JP2011232391A - Electrophotographic receptor, image forming apparatus and image forming method - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a highly reliable electrophotographic receptor having high charge potential, high sensitivity, sufficient light responsivity, and excellent endurance without deterioration of the characteristics even when being used under a low temperature circumstance or in a high electrophotographic speed process, and further to provide an image forming apparatus.SOLUTION: An electrophotographic photoreceptor includes: a laminated photosensitive layer formed by laminating a charge generating layer containing a charge generating substance and a charge transportation layer containing a charge transportation substance in this order on a conductive support; or a monolayer photosensitive layer, which contains the charge generating substance and the charge transportation substance, formed on the conductive support. And the charge transportation layer or the monolayer photosensitive layer contains a 2,2-diphenylvinylamine derivative compound represented by the following general formula (I) as the charge transportation substance.

Description

  The present invention relates to an electrophotographic photoreceptor and an image forming apparatus using an organic compound exhibiting a high charge transport capability as a charge transport material.

In recent years, organic photoconductive materials have been widely researched and developed and used not only for electrophotographic photoreceptors (hereinafter also simply referred to as “photoreceptors”), but also for electrostatic recording elements, sensor materials, or organic electroluminescent (Electro Luminescent (EL) devices are beginning to be applied.
In addition, electrophotographic photoreceptors using organic photoconductive materials are used not only in the field of copying machines, but also in fields such as printing plate materials, slide films, and microfilms in which photographic technology has been used. It is also applied to a high-speed printer using a laser, a light emitting diode (LED) or a cathode ray tube (CRT) as a light source.

Therefore, the demand for organic photoconductive materials and electrophotographic photoreceptors using the same is becoming high and wide.
Organic photoconductors using organic photoconductive materials have good film-forming properties, excellent flexibility, light weight, good transparency, and a wide wavelength range by appropriate sensitization methods. For example, it is possible to easily design a photoconductor showing good sensitivity.
Accordingly, organic photoreceptors are gradually being developed as the mainstay of electrophotographic photoreceptors.

Early organic photoreceptors had drawbacks in sensitivity and durability, but these drawbacks were due to the development of a function-separated electrophotographic photoreceptor in which the charge generation function and the charge transport function were assigned to separate substances. Significant improvement.
The above-described function-separated type photoconductor has a wide material selection range for each of the charge generation material having the charge generation function and the charge transport material having the charge transport function, and an electrophotographic photoconductor having arbitrary characteristics can be relatively easily produced. It also has the advantage.

  Examples of the charge generating material used in such a function-separated type photoreceptor include various types such as phthalocyanine pigments, squarylium dyes, azo pigments, perylene pigments, polycyclic quinone pigments, cyanine dyes, squaric acid dyes and pyrylium salt dyes. Substances have been studied, and various materials having high light resistance and high charge generation ability have been proposed.

  On the other hand, examples of the charge transport material include pyrazoline compounds (for example, Patent Document 1), hydrazone compounds (for example, Patent Document 2), triphenylamine compounds (for example, Patent Document 3), stilbene compounds (for example, Patent Document 4 and Various compounds such as 5) and enamine compounds (for example, Patent Document 6) are known.

For charge transport materials, the following are described:
(1) being stable to light and heat;
(2) being stable against ozone, nitrogen oxides (NO _x ), nitric acid, etc. generated by corona discharge when charging the surface of the photoreceptor;
(3) having a high charge transport capability;
(4) High compatibility with organic solvents and binders,
(5) Easy and inexpensive to manufacture,
However, the above-mentioned conventional charge transport material satisfies some of these items, but has not yet satisfied all items at a high level.

Among the above five items, in particular, (3) “having high charge transport capability” is required.
This is because when the charge transport layer formed by dispersing the charge transport material together with the binder resin is the surface layer of the photoreceptor, a high charge transport capability is added to the charge transport material in order to ensure sufficient photoresponsiveness. Because it is required.

  When the photoconductor is mounted and used in a copying machine or a laser beam printer, a part of the surface layer of the photoconductor is forced to be scraped off by a contact member such as a cleaning blade or a charging roller. Therefore, in order to increase the durability of copying machines and laser beam printers, a surface layer that is strong against the contact members, that is, a surface layer that is less likely to be scraped off by the contact members, is required. It is done.

Therefore, when the content of the binder resin in the charge transport layer, which is the surface layer, is increased for the purpose of strengthening the surface layer and improving durability, the photoresponsiveness decreases. This is due to the low charge transport capability of the charge transport material.
That is, as the binder resin content increases, the charge transport material in the charge transport layer is diluted, and the charge transport capability of the charge transport layer is further reduced, resulting in poor photoresponsiveness.

If the photoresponsiveness is poor, the residual potential increases and the surface potential of the photoreceptor is repeatedly attenuated, so that the surface charge of the portion that should be erased by exposure is sufficiently erased. This will cause problems such as image quality deterioration at an early stage.
Therefore, in order to ensure sufficient photoresponsiveness, the charge transport material is required to have a high charge transport capability.

  In addition, since the time from exposure to development is short in a high-speed process, a photoconductor with good photoresponsiveness is required. As described above, since the photoresponsiveness depends on the charge transporting ability of the charge transporting substance, a charge transporting substance having a higher charge transporting ability is also demanded from this point.

  Furthermore, recently, electrophotographic apparatuses such as digital copiers and printers have been miniaturized and speeded up, and it has been demanded that the photoconductor characteristics have higher sensitivity corresponding to the speeding up. Even when it is used, the sensitivity is not lowered, and it is required that the change in characteristics is small and the reliability is high under various environments. Therefore, the charge transport material is required to have a higher charge transport capability.

  Conventionally, various molecular designs have been performed for the purpose of developing charge transport materials that meet these requirements, and hydrazone structures and styryl structures that have a broader conjugated system in the basic structure as compounds with superior performance. Have been proposed (for example, Patent Documents 7, 8, and 9). However, since the sensitivity of these compounds decreases in a low temperature environment, improvement is required from the viewpoint of sufficient charge transport capability in a low temperature environment.

JP-A 61-189547 JP 2000-143654 A Japanese Patent Publication No.58-32372 JP 58-198043 A JP-A-2-190862 Japanese Patent Laid-Open No. 2-51162 JP-A-5-66587 JP-A-6-348045 JP 2000-235272 A

  Therefore, the present invention can be used in a low temperature environment or in a high-speed process by using an organic photoconductive material having a high charging potential, high sensitivity, sufficient photoresponsiveness, and high charge transport capability. An object of the present invention is to provide a highly reliable electrophotographic photosensitive member and an image forming apparatus in which these characteristics do not deteriorate.

  As a result of intensive research, the inventors of the present invention have found that the charge transport layer or the single layer type photosensitive layer of the laminated type photosensitive layer is a specific 2,2-diphenylvinylamine having both an enamine structure and a hydrazone structure in the molecule. By containing the derivative compound as a charge transport material, it has excellent compatibility with the binder resin, high charging potential, high sensitivity and sufficient photoresponsiveness, excellent durability, low temperature environment or high speed Discovered that it is possible to provide a highly reliable electrophotographic photosensitive member that does not deteriorate those characteristics even when used in a process and that does not deteriorate even when exposed to light, and completed the present invention. It came to do.

（式中、Ａｒ¹およびＡｒ²は、独立して、置換基を有してもよいアリレン基または二価の複素環式基であり、Ａｒ³およびＡｒ⁴は、独立して、置換基を有してもよいアルキル基、アラルキル基、アリール基もしくは一価の複素環式基である。ただしＡｒ³およびＡｒ⁴のどちらか一方はアリール基もしくは一価の複素環式基であるか、またはＡｒ³およびＡｒ⁴は、互いが結合する窒素原子と一緒になって、置換基を有してもよい複素環式基を形成することができる）
で示される２,２−ジフェニルビニルアミン誘導体化合物を含む電子写真感光体が提供される。 However, according to the present invention, a layered photosensitive layer in which a charge generation layer containing a charge generation material and a charge transport layer containing a charge transport material are laminated in this order, or a single layer containing a charge generation material and a charge transport material. A layer type photosensitive layer is formed on a conductive support, and the charge transport layer or the single layer type photosensitive layer is represented by the following general formula (I):

(In the formula, Ar ¹ and Ar ² are each independently an arylene group or divalent heterocyclic group which may have a substituent, and Ar ³ and Ar ⁴ independently represent a substituent. An alkyl group, an aralkyl group, an aryl group or a monovalent heterocyclic group which may have, provided that either Ar ³ or Ar ⁴ is an aryl group or a monovalent heterocyclic group, or Ar ³ and Ar ⁴ can be combined with the nitrogen atom to which they are bonded to each other to form an optionally substituted heterocyclic group)
An electrophotographic photoreceptor comprising the 2,2-diphenylvinylamine derivative compound represented by the formula:

Further, according to the present invention, an image forming apparatus provided with the electrophotographic photosensitive member is provided.
Furthermore, according to the present invention, there is provided an image forming method using the above-described image forming apparatus.

The electrophotographic photosensitive member of the present invention contains the compound according to the present invention having a high charge mobility as a charge transport material, so that even if a binder resin is added at a higher ratio than when a conventional charge transport material is used, The body's photoresponsiveness can be maintained.
Therefore, an electrophotographic photosensitive member that improves the printing durability of the charge transport layer without lowering the photoresponsiveness and further improves the durability due to a synergistic effect with the excellent wear resistance of the compound itself according to the present invention. Can be provided.

  More specifically, according to the present invention, the 2,2-diphenylvinylamine derivative compound used as a charge transport material has a structure in which an extended conjugated system having two enamine structures and hydrazone structures in the molecule is formed. Since it has many hole hopping sites in its structure, it can be used as a charge transport material having a high charge transport capability even in a low temperature environment, so it has a high charging potential, high sensitivity, and sufficient photoresponsiveness. Thus, even when used in a low-temperature environment or in a high-speed process, a highly reliable electrophotographic photosensitive member that does not deteriorate these characteristics and an image forming apparatus including the same can be obtained.

By using the 2,2-diphenylvinylamine derivative compound of the present invention having a high charge transporting capability together with a binder resin as a charge transporting material in the photoreceptor, it becomes possible to increase the content of the binder resin, and as a result, durability Therefore, it is possible to obtain an electrophotographic photosensitive member and an image forming apparatus with high reliability, which do not deteriorate the above characteristics even when used in a low temperature environment or a high-speed process.
Further, when the compound of the present invention is used for a sensor material, an EL element, an electrostatic recording element or the like, it is possible to provide a device with high sensitivity and excellent photoresponsiveness.

（式中、Ａｒ¹およびＡｒ²は、独立して、置換基を有してもよいアリレン基または二価の複素環式基であり、Ａｒ³およびＡｒ⁴は、独立して、置換基を有してもよいアルキル基、アラルキル基、アリール基もしくは一価の複素環式基である。ただしＡｒ³およびＡｒ⁴のどちらか一方はアリール基もしくは一価の複素環式基であるか、またはＡｒ³およびＡｒ⁴は、互いが結合する窒素原子と一緒になって、置換基を有してもよい複素環式基を形成することができる）
で表される。 [Organic photoconductive material]
The 2,2-diphenylvinylamine derivative compound contained in the electrophotographic photoreceptor according to the present invention as a charge transport material has the following general formula (I):

(In the formula, Ar ¹ and Ar ² are each independently an arylene group or divalent heterocyclic group which may have a substituent, and Ar ³ and Ar ⁴ independently represent a substituent. An alkyl group, an aralkyl group, an aryl group or a monovalent heterocyclic group which may have, provided that either Ar ³ or Ar ⁴ is an aryl group or a monovalent heterocyclic group, or Ar ³ and Ar ⁴ can be combined with the nitrogen atom to which they are bonded to each other to form an optionally substituted heterocyclic group)
It is represented by

In the general formula (I),
Ar ¹ and Ar ² are each independently an arylene group or divalent heterocyclic group which may have a substituent.

Examples of arylene groups of Ar ¹ and Ar ^2, p-phenylene, m- phenylene, 1,4-naphthylene, 2,6-naphthylene, mention may be made of biphenylene, fluorenylene, an arylene group such as Suchirubeniren.

Examples of the heterocyclic group represented by Ar ¹ and Ar ² include divalent heterocyclic groups such as furylene, thienylene, thiazolylene, benzofurylene, phenylbenzofurylene, and carbazolylene.

The above arylene group and divalent heterocyclic group may optionally have one or more substituents.
As the substituent, for example, a linear or branched alkyl group having 1 to 4 carbon atoms (which may be further substituted with one or more halogen atoms or an alkoxy group having 1 to 4 carbon atoms), A linear or branched alkoxy group having 1 to 4 carbon atoms (which may be further substituted with one or more halogen atoms or an alkyl group having 1 to 4 carbon atoms), a halogen atom (preferably a fluorine atom) ), Phenoxy group and phenylthio group, but are not limited thereto.

Arylene groups and heterocyclic groups may also be partially hydrogenated.
Ar ¹ and Ar ² may be different from each other or the same.

Specific examples of Ar ¹ include biphenylene, 3,5′-dimethylbiphenylene, stilbenylene, phenylbenzofurylene, p-phenylene, m-phenylene, methoxy-p-phenylene, 1,4-naphthylene, and 9-dimethylfluorene. Examples include nylene, 9-ethylcarbazolylene, and 3,5′-difluorobiphenylene group.

Specific examples of Ar ² include p-phenylene, 1,4-naphthylene, methyl-p-phenylene, 2,6-naphthylene, methyl-1,4-naphthylene, thienylene, 5,6,7,8-tetrahydro. -1,4-naphthylene, methoxy-p-phenylene, 5-methoxy-1,4-naphthylene and biphenylene groups.

Ar ³ and Ar ⁴ are each independently an alkyl group, aralkyl group, aryl group or monovalent heterocyclic group which may have a substituent.
Examples of the alkyl group of Ar ³ and Ar ⁴ include alkyl groups such as methyl, ethyl, n-propyl, isopropyl, t-butyl, cyclohexyl and cyclopentyl groups.

Examples of Ar ³ and Ar ⁴ aralkyl groups include aralkyl groups such as benzyl, p-methoxybenzyl, phenethyl and 1-naphthylmethyl groups.

Examples of the aryl group of Ar ³ and Ar ⁴ include aryl groups such as phenyl, tolyl, naphthyl, pyrenyl, and biphenyl groups.

Examples of Ar ³ and Ar ⁴ heterocyclic groups include monovalent heterocyclic groups such as furyl, thienyl, thiazoyl, benzofuryl, benzothiophenyl and benzothiazoyl groups.

The alkyl group, aralkyl group, aryl group and monovalent heterocyclic group optionally have one or more substituents.
Examples of such a substituent include, for example, an alkyl group having 1 to 4 carbon atoms which may be further substituted with one or more halogen atoms or an alkoxy group having 1 to 4 carbon atoms; Examples thereof include, but are not limited to, an alkoxy group having 1 to 4 carbon atoms which may be substituted with an alkyl group of ˜4; a halogen atom (preferably a fluorine atom); a phenoxy group and a phenylthio group.

The above aryl group and heterocyclic group may be partially hydrogenated.
Ar ³ and Ar ⁴ may be different from each other or the same, but either one is an aryl group or a monovalent heterocyclic group.

More specific examples of Ar ³ and Ar ⁴ include methyl, ethyl, cyclohexyl, benzyl, phenyl, methoxy-phenyl, trifluoromethyl-phenyl, methyl-phenyl, thienyl, methoxy-naphthyl and benzothiazoyl groups It is done.

Alternatively, Ar ³ and Ar ⁴ may be combined with a nitrogen atom bonded to each other to form a heterocyclic group.
Ar ³ and Ar ⁴ may be formed together with nitrogen atoms bonded to each other.
Examples of the above heterocyclic groups include monocyclic heterocyclic groups and condensed heterocyclic groups, for example, one 5-membered or 6-membered heterocyclic ring condensed with 1 or 2 benzene rings. Can do.
Any of the above heterocyclic groups may be an aromatic group or may be hydrogenated.

  Examples of the heterocyclic group include pyrrolyl, tetrahydropyrrolyl, pyridyl, pentahydropyridyl, indolyl, dihydroindolyl, quinolyl, tetrahydroquinolyl, carbazolyl, acridinyl and dihydroacridinyl groups.

The above monocyclic heterocyclic group or condensed heterocyclic group may optionally have one or more substituents.
Such substituents include for example further one or more halogen atoms or linear or branched alkyl group having 1 to 4 carbon atoms which may be substituted with an alkoxy group having 1 to 4 carbon atoms; and 1 A linear or branched alkoxy group having 1 to 4 carbon atoms which may be substituted with the above halogen atom or an alkyl group having 1 to 4 carbon atoms; a halogen atom (preferably a fluorine atom); a phenoxy group and phenylthio Groups, but not limited thereto.

の場合（以下の表に示す化合物（２９））には分子内に２つのエナミン構造と２つのヒドラゾン構造と１つのスチルベン構造を有することになる。
このような化合物は、その構造上多くのホールのホッピングサイトを有しするため、高い電荷輸送能力を有し、有機光導電性材料として適切である。 The 2,2-diphenylvinylamine derivative compound used as a charge transport material in the present invention forms an extended conjugated system having two enamine structures and hydrazine structures in the molecule.
For example, the compound (29) shown below, wherein Ar ¹ is a stilbenylene group:

In this case (compound (29) shown in the following table), the molecule has two enamine structures, two hydrazone structures, and one stilbene structure.
Since such a compound has many hole hopping sites in its structure, it has a high charge transport capability and is suitable as an organic photoconductive material.

  In the present invention, the compound represented by the general formula (I) is a novel compound and can be produced, for example, as follows.

（式中、Ａｒ¹およびＡｒ²は、前記一般式（Ｉ）において定義したものと同義である）
で表されるビスエナミン化合物を、特開平６−３４８０４５号公報段落〔００１４〕に記載されている方法に従って同様に合成できる。 For example, the following general formula (II):

(In the formula, Ar ¹ and Ar ² have the same meaning as defined in the general formula (I)).
Can be synthesized in the same manner according to the method described in paragraph [0014] of JP-A-6-348045.

（式中、Ａｒ¹およびＡｒ²は、前記一般式（Ｉ）において定義したものと同義である）
で表されるアルデヒド体とする。 Next, the compound represented by the above general formula (II) is formylated by a Vilsmeier reaction, and the following general formula (III):

(In the formula, Ar ¹ and Ar ² have the same meaning as defined in the general formula (I)).
It is set as the aldehyde body represented by these.

The Vilsmeier reaction can be performed, for example, as follows.
First, in a solvent such as N, N-dimethylformamide (DMF) or 1,2-dichloroethane, phosphorus oxychloride and N, N-dimethylformamide, phosphorus oxychloride and N-methyl-N-phenylformamide, or oxychloride Phosphorus and N, N-diphenylformamide are added, and a Vilsmeier reagent is prepared according to a known method.

  1.0 equivalent of the bisenamine compound represented by the general formula (II) is added to 1.0 to 1.3 equivalent of the prepared Vilsmeier reagent, and the mixture is stirred for 2 to 8 hours under heating at 60 to 110 ° C. To do. Then, alkali hydrolysis is performed using 1-8 N sodium hydroxide or potassium hydroxide aqueous solution.

  By this alkaline hydrolysis, the aldehyde represented by the general formula (III) can be produced in a high yield.

（式中、Ａｒ³およびＡｒ⁴は、前記一般式（Ｉ）において定義したものと同義である）
で示されるヒドラジン試薬と、例えば、エタノール、メタノール、テトラヒドロフラン、エチレングリコールジメチルエーテルまたは１,４‐ジオキサン等の溶剤中において、上記一般式（ＩＩＩ）で表されるエナミン‐アルデヒド化合物１.０当量と、上記一般式（ＩＶ）で表されるヒドラジン試薬あるいはその塩酸塩３.０〜３.３当量とを、酢酸等の有機酸、あるいは酢酸ナトリウム、酢酸カリウム等の有機塩の触媒を触媒量（０.００１〜０.１当量）と共に６０〜１１０℃で２〜８時間加熱撹拌することにより、本発明の一般式（Ｉ）： Finally, the aldehyde compound represented by the above general formula (III) and the following general formula (IV):

(In the formula, Ar ³ and Ar ⁴ have the same meanings as defined in the general formula (I)).
In a solvent such as ethanol, methanol, tetrahydrofuran, ethylene glycol dimethyl ether or 1,4-dioxane, 1.0 equivalent of an enamine-aldehyde compound represented by the above general formula (III), A hydrazine reagent represented by the above general formula (IV) or its hydrochloride (3.0 to 3.3 equivalents) and an organic acid such as acetic acid or a catalyst of an organic salt such as sodium acetate or potassium acetate in a catalytic amount (0 (0.001 to 0.1 equivalent) together with heating and stirring at 60 to 110 ° C. for 2 to 8 hours, the general formula (I) of the present invention:

（式中、Ａｒ¹およびＡｒ²は、独立して、置換基を有してもよいアリレン基または二価の複素環式基であり、Ａｒ³およびＡｒ⁴は、独立して、置換基を有してもよいアルキル基、アラルキル基、アリール基もしくは一価の複素環式基である。ただしＡｒ³およびＡｒ⁴のどちらか一方はアリール基もしくは一価の複素環式基であるか、またはＡｒ³およびＡｒ⁴は、互いが結合する窒素原子と一緒になって、置換基を有してもよい複素環式基を形成することができる）
で表される２,２−ジフェニルビニルアミン誘導体化合物を製造できる。

(In the formula, Ar ¹ and Ar ² are each independently an arylene group or divalent heterocyclic group which may have a substituent, and Ar ³ and Ar ⁴ independently represent a substituent. An alkyl group, an aralkyl group, an aryl group or a monovalent heterocyclic group which may have, provided that either Ar ³ or Ar ⁴ is an aryl group or a monovalent heterocyclic group, or Ar ³ and Ar ⁴ can be combined with the nitrogen atom to which they are bonded to each other to form an optionally substituted heterocyclic group)
The 2,2-diphenylvinylamine derivative compound represented by these can be manufactured.

で表される基であり、 Specifically, in the compound of the general formula (I), in the general formula (I), the Ar ¹ is represented by the following formula:

A group represented by

で表される基であり、 The Ar ² is represented by the following formula:

A group represented by

で表される基であるか、または
Ａｒ³およびＡｒ⁴は、互いに結合する窒素原子と一緒になって、次の式：

で表される２,２−ジフェニルビニルアミン誘導体化合物である。 Ar ³ and Ar ⁴ are represented by the following formula:

Or Ar ³ and Ar ⁴ together with a nitrogen atom bonded to each other can be represented by the following formula:

It is a 2,2-diphenylvinylamine derivative compound represented by these.

で表される基であり、 More specifically, in the compound of the general formula (I), in the general formula (I), the Ar ¹ is represented by the following formula:

A group represented by

で表される基であり、 The Ar ² is represented by the following formula:

A group represented by

で表される基であり、 The Ar ³ is represented by the following formula:

A group represented by

で表される基であるか、または
Ａｒ³およびＡｒ⁴は、互いに結合する窒素原子と一緒になって、次の式：

で表される２,２−ジフェニルビニルアミン誘導体化合物である。 The Ar ⁴ has the following formula:

Or Ar ³ and Ar ⁴ together with a nitrogen atom bonded to each other can be represented by the following formula:

It is a 2,2-diphenylvinylamine derivative compound represented by these.

で表される基であり、
前記Ａｒ²が、

で表される基であり、 More specifically, in the general formula (I), the Ar ¹ is represented by the following formula:

A group represented by
Ar ² is

A group represented by

で表される２,２−ジフェニルビニルアミン誘導体化合物である。 Ar ³ and Ar ⁴ are represented by the following formula:

It is a 2,2-diphenylvinylamine derivative compound represented by these.

で表される基であり、前記Ａｒ²が、次の式： More specifically, the compound represented by the general formula (I) is
The Ar ¹ is represented by the following formula:

Wherein Ar ² is a group represented by the following formula:

で表される基であり、前記Ａｒ³およびＡｒ⁴が、次の式：

で表される次の式（３）：

Wherein Ar ³ and Ar ⁴ are represented by the following formula:

The following formula (3):

で表されるか、
前記Ａｒ¹が、次の式：

で表される基であり、前記Ａｒ²が、次の式：

Or
The Ar ¹ is represented by the following formula:

Wherein Ar ² is a group represented by the following formula:

で表される基であり、前記Ａｒ³およびＡｒ⁴が、互いに同一になることはなく、次の式：

で表される次の式（２４）：

The Ar ³ and Ar ⁴ are not the same as each other, and the following formula:

The following formula (24):

で表されるか、あるいは、
前記Ａｒ¹が、次の式：

で表される基であり、前記Ａｒ²が、次の式：

Or
The Ar ¹ is represented by the following formula:

Wherein Ar ² is a group represented by the following formula:

で表される基であり、前記Ａｒ³およびＡｒ⁴が、次の式：

で表され、次の式（３５）：

で表されるか、あるいは、

Wherein Ar ³ and Ar ⁴ are represented by the following formula:

And the following equation (35):

Or

で表される基であり、前記Ａｒ²が、次の式：

で表される基であり、前記Ａｒ³およびＡｒ⁴が、互いに同一になることはなく、次の式： The Ar ¹ is represented by the following formula:

Wherein Ar ² is a group represented by the following formula:

The Ar ³ and Ar ⁴ are not the same as each other, and the following formula:

で表される次の式（４５）：

で表される２,２−ジフェニルビニルアミン誘導体化合物である。

The following formula (45):

It is a 2,2-diphenylvinylamine derivative compound represented by these.

で示される２,２−ジフェニルビニルアミン誘導体化合物の他の具体例としては、例えば以下の表に示す基を有する化合物（１）〜（５０）を挙げることができるが、これらに限定されるものではない。なお、以下の表に示す各基は、上記一般式（Ｉ）の各基に対応する。
なお、以下の表に示す各基は、上記一般式（Ｉ）の各基に対応するが、該一般式（Ｉ）における置換基Ａｒ₃とＡｒ₄とは、互いに固定されたものではなく、それぞれ入れ替わることができるものと理解される。 General formula (I) according to the invention:

Other specific examples of the 2,2-diphenylvinylamine derivative compound represented by formula (1) to (50) having the groups shown in the following table include, but are not limited to, is not. In addition, each group shown in the following table | surfaces respond | corresponds to each group of the said general formula (I).
Each group shown in the following table corresponds to each group of the above general formula (I), but the substituents Ar ₃ and Ar ₄ in the general formula (I) are not fixed to each other, It is understood that each can be replaced.

  Among the compounds represented by the general formula (I), the compounds (3), (24), () which are particularly excellent as organic photoconductive materials from the viewpoints of their electrical properties, cost, productivity, etc. 35) and (45).

[Electrophotographic photoreceptor]
The electrophotographic photoreceptor of the present invention includes a layered photosensitive layer in which a charge generation layer containing a charge generation material and a charge transport layer containing a charge transport material are laminated in this order, or a charge generation material and a charge transport material. A single-layer type photosensitive layer is formed on a conductive support, and the charge transport layer or the single-layer type photosensitive layer has the general formula (I), particularly the compound (3), ( 24), (35) or (45), a laminated electrophotographic photoreceptor or a single-layer electrophotographic photoreceptor.

Embodiments of an electrophotographic photosensitive member and an image forming apparatus according to the present invention will be described below with reference to the accompanying drawings.
The electrophotographic photosensitive member and the image forming apparatus of the present invention are not limited to the embodiments described below, and include other forms in which various modifications are made without departing from the gist of the present invention. Of course, such other forms are easily understood by those skilled in the art based on the description of the present specification and the drawings.

[Laminated electrophotographic photoreceptor]
Embodiment 1
FIG. 1 is a partial cross-sectional view showing a simplified configuration of an electrophotographic photoreceptor 1 which is a first embodiment of the electrophotographic photoreceptor according to the present invention. In the present embodiment, the photosensitive layer has a laminated structure of a charge generation layer and a charge transport layer.

  The electrophotographic photosensitive member 1 includes a sheet-like conductive support 11 made of a conductive material, a charge generation layer 15 that is a layer laminated on the conductive support 11 and contains a charge generation material 12, a charge A charge transport layer 16 that is stacked on the generation layer 15 and contains the charge transport material 13. The charge generation layer 15 and the charge transport layer 16 constitute a stacked photosensitive layer 14 that is a photosensitive layer. That is, the photoreceptor 1 is a laminated photoreceptor.

<Conductive support>
The conductive support 11 serves as an electrode for the photoreceptor 1 and also functions as a support member for the other layers 15 and 16. The shape of the conductive support 11 is illustrated as a sheet, but is not limited thereto, and may be, for example, a columnar shape, a cylindrical shape, or an endless belt shape.

In the present invention, the conductive support may be any conductive support that can be used for the photoreceptor. As the conductive material constituting the conductive support 11, for example, a single metal such as aluminum, copper, zinc, or titanium, or an alloy such as an aluminum alloy or stainless steel can be used.
Furthermore, without being limited to these metal materials, for example, a polymer material such as polyethylene terephthalate, nylon or polystyrene, a laminate of metal foil on the surface of a substrate such as hard paper or glass, or a metal material is deposited. Or a layer obtained by depositing or coating a layer of a conductive compound such as a conductive polymer, tin oxide, or indium oxide can also be used. These conductive materials are processed into an appropriate shape and used as a conductive support for the photoreceptor.

  If necessary, the surface of the conductive support 11 may be subjected to an anodic oxide coating treatment, surface treatment with chemicals or hot water, coloring treatment, or surface roughening within a range that does not affect the image quality. You may perform an irregular reflection process. In an electrophotographic process using a laser as an exposure light source, the wavelengths of the laser light are uniform, so the laser light reflected on the surface of the photoconductor and the laser light reflected inside the photoconductor cause interference, and the interference due to this interference. Stripes may appear on the image and cause image defects. By performing the above-described treatment on the surface of the conductive support 11, image defects due to interference of laser light having the same wavelength can be prevented.

<Charge generation layer>
The charge generation layer 15 provided on the conductive support 11 contains a charge generation material 12 that generates charges by absorbing light.

(Charge generating material)
Examples of the charge generation material include azo pigments such as monoazo pigments, bisazo pigments and trisazo pigments, indigo pigments such as indigo and thioindigo, perylene pigments such as peryleneimide and perylene anhydride, anthraquinone and pyrenequinone, etc. Polycyclic quinone pigments, metal phthalocyanines such as oxotitanium phthalocyanine compounds and phthalocyanine compounds such as metal-free phthalocyanines, squarylium dyes, pyrylium salts and thiopyrylium salts, organic photoconductive materials such as triphenylmethane dyes, and selenium and non- Examples thereof include inorganic photoconductive materials such as crystalline silicon.
One of these charge generation materials may be used alone, or two or more of these charge generation materials may be used in combination.

Among these charge generation materials, it is preferable to use phthalocyanine compounds, particularly oxotitanium phthalocyanine compounds.
The oxotitanium phthalocyanine compound used in the present invention is oxotitanium phthalocyanine and its derivatives. As the oxotitanium phthalocyanine derivative, for example, a hydrogen atom of an aromatic ring contained in a phthalocyanine group of oxotitanium phthalocyanine is substituted with a halogen atom such as a chlorine atom or a fluorine atom, a substituent such as a nitro group, a cyano group or a sulfonic acid group. And those in which a ligand such as a chlorine atom is coordinated to a titanium atom which is a central metal of oxotitanium phthalocyanine.

  The oxotitanium phthalocyanine compound preferably has a specific crystal structure. Of the oxotitanium phthalocyanine compounds, the X-ray diffraction spectrum for Cu-Kα characteristic X-ray (wavelength: 1.54 Å) is preferably diffracted at a Bragg angle 2θ (error: ± 0.2 °) 27.2 °. The thing which has the crystal structure which shows a peak is mentioned. Here, the Bragg angle 2θ is an angle formed by incident X-rays and diffracted X-rays, and represents a so-called diffraction angle.

It is particularly preferable to use such an oxotitanium phthalocyanine compound as a charge generating material in combination with the charge transporting material represented by the general formula (I) because a photoconductor further excellent in sensitivity and resolution can be realized.
That is, since the oxotitanium phthalocyanine compound is excellent in charge generation capability and charge injection capability, it generates a large amount of charge by absorbing light, and does not accumulate the generated charge in the charge transport layer 16. Can be injected efficiently.
On the other hand, since the charge transport material 13 is a compound having a high charge mobility represented by the general formula (I), the charge generated in the charge generation material 12 due to light absorption is efficiently transferred to the charge transport material 13. Therefore, it is possible to obtain a high-sensitivity and high-resolution electrophotographic photosensitive member.

The oxotitanium phthalocyanine compound can be produced according to a conventionally known production method such as, for example, a method described in Phthhalocyanine Compounds by Moser and Thomas, Reinhold Publishing Corp., New York, 1963.
For example, oxotitanium phthalocyanine synthesizes dichlorotitanium phthalocyanine by melting and melting phthalonitrile and titanium tetrachloride in a suitable solvent such as α-chloronaphthalene, followed by base or water. It can be produced by hydrolysis. Alternatively, oxotitanium phthalocyanine can also be produced by reacting isoindoline with titanium tetraalkoxide such as tetrabutoxytitanium in a suitable solvent such as N-methylpyrrolidone.

(Sensitizer)
The charge generating substance may be used in combination with other sensitizing dyes (sensitizers). By adding a sensitizer, the sensitivity of the photoreceptor can be improved, and further, increase in residual potential and decrease in charging potential due to repeated use can be suppressed, and electrical durability can be improved.
Examples of such sensitizing dyes include triphenylmethane dyes typified by methyl violet, crystal violet, knight blue and victoria blue, erythrosine, rhodamine B, rhodamine 3R, acridine orange and frapeosin. Examples include sensitizing dyes such as acridine dyes, thiazine dyes typified by methylene blue and methylene green, oxazine dyes typified by capri blue and meldra blue, cyanine dyes, styryl dyes, pyrylium salt dyes or thiopyrylium salt dyes. .

(Binder resin for charge generation layer)
The charge generation layer 15 may contain a binder resin in order to improve the binding property. Examples of the binder resin include polyester resin, polystyrene resin, polyurethane resin, phenol resin, alkyd resin, melamine resin, epoxy resin, silicone resin, acrylic resin, methacrylic resin, polycarbonate resin, polyarylate resin, phenoxy resin, and polyvinyl butyral resin. And a resin such as polyvinyl formal resin, and a copolymer resin containing two or more repeating units constituting these resins.

  Specific examples of the copolymer resin include insulating resins such as vinyl chloride-vinyl acetate copolymer resin, vinyl chloride-vinyl acetate-maleic anhydride copolymer resin, and acrylonitrile-styrene copolymer resin. Can be mentioned.

  The binder resin is not limited to the above, and a resin generally used in this field can be used as the binder resin. Binder resin may be used individually by 1 type, or 2 or more types may be used together.

The ratio of the charge generation material in the charge generation layer 15 is preferably 10 wt% or more and 99 wt% or less.
If the ratio of the charge generation material is less than 10% by weight, the sensitivity of the photoreceptor may be lowered.
On the other hand, if the ratio of the charge generation material exceeds 99% by weight, the binder resin content is too low, and the film strength of the charge generation layer 15 may be reduced.
Further, the dispersibility of the charge generation material in the charge generation layer 15 is reduced, the coarse particles of the charge generation material are increased, the surface charge other than the portion to be erased is reduced by exposure, and the image defect, particularly the toner on the white background There is a possibility that the fogging of an image called so-called black spots, which adhere and form minute black spots, increases.

  The coating solution for the charge generation layer can be prepared, for example, by adding the above-described charge generation material and, if necessary, the above-described binder resin in a suitable solvent and dispersing by a conventionally known method.

(Solvent for charge generation layer coating solution)
Solvents used in the coating solution for the charge generation layer include, for example, halogenated hydrocarbons such as dichloromethane and dichloroethane; ketones such as acetone, methyl ethyl ketone and cyclohexanone; esters such as ethyl acetate and butyl acetate; tetrahydrofuran and dioxane Ethers such as 1,2-dimethoxyethane, etc .; alkyl ethers of ethylene glycol; aromatic hydrocarbons such as benzene, toluene, xylene; and aprotic substances such as N, N-dimethylformamide and N, N-dimethylacetamide Polar solvents and the like.
One of these solvents may be used alone, or two or more thereof may be mixed and used as a mixed solvent.

(Coating solution for charge generation layer)
The charge generation material may be pulverized in advance by a pulverizer before being dispersed in the solvent. Examples of the pulverizer used for the pulverization treatment include a ball mill, a sand mill, an attritor, a vibration mill, and an ultrasonic disperser.

  Examples of the disperser used when dispersing the charge generating substance in the solvent include a paint shaker, a ball mill, and a sand mill. As a dispersion condition at this time, an appropriate condition is selected so that impurities are not mixed due to wear of a container and a member constituting the disperser.

(Method for forming charge generation layer)
As a method for forming the charge generation layer 15, a vacuum deposition method in which the above-described charge generation material is vacuum-deposited on the surface of the conductive support 11, and a charge generation layer coating solution containing the charge generation material is used as the conductive support 11. The coating method etc. which apply | coat to the surface of this. Among these, a simple coating method is preferably used.

  Examples of the coating method for the charge generation layer coating liquid include a spray method, a bar coating method, a roll coating method, a blade method, a ring method, and a dip coating method. Among these coating methods, in particular, the dip coating method is a method of forming a layer on the surface of the substrate by immersing the substrate in a coating tank filled with a coating solution and then pulling it up at a constant speed or a sequentially changing speed. It is relatively simple and excellent in terms of productivity and cost, and is therefore preferably used.

  In order to stabilize the dispersibility of the coating liquid, the apparatus used for the dip coating method may be provided with a coating liquid dispersing apparatus represented by an ultrasonic generator. Note that the coating method is not limited to these, and an optimum method can be appropriately selected in consideration of physical properties and productivity of the coating solution.

  The layer thickness of the charge generation layer 15 is preferably 0.05 μm or more and 5 μm or less, and more preferably 0.1 μm or more and 1 μm or less. If the layer thickness of the charge generation layer 15 is less than 0.05 μm, the light absorption efficiency is lowered, and the sensitivity of the photoreceptor 1 may be lowered. If the thickness of the charge generation layer 15 exceeds 5 μm, the charge transfer inside the charge generation layer 15 becomes a rate-determining step in the process of erasing the charge on the surface of the photosensitive layer 14, and the sensitivity of the photoreceptor 1 may be reduced. is there.

<Charge transport layer>
The charge transport layer 16 includes the charge transport material 13 in the binder resin and has a function of transporting charges generated in the charge generation layer 15.
As the charge transport material represented by the general formula (I), one kind selected from the group consisting of the compounds (1) to (50) shown in Table 1 is used alone, or two or more kinds are used in combination. obtain.

The charge transport layer 16 receives the general formula (I), particularly the compound (3), (24), (35) or (45) as the charge transport material 13 that accepts and transports the charge generated in the charge generation material 12. , And is contained in the binder resin 17.
The compound represented by the general formula (I) may be used as a mixture with another charge transport material.

  Examples of such other charge transport materials include carbazole derivatives, oxazole derivatives, oxadiazole derivatives, thiazole derivatives, thiadiazole derivatives, triazole derivatives, imidazole derivatives, imidazolone derivatives, imidazolidine derivatives, bisimidazolidine derivatives, and styryl compounds. , Hydrazone compounds, polycyclic aromatic compounds, indole derivatives, pyrazoline derivatives, oxazolone derivatives, benzimidazole derivatives, quinazoline derivatives, benzofuran derivatives, acridine derivatives, phenazine derivatives, aminostilbene derivatives, triarylamine derivatives, triarylmethane derivatives, phenylene Examples thereof include diamine derivatives, stilbene derivatives, and benzidine derivatives.

  Also included are polymers having groups derived from these compounds in the main chain or side chain, such as poly-N-vinylcarbazole, poly-1-vinylpyrene and poly-9-vinylanthracene.

  In order to achieve a particularly high charge transporting ability, the total amount of the charge transporting substance 13 is the compound of the present invention represented by the general formula (I), particularly the compounds (3), (24), (35) or ( 45).

(Binder resin for charge transport layer coating solution)
As the binder resin 17 for forming the charge transport layer 16, a resin having excellent compatibility with the charge transport material 13 is selected.
Specific examples of such a binder resin include, for example, a vinyl polymer resin such as a polymethyl methacrylate resin, a polystyrene resin, and a polyvinyl chloride resin, and a copolymer resin including two or more of repeating units constituting them. And polycarbonate resin, polyester resin, polyester carbonate resin, polysulfone resin, phenoxy resin, epoxy resin, silicone resin, polyarylate resin, polyamide resin, polyether resin, polyurethane resin, polyacrylamide resin, and phenol resin. Moreover, the thermosetting resin which partially bridge | crosslinked these resin is also mentioned.
One of these resins may be used alone, or two or more of these resins may be mixed and used.

Among the above resins, polystyrene resin, polycarbonate resin, polyarylate resin or polyphenylene oxide has a volume resistivity of 10 ¹³ Ω · cm or more, excellent electrical insulation, and also has film property and potential characteristics. Since it is excellent, it is preferably used.

In the charge transport layer 16, the weight ratio (A / B) of the binder resin weight (B) to the weight (A) of the charge transport material is preferably 10/12 to 10/30.
The printing durability of the charge transport layer 16 can be improved by setting the ratio A / B to 10/12 or less and including the binder resin in the charge transport layer 16 at a high ratio.
When a conventionally known charge transport material is used, if the binder resin ratio is increased in this way, the content of the charge transport material decreases as a result, resulting in insufficient photoresponsiveness of the photoreceptor and image defects. There was a thing.

On the other hand, since the compound represented by the general formula (I) of the present invention has an excellent charge transport capability, the ratio B / A is 1.2 or more, and the ratio of the binder resin in the charge transport layer 16 is as follows. Even if the height of the photosensitive member 1 is increased, the photosensitive member 1 exhibits sufficiently high photoresponsiveness and can provide a high-quality image.
That is, by using the compound represented by the general formula (I) according to the present invention as a charge transport material, the photoreceptor 1 can improve the printing durability of the charge transport layer 16 without decreasing the photoresponsiveness. And mechanical durability is improved.

On the other hand, if the ratio B / A exceeds 3.0, the binder resin ratio becomes too high, and the sensitivity of the photoreceptor 1 may decrease.
Further, when the charge transport layer 16 is formed by a dip coating method, the viscosity of the coating solution increases, the coating speed decreases, and the productivity may be remarkably deteriorated. If the amount of the solvent in the coating solution is increased in order to suppress an increase in the viscosity of the coating solution, a brushing phenomenon occurs, and the formed charge transport layer 16 may become cloudy.

  When the ratio B / A is less than 1.2, the binder resin ratio becomes too low, the printing durability of the charge transport layer 16 decreases, the amount of film loss of the photosensitive layer 14 increases, and the charge of the photosensitive member 1 increases. May decrease.

(Additive for charge transport layer)
In order to improve the film formability, flexibility and surface smoothness, an additive such as a plasticizer and / or a leveling agent may be added to the charge transport layer 16 as necessary.

  Examples of the plasticizer include dibasic acid esters such as phthalate esters, fatty acid esters, phosphate esters, chlorinated paraffins, and epoxy type plasticizers.

  Examples of the leveling agent include silicone type leveling agents such as dimethyl silicone, diphenyl silicone, and phenylmethyl silicone.

  In addition, fine particles of an inorganic compound and / or an organic compound may be added to the charge transport layer 16 in order to increase mechanical strength and improve electrical characteristics. Specific examples of such an inorganic compound include fine metal oxide particles such as titanium oxide. Specific examples of organic compound fine particles include fine particles of fluorine atom-containing polymers such as tetrafluoroethylene polymer fine particles.

  The charge transport layer 16 may contain various additives such as an antioxidant and / or a sensitizer as necessary. As a result, the potential characteristics are improved, the stability as a coating solution is increased, fatigue deterioration when the photoreceptor is repeatedly used can be reduced, and durability can be improved.

As the antioxidant, a hindered phenol derivative or a hindered amine derivative is preferably used. The hindered phenol derivative and the hindered amine derivative may be used as a mixture in any ratio.
The amount of hindered phenol derivative or hindered amine derivative used, or the total amount of hindered phenol derivative and hindered amine derivative used is preferably in the range of 0.1 wt% or more and 50 wt% or less with respect to charge transport material 13.
By making the amount used 0.1% by weight or more, further effects can be obtained in improving the stability of the coating solution and improving the durability of the photoreceptor. If the amount used exceeds 50% by weight, the photoreceptor characteristics may be adversely affected.

(Solvent for charge transport layer coating solution)
Examples of the solvent used in the coating solution for the charge transport layer include aromatic hydrocarbons such as benzene, toluene, xylene and monochlorobenzene, halogenated hydrocarbons such as dichloromethane and dichloroethane, ethers such as THF, dioxane and dimethoxymethyl ether. And aprotic polar solvents such as N, N-dimethylformamide.
A solvent may be used individually by 1 type, or 2 or more types may be mixed and used for it.
Further, if necessary, a solvent such as alcohols, acetonitrile or methyl ethyl ketone can be further added to the above solvent.

(Method for forming charge transport layer)
The charge transport layer 16 is prepared by, for example, dissolving or dispersing the charge transport material 13 and the binder resin 17 and, if necessary, the aforementioned additives in an appropriate solvent, as in the case of forming the aforementioned charge generation layer 15. It is formed by preparing a coating solution for charge transport layer and coating the coating solution on the charge generation layer 15 by spray method, bar coating method, roll coating method, blade method, ring method or dip coating method. . Among these coating methods, the dip coating method is particularly excellent in various respects as described above, and is often used when the charge transport layer 16 is formed.

The film thickness of the charge transport layer 16 is preferably 5 μm or more and 50 μm or less, and more preferably 10 μm or more and 40 μm or less.
If the thickness of the charge transport layer 16 is less than 5 μm, the charge holding ability of the surface of the photoreceptor may be lowered. If the thickness of the charge transport layer 16 exceeds 50 μm, the resolution of the photoreceptor 1 may be lowered.

(Sensitizer for charge transport layer)
Each layer of the photosensitive layer 14, that is, the charge generation layer 15 and / or the charge transport layer 16, includes one or more sensitizers such as an electron acceptor and a dye within a range that does not impair the preferred characteristics of the present invention. It may be added.
By adding the sensitizer, the sensitivity of the photoreceptor is improved, and the increase in residual potential and fatigue due to repeated use are suppressed, and the electrical durability is improved.

  Examples of the electron acceptor include acid anhydrides such as succinic anhydride, maleic anhydride, phthalic anhydride, 4-chloronaphthalic anhydride, cyano compounds such as tetracyanoethylene and terephthalmalondinitrile, 4-nitrobenzaldehyde, and the like. Aldehydes, anthraquinones such as anthraquinone and 1-nitroanthraquinone, polycyclic or heterocyclic nitro compounds such as 2,4,7-trinitrofluorenone, 2,4,5,7-tetranitrofluorenone, and diphenoquinone compounds The electron-withdrawing material can be used. Moreover, what polymerized these electron-withdrawing materials can also be used.

  As a sensitizer such as a dye, for example, an organic photoconductive compound such as a xanthene dye, a thiazine dye, a triphenylmethane dye, a quinoline pigment, or copper phthalocyanine can be used. These organic photoconductive compounds function as optical sensitizers.

  In the present embodiment, the photosensitive layer 14 has a stacked structure in which the charge generation layer 15 and the charge transport layer 16 formed as described above are stacked. Since the charge generation function and the charge transport function are assigned to separate layers as described above, the materials constituting each layer can be independently selected. Therefore, the most suitable materials for the charge generation function and the charge transport function can be selected. You can choose. Therefore, the photoreceptor 1 is particularly excellent in electrical characteristics such as chargeability, sensitivity, and photoresponsiveness, and electrical and mechanical durability.

Embodiment 2
FIG. 2 is a partial cross-sectional view showing a simplified configuration of an electrophotographic photoreceptor 2 which is a second embodiment of the electrophotographic photoreceptor according to the present invention. The electrophotographic photosensitive member 2 of this embodiment is similar to the electrophotographic photosensitive member 1 of the first embodiment shown in FIG. 1, and corresponding portions are denoted by the same reference numerals and description thereof is omitted.

<Intermediate layer>
What should be noted in the electrophotographic photoreceptor 2 is that an intermediate layer 18 is provided between the conductive support 11 and the photosensitive layer 14.

  When there is no intermediate layer 18 between the conductive support 11 and the photosensitive layer 14, charges are injected from the conductive support 11 into the photosensitive layer 14, and the chargeability of the photosensitive layer 14 is reduced, so that the portion other than the exposed portion is not exposed. The surface charge of the image may be reduced and defects such as fogging may occur in the image. In particular, when an image is formed by using a reversal development process, a toner image is formed by attaching toner to a portion where the surface charge has been reduced by exposure. Therefore, if the surface charge decreases due to a factor other than exposure, There is a possibility that fogging of an image called black spots where toner adheres to the surface and minute black spots are formed may cause a significant deterioration in image quality.

  In the present photoreceptor 2, as described above, the intermediate layer 18 is provided between the conductive support 11 and the photosensitive layer 14, thereby preventing charge injection from the conductive support 11 to the photosensitive layer 14. . Therefore, it is possible to prevent the chargeability of the photosensitive layer 14 from being lowered, to suppress the reduction of the surface charge at portions other than the exposed portion, and to prevent the occurrence of defects such as fogging on the image.

Further, by providing the intermediate layer 18, it is possible to cover the defects on the surface of the conductive support 11 and obtain a uniform surface, so that the film formability of the photosensitive layer 14 can be improved.
Furthermore, since the intermediate layer 18 functions as an adhesive that bonds the conductive support 11 and the photosensitive layer 14, peeling of the photosensitive layer 14 from the conductive support 11 can be suppressed.

  Conventionally, when the intermediate layer 18 is provided between the conductive support 11 and the photosensitive layer 14 as described above, the sensitivity of the photosensitive member may be lowered. However, in this photoreceptor 2, since the photosensitive layer 14 contains the charge transport material according to the present invention having an excellent charge transport capability, the sensitivity is not lowered by providing the intermediate layer 15. That is, according to the present invention, the intermediate layer can be provided on the photoreceptor without reducing the sensitivity.

(Resin material for intermediate layer)
As the intermediate layer 18, a resin layer made of various resin materials, an alumite layer, or the like is used.
Examples of the resin material constituting the resin layer include polyethylene resin, polypropylene resin, polystyrene resin, acrylic resin, vinyl chloride resin, vinyl acetate resin, polyurethane resin, epoxy resin, polyester resin, melamine resin, silicone resin, and polyvinyl butyral resin. And synthetic resins such as polyamide resins, and copolymer resins containing two or more of the repeating units constituting these synthetic resins. Moreover, casein, gelatin, polyvinyl alcohol, ethyl cellulose, and the like are also included.

  Of these resins, polyamide resins are preferably used, and alcohol-soluble nylon resins are particularly preferably used. Preferred alcohol-soluble nylon resins include, for example, so-called copolymer nylon obtained by copolymerizing 6-nylon, 6,6-nylon, 6,10-nylon, 11-nylon, 12-nylon, and the like, and N-alkoxymethyl. Examples thereof include resins obtained by chemically modifying nylon such as modified nylon and N-alkoxyethyl-modified nylon.

(Intermediate layer additive)
Further, the intermediate layer 18 may contain particles such as metal oxide particles. By containing these particles in the intermediate layer 18, the volume resistance value of the intermediate layer can be adjusted, and the effect of preventing the injection of charges from the conductive support 11 to the photosensitive layer 14 can be enhanced. In addition, the electrical characteristics of the photoreceptor 2 can be maintained under various environments, and environmental stability can be improved. Examples of the metal oxide particles that can be included include particles of titanium oxide, aluminum oxide, aluminum hydroxide, tin oxide, and the like.

  The intermediate layer 18 can be formed by, for example, preparing an intermediate layer coating solution by dissolving or dispersing the resin in a suitable solvent and applying the coating solution to the surface of the conductive support 11. it can. When the intermediate layer 18 contains particles such as the above-described metal oxide particles, for example, these particles are dispersed in a resin solution obtained by dissolving the resin in an appropriate solvent. The intermediate layer 18 can be formed by preparing a coating solution and coating the coating solution on the surface of the conductive support 11.

(Solvent for intermediate layer coating solution)
As the solvent for the intermediate layer coating solution, water, various organic solvents, or a mixed solvent thereof is used. Among them, single solvents such as water, methanol, ethanol or butanol, water and alcohols, two or more alcohols, acetone or dioxolane and alcohols, chlorinated solvents such as dichloroethane, chloroform or trichloroethane and alcohols, etc. These mixed solvents are preferably used.

(Method for forming intermediate layer)
As a method for dispersing the metal oxide particles in the resin solution, a known dispersion method using a ball mill, a sand mill, an attritor, a vibration mill, an ultrasonic disperser, a paint shaker, or the like can be used.

In the intermediate layer coating solution, the weight ratio (C / D) of the total weight (C) of the resin and metal oxide to the weight (D) of the solvent used in the intermediate layer coating solution is 1/99 to The ratio is preferably 40/60, more preferably 2/98 to 30/70.
The weight ratio (E / F) of the resin weight (E) to the metal oxide weight (F) is preferably 90/10 to 1/99, more preferably 70/30 to 5 /. 95.

  Examples of the coating method of the intermediate layer coating liquid include a spray method, a bar coating method, a roll coating method, a blade method, a ring method, and a dip coating method. Among these, the dip coating method is relatively simple as described above, and is excellent in terms of productivity and cost. Therefore, the dip coating method is also preferably used when forming an intermediate layer.

  The film thickness of the intermediate layer 18 is preferably 0.01 μm or more and 20 μm or less, and more preferably 0.05 μm or more and 10 μm or less. If the thickness of the intermediate layer 15 is less than 0.01 μm, it will not substantially function as the intermediate layer 18, and it will not be possible to obtain uniform surface properties by covering the defects of the conductive support 11. There is a possibility that the injection of charges from the support 11 to the photosensitive layer 14 cannot be sufficiently prevented, and there is a possibility that a decrease in the chargeability of the photosensitive layer 14 cannot be suppressed.

  Making the thickness of the intermediate layer 18 greater than 20 μm makes it difficult to form the intermediate layer when formed by dip coating, and allows the photosensitive layer 14 to be uniformly formed on the intermediate layer. Therefore, the sensitivity of the photoreceptor 2 may be lowered, which is not preferable.

Also in the present embodiment, various additives such as plasticizers, leveling agents, and / or fine particles of inorganic compounds and / or organic compounds are added to the charge transport layer 16 in the same manner as in the first embodiment. Also good. Further, an additive such as a sensitizer such as an electron accepting substance and / or a dye, an antioxidant, and / or an ultraviolet absorber is added to the charge generation layer 15 and / or the charge transport layer 16 of the photosensitive layer 14. Also good.
Embodiment 3
[Single-layer type electrophotographic photoreceptor]
FIG. 3 is a partial cross-sectional view showing a simplified configuration of an electrophotographic photosensitive member 3 as a third embodiment of the electrophotographic photosensitive member according to the present invention. The electrophotographic photosensitive member 3 of the present embodiment is similar to the electrophotographic photosensitive member 2 of the second embodiment shown in FIG. 2, and corresponding portions are denoted by the same reference numerals and description thereof is omitted.

  It should be noted in the electrophotographic photoreceptor 3 that the photosensitive layer 14 has a single layer structure composed of a single layer containing both a charge generating material and a charge transport material. That is, the photoconductor 3 is a single layer type photoconductor.

  The single-layer type photoreceptor 3 of the present embodiment is suitable as a photoreceptor for a positively charged image forming apparatus that generates less ozone, and has only one photosensitive layer 14 to be coated. In addition, the yield is superior to that of the multilayer photoreceptors 1 and 2 of the first and second embodiments.

  The photosensitive layer 14 binds the above-described general formula (I), particularly the compound (3), (24), (35) or (45) as a charge transporting substance and the above-described charge generating substance with a binder resin. Can be formed. As the binder resin, for example, those exemplified as the binder resin of the charge transport layer 13 in the first embodiment can be used.

  The photosensitive layer 14 has a sensitizer such as a plasticizer, a leveling agent, fine particles of an inorganic compound and / or an organic compound, an electron accepting substance and / or a dye, as in the photosensitive layer 14 in the first embodiment. Various additives such as an antioxidant and / or an ultraviolet absorber may be added.

  The photosensitive layer 14 can be formed by the same method as the charge transport layer 16 provided on the photoreceptor 1 of the first embodiment. For example, the charge generating material, the charge transport material according to the present invention represented by the general formula (I) and appropriate amounts of the binder resin, and various charge transport materials other than the charge transport material of the present invention as required An appropriate amount of the additive is dissolved or dispersed in an appropriate solvent similar to the charge transport layer coating solution of the first embodiment to prepare a photosensitive layer coating solution, and this photosensitive layer coating solution is dip coated. The photosensitive layer 14 can be formed by coating on the intermediate layer 18 by, for example.

  The weight ratio (B ′ / A ′) of the weight (B ′) of the binder resin to the weight (A ′) of the charge transport material in the photosensitive layer 14 is the weight of the charge transport material in the charge transport layer 16 of the first embodiment. Like the weight ratio A / B of the weight (B) of the binder resin to (A), it is preferably 10/12 to 10/30. The ratio of the charge generating material in the photosensitive layer 14 is preferably 1.5% by weight or more and 10% by weight or less.

  The film thickness of the photosensitive layer 14 is preferably 5 μm to 100 μm, more preferably 10 μm to 50 μm. If the film thickness of the photosensitive layer 14 is less than 5 μm, the charge holding ability on the surface of the photoreceptor may be lowered. If the film thickness of the photosensitive layer 14 exceeds 100 μm, the productivity may decrease.

  In the photoreceptor 3 of the third embodiment, a compound having a high charge transport ability represented by the general formula (I) according to the present invention is used as a charge transport material, whereby a binder resin is contained in the photosensitive layer 14 at a high ratio. Since it can be contained, the printing durability of the charge transport layer 16 is improved and the mechanical durability is improved without lowering the photoresponsiveness.

  The electrophotographic photoreceptor according to the present invention is not limited to the configuration of the electrophotographic photoreceptors 1, 2, and 3 of Embodiments 1 to 3 described above, and is represented by the general formula (I) according to the present invention. Other constitutions may be used as long as the compound to be contained is contained in the photosensitive layer as a charge transport material.

(Surface protective layer)
For example, a configuration in which a surface protective layer is provided on the surface of each photosensitive layer 14 in the first to third embodiments may be employed. By providing a surface protective layer on the surface of these photosensitive layers, the mechanical durability of the photoreceptor can be further improved. Further, it prevents chemical adverse effects on the photosensitive layer of active gas such as ozone and / or nitrogen oxide (NOx) generated by corona discharge when charging the surface of the photosensitive member, and further enhances the electrical durability of the photosensitive member. Can be improved.

  For the surface protective layer, for example, a layer made of a resin, an inorganic filler-containing resin, an inorganic oxide, or the like is used.

Embodiment 4
[Image forming apparatus]
The image forming apparatus of the present invention includes the electrophotographic photosensitive member according to the present invention.
As described above, an electrophotographic photosensitive member having a high charging potential, high sensitivity, sufficient photoresponsiveness, excellent durability, and characteristics do not deteriorate even when used in a low temperature environment or in a high-speed process. Therefore, a highly reliable image forming apparatus capable of providing high-quality images under various environments is provided.

The image forming apparatus of the present invention can be various printers, copiers, facsimiles, multifunction peripherals, etc. using an electrophotographic process regardless of monochrome or color.
Embodiments of an image forming apparatus including an electrophotographic photosensitive member according to the present invention will be described below. The image forming apparatus according to the present invention is not limited to the following description.

  FIG. 4 is an arrangement side view showing a simplified configuration of an image forming apparatus 100 as an embodiment of the image forming apparatus according to the present invention. An image forming apparatus 100 shown in FIG. 4 mounts a photoreceptor 1 that is a first embodiment of the electrophotographic photoreceptor according to the present invention. Hereinafter, the configuration and image forming operation of the image forming apparatus 100 will be described with reference to FIG.

  The image forming apparatus 100 includes a photoconductor 1 that is rotatably supported by an apparatus main body (not shown), and a drive unit (not shown) that rotates the photoconductor 1 around a rotation axis 44 in the direction of an arrow 41. The drive means includes, for example, a motor as a power source, and rotates the photosensitive member 1 at a predetermined peripheral speed Vp by transmitting the power from the motor to a support member constituting the core of the photosensitive member 1 via a gear (not shown). Driven (hereinafter, this peripheral speed Vp is also referred to as a rotational peripheral speed Vp).

  Around the photosensitive member 1, a charger 32, an exposure unit 30, a developing device 33, a transfer device 34, and a cleaner 36 are downstream from the upstream side in the rotation direction of the photosensitive member 1 indicated by an arrow 41. In this order towards the side.

The charger 32 is a charging unit that charges the surface 43 of the photoreceptor 1 to a predetermined potential.
In FIG. 4, the charger 32 is shown as a contact-type charging unit such as a charging roller. However, the charger 32 is not limited to this and is a non-contact type charging unit (for example, a scorotron charger) such as a corona discharger. May be.

  The exposure unit 30 includes, for example, a semiconductor laser as a light source, and exposes the charged surface 43 of the photosensitive member 1 with light 31 such as a laser beam output according to image information from the light source. An electrostatic latent image corresponding to image information is formed on the surface 43 of the substrate.

  The developing device 33 is a developing unit that develops the electrostatic latent image formed on the surface 43 of the photoreceptor 1 with a developer (for example, toner) to form a visible toner image, and faces the photoreceptor 1. Provided. The developing device 33 includes, for example, a developing roller 33a that supplies a developer to the surface 43 of the photoreceptor 1, and supports the developing roller 33a so that the developing roller 33a can rotate around a rotation axis parallel to the rotation axis 44 of the photoreceptor 1 and the inside thereof. And a casing 33b for accommodating the developer in the space.

  The transfer unit 34 is a transfer unit that transfers the toner image formed on the surface 43 of the photoreceptor 1 from the surface 43 of the photoreceptor 1 onto the recording paper 51 that is a transfer material. In FIG. 4, the transfer unit 34 is a non-contact type transfer unit that includes a charging unit such as a corona discharger and transfers a toner image onto the recording paper 51 by applying a charge having a polarity opposite to that of the toner to the recording paper 51. is there. However, the transfer unit 34 may be a contact-type transfer unit that performs transfer using a pressing force. As the contact-type transfer means, for example, a transfer roller is provided, and the transfer roller is pressed against the photosensitive member 1 from the opposite side of the contact surface of the recording paper 51 that is in contact with the surface 43 of the photosensitive member 1. For example, a toner image can be transferred onto the recording paper 51 by applying a voltage to the transfer roller while the photosensitive member 1 and the recording paper 51 are in pressure contact with each other.

  The cleaner 36 is a cleaning unit that cleans the surface of the photoreceptor 1 after image transfer. For example, the cleaner 36 is pressed against the surface 43 of the photoconductor, and is removed by the cleaning blade 36a that removes toner remaining on the surface 43 of the photoconductor 1 after the transfer operation by the transfer unit 34 from the surface 43. A recovery casing 36b for storing the developer.

  The cleaner 36 is provided together with a static elimination lamp (not shown). The static eliminator is a means for removing the charges accumulated on the surface of the photoreceptor 1. The static eliminator is, for example, a static elimination lamp.

  In the direction in which the recording paper 51 is conveyed after passing between the photoreceptor 1 and the transfer device 34, a fixing device 35 is provided as a fixing means for fixing the transferred toner image. The fixing device 35 includes, for example, a heating roller 35a having a heating unit (not shown), and a pressure roller 35b that is provided to face the heating roller 35a and that is pressed by the heating roller 35a to form a contact portion.

Hereinafter, an image forming operation by the image forming apparatus 100 will be described.
First, in response to an instruction from a control unit (not shown), the photosensitive member 1 is rotationally driven in the direction of an arrow 41 by a driving unit, and is upstream of the image forming point of the light 31 from the exposure unit 30 in the rotational direction of the photosensitive member 1. The surface 43 is uniformly charged to a predetermined positive or negative potential by the charger 32 provided on the side.

  Next, in response to an instruction from the control unit, light 31 is irradiated from the exposure unit 30 to the charged surface 43 of the photoreceptor 1. The light 31 from the light source is repeatedly scanned in the longitudinal direction of the photoreceptor 1 which is the main scanning direction based on the image information. By repeatedly scanning the light 31 from the light source based on the image information while rotating the photoconductor 1, the surface 43 of the photoconductor 1 can be exposed according to the image information. By this exposure, the surface charge of the portion irradiated with the light 31 is reduced, and a difference occurs between the surface potential of the portion irradiated with the light 31 and the surface potential of the portion not irradiated with the light 31. An electrostatic latent image is formed on the surface 43.

  In synchronism with the exposure of the photoreceptor 1, the recording paper 51 is supplied to the transfer position between the transfer device 34 and the photoreceptor 1 from the direction of the arrow 42 by the conveying means.

  Next, toner is applied from the developing roller 33a of the developing device 33 provided downstream of the image forming point of the light 31 from the light source to the surface 43 of the photosensitive member 1 on which the electrostatic latent image is formed. Is supplied. As a result, the electrostatic latent image is developed and a visible toner image is formed on the surface 43 of the photoreceptor 1. When the recording paper 51 is supplied between the photoconductor 1 and the transfer device 34, the transfer device 34 gives a charge having a polarity opposite to that of the toner to the recording paper 51, thereby forming the surface 43 of the photoconductor 1. The toner image is transferred onto the recording paper 51.

  The recording paper 51 onto which the toner image has been transferred is conveyed to the fixing device 35 by the conveying means, and is heated and pressed when passing through the contact portion between the heating roller 35a and the pressure roller 35b of the fixing device 35. As a result, the toner image on the recording paper 51 is fixed on the recording paper 51 and becomes a robust image. The recording paper 51 on which the image is formed in this way is discharged to the outside of the image forming apparatus 100 by the conveying means.

  On the other hand, after the toner image is transferred to the recording paper 51, the photosensitive member 1 that further rotates in the direction of the arrow 41 is scraped and cleaned by the cleaning blade 36 a provided on the cleaner 36. The charge 43 is removed from the surface 43 of the photoreceptor 1 from which the toner has been removed in this manner by the light from the static elimination lamp, and thereby the electrostatic latent image on the surface 43 of the photoreceptor 1 disappears. Thereafter, the photosensitive member 1 is further rotated and a series of operations starting from charging of the photosensitive member 1 is repeated. As described above, images are continuously formed.

  As described above, the photoreceptor 1 provided in the image forming apparatus 100 contains the compound according to the present invention represented by the general formula (I) in the photosensitive layer 14 as a charge transport material. Excellent electrical characteristics such as photoresponsiveness, electrical and mechanical durability, and environmental stability. Therefore, a highly reliable image forming apparatus 100 capable of stably forming a high-quality image over a long period of time in various environments is realized.

  In addition, even when the photoreceptor 1 is used in a high-speed electrophotographic process, the image forming apparatus 100 can increase the image forming speed because the image quality does not deteriorate. For example, the photosensitive member 1 having a diameter of 30 mm and a longitudinal length of 340 mm is used, the rotational peripheral speed Vp of the photosensitive member 1 is set to about 100 to 140 mm per second, and an electrophotographic process is performed at a high speed. High-quality images can be provided even when images are formed at a high image forming speed of about 25 A4 sheets / minute as defined in JIS P0138.

  The image forming apparatus of the present invention is not limited to the above-described configuration described with reference to FIG. 4, and may have another configuration as long as the photoconductor of the present invention is used.

  EXAMPLES Hereinafter, although a manufacture example, an Example, and a comparative example are given and this invention is demonstrated further in detail, this invention is not limited at all by these.

Production Example 1
Preparation of Compound (3) N, N′-diphenylbenzidine (33.6 g; 1.0 molar equivalent), diphenylacetaldehyde (40.2 g; 2.05 mole) was added to 300 mL of toluene in a reactor equipped with Dean-Stark. Equivalent)), DL-10-camphorsulfonic acid (0.23 g; 0.01 molar equivalent) was added and heated to reflux, and the reaction was carried out for 6 hours while removing water azeotroped with toluene out of the system. After completion of the reaction, the reaction solution was concentrated to about 1/10 (1/10), and gradually dropped into 100 mL of hexane with vigorous stirring. The produced crystals are collected by filtration, washed with cold ethanol, recrystallized with a mixed solvent of toluene-ethyl acetate (1: 3), and the following formula (a):

で表されるエナミン化合物（ａ）の結晶５６.８ｇを得た。
ｍｐ.１９１.０〜１９４.０℃、収率５８％。
ＮＭＲ（δ、ｐｐｍ、ＣＤＣｌ₃）７.２−７.３（ｍ、１４Ｈ）、７.１５−６.８５（ｍ、２４Ｈ）、６.７６（ｓ，２Ｈ）。

56.8 g of crystals of the enamine compound (a) represented by
mp.191.0-194.0 ° C., yield 58%.
_{NMR (δ, ppm, CDCl 3} ) 7.2-7.3 (m, 14H), 7.15-6.85 (m, 24H), 6.76 (s, 2H).

  In 200 mL of anhydrous N, N-dimethylformamide (DMF), 16.9 g (2.2 molar equivalents) of phosphorus oxychloride was gradually added under ice-cooling, and the mixture was stirred for about 30 minutes to prepare a Vilsmeier reagent. To this solution, 34.6 g (1.0 molar equivalent) of the enamine compound was gradually added under ice cooling. Thereafter, the reaction solution was gradually heated to raise the temperature of the reaction solution to 80 ° C. and stirred for 6 hours while reacting to maintain 80 to 90 ° C. for reaction. After completion of the reaction, the reaction solution was allowed to cool and gradually added to 800 mL of a cooled 4N (4N) aqueous sodium hydroxide solution to cause precipitation. The resulting precipitate was collected by filtration and sufficiently washed with water, and then recrystallized with a mixed solvent of ethanol and ethyl acetate to obtain 30.0 g of a yellow powdery compound.

で表されるアルデヒド体（ｂ）（分子量の計算値：７４８.３１）の分子イオン［Ｍ］⁺に相当するピークが７４８.９に観測された。このことから、得られた化合物は上記式（ｂ）で表される構造を有するアルデヒド体であることが確認された（収率：８０％）。また、ＬＣ−ＭＳの分析結果から、得られたアルデヒド体の純度が９８.７％であることが判った。 As a result of analyzing the obtained crystals by liquid chromatography-mass spectrometry (LC-MS), the following compound (b), which is the target compound:

A peak corresponding to the molecular ion [M] ⁺ of the aldehyde (b) (calculated molecular weight: 748.31) represented by the following was observed at 748.9. From this, it was confirmed that the obtained compound was an aldehyde having the structure represented by the above formula (b) (yield: 80%). Further, the analysis result of LC-MS showed that the purity of the obtained aldehyde compound was 98.7%.

で表される化合物（３）９.９ｇを黄色結晶として得た。 Next, 7.5 g (1.0 equivalent) of the aldehyde obtained above was dissolved in 80 ml of ethanol, 6.1 g (3.3 equivalent) of N, N-diphenylhydrazine was added to the solution, and acetic acid was added as a catalyst. 2 ml was added at room temperature and then heated and stirred at 60-70 ° C. for 5 hours. After completion of the reaction, the mixture is allowed to cool, and the resulting solid is filtered off and recrystallized with ethanol to obtain the following formula:

9.9 g of the compound (3) represented by formula (1) was obtained as yellow crystals.

<LC-MS>
As a result of analyzing the obtained crystals by LC-MS, a peak corresponding to the molecular ion [M] ⁺ of the compound (calculated molecular weight: 1080.49) of the compound (3) shown in Table 1 below, which is the target compound. Was observed at 1080.9, and the following fragment peaks were also observed:
MW = 1003: [M−φ] ⁺ <corresponding to a form in which the benzene ring is eliminated>
MW = 885: [M- (φ ₂ -NN = C)] ⁺ <corresponding to a form in which diphenylhydrazone is eliminated>
MW = 901: [M- (CH = C (φ) ₂ )] ⁺ <corresponding to the form in which the enamine unit is detached>
MW = 809: [M- (φ-C = NN-φ ₂ )] ⁺ <corresponding to a form in which the diphenylhydrazone unit is detached>
MW = 616: [M-([phi] _2- N-N = C- [phi] -N-CH = C ([phi]) ₂ )] ⁺ <corresponding to the form in which the amine unit is eliminated>
MW = 168: [φ ₂ -N] ⁺ <part of diphenylhydrazone>
(Φ represents a benzene ring.)
From this, it was confirmed that the obtained crystal was the compound (3) (yield: 92%).
Further, from the analysis result of LC-MS, it was found that the purity of the obtained compound (3) was 99.1%.

  Elemental analysis of the obtained compound (3) was performed using a simultaneous determination method of carbon (C), hydrogen (H) and nitrogen (N) by a differential thermal conductivity method. The same applies to the following production examples.

Elemental analysis value of compound (3):
Theoretical values: C: 86.64%, H: 5.59%, N: 7.77%
Actual value: C: 86.05%, H: 6.06%, N: 7.89%

で表されるエナミン化合物（ｃ）（３６.８ｇ）を合成した。このエナミン化合物を原料として、前記製造例１と同様にして、以下の式： Production Example 2
Preparation of Compound (24) From N, N′-dinaphthyl-3,3′dimethylbenzidine (23.2 g) and diphenylacetaldehyde (20.1 g) according to the method described in Preparation Example 1 above, formula (c):

The enamine compound (c) (36.8 g) represented by Using this enamine compound as a raw material, the following formula:

で表される化合物（２４）（９.５ｇ）を得た（収率：７５％）。

The compound (24) (9.5g) represented by this was obtained (yield: 75%).

  The obtained compound was subjected to LC-MS analysis and elemental analysis. As a result, the following results were obtained, and it was confirmed that the compound was compound (24).

Compound (24)
<LC-MS>
Purity: 98.9%
[M] ⁺ : Actual value: 1084.9 (Calculated value of molecular weight: 1084.50)
Fragment ion peak MW = 1069: [M-Me] ⁺ <corresponding to a form in which a methyl group is eliminated>
MW = 1007: [M−φ] ⁺ <corresponding to a form in which the phenyl group is eliminated>
MW = 951: [M- (C = NN- (Me) φ)] ⁺ <corresponding to a form in which phenylmethylhydrazone is eliminated>
MW = 905: [M- (CH = C (φ) ₂ )] ⁺ <corresponding to the form in which the enamine unit is detached>
MW = 632: [M- (φ (Me) -N—N—C—Np—N—CH═C (φ) ₂ )] ⁺ <corresponding to the form in which the amine unit is eliminated>
MW = 106: [φ (Me) -N] ⁺ <Part of phenylmethylhydrazone>
(Φ represents a benzene ring, Np represents a naphthalene ring, and Me represents a methyl group.)
<Elemental analysis> Theoretical values: C: 86.31%, H: 5.94%, N: 7.74%
Actual value: C: 86.21%, H: 5.91%, N: 7.88%

で表されるエナミン化合物（ｄ）（３１.９ｇ）を合成した。このエナミン化合物を原料として、前記製造例１と同様にして、以下の式： Production Example 3
Preparation of Compound (35) From 1- (4-phenylaminophenyl) -4-phenylaminobenzofuran (18.8 g) and diphenylacetaldehyde (20.1 g) according to the method described in Preparation Example 1 above, the compound of formula (d) :

An enamine compound (d) (31.9 g) represented by the following formula was synthesized. Using this enamine compound as a raw material, the following formula:

で表される化合物（３５）（８.５ｇ）を得た（収率：７４％）。

(35) (8.5 g) represented by the following yield was obtained (yield: 74%).

  The obtained compound was subjected to LC-MS analysis and elemental analysis. As a result, the following results were obtained, and it was confirmed that the compound was the compound (35).

Compound (35)
<LC-MS>
Purity: 99.0%
[M] ⁺ : 110.9 (calculated molecular weight: 110.5)
Fragment ion peak MW = 1043: [M−φ] ⁺ <corresponding to a form in which a benzene ring is eliminated>
MW = 925: [M- (φ ₂ -N—N═C)] ⁺ <corresponding to a form in which diphenylhydrazone is eliminated>
MW = 941: [M- (CH = C (φ) ₂ )] ⁺ <corresponding to the form in which the enamine unit is detached>
MW = 861: [M- (φ-C = NN-φ ₂ )] ⁺ <corresponding to a form in which the diphenylhydrazone unit is detached>
MW = 656: [M-([phi] ₂ -NN = C- [phi] -N-CH = C ([phi]) ₂ )] ⁺ <corresponding to the form in which the amine unit is eliminated>
MW = 168: [φ ₂ -N] ⁺ <part of diphenylhydrazone>
(Φ represents a benzene ring.)
<Elemental analysis> Theoretical values: C: 85.69%, H: 5.39%, N: 7.49%
Actual value: C: 85.41%, H: 5.49%, N: 7.59%

で表されるエナミン化合物（ｅ）を原料として、前記製造例１と同様にして、以下の式： Production Example 4
Preparation of Compound (45) Compound (e) synthesized from 3,6-phenylamino-N-ethylcarbazole (18.9 g) and diphenylacetaldehyde (20.1 g) according to the method described in Preparation Example 1 above:

In the same manner as in Production Example 1, using the enamine compound (e) represented by the following formula:

で表される化合物（４５）（９.８ｇ）を得た（収率：８２％）。

Compound (45) (9.8 g) represented by the following yield was obtained (yield: 82%).

The obtained compound was subjected to LC-MS analysis and elemental analysis. The results were as follows, and it was confirmed that the compound was the compound (45).
Compound (45)
<LC-MS>
Purity: 98.9%
[M + H] ⁺ : 997.9 (calculated molecular weight: 997.5)
Fragment ion peak MW = 982: [M-Me] ⁺ <corresponding to a form in which a methyl group is eliminated>
MW = 968: [M-CH ₂ CH ₃ ] ⁺ <corresponding to the form in which the ethyl group is eliminated>
MW = 920: [M−φ] ⁺ <corresponding to the form in which the benzene ring is eliminated>
MW = 864: [M- (C = NN- (Me) φ)] ⁺ <corresponding to a form in which phenylmethylhydrazone is eliminated>
MW = 818: [M- (CH = C (φ) ₂ )] ⁺ <corresponding to the form in which the enamine unit is detached>
MW = 595: [M- (φ (Me) -N—N—C—Np—N—CH═C (φ) ₂ )] ⁺ <corresponding to the form in which the amine unit is eliminated>
MW = 106: [φ (Me) -N] ⁺ <Part of phenylmethylhydrazone>
(Φ represents a benzene ring, and Me represents a methyl group.)
<Elemental analysis> Theoretical values: C: 84.22%, H: 5.96%, N: 9.82%
Actual value: C: 84.08%, H: 6.05%, N: 9.87%

Example 1
9 parts by weight of dendritic titanium oxide (Ishihara Sangyo Co., Ltd .: TTO-D-1) surface-treated with aluminum oxide (Al ₂ O ₃ ) and zirconium dioxide (ZrO ₂ ), copolymer nylon resin (Toray Industries, Inc.) 9 parts by weight (manufactured by Co., Ltd .: CM8000) is added to a mixed solvent of 41 parts by weight of 1,3-dioxolane and 41 parts by weight of methanol, and dispersed for 12 hours using a paint shaker. Was prepared. The prepared coating solution for intermediate layer was applied on a 0.2 mm thick aluminum plate-like conductive support with a baker applicator and then dried to form an intermediate layer having a thickness of 1 μm.

  Next, 2 parts by weight of an X-type metal-free phthalocyanine (Dainippon Ink Chemical Co., Ltd .: Fastgen Blue 8120BS) as a charge generating substance, and polyvinyl butyral resin (Sekisui Chemical Co., Ltd .: BX-1) 1 in 97 parts by weight of THF 1 The resin solution obtained by dissolving parts by weight was added and then dispersed for 10 hours with a paint shaker to prepare a coating solution for charge generation layer (100 g). The charge generation layer coating solution was applied onto the intermediate layer formed previously by a bakery applicator and then dried to form a charge generation layer having a thickness of 0.3 μm.

Next, 10 parts by weight of the compound (3) obtained in Production Example 1 as a charge transport material, 18 parts by weight of a polycarbonate resin (manufactured by Mitsubishi Gas Chemical Co., Inc .: Z200) as a binder resin, and 2,6-di-t- 0.2 part by weight of butyl-4-methylphenol was dissolved in 115 parts by weight of THF to prepare a coating solution for charge transport layer (100 g). This coating solution for charge transport layer was applied on the charge generation layer formed previously by a baker applicator and then dried to form a charge transport layer having a thickness of 20 μm.
As described above, the electrophotographic photosensitive member of Example 1 having the stacked layer structure shown in FIG. 2 was produced.

Example 2
In the same manner as in Example 1, except that the compound (24) obtained in Production Example 2 was used instead of the compound (3) used as the charge transport material in Example 1, the electrophotographic photosensitive material of Example 2 was used. The body was made.

Example 3
The electrophotographic photosensitive material of Example 3 was obtained in the same manner as in Example 1 except that the compound (35) obtained in Production Example 3 was used instead of the compound (3) used as the charge transport material in Example 1. The body was made.

で表される化合物（Ａ）（トリフェニルアミンダイマー；ＴＰＤ）を用いる以外は、実施例１と同様にして、比較例１の電子写真感光体を作製した。 Comparative Example 1
As a charge transport material, instead of the compound (3), the following formula (A):

An electrophotographic photosensitive member of Comparative Example 1 was produced in the same manner as in Example 1 except that the compound (A) represented by the formula (triphenylamine dimer; TPD) was used.

Example 4
In the same manner as in Example 1, an intermediate layer having a thickness of 1 μm was formed on an aluminum plate-like conductive support having a thickness of 0.2 mm.
Next, 1 part by weight of an X-type metal-free phthalocyanine (Dainippon Ink Chemical Co., Ltd .: Fastgen Blue 8120BS) as a charge generating substance and 18 parts by weight of a polycarbonate resin (Mitsubishi Gas Chemical Co., Ltd .: Z-400) as a binder resin 10 parts by weight of a compound (3) shown in Table 1 as a charge transport material, 5 parts by weight of 3,5-dimethyl-3 ′, 5′-di-t-butyldiphenoquinone, and 2,6 -0.5 part by weight of di-t-butyl-4-methylphenol and 115 parts by weight of THF were dispersed in a ball mill for 12 hours to prepare a coating solution for a photosensitive layer. This photosensitive layer coating solution was applied onto the previously formed intermediate layer with a baker applicator and then dried with hot air at a temperature of 110 ° C. for 1 hour to form a photosensitive layer having a thickness of 20 μm.
As described above, the electrophotographic photosensitive member of Example 4 having the single-layer structure shown in FIG. 3 was produced.

[Evaluation 1]
For each of the photoreceptors of Examples 1 to 4 and Comparative Example 1 manufactured as described above, initial characteristics and repeat characteristics were measured using an electrostatic copying paper test apparatus (manufactured by Kawaguchi Electric Co., Ltd .: EPA-8200). evaluated. Evaluation is conducted at a normal temperature / normal humidity (N / N) environment at a temperature of 22 ° C. and a relative humidity of 65% (65% RH), and at a temperature of 5 ° C. and a relative humidity of 20% (20% RH). The test was carried out in each environment under a low temperature / low humidity (L / L) environment.

Initial characteristics were evaluated as follows. Minus the photoreceptor (-) 5 kV voltage charges the photosensitive member surface by applying a, the surface potential of the photosensitive member at that time was measured as the charging potential V ₀ which [V], the absolute value of the charge potential V ₀ which is It was evaluated that the larger the value, the better the chargeability. However, in the case of the single layer type photoreceptor of Example 4, the surface of the photoreceptor was charged by applying a voltage of plus (+) 5 kV.

Next, the charged photoreceptor surface was exposed. At this time, the exposure energy required to halve the surface potential of the photoreceptor from the charging potential V ₀ is measured as a half exposure E _1/2 [μJ / cm ² ], and the smaller the half exposure E _1/2 is, the smaller the half exposure E _1/2 is. It was evaluated that the sensitivity was excellent. Further, the surface potential of the photoconductor after 10 seconds from the start of exposure was measured as the residual potential V _r [V], and it was evaluated that the smaller the absolute value of the residual potential V _r , the better the photoresponsiveness.
A monochromatic light of 1 μW / cm ² of energy was used.

The repeatability was evaluated as follows. After the above-described charging and exposure operations were repeated 5000 times as one cycle, the charging potential V ₀ , half-exposure amount E _1/2 and residual potential V _r were measured in the same manner as in the evaluation of the initial characteristics, and the charging property, Sensitivity and photoresponsiveness were evaluated.

表２から、電荷輸送物質として一般式（Ｉ）で表される本発明に係る化合物を用いた実施例１〜４の感光体は、Ｎ／Ｎ環境下およびＬ／Ｌ環境下のいずれにおいても、帯電性、感度および光応答性に優れることが判る。また、実施例１〜４の感光体は、繰返し使用されても初期と同様に優れた電気特性を有することが判る。 The measurement results are shown in Table 2.

From Table 2, the photoreceptors of Examples 1 to 4 using the compound according to the present invention represented by the general formula (I) as the charge transporting substance can be used in both N / N environment and L / L environment. It can be seen that it is excellent in chargeability, sensitivity and photoresponsiveness. In addition, it can be seen that the photoreceptors of Examples 1 to 4 have excellent electrical characteristics as in the initial stage even when used repeatedly.

Example 5
9 parts by weight of dendritic titanium oxide (Ishihara Sangyo Co., Ltd .: TTO-D-1) surface-treated with aluminum oxide (Al ₂ O ₃ ) and zirconium dioxide (ZrO ₂ ), copolymer nylon resin (Toray Industries, Inc.) After adding 9 parts by weight to a mixed solvent of 41 parts by weight of 1,3-dioxolane and 41 parts by weight of methanol, dispersion treatment was carried out with a paint shaker for 8 hours. 1 kg) was prepared. The intermediate layer coating solution is filled in a coating tank, and an aluminum cylindrical conductive support having a diameter of 30 mm × length of 357 mm × thickness of 0.8 mm is immersed in the coating tank, and then pulled up and dried to obtain a film thickness of 1 A 0.0 μm intermediate layer was formed on the conductive support.

Next, 2 parts by weight of oxotitanium phthalocyanine (produced by Orient Chemical Co., Ltd .: TPL-3), 1 part by weight of polyvinyl butyral resin (manufactured by Sekisui Chemical Co., Ltd .: ESREC BM-S), which is the charge generation material 12, and 97 parts by weight of methyl ethyl ketone Were mixed with a paint shaker to prepare a charge generation layer coating solution (1 kg). This charge generation layer coating solution was applied onto the intermediate layer by the same dip coating method as that for the previously formed intermediate layer and dried to form a charge generation layer having a thickness of 0.4 μm.
As a result of measuring an X-ray diffraction spectrum by Cu-Kα characteristic X-ray (wavelength: 1.54 波長) of the charge generation layer, a clear diffraction peak was observed at a Bragg angle (2θ ± 0.2 °) of 27.2 °. Indicated.

Next, 10 parts by weight of the compound (3) obtained in Production Example 1 as a charge transport material, 20 parts by weight of a polycarbonate resin (manufactured by Mitsubishi Engineering Plastics Co., Ltd .: Iupilon Z200) as a binder resin, and 2,6-di- 1 part by weight of t-butyl-4-methylphenol and 0.004 part by weight of dimethylpolysiloxane (manufactured by Shin-Etsu Chemical Co., Ltd .: KF-96) are dissolved in 120 parts by weight of THF, and a coating solution for a charge transport layer ( 1 kg) was prepared.
This charge transport layer coating solution was applied on the charge generation layer formed earlier by the same dip coating method as that for the previously formed intermediate layer, and then dried at a temperature of 130 ° C. for 1 hour. A charge transport layer was formed.
As described above, the electrophotographic photosensitive member of Example 5 was produced.

Example 6
The electrophotographic photosensitive material of Example 6 was obtained in the same manner as in Example 5 except that the compound (24) obtained in Production Example 2 was used in place of the compound (3) used as the charge transport material in Example 5. The body was made.

Example 7
The electrophotographic photosensitive material of Example 6 was obtained in the same manner as in Example 5 except that the compound (45) obtained in Production Example 4 was used instead of the compound (3) used as the charge transport material in Example 5. The body was made.

Comparative Example 2
An electrophotographic photoreceptor of Comparative Example 2 was produced in the same manner as in Example 5 except that the compound (A) was used instead of the compound (3) used as the charge transport material in Example 5.

Example 8
An electrophotographic photosensitive member of Example 8 was produced in the same manner as in Example 5 except that the amount of the polycarbonate resin as the binder resin was changed to 25 parts by weight when forming the charge transport layer in Example 5.

Example 9
In the formation of the charge transport layer in Example 5, the amount of the polycarbonate resin as the binder resin was changed to 25 parts by weight, and the compound (24) obtained in Production Example 2 was used instead of the compound (3) as the charge transport material. The electrophotographic photosensitive member of Example 9 was produced in the same manner as in Example 5 except that.

Example 10
In forming the charge transport layer in Example 5, the amount of the polycarbonate resin as the binder resin was changed to 25 parts by weight, and the compound (45) obtained in Production Example 4 was used instead of the compound (3) as the charge transport material. The electrophotographic photosensitive member of Example 10 was produced in the same manner as in Example 5 except that.

Example 11 (Reference Example 1)
An electrophotographic photosensitive member of Example 11 was produced in the same manner as in Example 5 except that the amount of the polycarbonate resin as the binder resin was changed to 10 parts by weight when forming the charge transport layer in Example 5.

Reference example 2
An electrophotographic photosensitive member was produced in the same manner as in Example 5 except that the amount of the polycarbonate resin as the binder resin was changed to 31 parts by weight when forming the charge transport layer in Example 5. However, the same amount of THF as in Example 5 increased the viscosity of the charge transport layer coating solution. Therefore, THF (150 g) was added, and a sufficiently diluted charge transport layer coating solution was prepared again. Used to form a charge transport layer.

  However, white turbidity due to the brushing phenomenon occurred at the longitudinal end of the cylindrical photoconductor, and the characteristic evaluation shown in Evaluation 2 below could not be performed. This brushing phenomenon is presumed to have occurred because the amount of the solvent in the charge transport layer coating solution was excessive.

Reference example 3
In forming the charge transport layer, the compound A represented by the structural formula (A) is used as the charge transport material instead of the compound (3), and the amount of the polycarbonate resin as the binder resin is changed to 10 parts by weight. An electrophotographic photoreceptor of Reference Example 3 was produced in the same manner as Example 5 except that.
[Evaluation 2]
Each of the photoreceptors of Examples 5 to 7 and Comparative Example 2 manufactured as described above was subjected to an X-TOF mode in a drum checker (Gentech Co., Ltd .: CYNCYA) and an electric field strength of 2.5 × 10 ⁵ V / The hole mobility at cm, temperature of 25 ° C. and relative humidity of 50% was measured.

  Each photoconductor was mounted on a commercially available digital copying machine MX-3100 (manufactured by Sharp Corporation), and the printing durability, electrical characteristics, and environmental stability of each photoconductor were evaluated as follows. The digital copying machine MX-3100 is a negatively charged image forming apparatus that performs an electrophotographic process by negatively charging the surface of the photoreceptor.

(Print life)
Using the above-described test copying machine, a test image having a predetermined pattern was formed on 40,000 sheets of recording paper, the mounted photoconductor was taken out, and the film thickness d1 [μm] of the photosensitive layer was measured. A value (d0−d1) obtained by subtracting d1 from the film thickness d0 of the photosensitive layer at the time of production was obtained as a film reduction amount Δd and used as an evaluation index for printing durability. The film thickness was measured with a film thickness measuring device F20-EXR (manufactured by Filmetrics).

(Electrical properties and environmental stability)
A surface potentiometer (manufactured by Gentec Corporation: CATE751) was provided in the test copying machine so that the surface potential of the photoreceptor in the image forming process could be measured. Using this copying machine, the surface potential of each photoconductor immediately after the charging operation by the charger was measured as a charging potential V1 [V] in an N / N environment at a temperature of 22 ° C. and a relative humidity of 65%. Further, measuring the surface potential of the photosensitive member immediately after subjected to exposure by a laser beam as a residual potential VL [V], which was used as a residual potential VL _N under the N / N environment. The larger the absolute value of the charging potential V1, the better the charging property, and the smaller the absolute value of the residual potential VL _N , the better the photoresponsiveness.

Further, a temperature 5 ° C., under a relative humidity of 20% of the L / L environment, N / N in the same manner as environment, to measure the residual potential VL [V], the residual potential VL _L this under the L / L environment It was. The absolute value (| VL _L −VL _N |) of the value obtained by subtracting the residual potential VL _N under the N / N environment from the residual potential VL _L under the L / L environment was determined as the potential fluctuation ΔVL. It was evaluated that the smaller the potential fluctuation ΔVL, the better the stability of the electrical characteristics.

These evaluation results are shown in Table 3.

  From comparison between Examples 5 to 7 and Comparative Example 2, the compound of the present invention represented by the general formula (I) is higher by 1 to 2 digits than the triphenylamine dimer (TPD) of Comparative Compound A. It was found to have charge mobility.

From the comparison between Examples 5 to 10 and Comparative Example 2, the photoreceptor using the compound of the present invention represented by the general formula (I) as the charge transport material is a comparative example using Comparative Compound A as the charge transport material. It can be seen that the absolute value of the exposure potential VL _N under the N / N environment is smaller than that of the photosensitive member 2. Therefore, in the photoreceptors of Examples 5 to 10, even when the ratio (B / A) of the weight (B) of the binder resin to the weight (A) of the charge transport material in the charge transport layer is 1.2 or more. It was found to have excellent photoresponsiveness. Further, the photoconductors of Examples 5 to 10 have a small potential fluctuation ΔVL value and excellent environmental stability as compared with the photoconductor of Comparative Example 2, and exhibit sufficient photoresponsiveness even in an L / L environment. understood.

  Further, from comparison between Examples 5 to 10 and Example 11, the photoconductors of Examples 5 to 10 in which the ratio B / A is in the range of 1.2 to 3.0 are more preferable than the ratio B / A. It was found that the film reduction amount Δd was smaller and the printing durability was superior to that of the photoreceptor of Example 11 in which A was less than 1.2.

  From a comparison between Example 11 and Comparative Example 2 and Reference Example 3, the photoconductor of Example 11 is inferior to the photoconductor of Comparative Example 2 in which the ratio B / A is high, but the ratio is the same. It was superior to a certain reference example 3, and it was found that the chargeability was almost comparable to that of comparative example 2.

  As described above, by using the compound of the present invention as a charge transport material, the photosensitive layer (when the photosensitive layer has a carbon layer structure) or the charge transport layer (the photosensitive layer is a laminated structure) without reducing the photoresponsiveness. In the case of (), the printing durability can be improved.

  According to the present invention, each of the compounds represented by the general formula (I), for example, (2) or (3) has a structure in which a conjugated system expanded by having two enamine structures and hydrazone structures in the molecule is formed. Can be used as an organic photoconductive material exhibiting a high charge (hole) transport capability.

  By incorporating this compound into the photosensitive layer as a charge transport material, it has a high charging potential, high sensitivity and sufficient photoresponsiveness, and even when used in various environments such as low temperature environments or high-speed processes. A highly reliable electrophotographic photosensitive member whose characteristics do not deteriorate and an image forming apparatus using the same are obtained.

  In addition, when this compound is contained in the photosensitive layer together with the binder resin, it becomes possible to increase the content ratio of the binder resin, and the durability is further improved by a synergistic effect with the excellent wear resistance of the compound itself. An electrophotographic photosensitive member and an image forming apparatus can be obtained.

  Furthermore, if the compound represented by the general formula (I) is used for a sensor material, an EL element, an electrostatic recording element or the like, a device having excellent responsiveness can be provided.

BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is a partial cross-sectional view showing a simplified configuration of an electrophotographic photoreceptor 1 that is a first embodiment of an electrophotographic photoreceptor according to the present invention. It is a fragmentary sectional view which simplifies and shows the structure of the electrophotographic photoreceptor 2 which is the 2nd Embodiment of the electrophotographic photoreceptor by this invention. It is a fragmentary sectional view which simplifies and shows the structure of the electrophotographic photosensitive member 3 which is the 3rd Embodiment of the electrophotographic photosensitive member by this invention. 1 is a side view schematically illustrating a configuration of an image forming apparatus 100 that is an embodiment of an image forming apparatus according to the present invention.

1, 2, 3 Electrophotographic photoreceptor 11 Conductive support 12 Charge generating material 13 Charge transporting material 14 Photosensitive layer 15 Charge generating layer 16 Charge transporting layer 17 Binder resin 18 Intermediate layer 30 Exposure means 31 Light 32 from exposure means Charging Device 33 developing device 34 transfer device 35 fixing device 36 cleaner 100 image forming apparatus

Claims (10)

A layered photosensitive layer in which a charge generating layer containing a charge generating material and a charge transporting layer containing a charge transporting material are laminated in this order, or a single layer type photosensitive layer containing a charge generating material and a charge transporting material is conductively supported The charge transport layer or the single-layer type photosensitive layer is formed on the body as the charge transport material and has the following general formula (I):

(In the formula, Ar ¹ and Ar ² are each independently an arylene group or divalent heterocyclic group which may have a substituent, and Ar ³ and Ar ⁴ independently represent a substituent. An alkyl group, an aralkyl group, an aryl group or a monovalent heterocyclic group which may have, provided that either Ar ³ or Ar ⁴ is an aryl group or a monovalent heterocyclic group, or Ar ³ and Ar ⁴ can be combined with the nitrogen atom to which they are bonded to each other to form an optionally substituted heterocyclic group)
An electrophotographic photoreceptor containing a 2,2-diphenylvinylamine derivative compound represented by the formula: In the general formula (I), the Ar ¹ is represented by the following formula:

A group represented by
The Ar ² is represented by the following formula:

A group represented by
Ar ³ and Ar ⁴ are represented by the following formula:

Or Ar ³ and Ar ⁴ together with a nitrogen atom bonded to each other can be represented by the following formula:

The photoreceptor according to claim 1, which is a 2,2-diphenylvinylamine derivative compound represented by the formula: In the general formula (I), the Ar ¹ is represented by the following formula:

A group represented by
The Ar ² is represented by the following formula:

A group represented by
The Ar ³ is represented by the following formula:

A group represented by
The Ar ⁴ has the following formula:

Or Ar ³ and Ar ⁴ together with a nitrogen atom bonded to each other can be represented by the following formula:

The photoreceptor according to claim 1, which is a 2,2-diphenylvinylamine derivative compound represented by the formula: In the general formula (I), the Ar ¹ is represented by the following formula:

A group represented by
Ar ² is

A group represented by
Ar ³ and Ar ⁴ are represented by the following formula:

The photoconductor according to claim 1, which is a 2,2-diphenylvinylamine derivative compound represented by the formula: The compound represented by the general formula (I) is:
The Ar ¹ is represented by the following formula:

Wherein Ar ² is a group represented by the following formula:

Wherein Ar ³ and Ar ⁴ are represented by the following formula:

The following formula (3):

Or
The Ar ¹ is represented by the following formula:

Wherein Ar ² is a group represented by the following formula:

The Ar ³ and Ar ⁴ are not the same as each other, and the following formula:

The following formula (24):

Or
The Ar ¹ is represented by the following formula:

Wherein Ar ² is a group represented by the following formula:

Wherein Ar ³ and Ar ⁴ are represented by the following formula:

And the following equation (35):

Or
The Ar ¹ is represented by the following formula:

Wherein Ar ² is a group represented by the following formula:

The Ar ³ and Ar ⁴ are not the same as each other, and the following formula:

The following formula (45):

The photoconductor according to claim 1, which is a 2,2-diphenylvinylamine derivative compound represented by the formula:   The charge generation layer or the single-layer type photosensitive layer contains a binder resin, and in the charge transport layer or the single-layer type photosensitive layer, the weight ratio of the charge transport material (A) and the binder resin (B). The electrophotographic photosensitive member according to any one of claims 1 to 5, wherein A / B is 10/12 to 10/30.   The charge generation layer or the single-layer type photosensitive layer diffracts as a charge generation material at a Bragg angle (2θ ± 0.2 °) of at least 27.2 ° in Cu-Kα characteristic X-ray diffraction (wavelength: 1.54Å). The electrophotographic photosensitive member according to any one of claims 1 to 6, comprising oxotitanium phthalocyanine having a peak.   The electrophotographic photosensitive member according to claim 1, wherein the photoreceptor further comprises an intermediate layer between the laminated photosensitive layer or the single-layer photosensitive layer and the conductive support. body.   An image forming apparatus comprising the electrophotographic photosensitive member according to claim 1.   An image forming method using the image forming apparatus according to claim 9.

Images