protective layer having a hole transporting ability. Since this surface protective layer has a hole transporting ability, it is included within the definition of the photosensitive layer.

In any case, it is preferable to carry out a polymerization / crosslinking reaction after applying the solution containing the hole transporting compound, but a solution containing the hole transporting compound is reacted in advance to obtain a cured product. Later, it is also possible to form the surface layer using a material dispersed or dissolved in a solvent again.

When a hole transporting compound having a chain polymerizable group is used as the charge transporting layer, the amount of the hole transporting compound is based on the total weight of the cured charge transporting layer. (For example, it is preferable that the hydrogenated product of A in the general formula (1) is contained in an amount of 20% by weight or more, preferably 40% by weight or more. If the content is less than 20% by weight, the charge transport ability is reduced, and problems such as a decrease in sensitivity and an increase in residual potential are liable to occur. The thickness of the charge transport layer is preferably from 1 to 50 μm, and particularly preferably from 3 to 30 μm.

When a hole transporting compound is used as a surface protective layer on the charge generating layer / charge transporting layer, the underlying charge transporting layer may be made of a suitable charge transporting material such as poly-N-vinylcarbazole and polystyrylanthracene. Polymer compounds having a heterocyclic ring or a condensed polycyclic aromatic compound, such as pyrazoline, imidazole, oxazole, triazole, and carbazole; triarylalkane derivatives such as triphenylmethane; and triarylamines such as triphenylamine Derivatives, phenylenediamine derivatives, N-phenylcarbazole derivatives, low molecular compounds such as stilbene derivatives and hydrazine derivatives, etc., are suitable binder resins (can be selected from the above-mentioned resins for the charge generation layer).
It can also be formed by applying and drying a solution dispersed / dissolved in a solvent.

In this case, the ratio of the charge transporting substance to the binder resin is preferably 30 to 100, and more preferably 50 to 100, when the total weight of both is 100.
It is preferably from 100 to 100. The amount of charge transport material is 3
If it is less than 0, the charge transporting ability is reduced, and problems such as a decrease in sensitivity and an increase in residual potential are likely to occur. The total thickness of the charge transport layer including the upper surface protective layer is 1 to 5
It is preferably 0 μm, particularly preferably 5 to 30 μm.

In any of the cases described above, in the present invention, the photosensitive layer containing a cured product of a hole transporting compound having a chain polymerizable group can contain the charge transporting substance.

In the case of a single-layer type photosensitive layer, it is formed by polymerizing / crosslinking a solution containing both a hole transporting compound and a charge generating substance, or a single layer containing a charge generating substance and a charge transporting substance. It is formed by applying a solution containing a hole transporting compound on the photosensitive layer and then polymerizing / crosslinking the solution.

Various additives can be added to the photosensitive layer in the present invention. Additives include deterioration inhibitors such as antioxidants and ultraviolet absorbers, and lubricants such as fine particles of fluorine atom-containing resin.

Examples of the method of applying the solution for each layer include a dip coating method, a spray coating method, a curtain coating method and a spin coating method. From the viewpoint of efficiency / productivity, the dip coating method is used. preferable. In addition, vapor deposition, plasma, and other known film forming methods can be appropriately selected.

In the present invention, the polymerization / crosslinking of the hole transporting compound having a chain polymerizable group is preferably carried out by radiation.

The greatest advantage of polymerization by radiation is that no polymerization initiator is required, which makes it possible to prepare a three-dimensional photosensitive layer matrix of very high purity and to ensure good electrophotographic properties. Can be. In addition, productivity is high because the polymerization reaction is efficient in a short time. Further, since radiation is excellent in transparency, the effect of curing inhibition when a shielding substance such as an additive is present in a layer or a thick layer is formed is very small.

However, depending on the type of the chain polymerizable group and the type of the central skeleton, the polymerization reaction may not easily proceed, and in that case, it is possible to add a polymerization initiator within a range that does not affect the polymerization reaction.

The radiation to be used includes an electron beam and a γ-ray, and an electron beam is preferable in terms of efficiency. When performing electron beam irradiation, any type of accelerator such as a scanning type, an electro curtain type, a broad beam type, a pulse type, and a laminar type can be used. Further, in the case of irradiating an electron beam, in the present invention, irradiation conditions are very important for developing electrical characteristics and durability. The acceleration voltage is preferably 300 KV or less, and most preferably 150 KV or less. The dose is preferably 1
Mrad in the range of 10 to 10 Mrad, more preferably 3 Mr
The range is from ad to 50 Mrad. Acceleration voltage is 300K
If it exceeds V, the damage of the electron beam irradiation on the characteristics of the photoreceptor tends to increase. If the dose is less than 1 Mrad, the crosslinking is likely to be insufficient, and
Care must be taken because if d exceeds d, the photoconductor is likely to deteriorate.

FIG. 1 shows a schematic configuration of an electrophotographic apparatus having a process cartridge having the electrophotographic photosensitive member of the present invention. In FIG. 1, reference numeral 1 denotes a drum-shaped electrophotographic photosensitive member of the present invention, which is driven to rotate around an axis 2 at a predetermined peripheral speed in a direction indicated by an arrow. In the rotation process, the photosensitive member 1 is uniformly charged with a predetermined positive or negative potential on its peripheral surface by the primary charging means 3, and then exposure light from exposure means (not shown) such as slit exposure or laser beam scanning exposure. Receive 4. Thus, an electrostatic latent image is sequentially formed on the peripheral surface of the photoconductor 1.

The formed electrostatic latent image is then transferred to developing means 5
The toner-developed image developed by the toner image is transferred from a paper supply unit (not shown) between the photoconductor 1 and the transfer unit 6 in synchronization with the rotation of the photoconductor 1 and fed to a transfer material 7 fed therefrom. The image is sequentially transferred by the transfer unit 6. The transfer material 7 having undergone the image transfer is separated from the photoreceptor surface, introduced into the image fixing means 8 and subjected to image fixation, so that it is printed out of the apparatus as a copy.

After the transfer of the image, the surface of the photoreceptor 1 is cleaned by the cleaning unit 9 to remove the untransferred toner, and the pre-exposure light 10 from the pre-exposure unit (not shown).
Is used for image formation repeatedly after the charge removal processing. When the primary charging unit 3 is a contact charging unit using a charging roller or the like, the pre-exposure is not necessarily required.

In the present invention, a plurality of components such as the electrophotographic photosensitive member 1, the primary charging means 3, the developing means 5 and the cleaning means 9 are integrally connected as a process cartridge. The process cartridge may be configured to be detachable from a main body of an electrophotographic apparatus such as a copying machine or a laser beam printer. For example, at least one of the primary charging unit 3, the developing unit 5, and the cleaning unit 9 is integrally supported together with the photoreceptor 1 to form a cartridge, which can be attached to and detached from the apparatus main body using a guide unit such as a rail 12 of the apparatus main body. Process cartridge 1
It can be 1.

When the electrophotographic apparatus is a copying machine or a printer, the exposure light 4 is reflected light or transmitted light from the original, or the original is read by a sensor and converted into a signal. , Light emitted by driving the LED array, driving the liquid crystal shutter array, and the like.

The electrophotographic photosensitive member of the present invention can be used not only for an electrophotographic copying machine but also for a laser beam printer,
It can be widely used in electrophotographic applications such as RT printers, LED printers, liquid crystal printers, and laser plate making.

Hereinafter, description will be made in accordance with embodiments. In the examples, "parts" represents parts by weight.

Example 1 First, a paint for a conductive layer was prepared by the following procedure. 50 parts of conductive titanium oxide powder coated with tin oxide containing 10% antimony oxide, 25 parts of phenolic resin, 20 parts of methyl cellosolve, 5 parts of methanol, and silicone oil (polydimethylsiloxane polyoxyalkylene copolymer, average (Molecular weight 3000)
It was prepared by dispersing 0.002 parts in a sand mill using φ1 mm glass beads for 2 hours. This paint is φ30m
The resultant was coated on an aluminum cylinder having a thickness of 20 m by a dip coating method and dried at 140 ° C. for 30 minutes to form a conductive layer having a thickness of 20 μm.

Next, 5 parts of N-methoxymethylated nylon was dissolved in 95 parts of methanol to prepare a coating for an intermediate layer. This paint was applied on the conductive layer by dip coating, dried at 100 ° C. for 20 minutes,
m of intermediate layers were formed.

Next, bisazo pigment 5 represented by the following structural formula (A)
Parts, 2 parts of polyvinyl butyral resin and 60 parts of cyclohexanone were dispersed in a sand mill using φ1 mm glass beads for 24 hours, and 60 parts of tetrahydrofuran was further added to prepare a paint for a charge generation layer. This paint was applied on the above-mentioned intermediate layer by a dip coating method and dried at 100 ° C. for 15 minutes to form a 0.2 μm-thick charge generation layer.

[0134]

[Outside 28]

Next, Compound Example No. 60 parts of the hole transporting compound of No. 6 were dissolved in a mixed solvent of 30 parts of monochlorobenzene / 30 parts of dichloromethane to prepare a paint for a charge transport layer. This paint was coated on the charge generation layer, and irradiated with an electron beam under the conditions of an acceleration voltage of 150 KV and a dose of 30 Mrad to cure the resin, thereby forming a charge transport layer having a thickness of 15 μm to obtain an electrophotographic photoreceptor. .

The produced electrophotographic photoreceptor was evaluated for its sedimentability with time, electrophotographic characteristics and durability. With respect to the sedimentability with time, a urethane rubber cleaning blade for a copying machine was pressed against the surface of the photoreceptor, stored at 75 ° C., and an accelerated test for the sedimentability was performed. After 14 days, the surface of the photoreceptor was observed under a microscope to determine the presence or absence of precipitation. When there was no precipitation, the test was continued until further 30 days later.

The electrophotographic characteristics and durability were evaluated by mounting this photoreceptor on LBP-SX manufactured by Canon Inc. Initial photoreceptor characteristics [dark portion potential Vd, light attenuation sensitivity (light amount required to attenuate light to -150 V at dark portion potential -700 V setting) and residual potential Vs1 (light amount three times the light attenuation sensitivity amount) Potential), and then 1000
A paper passing durability test was performed for zero sheets, the presence or absence of occurrence of image defects was visually observed, the abrasion amount of the photoconductor and the photoconductor characteristics after the durability were measured, and the respective change values ΔVd, ΔVl (initial V
difference between Vl and Vl when the same amount of light required to bring Vl to -150 V at the beginning is irradiated after endurance) and Δ
Vsl was determined.

The results are shown in Table 1. The photoreceptor of the present invention did not precipitate, had good photoreceptor characteristics, had a small amount of abrasion at endurance, and had low photoreceptor characteristics at endurance. It shows very stable and good properties, with little change.

(Examples 2 to 25) Hole transporting compound N
o. Example 1 was repeated except that 6 was replaced with the compounds shown in the following table.
An electrophotographic photoreceptor was prepared in the same manner as described above and evaluated. The results are shown in Table 1.

[0140]

[Table 20]

Example 26 The hole transporting compound no. 6
Example 1 was carried out except that the amount of was 48 parts and that 12 parts of an acrylic monomer having the structure of the following structural formula (B) were further added.
An electrophotographic photoreceptor was prepared in the same manner as described above and evaluated. The results are shown in Table 1.

[0142]

[Outside 29]

Example 27 The hole transporting compound No. 1
An electrophotographic photoreceptor was prepared and evaluated in the same manner as in Example 7, except that the amount of 1 was changed to 48 parts and further 12 parts of an acrylate monomer having the structure of the following structural formula (C) was added. The results are shown in Table 1.

[0144]

[Outside 30]

Example 28 The hole transporting compound No. 6
Of an acrylic oligomer (number-average molecular weight: 2,000) having a structure represented by the following structural formula (D):
An electrophotographic photosensitive member was prepared and evaluated in the same manner as in Example 1 except that 2 parts were added. The results are shown in Table 1.

[0146]

[Outside 31]

(Examples 29 to 33) Electrophotographic photosensitive members were prepared and evaluated in the same manner as in Example 1 except that the irradiation conditions of the electron beam were changed as shown in the following table. Result, amount of shaving,
Although the durability image was good, the sensitivity was slightly lowered and the residual potential was slightly increased in the initial electrophotographic characteristics by increasing the dose. The results are shown in Table 1.

[0148]

[Table 21]

Example 34 A charge generation layer was formed in the same manner as in Example 1.

Then, 20 parts of a styryl compound represented by the following structural formula (E),

[0151]

[Outside 32] And 10 parts of a polycarbonate resin having a repeating unit of the following structural formula (F) (number average molecular weight: 20,000)

[0152]

[Outside 33] Was dissolved in a mixed solvent of 50 parts of monochlorobenzene / 20 parts of dichloromethane to prepare a charge transport layer on the charge generation layer using a charge transport layer paint. At this time, the thickness of the charge transport layer was 10 μm.

Next, the hole transporting compound No. 6 of 60
Was dissolved in a mixed solvent of 50 parts of monochlorobenzene / 50 parts of dichloromethane to prepare a coating for a surface protective layer.
This paint is applied on the previous charge transport layer by a spray coating method, and the acceleration voltage is 150 KV and the dose is 30 Mrad.
The resin was cured by irradiating an electron beam under the conditions described above to form a surface protective layer having a thickness of 5 μm to obtain an electrophotographic photosensitive member. This photoreceptor was evaluated in the same manner as in Example 1. The results are shown in Table 1.

Example 35 The hole transporting compound no. 6
Is a hole transporting compound No. Example 3 except that it was changed to 7.
An electrophotographic photoreceptor was prepared in the same manner as in No. 4 and evaluated. The results are shown in Table 1.

Example 36 The hole transporting compound No. 6
Of Example 34, except that the amount of the monomer was 30 parts and 30 parts of the acrylic monomer of the structural formula (B) used in Example 26 was added.
An electrophotographic photoreceptor was prepared in the same manner as described above and evaluated. The results are shown in Table 1.

Example 37 The hole transporting compound no. 6
Example 3 was repeated except that the amount of acryl was 30 parts and 30 parts of the acrylic oligomer of the structural formula (D) used in Example 28 was added.
An electrophotographic photoreceptor was prepared in the same manner as in No. 4 and evaluated. The results are shown in Table 1.

[0157]

[Table 22]

Comparative Example 1 A charge generation layer was formed in the same manner as in Example 1.

Next, styryl compound 1 of structural formula (E)
Polymethyl methacrylate resin having 5 parts and a repeating unit represented by the following structural formula (G) (number average molecular weight: 40,000)
15 parts of monochlorobenzene 50 parts / dichloromethane 2
A charge transport layer was formed on the charge generation layer using a charge transport layer paint prepared by dissolving in 0 parts of a mixed solvent.
At this time, the thickness of the charge transport layer was 15 μm.

[0160]

[Outside 34]

The electrophotographic photosensitive member was evaluated in the same manner as in Example 1. As a result, deposition was observed after 14 days. On the other hand, the electrophotographic characteristics in the initial stage were good, but the amount of surface layer shaved in durability was large, and image defects such as fogging and scratches occurred. Further, after 8000 sheets were cut, the thickness of the charge transport layer was reduced by shaving, and poor charging occurred, making image formation impossible. The results are shown in Table 2.

Comparative Example 2 Instead of the polymethyl methacrylate resin represented by the structural formula (G), a polycarbonate resin represented by the structural formula (F) (number average molecular weight: 2000
An electrophotographic photosensitive member was prepared and evaluated in the same manner as in Comparative Example 1, except that 0) was used. As a result, precipitation was observed after 30 days. In addition, although the durability was slightly improved as compared with the case of the polymethyl methacrylate resin, it was not sufficient, and image defects after the durability also occurred. The results are shown in Table 2.

Comparative Example 3 10 parts of the styryl compound of the structural formula (E) and 1 part of the polycarbonate resin of the structural formula (F)
An electrophotographic photosensitive member was prepared and evaluated in the same manner as in Comparative Example 2 except that the amount was changed to 5 parts. As a result, although the durability was improved as compared with Comparative Example 2, the charge transporting ability was reduced due to the increase in the distance between the charge transporting substances, and the sensitivity was reduced and the residual potential was increased. As a result, a ghost was observed in the image. The results are shown in Table 2.

Comparative Example 4 A charge transport layer was formed in the same manner as in Example 34.

Next, 10 parts of the styryl compound represented by the structural formula (E) and 15 parts of the polycarbonate resin represented by the structural formula (F) were dissolved in a mixed solvent of 50 parts of monochlorobenzene / 30 parts of dichloromethane to obtain a surface protective layer. Paint was prepared. This paint is applied on the previous charge transport layer by a spray coating method, dried at 120 ° C. for 1 hour,
A 5 μm surface protection layer was formed.

This photosensitive member was evaluated in the same manner as in Example 34. As a result, no lowering of the sensitivity and no increase in the residual potential were observed, and no image ghost was generated because the charge transporting layer having a high charge transporting ability was in the lower layer. The image after the durability test still had scratches / fog, and sufficient durability could not be secured. The results are shown in Table 2.

(Comparative Example 5) Example 1 was repeated except that the compound of the following structural formula (H) disclosed in JP-A-5-216249 was used instead of 6.
An electrophotographic photoreceptor was prepared in the same manner as described above and evaluated. As a result, the initial electrophotographic characteristics were good.
The durability was greatly reduced as compared with. The results are shown in Table 2.

[0168]

[Outside 35]

Comparative Example 6 The hole transporting compound No. An electrophotographic photosensitive member was prepared and evaluated in the same manner as in Example 26, except that the compound of the structural formula (H) was used instead of 6. As a result, the initial electrophotographic properties were good,
The durability was significantly reduced as compared with Example 26. The results are shown in Table 2.

Comparative Example 7 A charge generation layer was formed in the same manner as in Example 1.

Next, 20 parts of a polycarbonate resin (number average molecular weight 20,000) of the following structural formula (I) synthesized according to the production method described in pages 10 to 11 of JP-A-8-248649 was dissolved in 80 parts of tetrahydrofuran. The charge transport layer was formed on the charge generation layer using the charge transport layer paint prepared in the above manner.

The film thickness of this charge transport layer was 15 μm. The electrophotographic photoreceptor was evaluated in the same manner as in Example 1. As a result, although the mechanical strength was improved as compared with Comparative Examples 1 and 2, sufficient durability could not be secured. The results are shown in Table 2.

[0173]

[Outside 36]

[0174]

[Table 23]

[0175]

As described above, the electrophotographic photoreceptor of the present invention has excellent effects on deposition resistance, abrasion resistance and scratch resistance. Further, electrophotographic characteristics such as sensitivity and residual potential are very good, and stable performance can be exhibited even when repeatedly used.

Further, the effect of the electrophotographic photosensitive member is naturally exerted also in a process cartridge and an electrophotographic apparatus having the electrophotographic photosensitive member, and high image quality is maintained for a long time.

[Brief description of the drawings]

FIG. 1 is a diagram illustrating an example of a schematic configuration of an electrophotographic apparatus including a process cartridge having an electrophotographic photosensitive member according to the present invention.

Claims (31)

[Claims] 1. An electrophotographic photosensitive member having a photosensitive layer on a support, wherein the photosensitive layer has a hole transporting compound having two or more chain-polymerizable functional groups in the same molecule and the hole transporting compound. An electrophotographic photoreceptor comprising at least one of a compound cured by polymerizing or crosslinking a compound. 2. The method according to claim 1, wherein the hole transporting compound is represented by the following general formula (1):
The electrophotographic photoreceptor according to claim 1, wherein [Outside 1] (In the formula, A represents a hole-transporting group; P ¹ and P ² represent a chain-polymerizable functional group; P ¹ and P ² may be the same or different. Z may have a substituent. Y represents a hydrogen atom, a, b, and d each represent 0 or an integer of 1 or more, provided that when a = 0, b + d is an integer of 3 or more; In the case of a, a is an integer of 2 or more, and in other cases, a + b + d is an integer of 3 or more.When a is 2 or more, P ¹ may be the same or different, and when d is 2 or more, P ² is May be the same or different, and when b is 2 or more, Z may be the same or different) 3. Z is an alkylene group which may have a substituent, an arylene group which may have a substituent, and CR ¹ ＣＲCR
² (R ¹ and R ² are an alkyl group which may have a substituent,
Represents an aryl group and a hydrogen atom which may have a substituent,
R ¹ and R ² may be the same or different), C ＝ O, S
3. The electrophotographic photoreceptor according to claim 2, wherein を represents an organic residue selected from one selected from O, SO ₂ , an oxygen atom and a sulfur atom, or an arbitrary combination thereof. 4. The electrophotographic photosensitive member according to claim 2, wherein Z is represented by the following general formula (2). [Outside 2] (Wherein, X ^{1 to} X ³ are an alkylene group which may have a substituent, (CR ¹ ＣＲCR ² ) m, C ＝ O, S ＝ O, SO ₂ ,
It represents an oxygen atom and a sulfur atom, and Ar ¹ and Ar ² represent an arylene group which may have a substituent. R ¹ and R ² represent an alkyl group which may have a substituent, an aryl group which may have a substituent and a hydrogen atom, and R ¹ and R ² may be the same or different. m is an integer of 1 to 5;
Indicates an integer of 10. However, p to t are not simultaneously 0. 5. The electrophotographic photosensitive member according to claim 2, wherein Z is represented by the following general formula (3). [Outside 3] (Wherein, Ar ³ represents an arylene group which may have a substituent. X ⁴ and X ⁵ represent (CH ₂ ) m ′, (CH ＝ CR
³ ) n ', C = O and oxygen atom. R ³ represents an alkyl group which may have a substituent, an aryl group which may have a substituent and a hydrogen atom, m ′ is an integer of 1 to 10, n ′
Represents an integer of 1 to 5, and u to w represent an integer of 0 to 10. However, u to w are not 0 at the same time.) 6. The electrophotographic photoreceptor according to claim 2, wherein a hydrogenated product obtained by replacing the bonding site of A with P ¹ and Z by a hydrogen atom is represented by the following general formula (4). . [Outside 4] (Wherein, R ⁴ , R ⁵ and R ⁶ represent an alkyl group which may have a substituent, an aralkyl group which may have a substituent, and an aryl group which may have a substituent. At least two of them represent an aryl group, and R ⁴ , R ⁵ and R ⁶ may be the same or different.) 7. The electrophotographic photosensitive member according to claim 6, wherein all of R ⁴ , R ⁵ and R ⁶ are an aryl group which may have a substituent. 8. The electrophotographic photoreceptor according to claim 1, wherein at least one of P ¹ and P ² is an unsaturated polymerizable functional group represented by the following general formula (5). [Outside 5] (Wherein E is a hydrogen atom, a halogen atom, an alkyl group which may have a substituent, an aralkyl group which may have a substituent, an aryl group which may have a substituent, a cyano group, a nitro group , An alkoxy group, -COOR ⁷ (R ⁷ is a hydrogen atom,
A halogen atom, an alkyl group which may have a substituent, an aralkyl group which may have a substituent and an aryl group which may have a substituent, and CONR ⁸ R ⁹ (R ⁸ and R ⁹ are hydrogen atoms A halogen atom, an alkyl group which may have a substituent, an aralkyl group which may have a substituent, and an aryl group which may have a substituent, which may be the same or different from each other. W is an arylene group which may have a substituent, an alkylene group which may have a substituent,-
COO-, -C-, -O-, -OO-, -S- and -C
ONR ¹⁰ - (R ¹⁰ is a hydrogen atom, a halogen atom, an optionally substituted alkyl group, an aryl group which may have a aralkyl group and a substituted group may have a substituent) shows a.
f represents 0 or 1) 9. The method according to claim 1, wherein at least one of P ¹ and P ² is a cyclic ether group represented by the following general formula (6).
8. The electrophotographic photosensitive member according to any one of items 1 to 7. [Outside 6] (Wherein, R ¹¹ and R ¹² represent a hydrogen atom, an alkyl group which may have a substituent, an aralkyl group which may have a substituent, and an aryl group which may have a substituent, and g is 1 to 10
Indicates an integer) 10. The electrophotographic photoreceptor according to claim 1, wherein at least one of P ¹ and P ² is an alicyclic epoxy group represented by the following general formula (7). [Outside 7] (Wherein, R ¹³ and R ¹⁴ represent a hydrogen atom, an alkyl group which may have a substituent, an aralkyl group which may have a substituent, and an aryl group which may have a substituent, and h is 0-10
Indicates an integer) 11. The method according to claim 1, wherein at least one of P ¹ and P ² is represented by any of the following formulas (8) to (14).
8. The electrophotographic photosensitive member according to any one of 7. [Outside 8] 12. The electrophotographic photoreceptor according to claim 11, wherein at least one of P ¹ and P ² is one of formulas (8) and (9). 13. An electrophotographic apparatus, wherein the electrophotographic photosensitive member according to claim 1 and at least one unit selected from the group consisting of a charging unit, a developing unit and a cleaning unit are integrally supported. A process cartridge which is detachable from a main body. 14. An electrophotographic apparatus comprising the electrophotographic photosensitive member according to claim 1, a charging unit, an image exposing unit, a developing unit, and a transferring unit. 15. A method for producing an electrophotographic photosensitive member in which a photosensitive layer is formed on a support, by polymerizing or crosslinking a hole transporting compound having two or more chain polymerizable functional groups in the same molecule. A method for producing an electrophotographic photosensitive member, comprising a step of curing. 16. The method according to claim 15, wherein the hole transporting compound is represented by the following general formula (1). [Outside 9] (In the formula, A represents a hole-transporting group; P ¹ and P ² represent a chain-polymerizable functional group; P ¹ and P ² may be the same or different. Z may have a substituent. Y represents a hydrogen atom, a, b, and d each represent 0 or an integer of 1 or more, provided that when a = 0, b + d is an integer of 3 or more; In the case of a, a is an integer of 2 or more, and in other cases, a + b + d is an integer of 3 or more.When a is 2 or more, P ¹ may be the same or different, and when d is 2 or more, P ² is May be the same or different, and when b is 2 or more, Z may be the same or different) 17. Z is an alkylene group which may have a substituent, an arylene group which may have a substituent, and CR ¹ ＣC
R ² (R ¹ and R ² represent an alkyl group which may have a substituent, an aryl group which may have a substituent and a hydrogen atom, and R ¹ and R ² may be the same or different), C =
_{O, S = O, SO 2} , one or a manufacturing method of the electrophotographic photoreceptor of the claim 16, wherein an organic residue in any combination selected from oxygen atom and sulfur atom. 18. The method for producing an electrophotographic photosensitive member according to claim 17, wherein Z is represented by the following general formula (2). [Outside 10] (Wherein, X ^{1 to} X ³ are an alkylene group which may have a substituent, (CR ¹ ＣＲCR ² ) m, C ＝ O, S ＝ O, SO ₂ ,
It represents an oxygen atom and a sulfur atom, and Ar ¹ and Ar ² represent an arylene group which may have a substituent. R ¹ and R ² represent an alkyl group which may have a substituent, an aryl group which may have a substituent, and a hydrogen atom, and R ¹ and R ² may be the same or different. m is an integer of 1 to 5;
Indicates an integer of 10. However, p to t are not simultaneously 0. 19. The method for producing an electrophotographic photoreceptor according to claim 16, wherein Z is represented by the following general formula (3). [Outside 11] (Wherein, Ar ³ represents an arylene group which may have a substituent. X ⁴ and X ⁵ represent (CH ₂ ) m ′, (CH ＝ CR
³ ) n ', C = O and oxygen atom. R ³ represents an alkyl group which may have a substituent, an aryl group which may have a substituent and a hydrogen atom, m ′ is an integer of 1 to 10, n ′
Represents an integer of 1 to 5, and u to w represent an integer of 0 to 10. However, u to w are not 0 at the same time.) 20. The electrophotographic photoreceptor according to claim 16, wherein a hydrogenated product obtained by replacing the bonding site of A with P ¹ and Z by a hydrogen atom is represented by the following general formula (4). Manufacturing method. [Outside 12] (Wherein, R ⁴ , R ⁵ and R ⁶ represent an alkyl group which may have a substituent, an aralkyl group which may have a substituent, and an aryl group which may have a substituent. At least two of them represent an aryl group, and R ⁴ , R ⁵ and R ⁶ may be the same or different.) 21. The method according to claim 20, wherein all of R ⁴ , R ⁵ and R ⁶ are an aryl group which may have a substituent. 22. The method for producing an electrophotographic photosensitive member according to claim 15, wherein at least one of P ¹ and P ² is an unsaturated polymerizable functional group represented by the following general formula (5). . [Outside 13] (Wherein E is a hydrogen atom, a halogen atom, an alkyl group which may have a substituent, an aralkyl group which may have a substituent, an aryl group which may have a substituent, a cyano group, a nitro group , An alkoxy group, -COOR ⁷ (R ⁷ is a hydrogen atom,
A halogen atom, an alkyl group which may have a substituent, an aralkyl group which may have a substituent and an aryl group which may have a substituent, and CONR ⁸ R ⁹ (R ⁸ and R ⁹ are hydrogen atoms A halogen atom, an alkyl group which may have a substituent, an aralkyl group which may have a substituent, and an aryl group which may have a substituent, which may be the same or different from each other. W is an arylene group which may have a substituent, an alkylene group which may have a substituent,-
COO-, -C-, -O-, -OO-, -S- and -C
ONR ¹⁰ - (R ¹⁰ is a hydrogen atom, a halogen atom, an optionally substituted alkyl group, an aryl group which may have a aralkyl group and a substituted group may have a substituent) shows a.
f represents 0 or 1) 23. The method for producing an electrophotographic photosensitive member according to claim 15, wherein at least one of P ¹ and P ² is a cyclic ether group represented by the following general formula (6). [Outside 14] (Wherein, R ¹¹ and R ¹² represent a hydrogen atom, an alkyl group which may have a substituent, an aralkyl group which may have a substituent, and an aryl group which may have a substituent, and g is 1 to 10
Indicates an integer) 24. The method for producing an electrophotographic photoreceptor according to claim 15, wherein at least one of P ¹ and P ² is an alicyclic epoxy group represented by the following general formula (7). [Outside 15] (Wherein, R ¹³ and R ¹⁴ represent a hydrogen atom, an alkyl group which may have a substituent, an aralkyl group which may have a substituent, and an aryl group which may have a substituent, and h is 0-10
Indicates an integer) 25. At least one of P ¹ and P ² is represented by any of the following formulas (8) to (14).
22. The method for producing an electrophotographic photosensitive member according to any one of items 21 to 21. [Outside 16] 26. The method according to claim 25, wherein at least one of P ¹ and P ² is one of formulas (8) and (9). 27. The method for producing an electrophotographic photosensitive member according to claim 15, wherein the polymerization and the crosslinking are performed by radiation. 28. The method according to claim 27, wherein the radiation is an electron beam. 29. The method according to claim 28, wherein the polymerization and the crosslinking are performed without using a polymerization initiator. 30. The method according to claim 28, wherein the accelerating voltage of the electron beam is 300 KV or less. 31. The method according to claim 28, wherein the dose is 1 to 100 Mrad.