JPH042184B2 - - Google Patents

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Publication number
JPH042184B2
JPH042184B2 JP58197343A JP19734383A JPH042184B2 JP H042184 B2 JPH042184 B2 JP H042184B2 JP 58197343 A JP58197343 A JP 58197343A JP 19734383 A JP19734383 A JP 19734383A JP H042184 B2 JPH042184 B2 JP H042184B2
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JP
Japan
Prior art keywords
group
photoreceptor
compound
charge
parts
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Expired - Lifetime
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JP58197343A
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Japanese (ja)
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JPS6088949A (en
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Priority to JP58197343A priority Critical patent/JPS6088949A/en
Publication of JPS6088949A publication Critical patent/JPS6088949A/en
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Granted legal-status Critical Current

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    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03GELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G5/00Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
    • G03G5/02Charge-receiving layers
    • G03G5/04Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
    • G03G5/06Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
    • G03G5/0601Acyclic or carbocyclic compounds
    • G03G5/0612Acyclic or carbocyclic compounds containing nitrogen
    • G03G5/0616Hydrazines; Hydrazones

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  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Photoreceptors In Electrophotography (AREA)
  • Light Receiving Elements (AREA)

Description

【発明の詳现な説明】[Detailed description of the invention]

本発明は電子写真感光䜓、詳しくはアゞン系化
合物から成る新芏な有機光導電性物質を含有する
電子写真甚感光䜓に関する。 電子写真法はすでにカヌル゜ンが米囜特蚱第
2297691号に明らかにしたように、画像露光の間
に受けた照射量に応じその電気抵抗が倉化する、
暗所で絶瞁性の物質をコヌテむングした支持䜓よ
りなる光導電性材料を甚いる。この光導電性材料
は䞀般に適圓な間の暗順応の埌、暗所で、たず䞀
様な衚面電荷を䞎えられる。次に、この材料は照
射パタヌンの皮々の郚分に含たれる盞察゚ネルギ
ヌに応じお衚面電荷を枛らす効果を有する照射の
パタヌンにより画像露光される。このようにしお
光導電性物質局感光局衚面に残぀た衚面電荷
又は静電朜像は次にその衚面が適圓な怜電衚瀺物
質、すなわちトナヌで接觊されお可芖像ずなる。
トナヌは絶瞁液䞭に含たれようず也燥担䜓䞭に含
たれようず、電荷パタヌンに応じお感光局衚面䞊
に付着させるこずができる。付着した衚瀺物質
は、熱、圧力、溶媒蒞気のような公知の手段によ
り定着するこずができる。又静電朜像は第の支
持䜓䟋えば玙、フむルムなどに転写するこず
ができる。同様に静電朜像を第の支持䜓に転写
し、そこで珟像するこずも可胜である。電子写真
法はこの様にしお画像を圢成するようにした画像
圢成法の䞀぀である。 このような電子写真法においお感光䜓に芁求さ
れる基本的な特性ずしおは、(1)暗所で適圓な電䜍
に垯電できるこず、(2)暗所においお電荷の逞散が
少ないこず、(3)光照射によ぀お速やかに電荷を逞
散せしめうるこずなどがあげられる。埓来甚いら
れおいるセレン、硫化カドミりム、酞化亜鉛など
の無機光導電物質は、倚くの長所を持぀おいるず
同時にさたざたな欠点を有しおいるこずは事実で
ある。䟋えば、珟圚広く甚いられおいるセレンは
前蚘(1)〜(3)の条件は十分に満足するが、補造する
条件がむずかしく、補造コストが高くなり、可撓
性がなく、ベルト状に加工するこずがむずかし
く、熱や機械的の衝撃に鋭敏なため取扱いに泚意
を芁するなどの欠点もある。硫化カドミりムや酞
化亜鋭は、結合剀ずしおの暹脂に分散させお感光
䜓ずしお甚いられおいるが、平滑性、硬床、匕匵
り匷床、耐摩擊性などの機械的な欠点があるため
にそのたたでは反埩しお䜿甚するこずができな
い。 近幎、これら無機光導電物質の欠点を排陀する
ためにいろいろの有機光導電物質を甚いた電子写
真甚感光䜓が提案され、実甚に䟛されおいるもの
もある。䟋えば、ポリ−−ビニルカルバゟヌル
ず−トリニトロフルオレン−−オン
ずからなる感光䜓米囜特蚱3484237、ポリ−
−ビニルカルバゟヌルをピリリりム塩系色玠で増
感したもの特公昭48−25658号公報、染料ず暹
脂ずからなる共晶錯䜓を䞻成分ずする感光䜓特
開昭47−10735号公報などである。 これらの有機光導電䜓を甚いた電子写真感光䜓
は、前蚘無機光導電䜓を甚いたものに比べお機械
的特性及び可撓性もある皋床たで改善したものの
抂しお光感床が䜎くたた繰り返し䜿甚に適さず電
子写真感光䜓ずしおの芁求を充分に満足するもの
ではなか぀た。 たた、さらに光により電荷を発生する物質電
荷発生物質ず呌ぶず、この発生した電荷を茞送
するこずのできる物質電荷茞送物質ず呌ぶず
を組合せた高感床の電子写真感光䜓が提案されお
いる。䟋えば米囜特蚱第3791826号には電荷発生
局䞊に電荷茞送局を蚭けた感光䜓が、米囜特蚱第
3573906号䞭には逆に電荷茞送局䞊に電荷発生局
を蚭けた感光䜓が、さらにたた米囜特蚱第
3764315号には電荷発生物質を電荷茞送物質䞭に
分散せしめた感光局を持぀感光䜓がそれぞれ蚘茉
されおいる。 この電荷発生局䞭に甚いる電荷茞送剀ずしお䟋
えば特開昭54−59143号公報米囜特蚱第4150987
号に察応蚘茉のヒドラゟン化合物、米囜特蚱第
3180729号蚘茉のピラゟリン化合物、米囜特蚱第
3567450号蚘茉のトリアリヌルアミン等を挙げる
こずができるが、いづれも感床の点で十分な性胜
を有する電子写真感光䜓を埗るこずはできなか぀
た。 たたアゞン系化合物に぀いおは特公昭42−5587
号公報に光導電性化合物ずしおたた特開昭58−
132240号公報には電荷茞送性化合物ずしおの蚘茉
がある。たた特開昭57−90634号公報には
4′−ゞ−ゞ眮換アミノベンゟプノンから
合成される察称圢のケタゞン化合物が光導電性及
び電荷茞送性を有するこずが瀺されおいる。 しかしこれらの特蚱蚘茉のアゞン系化合物を有
機光導電䜓ずしおもしくは電荷茞送物質ずしお甚
いおも十分な感床を有する電子写真感光䜓を埗る
こずができなか぀た。たたこれら特蚱蚘茉のアゞ
ン系化合物のうち特にケタゞン系化合物を甚いる
ず補䜜した感光䜓衚面にケタゞン化合物の結晶が
析出するずいう欠点を有しおいた。 本発明の目的は前述の問題点を解消した新芏な
電子写真感光䜓を提䟛するこずにある。 本発明の別の目的は新芏な有機光導電性材料を
提䟛するこずにある。 本発明の別の目的は、電荷発生局ず電荷茞送局
の積局構造から成る感光局で甚いる電荷茞送物質
に適した化合物を提䟛するこずにある。 本発明者らは鋭意研究の結果アゞン系化合物の
䞭で、4′−ゞ−ゞ眮換アミノベンゟフ
゚ノン及び4′−ゞ−ゞ眮換アミノベン
ゟプノン以倖の眮換ケトン又は眮換アルデヒド
の皮の異なる化合物から合成される非察称のア
ゞン系化合物が光導電性化合物ずしおもたた電荷
茞送化合物ずしおも特に勝れた性胜を有するこず
を芋い出したものである。 本発明のかかる目的は、䞋蚘䞀般匏(1)で瀺され
るアゞン系化合物を含有する局を有する電子写真
感光䜓によ぀お達成される。 匏䞭R1R2R3R4は同䞀であ぀おも又異぀
おいおも良くそれぞれメチル、゚チル、プロピ
ル、ブチルなどの盎鎖状又は分岐状の炭玠数〜
12のアルキル基、ベンゞル、プネチルなどのア
ラルキル基、プニル、ナフチルなどのアリヌル
基、たたはピロリゞノ、ピペリゞノ、モルホリノ
などの窒玠原子ず共に環状アミノ基を圢成する残
基を衚わす。又これらのアルキル基、アラルキル
基、アリヌル基は眮換基を有しおいおもよく、眮
換基ずしおはメチル、゚チルなどのアルキル基、
メトキシ、゚トキシなどの炭玠数〜のアルコ
キシ、塩玠、臭玠、などのハロゲン原子の他に氎
酞基、シアノ基等があげられる。 R5は氎玠、眮換又は非眮換の炭玠数〜12の、
アルキル基、アラルキル基、非眮換又は炭玠数
〜の、アルキル基、アルコキシ基、ハロゲン原
子、氎酞基、シアノ基を眮換基ずしお含むアリヌ
ル基を衚わす。 R6ずしおは炭玠数〜の、
The present invention relates to an electrophotographic photoreceptor, and more particularly to an electrophotographic photoreceptor containing a novel organic photoconductive substance comprising an azine compound. Electrophotography has already been covered by Carlson's U.S. Patent No.
As revealed in No. 2297691, its electrical resistance changes depending on the amount of radiation received during image exposure.
A photoconductive material consisting of a support coated with an insulating substance is used in the dark. The photoconductive material is generally first given a uniform surface charge in the dark after dark adaptation for a suitable period of time. The material is then imagewise exposed to a pattern of radiation that has the effect of reducing the surface charge depending on the relative energy contained in different parts of the radiation pattern. The surface charge or electrostatic latent image thus left on the surface of the photoconductive material layer (photosensitive layer) then becomes a visible image when that surface is contacted with a suitable electrometric indicator, ie, toner.
Toner, whether contained in an insulating liquid or in a dry carrier, can be deposited on the surface of the photosensitive layer depending on the charge pattern. The deposited display material can be fixed by known means such as heat, pressure, and solvent vapor. The electrostatic latent image can also be transferred to a second support (eg, paper, film, etc.). It is likewise possible to transfer the electrostatic latent image to a second support and develop it there. Electrophotography is one of the image forming methods in which images are formed in this manner. The basic characteristics required of the photoreceptor in such electrophotography are (1) ability to be charged to an appropriate potential in the dark, (2) low dissipation of charge in the dark, (3) For example, the charge can be quickly dissipated by light irradiation. It is true that conventionally used inorganic photoconductive materials such as selenium, cadmium sulfide, and zinc oxide have many advantages, but also have various disadvantages. For example, selenium, which is currently widely used, fully satisfies the conditions (1) to (3) above, but the manufacturing conditions are difficult, the manufacturing cost is high, it is not flexible, and it cannot be processed into a belt shape. It also has disadvantages, such as being difficult to handle and being sensitive to heat and mechanical shock, requiring careful handling. Cadmium sulfide and acertic oxide are used as photoreceptors by being dispersed in resin as a binder, but they have mechanical drawbacks such as smoothness, hardness, tensile strength, and abrasion resistance, so they cannot be used as is. and cannot be used. In recent years, in order to eliminate the drawbacks of these inorganic photoconductive materials, electrophotographic photoreceptors using various organic photoconductive materials have been proposed, and some of them are in practical use. For example, photoreceptors made of poly-N-vinylcarbazole and 2,4,7-trinitrofluoren-9-one (US Pat. No. 3,484,237), poly-N-
- Vinylcarbazole sensitized with pyrylium salt dyes (Japanese Patent Publication No. 48-25658), photoreceptors whose main component is a eutectic complex consisting of a dye and a resin (Japanese Patent Application Laid-open No. 10735-1987), etc. It is. Although electrophotographic photoreceptors using these organic photoconductors have improved mechanical properties and flexibility to some extent than those using the inorganic photoconductors, they generally have low photosensitivity and are not suitable for repeated use. First, it did not fully satisfy the requirements for an electrophotographic photoreceptor. Furthermore, a highly sensitive electrophotographic photoreceptor has been proposed that combines a substance that generates electric charges when exposed to light (called a charge-generating substance) and a substance that can transport the generated charges (called a charge-transporting substance). has been done. For example, US Pat. No. 3,791,826 discloses a photoreceptor in which a charge transport layer is provided on a charge generating layer.
No. 3,573,906 discloses a photoreceptor in which a charge generation layer is provided on a charge transport layer.
No. 3,764,315 describes a photoreceptor having a photosensitive layer in which a charge generating material is dispersed in a charge transporting material. Examples of charge transporting agents used in this charge generation layer include those disclosed in JP-A-54-59143 (U.S. Pat. No. 4,150,987).
hydrazone compounds described in U.S. Patent No.
Pyrazoline compounds described in 3180729, U.S. Pat.
Although triarylamine described in No. 3567450 can be mentioned, it has not been possible to obtain an electrophotographic photoreceptor having sufficient performance in terms of sensitivity. Regarding azine compounds, Japanese Patent Publication No. 42-5587
In JP-A No. 58-1989, it was also published as a photoconductive compound.
No. 132240 describes it as a charge transporting compound. Also, in Japanese Patent Application Laid-Open No. 57-90634,
Symmetrical ketazine compounds synthesized from 4'-di(N-disubstituted amino)benzophenones have been shown to have photoconductivity and charge transport properties. However, even when the azine compounds described in these patents are used as organic photoconductors or charge transport materials, it has not been possible to obtain electrophotographic photoreceptors with sufficient sensitivity. Furthermore, among the azine compounds described in these patents, the use of ketazine compounds in particular has the disadvantage that crystals of the ketazine compounds precipitate on the surface of the photoreceptor produced. An object of the present invention is to provide a new electrophotographic photoreceptor that solves the above-mentioned problems. Another object of the invention is to provide new organic photoconductive materials. Another object of the present invention is to provide a compound suitable as a charge transport material for use in a photosensitive layer having a laminated structure of a charge generation layer and a charge transport layer. As a result of extensive research, the present inventors found that among azine compounds, substituted ketones other than 4,4'-di(N-disubstituted amino)benzophenone and It has been discovered that an asymmetric azine compound synthesized from two different substituted aldehydes has particularly excellent performance both as a photoconductive compound and as a charge transport compound. This object of the present invention is achieved by an electrophotographic photoreceptor having a layer containing an azine compound represented by the following general formula (1). In the formula, R 1 , R 2 , R 3 , and R 4 may be the same or different, and each represents a linear or branched chain having 1 to 1 carbon atoms such as methyl, ethyl, propyl, butyl, etc.
12 alkyl groups, aralkyl groups such as benzyl and phenethyl, aryl groups such as phenyl and naphthyl, or residues that form a cyclic amino group together with nitrogen atoms such as pyrrolidino, piperidino and morpholino. In addition, these alkyl groups, aralkyl groups, and aryl groups may have a substituent, and examples of the substituent include alkyl groups such as methyl and ethyl;
In addition to alkoxy having 1 to 8 carbon atoms such as methoxy and ethoxy, halogen atoms such as chlorine and bromine, hydroxyl groups, cyano groups, etc. can be mentioned. R 5 is hydrogen, substituted or unsubstituted, having 1 to 12 carbon atoms,
Alkyl group, aralkyl group, unsubstituted or carbon number 1
-8 represents an aryl group containing an alkyl group, an alkoxy group, a halogen atom, a hydroxyl group, or a cyano group as a substituent. R 6 has 1 to 8 carbon atoms,

【匏】又は[Formula] or

【匏】で衚わされる−ゞ眮換アミノ基、メ トキシ、゚トキシなどの炭玠数〜のアルコキ
シ、ベンゞルオキシなどのアラルキルオキシ基、
プノキシなどのアリヌルオキシ基および塩玠、
臭玠などのハロゲン原子を衚わし、又はR6はR7
又はR8およびそれらが結合しおいるベンれン環
ず䞀緒にな぀お、ゞナロリゞノ環、カルバゟヌル
環、プノチアゞン環、プノキサゞン環等の耇
玠環を圢成しおいおも良い。 R7及びR8は同䞀でもたた盞違しおいおもよ
く氎玠、メチル、゚チルなどの炭玠数〜たで
のアルキル基、メトキシ、゚トキシなどの炭玠数
〜たでのアルコキシ基、塩玠、臭玠などのハ
ロゲン原子を衚わすか又は、R6ず共に耇玠環を
圢成しおいおも良い。 本発明に甚いられるアゞン系化合物の䞭で、特
に奜たしいものは䞋蚘䞀般匏(2)で瀺されるもので
ある。 匏䞭のR1R2R3R4R5R10は䞀般匏(1)
で説明したR1R2R3R4ず同じものを瀺す。 本発明で甚いる前蚘䞀般匏(1)で瀺される化合物
の具䜓䟋を䞋蚘に列挙する。 これらの化合物は䞋蚘䞀般匏(3)及び(4)で瀺され
る化合物ずヒドラゞンずにより公知の方法によ぀
お合成するこずができる。 次に本発明に甚いられるアゞン系化合物に぀い
お合成䟋で説明する。 䟋瀺化合物(1)の合成 4′−ビスゞメチルアミノベンゟプノ
ンヒドラゟン7.0及び−ゞ゚チルアミノベン
ズアルデヒド4.8を゚タノヌル䞭で時間加熱
還流した。 反応液を冷华埌生じた固䜓を過し也燥した。
次に゚タノヌルから再結晶を行い融点167〜167.5
℃の結晶8.8を埗た。収率78 元玠分析倀 C28H33N5ずしお 蚈算倀 76.15 7.98 
15.85 実枬倀 76.01 8.20 
15.76 䟋瀺化合物(3)の合成 4′−ビスゞメチルアミノベンゟプノ
ンヒドラゟン7.0および−−プニル−
−メチルアミノベンズアルデヒド5.3を゚タ
ノヌル䞭時間加熱還流した。 反応終了埌反応液を冷华し生じた固䜓を過し
也燥した。 次にベンれン、−ヘキサンの混合溶媒により
再結晶を行い融点133.5〜134℃の結晶9.2を埗
た。収率78 元玠分析倀 C31H33N5ずしお 蚈算倀 78.27 6.99 
14.72 実枬倀 78.19 7.22 
14.57 本発明で甚いられる他のアゞン系化合物も同様
にしお合成するこずができる。 䞀般匏(1)で瀺されるアゞン系化合物を電子写真
感光䜓に甚いる堎合(1)は有機光導電性化合物ずし
おもたた電荷茞送性化合物ずしおも機胜するため
に䞋蚘B2぀のタむプの電子写真感光䜓ずし
お甚いるこずができる。 タむプ 増感剀ず組み合わせお実質的に均䞀
で透明な感光局を有する電子写真感光䜓。 タむプ 電荷発生化合物ず組み合わせた電子
写真感光䜓。 タむプの電子写真感光䜓の感光局に甚いられ
る増感剀ずしおは−トリニトロフルオ
レン−−オン、クロラニル、テトラシアノ゚チ
レン、および米囜特蚱第3232755号蚘茉の電子吞
匕性化合物、米囜特蚱第3250615号蚘茉のピリリ
りム染料、米囜特蚱第4315983号、米囜特蚱第
4343948号、特開昭57−46980号公報蚘茉のチオピ
リリりム染料、特開昭56−81852号公報蚘茉のア
ザシアニン染料、トリアリヌルメタン染料、チア
ゞン染料、シアニン染料等の増感染料などがあ
る。 タむプの電子写真感光䜓は機胜分離型感光䜓
ず呌ばれるものであり、電荷発生化合物が電荷茞
送化合物ずしお甚いられる本発明のアゞン系化合
物䞭に分散された局の感光局からなる単局型感
光䜓ず、もしくは、電荷発生化合物を含有する電
荷発生局ず電荷茞送化合物ずしお甚いられる本発
明のアゞン系化合物を含む電荷茞送局の局の感
光局からなる積局型感光䜓ずがある。奜たしくは
電子写真感光䜓の感床、電荷保持率の点で積局型
の感光䜓が有甚である。 タむプの電荷発生化合物ずしおは、無機系の
ものでは、硫化カドミりム、セレン化カドミり
ム、酞化亜鉛、硫化亜鉛、二酞化チタン特にル
テル型、䞉方晶圢セレン等が、たた有機系のも
のでは䟋えば、スヌダンレツド、クロルダむアン
ブルヌ、ゞ゚ナスグリヌンなどのアゟ顔料、特
公昭56−11945号公報、特開昭53−133445号公報、
特開昭54−2738号、特開昭57−152091号公報、特
開昭58−123541号公報等に蚘茉のゞスアゟ顔料、
特開昭57−41642号公報、特開昭57−116345号公
報等に蚘茉のトリスアゟ顔料、アルゎヌルむ゚ロ
ヌ、ピレンキノン、むンダンスレンブリリアント
バむオレツトRRPなどのキノン顔料、ペリレン
顔料、むンゞゎ、チオむンゞゎ等のむンゞゎ顔料
むンドフアヌストオレンゞトナヌなどろビスベン
ゟむミダゟヌル顔料、銅フタロシアニンなどのフ
タロシアニン顔料、キナクリドン顔料、アントラ
キノン顔料、ナフトキノン顔料、スクアリりム顔
料、米囜特蚱第4264694号公報、特公昭56−774号
公報、特開昭49−1231号公報等に蚘茉のシアニン
顔料等がある。 本発明によるアゞン系化合物を含有する前述の
タむプの電子写真感光䜓は、アゞン系化合
物がそれ自身皮膜圢成胜を有しないためバむンダ
ヌず共に溶液に溶解し塗垃、也燥する方法で甚い
られる。 バむンダヌずしおは疎氎性で、か぀誘電率が高
く、電気絶瞁性のフむルム圢成性高分子重合䜓を
甚いるのが奜たしい。このような高分子重合䜓ず
しおは、䟋えば、次のものを挙げるこずができる
が、勿論これらに限るものではない。 ポリカヌボネヌト、ポリ゚ステル、メタクリル
暹脂、アクリル暹脂、ポリ塩化ビニル、ポリ塩化
ビニリデン、ポリスチレン、ポリビニヌルアセテ
ヌト、スチレン−ブタゞ゚ン共重合䜓、塩化ビニ
リデン−アクリロニトリル共重合䜓、塩化ビニル
−酢酞ビニル共重合䜓、塩化ビニル−酢酞ビニル
−無氎マレむン酞共重合䜓、シリコン暹脂、シリ
コン−アルキツド暹脂、プノヌル−ホルムアル
デヒド暹脂、スチレン−アルキツド暹脂、ポリ−
−ビニルカルバゟヌル これらのバむンダヌは、単独で或いは、皮以
䞊の混合物ずしお甚いるこずができる。 バむンダヌの量はいづれのタむプの感光
䜓においおも本発明の化合物重量郚に察し0.2
重量郚から20重量郚の範囲で甚いられる。バむン
ダヌの量が0.2重量郚未満だず感光局の膜ずしお
の性質が匱くなりたた20重量郚を越えるず感光局
の感床が悪くなる。奜たしくは0.5から10重量郹
の範囲である。 タむプの感光䜓においお増感染料の量は本発
明の化合物重量郚に察し0.0001重量郚から0.5
重量郚の範囲であり、奜たしくは0.001重量郚か
ら0.1重量郚の範囲である。 たた電子吞匕性化合物の量は本発明の化合物
重量郚に察し0.01重量郚から10重量郚、奜たしく
は0.1重量郚から重量郚の範囲で甚いられる。 タむプの感光䜓のうち単局型感光䜓においお
䜿甚される電荷発生化合物の量は本発明の化合物
重量郚に察しお0.01重量郚から重量郚の範囲
であり奜たしくは0.05〜重量郚の範囲である。 タむプの積局型感光䜓においお電荷発生局は
電荷発生化合物重量郚に察しお重量郚以䞋の
バむンダヌず共に圢成される。 感光局の膜厚はいづれのタむプの感光䜓
においおも〜30ミクロンの範囲が奜たしい。 感光局が電荷発生局ず電荷茞送局ずの局ずか
ら成るタむプの積局型感光䜓においおは電荷発
生局は0.01〜ミクロンの範囲であり、電荷茞送
局は11〜30ミクロンの範囲で䜿甚される。 本発明の感光局を蚭ける時に甚いる塗垃方法ず
しおはブレヌドコヌテむング法、ワむダヌバヌコ
ヌテむング法、スプレヌコヌテむング法、浞挬コ
ヌテむング法、ビヌドコヌテむング法、゚アヌナ
むフコヌテむング法、カヌテンコヌテむング法な
どの通垞の方法を甚いるこずができる。 本発明の感光局を蚭ける時に甚いる溶剀ずしお
は、倚数の有甚な有機溶剀を包含しおいる。代衚
的なものずしお、䟋えばベンれン、ナフタリン、
トル゚ン、キシレン、メシチレン、クロロベンれ
ンなどの芳銙族系炭化氎玠類、アセトン、−ブ
タノンなどのケトン類、塩化メチレン、クロロホ
ルム、塩化゚チレンなどのハロゲン化脂肪族系炭
化氎玠類、テトラヒドロフラン、゚チル゚テヌル
などの環状若しくは盎鎖状の゚ヌ゚ル類など、あ
るいはこれらの混合溶剀を挙げるこずができる。 たた電荷発生化合物を塗垃する際には、分散を
容易にするため゚チレンゞアミン、ゞ゚チレント
リアミン、トリゞメチルアミノメチルプノヌル
などのアミン系溶剀、−ゞメチルホルムア
ミドなどのアミド系溶剀を塗垃溶剀に加えるこず
ができる。 本発明の感光局には感光局の可塑性を増し膜匷
床を向䞊させるため皮々の添加剀を含有させるこ
ずができる。かかる添加剀ずしおは、ゞプニ
ル、塩化ゞプニル、−タヌプニル、−タ
ヌプニル、ゞブチルフタレヌト、ゞメチルグリ
コヌルフタレヌト、ゞオクチルフタレヌト、トリ
プニル燐酞、メチルナフタリン、ベンゟプノ
ン、塩玠化パラフむン、ゞラりリルチオプロピオ
ネヌト、−ゞニトロサリチル酞、各皮フル
オロカヌボン類、シリコンオむル、シリコンゎム
あるいはゞブチルヒドロキシトル゚ン、2′−
メチレン−ビス−−−ブチル−−メチル
プノヌル、α−トコプロヌル、−−オ
クチル−−クロロハむドロキノン、−ゞ
−−オクチルハむドロキノンなどのプノヌル
性化合物類などを挙げるこずができる。 本発明の感光䜓を構成する導電性支持䜓ずしお
は、酞化むンゞりム、ペり化第銅などの導電性
化合物あるいは金属薄局等を衚面に付しお導電性
化した玙、プラスチツク支持䜓たたは必芁に応じ
おパラゞりム、アルミニりム等を鍛金たたは真空
蒞着した金属板や、アルミニりム板等の任意のも
のが甚いられる。 たた、必芁に応じお蚭けられる接着局、バリダ
ヌ局などの䞭間局を構成する材料ずしおは、前述
した高分子バむンダヌの他、カれむン、れラチ
ン、柱粉、ポリビニルアルコヌル、ポリ酢酞ビニ
ル、゚チルセルロヌス、カルボキシメチルセルロ
ヌス、など他に特願昭57−194199、特願昭57−
225302明现曞蚘茉の元系から成る有機高分子化
合物あるいは酞化アルミニりム等の金属酞化物等
が甚いられる。 本発明の電子写真感光䜓は電子写真耇写機に利
甚するのみならず倪陜電池の他、マむクロフむル
ム、レヌザヌプリンタヌ、CRTプリンタヌ、電
子写真匏補版システムなどの電子写真応甚分野に
も広く甚いるこずができる。 次に本発明を実斜䟋により、曎に具䜓的に説明
するが、本発明はその芁旚を越えない限り、以䞋
の実斜䟋に限定されるものではない。尚、䞋蚘実
斜䟋においお郚はすべお重量郚を瀺す。 実斜䟋  75Όのポリ゚チレンテレフタレヌトフむルムに
アルミを蒞着した導電性支持䜓䞊に䞋蚘構造のビ
スアゟ顔料郚ずポリ゚ステル暹脂商品名 バ
むロン200東掋レヌペン(æ ª)補郚をテトラヒ
ドロフラン50郚に溶かした液ず共にペむントシ゚
むカヌで時間分散した埌ワむダヌバヌで塗垃
し、膜厚0.7Όの電荷発生局を圢成した。 次に、アゞン系化合物(1)郚、ポリカヌボネヌ
ト商品名レキサン121゚ンゞニアリングプラ
スチツク(æ ª)補郚を塩化メチレン40郚および塩
化゚チレン80郚の混合溶媒に溶解した塗垃液をワ
むダヌバヌで前蚘の電荷発生局䞊に塗垃し、電荷
発生局ず電荷茞送局の局からなる膜厚13Όの積
局型感光䜓を䜜成した。感光䜓衚面にはアゞン系
化合物による結晶析出は芋られなか぀た。 この感光䜓を静電耇写玙詊隓装眮川口電機(æ ª)
補、SP−428型−5kvのコロナ攟電により感光䜓
衚面の初期電䜍Voを−650vずした埌タング
ステン光を甚い光照射し、感光䜓衚面の電䜍が50
枛衰するのに必芁な露光量、半枛電光量E50
を枬定した。E50は2.5lux・secであ぀た。たた垯
電・露光のプロセスを連続しお1000回行぀た埌枬
定した所、Voは−645v、E50は2.4lux・secで
回目に比べお倧きな倉化はなか぀た。 実斜䟋 〜 アゞン系化合物(1)のかわりにそれぞれアゞン系
化合物(3)(6)(10)を甚いた他は実斜䟋ず同様にしお
積局型感光䜓を䜜成し、半枛露光量E50を枬
定した。結果を第衚に瀺す。
N-disubstituted amino group represented by the formula; alkoxy groups having 1 to 8 carbon atoms such as methoxy and ethoxy; aralkyloxy groups such as benzyloxy;
Aryloxy groups such as phenoxy and chlorine,
represents a halogen atom such as bromine, or R 6 is R 7
Alternatively, R 8 and the benzene ring to which they are bonded may be combined to form a heterocycle such as a diurolidino ring, a carbazole ring, a phenothiazine ring, or a phenoxazine ring. R 7 and R 8 may be the same or different; hydrogen, an alkyl group having 1 to 8 carbon atoms such as methyl and ethyl, an alkoxy group having 1 to 8 carbon atoms such as methoxy and ethoxy, chlorine, It may represent a halogen atom such as bromine, or it may form a heterocycle together with R 6 . Among the azine compounds used in the present invention, particularly preferred are those represented by the following general formula (2). R 1 , R 2 , R 3 , R 4 , R 5 , R 10 in the formula are general formula (1)
This shows the same as R 1 , R 2 , R 3 , and R 4 explained in . Specific examples of the compound represented by the general formula (1) used in the present invention are listed below. These compounds can be synthesized by a known method using compounds represented by the following general formulas (3) and (4) and hydrazine. Next, the azine compounds used in the present invention will be explained using synthesis examples. Synthesis of Exemplary Compound (1) 7.0 g of 4,4'-bis(dimethylamino)benzophenone hydrazone and 4.8 g of 4-diethylaminobenzaldehyde were heated under reflux in ethanol for 2 hours. After cooling the reaction solution, the resulting solid was filtered and dried.
Next, recrystallize from ethanol with a melting point of 167-167.5.
8.8 g of crystals were obtained. Yield 78% Elemental analysis value C 28 H 33 N 5 Calculated value C: 76.15% H: 7.98% N:
15.85% Actual value C: 76.01% H: 8.20% N:
15.76% Synthesis of Exemplified Compound (3) 7.0 g of 4,4'-bis(dimethylamino)benzophenone hydrazone and 4-(N-phenyl-N
-Methylamino)benzaldehyde (5.3 g) was heated under reflux in ethanol for 2 hours. After the reaction was completed, the reaction solution was cooled, and the resulting solid was filtered and dried. Next, recrystallization was performed using a mixed solvent of benzene and n-hexane to obtain 9.2 g of crystals with a melting point of 133.5 to 134°C. Yield 78% Elemental analysis value C 31 H 33 N Calculated value as 5 C: 78.27% H: 6.99% N:
14.72% Actual value C: 78.19% H: 7.22% N:
14.57% Other azine compounds used in the present invention can be synthesized in the same manner. When the azine compound represented by the general formula (1) is used in an electrophotographic photoreceptor, the azine compound (1) functions both as an organic photoconductive compound and as a charge transporting compound. It can be used as a photoreceptor. Type A: An electrophotographic photoreceptor having a substantially uniform and transparent photosensitive layer in combination with a sensitizer. Type B: Electrophotographic photoreceptor combined with a charge generating compound. Sensitizers used in the photosensitive layer of A-type electrophotographic photoreceptors include 2,4,7-trinitrofluoren-9-one, chloranil, tetracyanoethylene, and electron-withdrawing compounds described in U.S. Pat. No. 3,232,755. , pyrylium dyes described in U.S. Pat. No. 3,250,615, U.S. Pat. No. 4,315,983, U.S. Pat.
There are sensitizing dyes such as thiopyrylium dyes described in No. 4343948 and JP-A-57-46980, azacyanine dyes, triarylmethane dyes, thiazine dyes, and cyanine dyes described in JP-A-56-81852. The B-type electrophotographic photoreceptor is called a functionally separated photoreceptor, and is a single-layer type consisting of one photoreceptor layer in which a charge-generating compound is dispersed in the azine compound of the present invention, which is used as a charge-transporting compound. There is a photoreceptor, or a laminated photoreceptor consisting of two photosensitive layers: a charge generation layer containing a charge generation compound and a charge transport layer containing the azine compound of the present invention used as a charge transport compound. Preferably, a laminated type photoreceptor is useful in terms of sensitivity and charge retention of the electrophotographic photoreceptor. Type B charge generating compounds include inorganic ones such as cadmium sulfide, cadmium selenide, zinc oxide, zinc sulfide, titanium dioxide (especially lutherite type), and trigonal selenium, and organic ones such as: Azo pigments such as Sudan Red, Chlordiane Blue, and Jenas Green B;
Disazo pigments described in JP-A-54-2738, JP-A-57-152091, JP-A-58-123541, etc.;
Trisazo pigments described in JP-A-57-41642, JP-A-57-116345, etc., quinone pigments such as algol yellow, pyrenequinone, indanthrene brilliant violet RRP, perylene pigments, indigo such as indigo, thioindigo, etc. Pigments India First Orange Toner etc. Phthalocyanine pigments such as bisbenzimidazole pigments and copper phthalocyanine, quinacridone pigments, anthraquinone pigments, naphthoquinone pigments, squalium pigments, U.S. Pat. There are cyanine pigments and the like described in Publication No. 49-1231 and the like. The above-mentioned A and B types of electrophotographic photoreceptors containing the azine compound according to the present invention are used by a method in which the azine compound itself does not have a film-forming ability, so it is dissolved in a solution together with a binder, coated, and dried. As the binder, it is preferable to use a film-forming polymer that is hydrophobic, has a high dielectric constant, and is electrically insulating. Examples of such high molecular weight polymers include, but are not limited to, the following. Polycarbonate, polyester, methacrylic resin, acrylic resin, polyvinyl chloride, polyvinylidene chloride, polystyrene, polyvinyl acetate, styrene-butadiene copolymer, vinylidene chloride-acrylonitrile copolymer, vinyl chloride-vinyl acetate copolymer, vinyl chloride -Vinyl acetate-maleic anhydride copolymer, silicone resin, silicone-alkyd resin, phenol-formaldehyde resin, styrene-alkyd resin, poly-
N-Vinylcarbazole These binders can be used alone or as a mixture of two or more. The amount of binder is 0.2 parts by weight of the compound of the present invention in both type A and B photoreceptors.
It is used in a range of 20 parts by weight. If the amount of the binder is less than 0.2 parts by weight, the properties of the photosensitive layer as a film will be weakened, and if it exceeds 20 parts by weight, the sensitivity of the photosensitive layer will deteriorate. Preferably it is in the range of 0.5 to 10 parts by weight. In the A type photoreceptor, the amount of sensitizing dye is 0.0001 to 0.5 parts by weight per 1 part by weight of the compound of the present invention.
Parts by weight, preferably 0.001 parts by weight to 0.1 parts by weight. In addition, the amount of the electron-withdrawing compound is the compound 1 of the present invention.
It is used in an amount of 0.01 to 10 parts by weight, preferably 0.1 to 2 parts by weight. The amount of the charge generating compound used in the single-layer type photoreceptor among B type photoreceptors is in the range of 0.01 to 2 parts by weight, preferably 0.05 to 1 part by weight, per 1 part by weight of the compound of the present invention. is within the range of In the B type laminated photoreceptor, the charge generation layer is formed with 5 parts by weight or less of a binder per 1 part by weight of the charge generation compound. The thickness of the photosensitive layer is preferably in the range of 1 to 30 microns for both type A and B photoreceptors. In a type B laminated photoreceptor in which the photosensitive layer is composed of two layers, a charge generation layer and a charge transport layer, the charge generation layer has a thickness in the range of 0.01 to 5 microns, and the charge transport layer has a thickness in the range of 11 to 30 microns. used. As the coating method used to form the photosensitive layer of the present invention, a conventional method such as a blade coating method, a wire bar coating method, a spray coating method, a dip coating method, a bead coating method, an air knife coating method, a curtain coating method, etc. can be used. I can do it. The solvent used in forming the photosensitive layer of the present invention includes many useful organic solvents. Typical examples include benzene, naphthalene,
Aromatic hydrocarbons such as toluene, xylene, mesitylene, and chlorobenzene, ketones such as acetone and 2-butanone, halogenated aliphatic hydrocarbons such as methylene chloride, chloroform, and ethylene chloride, and cyclic hydrocarbons such as tetrahydrofuran and ethyl ether. or linear AELs, or a mixed solvent thereof. Furthermore, when coating a charge generating compound, an amine solvent such as ethylenediamine, diethylenetriamine, or tridimethylaminomethylphenol, or an amide solvent such as N,N-dimethylformamide may be added to the coating solvent to facilitate dispersion. can. The photosensitive layer of the present invention can contain various additives in order to increase the plasticity of the photosensitive layer and improve the film strength. Such additives include diphenyl, diphenyl chloride, o-terphenyl, P-terphenyl, dibutyl phthalate, dimethyl glycol phthalate, dioctyl phthalate, triphenyl phosphoric acid, methylnaphthalene, benzophenone, chlorinated paraffin, dilaurylthiopropionate, 3, 5-dinitrosalicylic acid, various fluorocarbons, silicone oil, silicone rubber or dibutylhydroxytoluene, 2,2'-
Phenolic compounds such as methylene-bis-(6-t-butyl-4-methylphenol), α-tocopherol, 2-t-octyl-5-chlorohydroquinone, 2,5-di-t-octylhydroquinone, etc. can be mentioned. The conductive support constituting the photoreceptor of the present invention may be a paper or plastic support made conductive by applying a conductive compound such as indium oxide or cuprous iodide or a thin metal layer to the surface, or a plastic support as required. Depending on the requirements, any material such as a metal plate made of forged or vacuum-deposited palladium, aluminum, or the like, or an aluminum plate may be used. In addition to the above-mentioned polymer binder, materials constituting intermediate layers such as adhesive layers and barrier layers that are provided as necessary include casein, gelatin, starch, polyvinyl alcohol, polyvinyl acetate, ethyl cellulose, carboxymethyl cellulose, Other patent applications include 194199, 1983, and
An organic polymer compound consisting of a ternary system or a metal oxide such as aluminum oxide described in the specification of No. 225302 is used. The electrophotographic photoreceptor of the present invention can be used not only in electrophotographic copying machines but also in a wide range of electrophotographic applications such as solar cells, microfilms, laser printers, CRT printers, and electrophotographic plate making systems. . Next, the present invention will be explained in more detail with reference to examples, but the present invention is not limited to the following examples unless it exceeds the gist thereof. In the following examples, all parts indicate parts by weight. Example 1 5 parts of a bisazo pigment with the following structure and 5 parts of a polyester resin (trade name: Vylon 200, manufactured by Toyo Rayon Co., Ltd.) were dissolved in 50 parts of tetrahydrofuran on a conductive support made of a 75Ό polyethylene terephthalate film with aluminum vapor-deposited. The mixture was dispersed with a paint shaker for 1 hour and then coated with a wire bar to form a charge generation layer with a thickness of 0.7 Όm. Next, a coating solution prepared by dissolving 7 parts of azine compound (1) and 7 parts of polycarbonate (trade name: Lexan 121, manufactured by Engineering Plastics Co., Ltd.) in a mixed solvent of 40 parts of methylene chloride and 80 parts of ethylene chloride was applied using a wire bar. A laminated photoreceptor having a thickness of 13 Όm was prepared by coating the above-mentioned charge generation layer with two layers: a charge generation layer and a charge transport layer. No crystal precipitation due to the azine compound was observed on the surface of the photoreceptor. This photoreceptor was tested using an electrostatic copying paper tester (Kawaguchi Electric Co., Ltd.).
After setting the initial potential (Vo) of the photoreceptor surface to -650V by corona discharge of -5kV (manufactured by SP-428, manufactured by Kogyo Co., Ltd., SP-428 type), the photoreceptor surface was irradiated with light using tungsten light, and the potential of the photoreceptor surface was set to 50V.
Exposure required to attenuate by %, halved amount of light (E 50 )
was measured. E 50 was 2.5 lux・sec. Also, when measured after performing the charging and exposure process 1000 times, Vo was -645v and E50 was 1 at 2.4lux・sec.
There were no major changes compared to the previous time. Examples 2 to 4 Laminated photoreceptors were prepared in the same manner as in Example 1, except that azine compounds (3), (6), and (10) were used instead of azine compound (1), and the half-decreased exposure amount was (E 50 ) was measured. The results are shown in Table 1.

【衚】 比范䟋 〜 実斜䟋で甚いたアゞン系化合物(1)のかわりに
本発明によるアゞン系化合物以倖の比范化合物
−−−を甚いた他は、
実斜䟋ず同様な方法にお感光䜓を䜜成した。 この感光䜓の垯電特性を実斜䟋(1)ず同様の方法
により枬定した。たた感光䜓の衚面状態を芳察し
た。結果を第衚に瀺す。
[Table] Comparative Examples 1 to 3 Comparative compounds (A-1), (A-2), (A-3) other than the azine compound according to the present invention in place of the azine compound (1) used in Example 1 In addition to using
A photoreceptor was produced in the same manner as in Example 1. The charging characteristics of this photoreceptor were measured in the same manner as in Example (1). The surface condition of the photoreceptor was also observed. The results are shown in Table 2.

【衚】 実斜䟋および比范䟋、から明らかなごず
く本発明による4′−ゞ−ゞ眮換アミノ
ベンゟプノンから合成される非察称のアゞン系
化合物は4′−−ゞ眮換アミノベンゟフ
゚ノン以倖のカルボニル化合物から合成されるア
ゞン系化合物にくらべお感床が良くか぀くり返し
埌の垯電特性にもすぐれおいる。 これは本発明による化合物が比范化合物−
−にくらべ−ゞ眮換アミノ基を䞀
぀倚く有するために化合物の最高被占準䜍が高く
な぀た結果電荷発生局から電荷茞送局ぞの正孔の
泚入効率が良くな぀たからだず考えられる。 たた実斜䟋および比范䟋から明らかなごず
く4′−ゞ−ゞ眮換アミノベンゟプノ
ンから合成される察称型をしたアゞン系化合物は
本発明による非察称型アゞン系化合物にくらべお
感床がおずるほか溶解床が悪いため感光䜓衚面に
結晶が析出しやすい欠点を有する。 実斜䟋  本発明によるアゞン系化合物(1)重量郚、−
〔−−−クロル゚チル、−−シアノ゚
チルスチリル〕−−ゞ−−ブチルチオ
ピリリりムフルオロボレヌト0.01郚およびポリカ
ヌボネヌトレキサン1211.5郚を塩化メチレン
40郚および塩化゚チレン80郚の混合溶媒に溶解し
塗垃液を調補した。この塗垃液をポリ゚チレンテ
レフタレヌトフむルム衚面にススがドヌプされた
酞化むンゞりムが蒞着された透明導電性フむルム
䞊にワむダヌバヌで塗垃、也燥し膜厚5Όの感光
局を有する感光䜓を埗た。 この感光䜓を実斜䟋ず同じ装眮を甚い
250vに垯電しE50を枬定した所10lux・secであ぀
た。 実斜䟋 〜 アゞン系化合物(1)をそれぞれ(2)(4)(8)にかえたほ
かは実斜䟋ず同様の方法で感光䜓を䜜成し感床
を枬定した。結果を第衚に瀺す。
[Table] As is clear from Example 1 and Comparative Examples 1 and 2, 4,4'-di(N-disubstituted amino) according to the present invention
Asymmetric azine-based compounds synthesized from benzophenone have better sensitivity and better charging characteristics after recycling than azine-based compounds synthesized from carbonyl compounds other than 4,4'-(N-disubstituted amino)benzophenone. ing. This indicates that the compound according to the present invention is different from the comparative compound (A-
Since it has one more N-disubstituted amino group than 1) and (A-2), the highest occupied level of the compound becomes higher, resulting in a higher hole injection efficiency from the charge generation layer to the charge transport layer. I think it's because he's getting better. Furthermore, as is clear from Example 1 and Comparative Example 3, the symmetric azine compound synthesized from 4,4'-di(N-disubstituted amino)benzophenone has a higher sensitivity than the asymmetric azine compound according to the present invention. In addition to its low solubility, it has the disadvantage that crystals tend to precipitate on the surface of the photoreceptor. Example 5 1 part by weight of azine compound (1) according to the present invention, 4-
0.01 part of [4-(N-2-chloroethyl, N-2-cyanoethyl)styryl]-2,6-di-t-butylthiopyrylium fluoroborate and 1.5 parts of polycarbonate (Lexan 121) were dissolved in methylene chloride.
A coating solution was prepared by dissolving in a mixed solvent of 40 parts of ethylene chloride and 80 parts of ethylene chloride. This coating solution was coated with a wire bar onto a transparent conductive film on which soot-doped indium oxide was deposited on the surface of a polyethylene terephthalate film, and dried to obtain a photoreceptor having a photosensitive layer with a film thickness of 5 ÎŒm. This photoreceptor was manufactured using the same equipment as in Example 1.
When charged to 250v and measured E50 , it was 10lux・sec. Examples 6 to 8 Photoreceptors were prepared in the same manner as in Example 5, except that azine compound (1) was replaced with (2), (4), and (8), respectively, and the sensitivity was measured. The results are shown in Table 3.

【衚】 比范䟋 〜 実斜䟋で甚いたアゞン系化合物(4)のかわりに
本発明の範囲に含たれないアゞン系化合物−
−−を甚いた他は実斜䟋ず同
様な方法にお感光䜓を䜜成した。 この感光䜓の垯電特性を実斜䟋ず同様の方法
により枬定した。結果を第衚に瀺すがいづれも
実斜䟋より感床が䜎か぀た。
[Table] Comparative Examples 4 to 6 Instead of the azine compound (4) used in Example 7, an azine compound (A-
4) A photoreceptor was produced in the same manner as in Example except that (A-5) and (A-6) were used. The charging characteristics of this photoreceptor were measured in the same manner as in Example 7. The results are shown in Table 4, and the sensitivity was lower than that of Example 7 in all cases.

【衚】 たた比范䟋で䜜成した感光䜓は宀枩で週間
攟眮埌感光䜓衚面に結晶が析出した。 実斜䟋  䞋蚘構造のビスアゟ顔料郚、アゞン系化合物
(3)郚、およびポリカヌボネヌトレキサン121
郚ずを塩化メチレン95郚に加え、これをペむン
トシ゚むカヌにお時間振ずうし塗垃液を調補し
た。この塗垃液をワむダヌバヌでポリ゚チレンテ
レフタレヌトフむルムにアルミを蒞着した導電性
支持䜓に塗垃し、也燥しお厚さ10Όの感光局を有
する単局型感光䜓を埗た。 この電子写真感光䜓に぀いお実斜䟋ず同じ装
眮を甚い5kvのコロナ攟電により450vに垯電
させタングステン光を甚いお露光した。半枛露光
量E50を枬定したずころ9lux・secであ぀た。 たた垯電ず露光の工皋を1000回繰返しおも
E50はほずんど倉化しなか぀た。 実斜䟋 10 実斜䟋で甚いたビスアゟ顔料郚、アゞン系
化合物郚および−クレゟヌルホルムアルデヒ
ド暹脂郚ずを゚チレングリコヌルモノメチル゚
ヌテル30郚に加え、これをボヌルミル䞭で粉砕、
混合し、この塗垃液を玄0.25mm厚の砂目立おされ
か぀陜極酞化及び封孔凊理されたアルミニりム板
䞊にワむダヌラりンドロツドを甚いお塗垃し、90
℃で10分間50℃で日也燥し、厚さ玄6ÎŒmの詊料
を䜜成した。 次にこの詊料に暗所で衚面電䜍が500Vになる
ようにコロナ攟電を行ない、タングステン光でネ
ガ像を露光100ルツクス・秒した埌、䞉菱ダ
むダフアツクスマスタヌLOM−EDトナ−䞉菱
補玙瀟補で反転珟像を行な぀たずころ、非垞に
鮮明なポゞ像を印刷原板䞊に埗るこずができた。
この印刷甚原板を゚ツチング液DP−富士写真
フむルム瀟補ケむ酞ナトリりム氎溶液の10倍
垌釈液䞭に䞀分間浞挬し、トナヌの付着しおいな
い郚分非画線郚の感光局を溶解陀去した。そ
の結果、非画線郚の顔料がバむンダヌず共に容易
に陀去され、鮮明な画像の印刷版を圢成するこず
ができた。
[Table] Crystals were deposited on the photoreceptor surface of the photoreceptor prepared in Comparative Example 6 after being left at room temperature for one week. Example 9 1 part of bisazo pigment with the following structure, azine compound
(3) 5 parts, and polycarbonate (Lexan 121)
5 parts of methylene chloride were added to 95 parts of methylene chloride, and the mixture was shaken for 1 hour in a paint shaker to prepare a coating solution. This coating solution was applied with a wire bar to a conductive support made of a polyethylene terephthalate film on which aluminum was vapor-deposited, and dried to obtain a single-layer photoreceptor having a photosensitive layer with a thickness of 10 Όm. Using the same apparatus as in Example 1, this electrophotographic photoreceptor was charged to +450V by +5kV corona discharge and exposed to tungsten light. The half-reduction exposure (E 50 ) was measured and found to be 9 lux·sec. Even if the two steps of charging and exposure are repeated 1000 times,
E 50 remained almost unchanged. Example 10 1 part of the bisazo pigment used in Example 9, 2 parts of the azine compound, and 6 parts of m-cresol formaldehyde resin were added to 30 parts of ethylene glycol monomethyl ether, and this was ground in a ball mill.
The coating solution was mixed and applied to a grained, anodized and sealed aluminum plate approximately 0.25 mm thick using a wire round rod.
It was dried at 50°C for 10 minutes and for 1 day to prepare a sample with a thickness of about 6 Όm. Next, corona discharge was applied to this sample in a dark place so that the surface potential became 500 V, and after exposing the negative image to tungsten light (100 lux seconds), Mitsubishi Diafax Master LOM-ED toner (Mitsubishi Paper When reversal development was performed using a printing press (manufactured by Co., Ltd.), a very clear positive image could be obtained on the original printing plate.
This printing original plate was immersed for 1 minute in a 10-fold diluted etching solution DP-1 (manufactured by Fuji Photo Film Co., Ltd.; sodium silicate aqueous solution), and the photosensitive layer was removed from the areas to which toner was not attached (non-image areas). was dissolved and removed. As a result, the pigment in the non-image area was easily removed together with the binder, and a printing plate with a clear image could be formed.

Claims (1)

【特蚱請求の範囲】  䞋蚘䞀般匏(1)で瀺される化合物を含有する感
光局を有するこずを特城ずする電子写真感光䜓。 䜆し、匏䞭R1、R2、R3、R4は眮換又は非眮換
の炭玠数〜12の、アルキル基、アラルキル基、
アリヌル基あるいは窒玠原子ず共に環状アミノ基
を圢成する残基を衚わし、 R5は氎玠、眮換又は非眮換の炭玠数〜12の、
アルキル基、アラルキル基、非眮換又は炭玠数
〜の、アルキル基、アルコキシ基、ハロゲン原
子、氎酞基、シアノ基を眮換基ずしお含むアリヌ
ル基を衚わす。 又R6ずしおは炭玠数〜の、【匏】又は 【匏】で衚わされる−ゞ眮換アミノ基、ア ルコキシ基、アラルキルオキシ基、アリヌルオキ
シ基、ハロゲン原子を衚わし、又はR6はR7又は
R8およびそれらが結合しおいるベンれン環ず䞀
緒にな぀お耇玠環を圢成するのに必芁な原子を衚
わす。 R7及びR8は同䞀でもたた盞違しおいおも良く、
氎玠、炭玠数〜の、アルキル基、アルコキシ
基、ハロゲン原子を衚わすか又はR6ず共に耇玠
環を圢成するのに必芁な原子を衚わす。
[Scope of Claims] 1. An electrophotographic photoreceptor comprising a photosensitive layer containing a compound represented by the following general formula (1). However, in the formula, R 1 , R 2 , R 3 , R 4 are substituted or unsubstituted alkyl groups, aralkyl groups, having 1 to 12 carbon atoms,
Represents a residue that forms a cyclic amino group with an aryl group or a nitrogen atom, R 5 is hydrogen, substituted or unsubstituted, having 1 to 12 carbon atoms,
Alkyl group, aralkyl group, unsubstituted or carbon number 1
-8 represents an aryl group containing an alkyl group, an alkoxy group, a halogen atom, a hydroxyl group, or a cyano group as a substituent. Further, R 6 represents an N-disubstituted amino group, an alkoxy group, an aralkyloxy group, an aryloxy group, or a halogen atom having 1 to 8 carbon atoms and represented by [Formula] or [Formula], or R 6 represents R 7 or
Represents the atoms necessary to form a heterocycle together with R 8 and the benzene ring to which they are bonded. R 7 and R 8 may be the same or different,
It represents hydrogen, an alkyl group, an alkoxy group, a halogen atom having 1 to 8 carbon atoms, or an atom necessary to form a heterocycle with R 6 .
JP58197343A 1983-10-21 1983-10-21 Electrophotographic sensitive body Granted JPS6088949A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58197343A JPS6088949A (en) 1983-10-21 1983-10-21 Electrophotographic sensitive body

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58197343A JPS6088949A (en) 1983-10-21 1983-10-21 Electrophotographic sensitive body

Publications (2)

Publication Number Publication Date
JPS6088949A JPS6088949A (en) 1985-05-18
JPH042184B2 true JPH042184B2 (en) 1992-01-16

Family

ID=16372893

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58197343A Granted JPS6088949A (en) 1983-10-21 1983-10-21 Electrophotographic sensitive body

Country Status (1)

Country Link
JP (1) JPS6088949A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS646143A (en) * 1987-06-26 1989-01-10 Unitika Ltd Manufacture of nylon 6 textile

Also Published As

Publication number Publication date
JPS6088949A (en) 1985-05-18

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