JPH07175250A - Electrophotographic photoreceptor - Google Patents

Electrophotographic photoreceptor

Info

Publication number
JPH07175250A
JPH07175250A JP34485293A JP34485293A JPH07175250A JP H07175250 A JPH07175250 A JP H07175250A JP 34485293 A JP34485293 A JP 34485293A JP 34485293 A JP34485293 A JP 34485293A JP H07175250 A JPH07175250 A JP H07175250A
Authority
JP
Japan
Prior art keywords
substituted
layer
electrophotographic photoreceptor
compound
group
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP34485293A
Other languages
Japanese (ja)
Inventor
Masayuki Shiyoji
正幸 所司
Yumi Ichikawa
由美 市川
Akio Kojima
明夫 小島
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Ricoh Co Ltd
Original Assignee
Ricoh Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Ricoh Co Ltd filed Critical Ricoh Co Ltd
Priority to JP34485293A priority Critical patent/JPH07175250A/en
Publication of JPH07175250A publication Critical patent/JPH07175250A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To obtain an electrophotographic photoreceptor having high sensitivity and high durability by incorporating a phthalimide compound into a primary coating layer. CONSTITUTION:In the function separating electrophotographic photoreceptor formed by successively laminating a charge generation layer (CGL) and a charge transport layer (CTL) containing a donor type compound having positive hole transportability on an electrically conductive substrate, the primary coat layer containing the phthalimide compound is provided between the electrically conductive substrate and the CGL. An electron transport material expressed by a formula is preferably used as the phthalimide compound. In the formula, each of R1 and R2 represents (un)substituted alkyl group, (un)substituted cycloalkyl group or (un)substituted phenyl group, X represents =O, =C(Y)(Z) or =N(CN) and each of Y and Z represents hydrogen atom, (un)substituted phenyl group, cyano group or (un)substituted alkoxycarbonyl group.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は電子写真プロセスを用い
た複写機、プリンター等に用いられる電子写真用感光体
に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an electrophotographic photosensitive member used in a copying machine, a printer or the like using an electrophotographic process.

【0002】[0002]

【従来の技術】電子写真プロセスは静電気力による潜像
の可視化を基本原理として用いたものであるため、その
プロセスに用いられる電子写真用感光体には良好な帯電
性と光照射による迅速な表面電位の減衰が必要となる。
これらプロセス上必要な特性は固有物性値である暗抵抗
の高さと、電荷担体生成の良好な量子効率、高い電荷移
動度に還元される。
2. Description of the Related Art Since the electrophotographic process uses the visualization of a latent image by electrostatic force as a basic principle, the electrophotographic photosensitive member used in the process has good chargeability and rapid surface irradiation by light irradiation. Potential decay is required.
The properties required for these processes are reduced to high dark resistance, which is a specific physical property value, good quantum efficiency for charge carrier generation, and high charge mobility.

【0003】これらの物性値を満足するものとして、従
来、セレン、セレン−テルル合金、砒素セレン等の無機
化合物から構成された感光体が採用され、多くの複写機
で用いられてきた。しかしながら、これらの材料は、毒
性が強い、アモルファス状態で用いられるため取扱いが
厄介である、蒸着法等により数10μmの膜厚にする必
要があるためコストが高くなる等の欠点があり、感光体
の必要機能を十分に満足していえるとは言えないもので
あった。
In order to satisfy these physical property values, a photoconductor composed of an inorganic compound such as selenium, selenium-tellurium alloy, arsenic selenium, etc. has been adopted and has been used in many copying machines. However, these materials have drawbacks that they are highly toxic, are difficult to handle because they are used in an amorphous state, and have a high cost because they require a film thickness of several tens of μm by a vapor deposition method. It cannot be said that it can be said that it fully satisfies the necessary functions of.

【0004】これらの欠点を改良するため、有機材料を
用いた電子写真用感光体(OPC)の開発が積極的にな
され、実用に供されるようになってきた。実用化された
OPCのほとんどは導電性基板上に電荷発生機能を有す
る層(CGL)と電荷輸送機能を有する層(CTL)と
を積層した構成の機能分離型感光体であり、機能を分離
することにより材料の選択幅も拡がり、電子写真感度、
繰返し安定性、機械的強度等の特性も向上し、複写基、
プリンター等に数多く搭載されるようになってきた。し
かし、このようなOPCにおいて導電性基板上に直接感
光層を設けた場合、導電性基板の欠陥、即ち傷、不純
物、腐食物といった表面欠陥が画像にそのまま反映し、
黒ポチや白抜けという異常画像の原因となる場合が多
い。特に機能分離型感光体におけるCGLは通常数μm
以下の薄膜にする必要があり、基板表面の欠陥を拾いや
すく、塗膜欠陥が生じやすく、生産性を低下させてい
る。また、導電性基板と感光層との接着性が悪い場合も
多くみられ、小さな感光層の傷から全体が剥がれてしま
う場合もある。
In order to improve these drawbacks, electrophotographic photoconductors (OPC) using organic materials have been actively developed and put into practical use. Most of the practically used OPCs are function-separated type photoconductors having a structure in which a layer having a charge generation function (CGL) and a layer having a charge transport function (CTL) are laminated on a conductive substrate, and separate the functions. As a result, the range of choice of materials is expanded, and the electrophotographic sensitivity,
The characteristics such as repeatability and mechanical strength are improved.
It has come to be installed in many printers and the like. However, when a photosensitive layer is directly provided on a conductive substrate in such an OPC, defects of the conductive substrate, that is, surface defects such as scratches, impurities, and corrosive substances are directly reflected in the image,
It often causes abnormal images such as black spots and white spots. In particular, the CGL of the function-separated type photoconductor is usually several μm.
It is necessary to form the following thin film, and defects on the surface of the substrate are easily picked up, defects in the coating film are likely to occur, and productivity is reduced. In many cases, the adhesiveness between the conductive substrate and the photosensitive layer is poor, and the entire surface may be peeled off from a scratch on the small photosensitive layer.

【0005】それらを防止する目的で、多くの感光体で
はバリヤー層、接着層として導電性基板と感光層との間
に下引層を設けている。下引層としては、主に絶縁性高
分子材料がサブミクロンの膜厚の薄膜で設けられている
が、絶縁性であるため、感度の低下、残留電位の増加を
引き起こすという致命的な欠点を有している。これらを
防ぐ目的で種々の方法が提案されている。一つは下引層
中に無機導電性フィラーを分散させる方法、また一つは
イオン導電性っ高分子を下引層中に含有させる方法、ま
た一つはアクセプター性の電子輸送物質を下引層中に含
有させる方法である。無機導電性フィラーとしては、酸
化チタンや酸化スズが用いられるが(特公昭63−19
869号)、これらは下引層塗布液中に分散させる必要
があり、その分散液の調整や、ポットライフに技術的な
困難を伴う。イオン導電性高分子としては、例えば可溶
性ナイロン、ポリアミド等の高分子が用いられるが(特
開昭52−25638号、特開昭58−30757
号)、導電率が低いため問題点を解消するには至ってい
ない。さらにこれらにアクセプター性の電子輸送物質を
含有させるのが3番目の方法であり、例えば、トリニト
ロフルオレノン、テトラシアノキノジメタン等のアクセ
プター性化合物が用いられるが、これらは安全性、安定
性、相溶性等に問題がある。このように、下引層を設け
た場合、感度、耐久性の低下という重要な問題点が残さ
れており、これらを改良した高性能な電子写真用感光体
の開発が当該技術分野で強く要望されているのが実情で
ある。
In order to prevent them, many photoreceptors have an undercoat layer as a barrier layer or an adhesive layer between the conductive substrate and the photosensitive layer. As the undercoat layer, an insulating polymer material is mainly provided as a thin film with a submicron thickness, but since it is insulating, it has the fatal drawback of causing a decrease in sensitivity and an increase in residual potential. Have Various methods have been proposed for the purpose of preventing these. One is a method of dispersing an inorganic conductive filler in the undercoat layer, one is a method of incorporating an ion conductive polymer in the undercoat layer, and another is a method of undercoating an electron transporting substance having an acceptor property. It is a method of including in a layer. Titanium oxide and tin oxide are used as the inorganic conductive filler (Japanese Patent Publication No. 63-19).
No. 869), it is necessary to disperse them in the coating liquid for the undercoat layer, which involves technical difficulties in adjusting the dispersion liquid and pot life. As the ion-conductive polymer, for example, polymers such as soluble nylon and polyamide are used (JP-A-52-25638, JP-A-58-30757).
No.) has not yet solved the problem due to its low conductivity. Further, the third method is to add an electron-transporting substance having an acceptor property to these, and for example, an acceptor compound such as trinitrofluorenone or tetracyanoquinodimethane is used. There is a problem with compatibility. As described above, when the undercoat layer is provided, there remains an important problem that the sensitivity and the durability are lowered, and the development of a high-performance electrophotographic photoreceptor that improves these is strongly demanded in the technical field. It is the actual situation that has been done.

【0006】[0006]

【発明が解決しようとする課題】本発明の目的は、かか
る課題を解決するものとして、画像欠陥の生じにくい下
引層を有する電子写真用感光体において、電子輸送能の
有る特定の化合物を下引層に含有させ、高感度、高耐久
性の電子写真用感光体を提供することにある。
SUMMARY OF THE INVENTION An object of the present invention is to solve the above problems by providing a specific compound having an electron transporting property in an electrophotographic photoreceptor having an undercoat layer which hardly causes image defects. The purpose of the present invention is to provide a high-sensitivity and high-durability electrophotographic photoreceptor by incorporating it in the undercoat layer.

【0007】[0007]

【課題を解決するための手段】本発明者らは上記課題を
解決すべく鋭意検討した結果、導電性基板と感光層との
間にフタルイミド化合物好ましくは下記一般式(I)で
示される化合物を含有する下引層を設けることにより、
上記課題が解決できることを見出し、本発明に至った。
As a result of intensive studies to solve the above problems, the present inventors have found that a phthalimide compound, preferably a compound represented by the following general formula (I), is provided between the conductive substrate and the photosensitive layer. By providing an undercoat layer to contain,
The inventors have found that the above problems can be solved and have reached the present invention.

【化1】 (式中、R1及びR2は置換または無置換のアルキル基、
置換または無置換のシクロアルキル基、置換または無置
換のフェニル基、Xは=O、=C(Y)(Z)、=N
(CN)であり、Y及びZは水素原子、置換または無置
換のフェニル基、シアノ基、置換または無置換のアルコ
キシカルボニル基を表す。) すなわち、本発明によれば、導電性基板上に電荷発生層
(CGL)、正孔輸送能を有するドナー性化合物を含有
する電荷輸送層(CTL)を順次積層して構成される機
能分離型電子写真用感光体において、該導電性基板と該
CGLの間にフタルイミド化合物を含有する下引層を設
けたことを特徴とする電子写真用感光体が提供される。
[Chemical 1] (In the formula, R 1 and R 2 are substituted or unsubstituted alkyl groups,
A substituted or unsubstituted cycloalkyl group, a substituted or unsubstituted phenyl group, X is ═O, ═C (Y) (Z), ═N
(CN), Y and Z each represent a hydrogen atom, a substituted or unsubstituted phenyl group, a cyano group, or a substituted or unsubstituted alkoxycarbonyl group. That is, according to the present invention, a function separation type structure in which a charge generation layer (CGL) and a charge transport layer (CTL) containing a donor compound having a hole transport ability are sequentially laminated on a conductive substrate. Provided is an electrophotographic photoreceptor, wherein an undercoat layer containing a phthalimide compound is provided between the conductive substrate and the CGL.

【0008】本発明の電子写真用感光体の下引層に使用
するフタルイミド化合物の代表例としては次のようなも
の(例示化合物1〜148)が挙げられるが、本発明は
それらに限定されるものではない。
Typical examples of the phthalimide compound used in the undercoat layer of the electrophotographic photoreceptor of the present invention include the following compounds (exemplified compounds 1 to 148), but the present invention is not limited thereto. Not a thing.

【0009】本発明の電子写真用感光体は、下引層にフ
タルイミド化合物を含有させたことから高感度で耐久性
に優れたものである。
The electrophotographic photoreceptor of the present invention has high sensitivity and excellent durability because it contains a phthalimide compound in the undercoat layer.

【0010】[0010]

【表1−(1)】 [Table 1- (1)]

【0011】[0011]

【表1−(2)】 [Table 1- (2)]

【0012】[0012]

【表1−(3)】 [Table 1- (3)]

【0013】[0013]

【表1−(4)】 [Table 1- (4)]

【0014】[0014]

【表1−(5)】 [Table 1- (5)]

【0015】[0015]

【表1−(6)】 [Table 1- (6)]

【0016】[0016]

【表1−(7)】 [Table 1- (7)]

【0017】[0017]

【表1−(8)】 [Table 1- (8)]

【0018】[0018]

【表1−(9)】 [Table 1- (9)]

【0019】[0019]

【表1−(10)】 [Table 1- (10)]

【0020】[0020]

【表1−(11)】 [Table 1- (11)]

【0021】[0021]

【表1−(12)】 [Table 1- (12)]

【0022】[0022]

【表1−(13)】 [Table 1- (13)]

【0023】[0023]

【表1−(14)】 [Table 1- (14)]

【0024】前記一般式(1)で示されるフタルイミド
化合物は電子輸送能を有し、多くの溶剤に可溶である。
このような溶剤としては、例えば、ベンゼン、トルエ
ン、キシレン、クロロベンゼン等の芳香族系溶剤、ジク
ロロメタン、1,2−ジクロロエタン、クロロホルム等
のハロゲン系溶剤、酢酸メチル、酢酸エチル、酢酸プロ
ピル、ギ酸エチル等のエステル系溶剤、アセトン、メチ
ルエチルケトン、シクロヘキサノン等のケトン系溶剤、
ジエチルーテル、ジオキサン、テトラヒドロフラン等の
エーテル系溶剤、メタノール、エタノール、イソプロパ
ノール等のアルコール系溶剤、及びジメチルホルムアミ
ド、ジメチルアセトアミド、ジメチルスルホキシド等が
挙げられる。
The phthalimide compound represented by the general formula (1) has an electron transporting ability and is soluble in many solvents.
Examples of such a solvent include aromatic solvents such as benzene, toluene, xylene and chlorobenzene, halogen solvents such as dichloromethane, 1,2-dichloroethane and chloroform, methyl acetate, ethyl acetate, propyl acetate and ethyl formate. Ester solvents, acetone, methyl ethyl ketone, cyclohexanone and other ketone solvents,
Examples thereof include ether solvents such as diethyl ether, dioxane and tetrahydrofuran, alcohol solvents such as methanol, ethanol and isopropanol, and dimethylformamide, dimethylacetamide and dimethylsulfoxide.

【0025】本発明の電子写真用感光体は導電性基板上
に好ましくは前記一般式(I)で示されるフタルイミド
化合物を結着樹脂中に含有させた下引層を設け、次いで
電荷発生層、電荷輸送層を順次積層することにより作製
される。
The electrophotographic photoreceptor of the present invention is preferably provided with an undercoat layer containing a phthalimide compound represented by the general formula (I) in a binder resin on a conductive substrate, and then a charge generation layer, It is manufactured by sequentially stacking charge transport layers.

【0026】本発明で使用される導電性基板としては、
アルミニウム、ニッケル、銅、ステンレス等の金属板、
金属ドラムまたは金属箔、アルミニウム、酸化錫、ヨウ
化銅等の薄膜を塗布したプラスチックフィルムあるいは
ガラス等が挙げられる。本発明の下引層に使用される結
着樹脂は、特に限定されることはなく、例えばポリエチ
レン樹脂、ポリプロピレン樹脂、アクリル樹脂、ポリス
チレン樹脂、塩化ビニル樹脂、酢酸ビニル樹脂、ポリカ
ーボネート樹脂、ポリアリレート樹脂、フェノキシ樹
脂、ポリウレタン樹脂、ブチラール樹脂、ポリアミド樹
脂、弗化ビニリデン樹脂、シリコーン樹脂、繊維素系樹
脂、シアノエチルプルラン、フェノール樹脂、メラミン
樹脂、アルキッド樹脂、エポキシ樹脂等の付加重合型樹
脂、重付加型樹脂、重縮合型樹脂、並びにこれらの繰返
し単位のうち2つ以上を含む共重合体樹脂等が挙げら
れ、単独もしくは2種以上のものを混合して用いること
ができる。
As the conductive substrate used in the present invention,
Metal plates such as aluminum, nickel, copper, stainless steel,
Examples thereof include a metal drum or a metal foil, a plastic film coated with a thin film of aluminum, tin oxide, copper iodide, or the like, or glass. The binder resin used in the undercoat layer of the present invention is not particularly limited, and examples thereof include polyethylene resin, polypropylene resin, acrylic resin, polystyrene resin, vinyl chloride resin, vinyl acetate resin, polycarbonate resin, polyarylate resin. , Phenoxy resin, polyurethane resin, butyral resin, polyamide resin, vinylidene fluoride resin, silicone resin, fibrin resin, cyanoethyl pullulan, phenol resin, melamine resin, alkyd resin, epoxy resin, etc. Examples thereof include resins, polycondensation resins, and copolymer resins containing two or more of these repeating units, and these can be used alone or in combination of two or more.

【0027】一般式(1)で示される化合物の使用量は
これらの結着樹脂に対して1〜50重量%、好ましくは
2〜30重量%である。1重量%以下であると効果が少
なく、また50重量%以上だと帯電性が悪くなる。下引
層の膜厚は0.1〜2.0μmが好ましい。
The amount of the compound represented by the general formula (1) used is 1 to 50% by weight, preferably 2 to 30% by weight, based on these binder resins. If it is 1% by weight or less, the effect is small, and if it is 50% by weight or more, the charging property is deteriorated. The thickness of the undercoat layer is preferably 0.1 to 2.0 μm.

【0028】本発明の電荷発生層は電荷発生物質を結着
樹脂に分散し塗布するか、蒸着することにより設けるこ
とができる。電荷発生物質としては、ビスアゾ色素、ト
リスアゾ色素、フタロシアニン色素、キナクリドン色
素、ペリレン色素、多環キノン色素、インジゴ色素、シ
アニン色素、ピリリウム色素、ビスベンズイミダゾール
色素、インダンスロン色素、トリアリールメタン色素、
チアジン色素、オキソジン色素、スクアリリウム色素、
アントラキノン色素、キサンテン色素等の有機色素、セ
レン、セレン合金、硫化カドミウム、硫セレン化カドミ
ウム、アモルファスシリコン等の無機化合物が挙げら
れ、結着樹脂とともに用いる場合は、電荷発生物質10
0重量部に対して結着樹脂は10〜400重量部、好ま
しくは25〜100重量部である。また、電荷発生層の
膜厚は0.05〜10μm、好ましくは0.1〜2μm
である。
The charge generating layer of the present invention can be provided by dispersing the charge generating substance in a binder resin and coating or vapor depositing it. As the charge generating substance, bisazo dye, trisazo dye, phthalocyanine dye, quinacridone dye, perylene dye, polycyclic quinone dye, indigo dye, cyanine dye, pyrylium dye, bisbenzimidazole dye, indanthrone dye, triarylmethane dye,
Thiazine dye, oxodine dye, squarylium dye,
Organic compounds such as anthraquinone dyes and xanthene dyes, inorganic compounds such as selenium, selenium alloys, cadmium sulfide, cadmium sulfide selenide, and amorphous silicon can be mentioned. When used with a binder resin, the charge generating substance 10
The binder resin is 10 to 400 parts by weight, preferably 25 to 100 parts by weight, based on 0 parts by weight. The thickness of the charge generation layer is 0.05 to 10 μm, preferably 0.1 to 2 μm.
Is.

【0029】本発明の電荷輸送層は少なくとも正孔輸送
物質、及び結着樹脂とからなり、必要に応じ、添加剤を
加えることができる。正孔輸送物質としては、分子中に
トリフェニルアミン部位を有する化合物、ヒドラゾン化
合物、ピラゾリン化合物、トリフェニルメタン化合物、
オキサゾール化合物、オキサジアゾール化合物、カルバ
ゾール基を含む化合物、スチリル化合物、ブタジエン化
合物、ポリシラン化合物、ポリ−N−ビニルカルバゾー
ル、ピレン−ホルマリン縮合物等のドナー性化合物を単
独もしくは複数で使用することができる。電荷輸送層の
構成は、結着樹脂100重量部に対して、正孔輸送物質
は25〜400重量部、好ましくは50〜200重量部
である。また、電荷輸送層の膜厚は5〜60μm、好ま
しくは10〜30μmである。また、必要に応じて用い
られる添加剤としては、消泡剤、酸化防止剤、接着補助
剤、可塑剤等を挙げることができる。電荷発生層及び電
荷輸送層の結着樹脂は下引層で使用される樹脂を使用す
ることができる。
The charge-transporting layer of the present invention comprises at least a hole-transporting substance and a binder resin, and an additive can be added if necessary. As the hole-transporting substance, a compound having a triphenylamine moiety in the molecule, a hydrazone compound, a pyrazoline compound, a triphenylmethane compound,
Donor compounds such as oxazole compounds, oxadiazole compounds, carbazole group-containing compounds, styryl compounds, butadiene compounds, polysilane compounds, poly-N-vinylcarbazole, and pyrene-formalin condensates can be used alone or in combination. . The structure of the charge transport layer is 25 to 400 parts by weight, preferably 50 to 200 parts by weight, based on 100 parts by weight of the binder resin. The thickness of the charge transport layer is 5 to 60 μm, preferably 10 to 30 μm. Further, examples of the additives used as necessary include antifoaming agents, antioxidants, adhesion aids, plasticizers and the like. As the binder resin for the charge generation layer and the charge transport layer, the resin used in the undercoat layer can be used.

【0030】本発明の電子写真用感光体は公知の塗布方
法、例えばディッピングコーター、カレンダーコータ
ー、キスコーター、グラビアコーター、ブレードコータ
ー、スプレーコーター、スピンコーター等で作製するこ
とができる。
The electrophotographic photoreceptor of the present invention can be produced by a known coating method, for example, a dipping coater, a calendar coater, a kiss coater, a gravure coater, a blade coater, a spray coater, a spin coater or the like.

【0031】[0031]

【実施例】以下本発明を実施例により説明するが、これ
により本発明の態様が限定されるわけではない。
EXAMPLES The present invention will be described below with reference to examples, but the embodiments of the present invention are not limited thereby.

【0032】実施例1 例示化合物No.4 1g、ナイロン樹脂(CM800
0 東レ(株)製)5gをエチルアルコール94gに溶
解し、アルミニウムを1000Åの厚さに蒸着した75
μm厚のポリエステルフィルム上にドクターブレードに
て塗布し、乾燥後の膜厚が0.5μmの下引層を設け
た。次に下記構造式のビスアゾ顔料1gをブチラール樹
脂(エスレックBL−S積水化学(株)製)の5重量%
テトラヒドロフラン溶液10gおよびテトラヒドロフラ
ン9gとともにボールミリングし、ミリング後テトラヒ
ドロフランを加え、2重量%に希釈し、下引層上にドク
ターブレードにて塗布し、乾燥後の膜厚が1.0μmの
電荷発生層を設けた。次に下記構造式の正孔輸送物質で
あるトリフェイルアミン系化合物6g、ポリカーボネー
トZ(帝人化成(株)製)9g、シリコンオイル(KF
50 信越化学(株)製)0.009gをテトラヒドロ
フラン85gに溶解し、電荷発生層上に塗布し、乾燥後
の膜厚が20μmの電荷輸送層を設け、導電性基板上に
下引層、電荷発生層、電荷輸送層を順次積層した電子写
真用感光体を作製した。
Example 1 Exemplified Compound No. 41 g, nylon resin (CM800
0 Toray Co., Ltd. 5 g was dissolved in ethyl alcohol 94 g, and aluminum was evaporated to a thickness of 1000 Å 75
It was coated on a polyester film having a thickness of μm with a doctor blade, and an undercoat layer having a film thickness after drying of 0.5 μm was provided. Next, 1 g of the bisazo pigment having the following structural formula was added to 5% by weight of butyral resin (S-REC BL-S Sekisui Chemical Co., Ltd.).
Ball-milling with 10 g of tetrahydrofuran solution and 9 g of tetrahydrofuran, adding tetrahydrofuran after milling, diluting to 2% by weight, and coating with a doctor blade on the undercoat layer to form a charge generation layer having a thickness of 1.0 μm after drying. Provided. Next, 6 g of a triphenylamine compound, which is a hole-transporting substance having the following structural formula, 9 g of polycarbonate Z (manufactured by Teijin Chemicals Ltd.), silicone oil (KF
50 manufactured by Shin-Etsu Chemical Co., Ltd.) was dissolved in 85 g of tetrahydrofuran, and the solution was applied on the charge generation layer, and a charge transport layer having a thickness of 20 μm after drying was provided. An electrophotographic photoreceptor was produced in which a generation layer and a charge transport layer were sequentially laminated.

【化2】 [Chemical 2]

【化3】[Chemical 3]

【0033】 実施例2 下引層に含有させる化合物である例示化合物No.4を
例示化合物No.−I−(7)に代えた以外は実施例1
と同様の条件で電子写真用感光体を作製した。
[0033] Example 2 Exemplified Compound No. which is a compound contained in the undercoat layer. No. 4 is exemplified compound No. Example 1 except that it was replaced with -I- (7)
An electrophotographic photosensitive member was produced under the same conditions as in.

【0034】実施例3 下引層に含有させる化合物である例示化合物No.4を
例示化合物No.36に代え、電荷発生物質としてX型
無金属フタロシアニン(Fastogen Blue
8120BS 大日本インキ(株)製)を用いた以外は
実施例1と同様の条件で電子写真用感光体を作製した。
Example 3 Exemplified Compound No. which is a compound contained in the undercoat layer. No. 4 is exemplified compound No. Instead of 36, X-type metal-free phthalocyanine (Fastogen Blue) is used as a charge generating substance.
An electrophotographic photoreceptor was prepared under the same conditions as in Example 1, except that 8120BS Dainippon Ink Co., Ltd. was used.

【0035】比較例 下引層を設けない以外は実施例1と同様の条件で電子写
真用感光体を作製した。
Comparative Example An electrophotographic photoreceptor was prepared under the same conditions as in Example 1 except that the subbing layer was not provided.

【0036】このようにして作製した電子写真用感光体
を川口電機(株)製の静電複写紙試験装置(SP−42
8)を用い、−6KVでコロナ放電を20秒間行なって
帯電し、さらに20秒間暗減衰させ、その後感光体表面
の照度が20ルックスになるようにタングステン光を3
0秒間照射した。以上の条件で連続500回の測定を行
ない、20秒間帯電後の表面電位Vs(V)、20秒間
暗減衰後の表面電位Vo(V)、Voが1/10になる
のに要する露光量E1/10(ルックス・秒)及び30秒間
露光後の表面電位V30(V)を測定した。測定結果を表
2に示す。
The electrophotographic photoconductor thus prepared was used as an electrostatic copying paper tester (SP-42) manufactured by Kawaguchi Electric Co., Ltd.
8), corona discharge was performed at -6 KV for 20 seconds to charge, dark decay was performed for 20 seconds, and then tungsten light was applied for 3 seconds so that the illuminance on the surface of the photoreceptor was 20 lux.
Irradiate for 0 seconds. The surface potential Vs (V) after being charged for 20 seconds, the surface potential Vo (V) after dark decay for 20 seconds, and the exposure amount E1 required for Vo to be 1/10 were measured under the above conditions continuously 500 times. The surface potential V30 (V) after exposure for / 10 (lux seconds) and 30 seconds was measured. The measurement results are shown in Table 2.

【0037】[0037]

【表2】 [Table 2]

【0038】[0038]

【発明の効果】本発明の電子写真用感光体は、下引層に
フタルイミド化合物を含有させたことから高感度で高耐
久性なものである。
The electrophotographic photoreceptor of the present invention has high sensitivity and high durability because it contains a phthalimide compound in the undercoat layer.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 導電性基板上に電荷発生層(CGL)、
正孔輸送能を有するドナー性化合物を含有する電荷輸送
層(CTL)を順次積層して構成される機能分離型電子
写真用感光体において、該導電性基板と該CGLの間に
フタルイミド化合物を含有する下引層を設けたことを特
徴とする電子写真用感光体。
1. A charge generation layer (CGL) on a conductive substrate,
A function-separated type electrophotographic photoreceptor comprising a charge-transporting layer (CTL) containing a donor compound having a hole-transporting ability, which is sequentially laminated, containing a phthalimide compound between the conductive substrate and the CGL. An electrophotographic photoreceptor, which is provided with an undercoat layer.
【請求項2】 フタルイミド化合物が下記一般式(1)
で示される電子輸送物質であることを特徴とする請求項
1記載の電子写真用感光体。 【化1】 (式中、R1及びR2は置換または無置換のアルキル基、
置換または無置換のシクロアルキル基、置換または無置
換のフェニル基、Xは=O、=C(Y)(Z)、=N
(CN)であり、Y及びZは水素原子、置換または無置
換のフェニル基、シアノ基、置換または無置換のアルコ
キシカルボニル基を表す。)
2. A phthalimide compound represented by the following general formula (1):
The electrophotographic photoreceptor according to claim 1, which is an electron-transporting substance represented by: [Chemical 1] (In the formula, R 1 and R 2 are substituted or unsubstituted alkyl groups,
A substituted or unsubstituted cycloalkyl group, a substituted or unsubstituted phenyl group, X is ═O, ═C (Y) (Z), ═N
(CN), Y and Z each represent a hydrogen atom, a substituted or unsubstituted phenyl group, a cyano group, or a substituted or unsubstituted alkoxycarbonyl group. )
JP34485293A 1993-12-20 1993-12-20 Electrophotographic photoreceptor Pending JPH07175250A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP34485293A JPH07175250A (en) 1993-12-20 1993-12-20 Electrophotographic photoreceptor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP34485293A JPH07175250A (en) 1993-12-20 1993-12-20 Electrophotographic photoreceptor

Publications (1)

Publication Number Publication Date
JPH07175250A true JPH07175250A (en) 1995-07-14

Family

ID=18372486

Family Applications (1)

Application Number Title Priority Date Filing Date
JP34485293A Pending JPH07175250A (en) 1993-12-20 1993-12-20 Electrophotographic photoreceptor

Country Status (1)

Country Link
JP (1) JPH07175250A (en)

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