Photosensitive material containing disazo compound for use in electrophotography

BACKGROUND OF THE INVENTION
1. Field of the Invention
This invention relates to a novel disazo compound useful as a charge generating material of a photosensitive material, particularly laminated type photosensitive material for use in electrophotography, a method for producing said disazo compound and a photosensitive material having a photosensitive layer containing said disazo compound as a charge generating material.
2. Description of the Prior Art
Heretofore, typically known photosensitive materials include inorganic type photosensitive materials using selenium and its alloy or dispersion of zinc oxide sensitized by coloring matter in binder resin, and organic type photosensitive materials using a charge transfer complex of 2,4,7-trinitro-9-fluorenone (hereinafter referred to as "TNF") and poly-N-vinylcarbazole (hereinafter referred to as "PVK").
However, these conventional photosensitive materials have not only advantages but also various disadvantages. For example, the selenium type photosensitive material widely used at present has such disadvantages as that the manufacturing cost is high due to the severity of the manufacturing conditions; that it is difficult to work the material into a belt-like product because of lack of flexibility; and that it is difficult to handle because the material is weak to heat and mechanical shock. The zinc oxide type photosensitive material can be manufactured at a low expense by coating cheap zinc oxide on a substrate, but has such disadvantages as that the sensitivity is low; that the smoothness of the surface, hardness, tensile strength, friction resistance and other mechanical properties are inferior; and that the durability for repeated use in a plain paper copier is poor. The photosensitive material using the charge transfer complex of TNF and PVK has a low sensitivity and is unsuitable as a photosensitive material for a high speed copier.
Recently, various studies have been carried out to remove disadvantages of these photosensitive materials, and many photosensitive materials, particularly organic type photosensitive materials have been proposed. Among them, a laminated type photosensitive material prepared by forming a thin film of organic pigment on an electro-conductive substrate (charge generating layer) and overlaying a charge transfer material-containing layer (charge transfer layer) on said charge generating layer has generally higher sensitivity and more stable chargeability than the conventional organic type photosensitive materials, and is practically used in part as a photosensitive material for a plain paper copier.
Examples of this kind of known conventional laminated type photosensitive materials include as follows:
(1) photosensitive material using a thin layer formed by vapor depositing perylene derivatives as a charge transfer layer (see U.S. Pat. No. 3,871,882);
(2) photosensitive material using a thin layer formed by coating an organic amine solution of Chloro Dian Blue as a charge generating layer and hydrazone compound as a charge transfer layer (see Japanese Patent Publication No. 55-42380);
(3) photosensitive material using a thin layer formed by coating an organic solvent dispersion of distyryl benzene type disazo compound, stilbene type disazo compound or benzidine type disazo compound as a charge generating layer and hydrazone compound as a charge transfer layer (see Japanese Patent Laid Open Nos. 55-84943, 52-8832 and 52-55643); and the like.
However, these conventional laminated type photosensitive materials have not only advantages but also various disadvantages as mentioned below.
(1) The above photosensitive material using perylene derivatives and oxadiazole derivatives has a disadvantage that the manufacturing cost is very high because of forming a charge generating layer by vapor deposition.
(2) The above photosensitive material using Chloro Dian Blue and hydrazone compound must use an organic amine (for example, ethylene diamine) as a coating solvent for forming a charge generating layer, which is difficult in handling. Furthermore, it has a disadvantage that the image reproducibility of a reddish original is poor because the photosensitive wavelength range of the visible light zone lies in the range of about 450-660 nm. Therefore, it is necessary to provide a filter to cut red light when used in a copier, thus being disadvantageous to the design of a copier.
(3) The above photosensitive materials using distyryl benzene type disazo compound, stilbene type disazo compound or benzidine type disazo compound and hydrazone compound have an advantage that the charge generating layer can easily be prepared simply by coating a dispersion of the disazo compound, but also have a disadvantage that the image reproducibility of a reddish original is poor in the same manner as in the above photosensitive material (2) since the photosensitive wave length lies in the range of about 450-700 nm.
SUMMARY OF THE INVENTION
An object of the present invention is to provide a novel disazo compound having a photosensitive wavelength range of the visible light zone in a shorter wavelength zone (about 450-600 nm) and therefore having an excellent image reproducibility of a reddish original, the sensitivity of which is higher when used as a charge generating material for a photosensitive material, particularly layered type photosensitive material for use in electrophotography, than those of the conventional disazo compounds, a method for preparing said novel disazo compound, and a photosensitive material containing said novel disazo compound for use in electrophotography.
The novel disazo compound of the present invention has the following general formula (I), ##STR4## wherein A represents ##STR5## (wherein R represents an alkyl, alkoxy, nitro, halogen, cyano or halomethyl group; n represents an integer of 0, 1, 2 or 3; and R may be the same or different when n is an integer of 2 or 3).
The method for preparing the novel disazo compound having the above general formula (I) of the present invention is characterized by comprising diazotizing a diamino compound having the formula (II), ##STR6## to prepare a tetrazonium salt having the general formula (III), ##STR7## (wherein X represents an anion functional group), and reacting the tetrazonium salt thus prepared with a compound (hereinafter referred to as a coupler) having the following general formula (IV), (V) or (VI), ##STR8## (wherein R represents an alkyl, alkoxy, nitro, halogen, cyano or halomethyl group; n represents an integer of 0, 1, 2 or 3; and R may be the same or different when n is an integer of 2 or 3).
The photosensitive material for use in electrophotography of the present invention is characterized by providing a photosensitive layer containing a disazo pigment having the following general formula (VII), ##STR9## wherein A.sub.1 represents a coupler residue and R' represents hydrogen or a lower alkyl group.

BRIEF DESCRIPTION OF THE DRAWINGS
FIGS. 1 to 16 show infrared absorption spectrums (KBr disk).
FIGS. 17 and 18 are enlarged sectional views showing a structure example of the electrophotographic element of the present invention.

DETAILED DESCRIPTION OF THE PRESENT INVENTION
We have studied for developing a photosensitive material having a high sensitivity for use in electrophotography, which can be easily prepared and has a photosensitive wave length zone residing in such a shorter wave length zone as to be suitable for reproducing an image of a reddish original. As the result of this study, we have found that the above mentioned object can be achieved by using the specific disazo compound having the above general formula (VII) of the present invention as a charge generating material.
Examples of the coupler of the disazo compounds expressed by the general formula (VII) include an aromatic hydrocarbon compound and heterocyclic compound having a phenolic hydroxyl group such as phenol type, naphthol type compounds and the like; an aromatic hydrocarbon compound and heterocyclic compound having an amino group; an aromatic hydrocarbon compound and heterocyclic compound having an amino group and a phenolic hydroxyl group such as aminophthols; a compound having an aliphatic or aromatic enol type ketone group (compound having an active methylene group) and the like. Preferably, the residue A.sub.1 of the coupler is expressed by the following general formula (VIII), (IX), (X), (XI), (XII), (XIII), (XIV), (XV), (XVI), (XVII) and (XVIII). ##STR10## wherein X.sub.1, Y.sub.1, Z, m and n in the above formula (VIII), (IX), (X) and (XI) represent the following groups: X.sub.1 : ##STR11## or --NHSO.sub.2 --R.sub.3 (wherein R.sub.1 and R.sub.2 represent hydrogen or a substituted or non-substituted alkyl group, and R.sub.3 represents a substituted or non-substituted alkyl or a substituted or non-substituted aryl group); Y.sub.1 : hydrogen, halogen, substituted or non-substituted alkyl group, substituted or non-substituted alkoxy group, carboxyl group, sulfo group, substituted or non-substituted sulfamoyl group or ##STR12## (wherein R.sub.4 represents hydrogen, alkyl group or its substituted compound, phenyl group or its substituted compound, and Y.sub.2 represents cyclic hydrocarbon or its substituted compound, heterocycle or its substituted compound, or ##STR13## wherein R.sub.5 represents a cyclic hydrocarbon or its substituted compound, heterocycle or its substituted compound, or styryl group or its substituted compound, and R.sub.6 represents hydrogen, alkyl group, phenyl group or their substituted compound, or R.sub.5 and R.sub.6 may form a ring with carbons bonded thereto);
Z: cyclic hydrocarbon or its substituted compound, or heterocycle or its substituted compound;
n: an integer of 1 or 2; and
m: an integer of 1 or 2. ##STR14## wherein R.sub.7 in the above formula (XII) and (XIII) represents a substituted or non-substituted hydrocarbonyl group, and X.sub.1 is the same as mentioned above. ##STR15## wherein R.sub.8 represents an alkyl group, carbamoyl group, carboxyl group or its ester, and Ar.sub.1 represents a cyclic hydrocarbon or its substituted compound, and X.sub.1 is the same as mentioned above. ##STR16## wherein R.sub.9 is the above formula (XV) and (XVI) represents hydrogen or substituted or non-substituted hydrocarbonyl group, and Ar.sub.2 represents cyclic hydrocarbon or its substituted compound.
Examples of the cyclic hydrocarbon expressed by Z in the above general formula (VIII), (IX), (X) or (XI) include benzene ring, naphthalene ring and the like, and examples of the heterocycle expressed by the same include indole ring, carbazole ring, benzofuran ring, ring and the like. Examples of the substituent of the ring expressed by Z include a halogen atom such as chlorine, bromine, and the like.
Examples of the cyclic hydrocarbon expressed by Y.sub.2 or R.sub.5 include phenyl, naphthyl, anthryl, pyrenyl and the like, and examples of the heterocyclic group expressed by the same include pyridyl, thienyl, furyl, indolyl, benzofuranyl, carbazolyl, dibenzofuranyl and the like. Examples of the ring formed by bonding R.sub.5 and R.sub.6 include fluorene ring.
Examples of the substituents for the cyclic hydrocarbon or heterocycle expressed by Y.sub.2 or R.sub.5 or for the ring formed by bonding R.sub.5 and R.sub.6 include an alkyl group such as methyl, ethyl, propyl, butyl or the like; an alkoxy group such as methoxy, ethoxy, propoxy, butoxy or the like; a halogen atom such as chlorine, bromine or the like; a dialkyl amino group such as dimethyl amino, diethyl amino or the like; a diaralkyl amino group such as dibenzyl amino or the like; a halomethyl group such trifluoromethyl or the like; nitro group; cyano group; carboxyl group or its ester; hydroxyl group; sulphonate group such as --SO.sub.3 Na; and the like.
Examples of the substituent for the phenyl group expressed by R.sub.4 include a halogen atom such as chlorine or bromine.
Examples of the hydrocarbonyl group expressed by R.sub.7 and R.sub.9 include an alkyl group such as methyl, ethyl, propyl, butyl and the like; an aralkyl group such as benzyl and the like; an aryl group such as phenyl; or their substituted compounds.
Examples of the substituent for the hydrocarbonyl group expressed by R.sub.7 or R.sub.9 include an alkyl group such as methyl, ethyl, propyl, butyl and the like; an alkoxy group such as methoxy, ethoxy, propoxy, butoxy and the like; a halogen atom such as chlorine, bromine and the like; hydroxyl group; nitro group; and the like.
Examples of the cyclic hydrocarbon expressed by Ar.sub.1 or Ar.sub.2 include phenyl, naphthyl and the like, and examples of the substituents for these groups include an alkyl group such as methyl, ethyl, propyl, butyl or the like; an alkoxy group such as methoxy, ethoxy, propoxy, butoxy or the like; nitro group; a halogen group such as chlorine, bromine or the like; cyano group; and a dialkyl amino group such as dimethyl amino, diethyl amino or the like.
Among the groups expressed by X.sub.1, hydroxyl group is particularly suitable.
Among the above coupler residues, preferable ones are expressed by the general formula (IX), (XII), (XIII), (XIV), (XV) and (XVI), and X.sub.1 in the general formula is preferably hydroxyl group. Among them, the coupler residue expressed by the general formula (XVII) ##STR17## (wherein Y.sub.1 and Z are the same as mentioned above) is preferable, and the coupler residue expressed by the general formula (XVIII) ##STR18## (wherein Z, Y.sub.2 and R.sub.2 are the same as mentioned above) is more preferable.
Still more preferable coupler residue among the above mentioned groups is expressed by the general formula (XIX) or (XX) ##STR19## (wherein Z, R.sub.2, R.sub.5 and R.sub.6 are the same as mentioned above, and R.sub.10 is the same as those illustrated with regard to the substituents for Y.sub.2).
Examples of the disazo compound of the present invention are illustrated by the following structural formulas.
__________________________________________________________________________ ##STR20## ##STR21##DisazoCompound No. R.sub.1 R.sub.2 R.sub.3 R.sub.4 R.sub.5 R.sub.6 R.sub.7__________________________________________________________________________1 H H H H H H H2 H NO.sub.2 H H H H H3 H H NO.sub.2 H H H H4 H H H NO.sub.2 H H H5 H CF.sub.3 H H H H H6 H H CF.sub.3 H H H H7 H H H CF.sub.3 H H H8 H CN H H H H H9 H H CN H H H H10 H H H CN H H H11 H I H H H H H12 H H I H H H H13 H H H I H H H14 H Br H H H H H15 H H Br H H H H16 H H H Br H H H17 H Cl H H H H H18 H H Cl H H H H19 H H H Cl H H H20 H F H H H H H21 H H F H H H H22 H H H F H H H23 H CH.sub.3 H H H H H24 H H CH.sub.3 H H H H25 H H H CH.sub.3 H H H26 H C.sub.2 H.sub.5 H H H H H27 H H H C.sub.2 H.sub.5 H H H28 H OCH.sub.3 H H H H H29 H H OCH.sub.3 H H H H30 H H H OCH.sub.3 H H H31 H OC.sub.2 H.sub.5 H H H H H32 H H OC.sub.2 H.sub.5 H H H H33 H H H OC.sub.2 H.sub.5 H H H34 H H H N(CH.sub.3).sub.2 H H H35 CH.sub.3 H H H H H H36 ##STR22## H H H H H H37 H OCH.sub.3 H H OCH.sub.3 H H38 H OC.sub.2 H.sub.5 H H OC.sub.2 H.sub.5 H H39 H CH.sub.3 H H CH.sub.3 H H40 H Cl H H Cl H H41 H CH.sub.3 H H Cl H H42 H OCH.sub.3 H OCH.sub.3 H H H43 H CH.sub.3 H CH.sub.3 H H H44 H CH.sub.3 H Cl H H H45 H NO.sub.2 H OCH.sub.3 H H H46 H H OCH.sub.3 H OCH.sub.3 H H47 H OCH.sub.3 H H Cl H H48 H OCH.sub.3 H Cl OCH.sub.3 H H49 H OCH.sub.3 H OCH.sub.3 Cl H H50 H CH.sub.3 H H H CH.sub.3 H51 H OCH.sub.3 H H Cl H H52 H CH.sub.3 H OCH.sub.3 H H H53 H OCH.sub.3 H Cl CH.sub.3 H H54 H H H H H H OCH.sub.355 H CH.sub.3 H H H H OCH.sub.356 H OCH.sub.3 H Cl OCH.sub.3 H OCH.sub.357 H OCH.sub.3 H H H H Br__________________________________________________________________________
______________________________________ ##STR23##DisazoCompoundNo. A______________________________________58 ##STR24##59 ##STR25##60 ##STR26##61 ##STR27##62 ##STR28##63 ##STR29##64 ##STR30##65 ##STR31##66 ##STR32##67 ##STR33##68 ##STR34##69 ##STR35##70 ##STR36##71 ##STR37##72 ##STR38##73 ##STR39##74 ##STR40##75 ##STR41##76 ##STR42##77 ##STR43##78 ##STR44##79 ##STR45##80 ##STR46##81 ##STR47##82 ##STR48##83 ##STR49##84 ##STR50##85 ##STR51##86 ##STR52##87 ##STR53##88 ##STR54##89 ##STR55##90 ##STR56##91 ##STR57##92 ##STR58##93 ##STR59##94 ##STR60##95 ##STR61##96 ##STR62##97 ##STR63##98 ##STR64##99 ##STR65##100 ##STR66##101 ##STR67##102 ##STR68##103 ##STR69##104 ##STR70##105 ##STR71##106 ##STR72##107 ##STR73##108 ##STR74##109 ##STR75##110 ##STR76##111 ##STR77##112 ##STR78##113 ##STR79##114 ##STR80##115 ##STR81##116 ##STR82##117 ##STR83##118 ##STR84##119 ##STR85##120 ##STR86##______________________________________
______________________________________ ##STR87## ##STR88##DisazoCompoundNo. R.sub.22 R.sub.33 R.sub.44 R.sub.55 R.sub.66______________________________________121 H H H H H122 NO.sub.2 H H H H123 H NO.sub.2 H H H124 H H NO.sub.2 H H125 Cl H H H H126 H Cl H H H127 H H Cl H H128 CH.sub.3 H H H H129 H CH.sub.3 H H H130 H H CH.sub.3 H H131 C.sub.2 H.sub.5 H H H H132 H H C.sub.2 H.sub.5 H H133 OCH.sub.3 H H H H134 H OCH.sub.3 H H H135 H H OCH.sub.3 H H136 OC.sub.2 H.sub.5 H H H H137 H H OC.sub.2 H.sub.5 H H138 CH.sub.3 H OCH.sub.3 H H139 CH.sub.3 H CH.sub.3 H H140 CH.sub.3 H H CH.sub.3 H141 CH.sub.3 H H H CH.sub.3142 OCH.sub.3 H OCH.sub.3 H H143 OCH.sub.3 H H OCH.sub.3 H144 H OCH.sub.3 H OCH.sub.3 H145 CH.sub.3 Cl H H H146 CH.sub.3 H Cl H H147 CH.sub.3 H H Cl H______________________________________
______________________________________ ##STR89## ##STR90##DisazoCompoundNo. R.sub.222 R.sub.333 R.sub.444 R.sub.555 R.sub.666______________________________________148 H H H H H149 NO.sub.2 H H H H150 H NO.sub.2 H H H151 H H NO.sub.2 H H152 Cl H H H H153 H Cl H H H154 H H Cl H H155 CH.sub.3 H H H H156 H CH.sub.3 H H H157 H H CH.sub.3 H H158 OCH.sub.3 H H H H159 H OCH.sub.3 H H H160 H H OCH.sub.3 H H161 CH.sub.3 H OCH.sub.3 H H162 OCH.sub.3 H Cl CH.sub.3 H163 CH.sub.3 H H H CH.sub.3______________________________________
__________________________________________________________________________ ##STR91## ##STR92##DisazoCompoundNo. R.sub.10 R.sub.20 R.sub.30 R.sub.40 R.sub.50 R.sub.60__________________________________________________________________________164 H H H H H H165 H NO.sub.2 H H H H166 H H NO.sub.2 H H H167 H H H NO.sub.2 H H168 H Cl H H H H169 H H Cl H H H170 H H H Cl H H171 H CH.sub.3 H H H H172 H H CH.sub.3 H H H173 H H H CH.sub.3 H H174 H OCH.sub.3 H H H H175 H H OCH.sub.3 H H H176 H H H OCH.sub.3 H H177 H H H N(CH.sub.3).sub.2 H H178 H F H H H H179 H H F H H H180 H H H F H H181 H Br H H H H182 H H Br H H H183 H H H Br H H184 H Cl H Cl H H185 H H Cl Cl H H186 H CN H H H H187 H H H CN H H188 H CH.sub.3 H CH.sub.3 H H189 H OCH.sub.3 H H OCH.sub.3 H190 H OCH.sub.3 OCH.sub.3 OCH.sub.3 H H191 H CH.sub.3 H H H CH.sub.3192 CH.sub.3 H H H H H193 ##STR93## H H H H H194 ##STR94## H H H H H195 H H H H ##STR95## H__________________________________________________________________________
______________________________________ ##STR96## ##STR97##DisazoCompoundNo. R.sub.8 R.sub.9______________________________________196 CH.sub.3 CH.sub.3197 H ##STR98##198 H ##STR99##199 H ##STR100##200 H ##STR101##201 H ##STR102##202 CH.sub.3 ##STR103##203 H ##STR104##204 H ##STR105##205 H ##STR106##206 H ##STR107##207 H ##STR108##______________________________________
______________________________________ ##STR109## ##STR110##DisazoCompoundNo. X.sub.1______________________________________208 ##STR111##209 ##STR112##210 ##STR113##______________________________________
__________________________________________________________________________ ##STR114## ##STR115##DisazoCompound No. R.sub.100 R.sub.200 R.sub.300 R.sub.400 R.sub.500 R.sub.600__________________________________________________________________________211 H H H H H H212 H NO.sub.2 H H H H213 H H NO.sub.2 H H H214 H H H NO.sub.2 H H215 H Cl H H H H216 H H Cl H H H217 H H H Cl H H218 H CH.sub.3 H H H H219 H H CH.sub.3 H H H220 H H H CH.sub.3 H H221 H OCH.sub.3 H H H H222 H H OCH.sub.3 H H H223 H H H OCH.sub.3 H H224 H H H N(CH.sub.3).sub.2 H H225 H F H H H H226 H H F H H H227 H H H F H H228 H Br H H H H229 H H Br H H H230 H H H Br H H231 H Cl H Cl H H232 H H Cl Cl H H233 H CN H H H H234 H H H CN H H235 H CH.sub.3 H CH.sub.3 H H236 H OCH.sub.3 H H OCH.sub.3 H237 H OCH.sub.3 OCH.sub.3 OCH.sub.3 H H238 H CH.sub.3 H H H CH.sub.3239 CH.sub.3 H H H H H240 ##STR116## H H H H H241 ##STR117## H H H H H242 H H H H ##STR118## H__________________________________________________________________________
______________________________________ ##STR119## ##STR120##DisazoCompound No. R.sub.80 R.sub.90______________________________________243 CH.sub.3 CH.sub.3244 H ##STR121##245 H ##STR122##246 H ##STR123##247 H ##STR124##248 H ##STR125##249 CH.sub.3 ##STR126##250 H ##STR127##251 H ##STR128##252 H ##STR129##253 H ##STR130##254 H ##STR131##______________________________________
______________________________________ ##STR132## ##STR133##DisazoCompound No. X.sub.2______________________________________255 ##STR134##256 ##STR135##257 ##STR136##______________________________________
A method for preparing the disazo compound of the present invention is illustrated hereinafter in detail.
The diazotization of the diamino compound having the above chemical formula (II), that is, 2,6-di(4-amino benzylidene)-4-methyl cyclohexanone prepared by reducing 2,6-di(4-nitrobenzylidene)-4-methyl cyclohexanone, is carried out in an inorganic acid such as hydrochloric acid or sulfuric acid by adding sodium nitrite at -10.degree. C. to 50.degree. C. This diazotization is completed in 30 minutes to 3 hours. To the reaction mixture, is added borofluoric acid, sodium borofluoride aqueous solution or the like to precipitate as a tetrazonium salt. The precipitated crystal is preferably filtered out to be used in a succeeding reaction. The tetrazonium salt thus obtained is subjected to a coupling reaction with a coupler having the general formulas (IV), (V) or (VI). From the stoichiometrical view point, one mole of a tetrazonium salt is reacted with two moles of a coupler, but from practical view point, 1.5-4 moles, preferably 2-3 moles of the coupler is supplied to one mole of the tetrazonium salt when taking manufacturing cost and the purity of pigment obtained into consideration. In practice, this reaction is carried out by dissolving a mixture of the tetrazonium salt and coupler in an organic solvent such as N,N-dimethylformamide (DMF), dimethylsulfoxide or the like, and adding drop-wise an alkaline aqueous solution to the reaction solution such as sodium acetate aqueous solution at about -10.degree. C. to 40.degree. C. This reaction is completed in about 5 minutes to 3 hours. After the completion of the reaction, the precipitated crystal is filtered out and is finally purified by an appropriate method (for example by washing, recrystalizing or the like with water and/or organic solvent).
The novel disazo compound prepared in accordance with the present invention as mentioned above, is a colored crystal at normal temperature. Examples of the novel disazo compound of the present invention are listed in the following Table 1 and 2, together with various datas including melting point, elemental analysis and infrared absorption spectrum.
TABLE 1__________________________________________________________________________ ##STR137## Decompo- InfraredDisazo Elemental Analysis sition AbsorptionCompound (Calculated Value) Point SpectrumNo. R.sub.1 R.sub.2 R.sub.3 R.sub.4 C % H % N % (.degree.C.) (KBr Disk)__________________________________________________________________________ 1 H H H H 75.98 4.67 9.53 286 FIG. 1 (76.28) (4.79) (9.71)28 OCH.sub.3 H H H 73.47 4.95 8.83 286 FIG. 2 (73.85) (5.00) (9.07)29 H OCH.sub.3 H H 73.35 4.83 8.89 284 FIG. 3 (73.85) (5.00) (9.07)30 H H OCH.sub.3 H 73.63 5.04 8.97 274 FIG. 4 (73.85) (5.00) (9.07)23 CH.sub.3 H H H 76.26 5.16 9.20 270 FIG. 5 (76.49) (5.18) (9.39)24 H CH.sub.3 H H 76.31 5.09 9.35 270 FIG. 6 (76.49) (5.18) (9.39)25 H H CH.sub.3 H 76.74 5.07 9.32 268 FIG. 7 (76.49) (5.18) (9.39)17 Cl H H H 70.17 4.45 8.68 268 FIG. 8 (70.66) (4.21) (8.99)18 H Cl H H 70.42 4.13 8.76 290 FIG. 9 (70.66) (4.21) (8.99)19 H H Cl H 70.40 4.12 8.81 282 FIG. 10 (70.66) (4.21) (8.99) 2 NO.sub.2 H H H 68.88 4.13 11.31 308 FIG. 11 (69.03) (4.21) (11.75) 3 H NO.sub.2 H H 69.20 4.10 11.61 280 FIG. 12 (69.03) (4.21) (11.75) 4 H H NO.sub.2 H 69.20 4.39 11.30 286 FIG. 13 (69.03) (4.21) (11.75)__________________________________________________________________________
TABLE 2__________________________________________________________________________ ##STR138## Decompo- InfraredDisazo Elemental Analysis sition AbsorptionCompound (Calculated Value) Point SpectrumNo. Ar C % H % N % (.degree.C.) (KBr Disk)__________________________________________________________________________121 ##STR139## 77.09 (76.99) 4.60 (4.63) 10.64 (10.72) 322 FIG. 14164 ##STR140## 74.31 (74.33) 4.79 (4.81) 12.20 (12.17) 268 FIG. 15 71 ##STR141## 71.02 (71.03) 4.27 (4.31) 10.43 (10.56) 294 FIG. 16__________________________________________________________________________
The preparation examples of the novel disazo compound of the present invention are illustrated hereinafter.
PREPARATION EXAMPLE 1
Preparation of Tetrazonium Salt
Sodium nitrite aqueous solution prepared by dissolving 7.47 g (0.105 mole) of 97% sodium nitrite in 30 ml of water was added drop-wise at a temperature of 0.degree.-5.degree. C. to a mixture of 2,6-bis(4-aminobenzylidene)-4-methylcyclohexanone 15.9 g (0.05 mole), 36% hydrochloric acid 100 ml and water 100 ml, and the resultant mixture was stirred at the same temperature for 1 hour. The solution thus obtained was filtered to removed undissolved portion (minute amount), and 42% borofluoric acid was added to the resultant filtrate to obtain a crystal. The precipitated crystal was filtered out, and the crystal was subjected to washing with water, washing with methanol and drying, thus obtaining a tetrazonium salt. The yield was 21.5 g (83.5%).
The infrared absorption spectrum (KBr Disk) was as follows:
.nu.N.sub.2.sup..sym. 2 2 6 0 cm.sup.-1
.nu.C=O 1 6 7 0 cm.sup.-1
Preparation of Disazo Compound No. 1
1.29 g of the tetrazonium salt thus obtained and 1.32 g of 2-hydroxy-3-naphthoic acid anilide as a coupler were dissolved in 150 ml of cooled N,N-dimethylformamide. To this solution, was added drop-wise a solution comprising sodium acetate 0.82 g and water 7 ml at a temperature of 5.degree.-10.degree. C. for 20 minutes. Thereafter, the resultant mixture was stirred for 3 hours at room temperature. The produced precipitate was filtered out, and was washed for 3 times with N,N-dimethylformamide 200 ml heated to 80.degree. C. and further with water 200 ml for 2 times. The washed precipitate was dried at 80.degree. C. under a reduced pressure of 2 mm Hg, thus obtaining 1.41 g (yield=65.0%) of the above disazo compound No. 1 shown in Table 1.
The appearance of disazo compound thus obtained was purplish red powder, the infrared absorption spectrum (KBr Disk) of which is shown in FIG. 1.
Preparation Examples 2 to 16
The same procedure as in the above Preparation Example 1 was repeated, except that compounds as mentioned in the following Table 3 were used as a coupler to prepare the disazo compounds shown in Tables 1 and 2. The results are shown in Table 3.
TABLE 3__________________________________________________________________________ DisazoExample CompoundNo. No. Coupling Component Yield (%) Appearance__________________________________________________________________________2 28 ##STR142## 78.9 purplish red3 29 ##STR143## 65.1 purplish red4 30 ##STR144## 68.5 purplish red5 23 ##STR145## 68.3 purplish red6 24 ##STR146## 70.5 purplish red7 25 ##STR147## 67.0 purplish red8 17 ##STR148## 82.1 red9 18 ##STR149## 66.7 purplish red10 19 ##STR150## 71.8 purplish red11 2 ##STR151## 70.7 purple12 3 ##STR152## 61.1 purple13 4 ##STR153## 74.9 purplish red14 121 ##STR154## 74.7 purple15 164 ##STR155## 65.2 purplish red16 71 ##STR156## 66.8 reddish brown__________________________________________________________________________
The disazo pigment of the present invention is used as a charge generating material in a photosensitive layer of an electrophotographic element. FIGS. 17 and 18 illustrate a typical structure of the electrophotographic element.
The electrophotographic element of FIG. 17 comprises a laminated type photosensitive layer 19 on an electroconductive substrate 11, said photosensitive layer 19 comprising a charge generating layer 15 containing disazo pigment 13 as the main component and a charge transfer layer 17 containing charge transfer material as the main component.
In the electrophotographic element of FIG. 17, exposed light passes through a charge transfer layer to a charge generating layer 15 wherein charge is generated in disazo pigment 13. The charge thus generated is transferred by the charge transfer layer 17. Thus, the generation of charge necessary for light decay is effected in disazo pigment 13, and the transfer of the generated charge is effected by the charge transfer layer 17.
The electrophotographic element shown in FIG. 18 is composed of a photosensitive layer 192 on an electroconductive substrate 11, the photosensitive layer 192 comprising essentially of disazo pigment 13, charge transfer material and insulative binder. The disazo pigment 13 is a charge generating material.
It is possible to modify the basic structure of the electrophotographic element of FIG. 17, for example, by applying the charge generating layer and the charge transfer layer in reverse order.
The thickness of the charge generating layer 15 of the photosensitive layer of FIG. 17 is preferably 0.01-5.mu., more preferably 0.05-2.mu.. If this thickness is less than 0.01.mu., the generation of charge is not satisfactory. On the other hand, if this thickness is more than 5.mu., the residual potential becomes too high for practical use.
The thickness of the charge transfer layer 17 is preferably 3-50.mu., more preferably 5-20.mu.. If this thickness is less than 3.mu., a charged amount is insufficient. On the other hand, if this thickness is more than 50.mu., the residual potential becomes too high for practical use.
The charge generating layer 15 contains disazo pigment expressed by the above general formula as the main component, and further binder, plasticizer and the like. The amount of disazo pigment in the charge generating layer is more than 30% by weight, more preferably 50% by weight.
The charge transfer layer 17 contains charge transfer material and binder as the main components and further plasticizer and the like. The amount of the charge transfer material in the charge transfer layer is 10-95% by weight, preferably 30-90% by weight. If the amount of the charge transfer material is less than 10% by weight, the transfer of the charge is not substantially carried out. On the other hand, if this amount is more than 95% by weight, the mechanical strength of the photosensitive film is too poor for practical use.
The photosensitive layer 192 of the photosensitive element of FIG. 18 is preferably 3-50.mu., more preferably 5-20.mu.. The amount of the disazo pigment in the photosensitive layer 192 is preferably less than 50% by weight, more preferably less than 20% by weight, and the amount of the charge transfer material is preferably 10-95% by weight, more preferably 30-90% by weight.
The essential feature of the present invention resides in the use of specific disazo pigments as expressed by the above general formula I, and other components such as electroconductive substrate, charge transfer material and the like are the same as the conventionally known materials. Examples of these materials are illustrated hereinafter.
Examples of the electroconductive substrate used in the electrophotgraphic element of the present invention include: metallic plates such as aluminum, copper, zinc and the like; plastic sheets such as polyester and the like; plastic film composite obtained by vapor depositing electroconductive materials such as aluminum, SnO.sub.2 and the like on a plastic film; or electroconductively treated paper and the like.
Examples of binders include: condensation type resins such as polyamide, polyurethane, polyester, epoxy resin, polyketone, polycarbonate and the like; vinyl polymers such as polyvinyl ketone, polystyrene, poly-N-vinyl carbazole, polyacrylamide, and the like. Any resin can be used if it is insulative and adhesive.
Examples of plasticizers include halogenated paraffin, polybiphenylchloride, dimethylnaphthalene, dibutyl phthalate and the like. Silicone oil may also be added to improve surface properties of the photosensitive material.
The charge transfer material includes a positive hole transfer material and an electron transfer material. Examples of the hole transfer material include compounds as expressed by the following general formula (1) to (11). ##STR157## (wherein R.sub.115 represents methyl, ethyl, 2-hydroxyethyl or 2-chloroethyl; R.sub.125 represents methyl, ethyl, benzyl or phenyl; and R.sub.135 represents hydrogen, chlorine, bromine, alkyl having 1 to 4 carbon atoms, alkoxy having 1 to 4 carbon atoms, dialkylamino or nitro.) ##STR158## (wherein Ar.sub.3 represents naphthalene ring, anthracene ring, styryl and their substituents or pyridine ring furan ring, or thiophene ring; and R.sub.145 represents alkyl or benzyl.) ##STR159## (wherein R.sub.155 represents alkyl, benzyl, phenyl or naphthyl; R.sub.165 represents hydrogen, alkyl having 1 to 3 carbon atoms, alkoxy having 1 to 3 carbon atoms, dialkylamino, diaralkylamino or diarylamino; n represents an integer of 1 to 4; when n is 2 or more, R.sub.165 may be the same or different; and R.sub.175 represents hydrogen or methoxy.) ##STR160## (wherein R.sub.185 represents alkyl having 1 to 11 carbon atoms, substituted or non-substituted phenyl or heterocyclic group; R.sub.195 and R.sub.205 may be the same or different and represent hydrogen, alkyl having 1 to 4 carbon atoms, hydroxyalkyl, chloroalkyl, substituted or non-substituted aralkyl; R.sub.195 and R.sub.205 may be bonded with each other to form a heterocyclic ring containing nitrogen; R.sub.215 may be the same or different and represents hydrogen alkyl having 1 to 4 carbon atoms, alkoxy or halogen.) ##STR161## (wherein R.sub.225 represents hydrogen or a halogen atom; and Ar.sub.4 represents substituted or non-substituted phenyl, naphthyl, anthryl or carbazolyl.) ##STR162## (wherein R.sub.235 represents hydrogen, halogen, cyano, alkoxy having 1 to 4 carbon atoms or alkyl having 1 to 4 carbon atoms; Ar.sub.5 represents ##STR163## wherein R.sub.245 represents alkyl having 1 to 4 carbon atoms, R.sub.255 represents hydrogen, halogen, alkyl having 1 to 4 carbon atoms, alkoxy having 1 to 4 carbon atoms or dialkyl amino, n is an integer of 1 or 2; when n is 2, R.sub.255 may be the same or different; R.sub.265 and R.sub.275 represent hydrogen, substituted or non-substituted alkyl having 1 to 4 carbon atoms or substituted or non-substituted benzyl group.) ##STR164## (wherein R.sub.285 and R.sub.295 represents carbazolyl, pyridyl, thienyl, indolyl, furyl, or substituted or non-substituted phenyl styryl, naphthyl or anthryl group; these substituents are selected from the group of dialkylamino, alkyl, alkoxy, carboxyl or its ester, halogen atom, cyano, aralkylamino, N-alkyl-N-aralkylamino, amino, nitro and acetyl amino groups.) ##STR165## (wherein R.sub.305 represents a lower alkyl or benzyl group; R.sub.315 represents hydrogen, lower alkyl, lower alkoxy, halogen, nitro, amino, or amino group substituted with lower alkyl or benzyl; and n is an integer of 1 or 2.) ##STR166## (wherein R.sub.325 represents hydrogen, alkyl, alkoxy or halogen; R.sub.335 and R.sub.345 represent alkyl, substituted or non-substituted aralkyl, or substituted or non-substituted aryl group; R.sub.355 represents hydrogen or substituted or non-substituted phenyl; and Ar.sub.6 represents phenyl or naphthyl group.) ##STR167## (wherein n is an integer of 0 or 1; R.sub.365 represents hydrogen, alkyl or substituted or non-substituted phenyl; A.sub.1 represents ##STR168## 9-anthryl, or substituted or non-substituted N-alkylcarbazolyl group, wherein R.sub.375 represents hydrogen, alkyl, alkoxy, halogen or ##STR169## wherein R.sub.385 and R.sub.395 represent alkyl, substituted or non-substituted aralkyl, or substituted or non-substituted aryl group, and R.sub.385 and R.sub.395 may form a ring; and m is an integer of 0, 1, 2 or 3, when m is 2 or more, R.sub.375 may be the same or different.) ##STR170## (wherein R.sub.405, R.sub.415 and R.sub.425 are hydrogen, lower alkyl, lower alkoxy, dialkylamino, or halogen; and n is 0 or 1.)
Examples of the compound expressed by the general formula (1) include: 9-ethylcarbazole-3-aldehyde-1-methyl-1-phenylhydrazone, 9-ethylcarbazole-3-aldehyde-1-benzyl-1-phenylhydrazone, 9-ethylcarbazole-3-aldehyde 1,1-diphenylhydrazone, and the like.
Examples of the compound expressed by the general formula (2) include: 4-diethylaminostyrene-.beta.-aldehyde-1-methyl-1-phenylhydrazone, 4-methoxynaphthalene-1-aldehyde-1-benzyl-1-phenylhydrazone, and the like.
Examples of the compound expressed by the general formula (3) include: 4-methoxybenzaldehyde 1-methyl-1-phenylhydrazone, 2,4-dimethoxybenzaldehyde 1-benzyl-1-phenylhydrazone, 4-diethylaminobenzaldehyde 1,1-diphenylhydrazone, 4-methoxybenzaldehyde 1-benzyl-1-(4-methoxy)phenyl hydrazone, 4-diphenylaminobenzaldehyde-1-benzyl-1-phenylhydrazone, 4-dibenzylaminobenzaldehyde 1,1-diphenylhydrazone and the like.
Examples of the compound expressed by the general formula (4) include: 1,1-bis(4-dibenzylaminophenyl)propane, tris(4-diethylaminophenyl)methane, 1,1-bis(4-dibenzylaminophenyl)propane, 2,2'-dimethyl-4,4'-bis(diethylamino)-triphenylmethane and the like.
Examples of the compound expressed by the general formula (5) include: 9-(4-diethylaminostyryl)anthracene, 9-bromo-10-(4-diethylaminostyryl)anthracene, and the like.
Examples of the compound expressed by the general formula (6) include: 9-(4-dimethylaminobenzylidene)fluorene, 3-(9-fluorenylidene)-9-ethylcarbazole, and the like.
Examples of the compound expressed by the general formula (7) include: 1,2-bis(4-diethylaminostyryl)benzene, 1,2-bis(2,4-dimethoxystyryl)benzene and the like.
Examples of the compound expressed by the general formula (8) include: 3-styryl-9-ethylcarbazole, 3-(4-methoxystyryl)-9-ethylcarbazole, and the like.
Examples of the compound expressed by the general formula (9) include: 4-diphenylaminostilbene, 4-dibenzylaminostilbene, 4-ditolylaminostilbene, 1-(4-diphenylaminostyryl)naphthalene, 1-(4-diethylaminostyryl)naphthalene, and the like.
Examples of the compound expressed by the general formula (10) include: 4'-diphenylaminoalpha-phenylstilbene, 4'-methylphenylamino-alphaphenylstilbene, and the like.
Examples of the compound expressed by the general formula (11) include: 1-phenyl-3-(4-diethylaminostyryl)-5-(4-diethylaminophenyl)pyrazoline, 1-phenyl-3-(4-dimethylaminostyryl)-5-(4-dimethylaminophenyl)pyrazoline, and the like.
Other examples of positive hole transfer material include: oxadiazole compounds such as 2,5-bis(4-diethylaminophenyl)-1,3,4-oxadiazole, 2,5-bis(4-(4-diethylaminostyryl)phenyl)-1,3,4-oxadiazole, 2-(9-ethylcarbazolyl-3)-5-(4-diethylaminophenyl)-1,3,4-oxadiazole, and the like; low molecular oxazole compounds such as 2-vinyl-4-(2-chlorophenyl)-5-(4-diethylaminophenyl)-oxazole, 2-(4-diethylaminophenyl)-4-phenyloxazole, and the like; and high molecular compounds such as poly-N-vinyl carbazole, halogenated poly-N-vinyl carbazole, polyvinyl pyrene, polyvinyl anthracene, pyrene formaldehyde resin, ethylcarbazole formaldehyde resin, and the like.
Examples of electron transfer material include: chloroanil, bromoanil, tetracyanoethylene, tetracyanoquinonedimethane, 2,4,7-trinitro-9-fluorenone, 2,4,5,7-tetranitro-9-fluorenone, 2,4,5,7-tetranitroxanthone, 2,4,8-trinitro-thioxanthone, 2,6,8-trinitro-4H-indeno(1,2-b)-thiophene-4-on, 1,3,7-trinitrodibenzothiophene-5,5-dioxide, and the like.
These charge transfer materials are used alone or in the form of a mixture of two or more.
With regard to the electrophotographic elements as prepared above, an adhesive layer or barrier layer may optionally be applied between an electroconductive substrate and a photosensitive layer. Examples of these layers include polyamide, nitrocellulose, aluminum oxide and the like. The thickness of the layer is preferably not more than 1.mu..
The electrophotographic element as shown in FIG. 17 is prepared by vapor-depositing disazo pigment on an electroconductive substrate in accordance with vacuum vapor depositing method as disclosed in U.S. Pat. Nos. 3,973,959 and 3,996,049 or coating and drying on an electroconductive substrate a dispersion of disazo pigment particles in an appropriate solvent optionally having a binder dissolved; and then coating and drying a solution containing charge transfer material and binder on the charge generating layer, the surface of which may optionally be subjected to a buff polishing as disclosed in Japanese Patent Laid Open No. 51-90827, or the thickness of which may be regulated.
The electrophotographic element as shown in FIG. 18 is prepared by dispersing disazo pigment particles in a solution having charge transfer material and binder dissolved, coating the dispersion on an electroconductive substrate and drying. In any case, disazo pigment used in the present invention is powdered by a ball mill or the like to a particle size of not more than 5.mu., preferably not more than 2.mu.. Coating can be effected by ordinary method by means of doctor blade, dipping, wire bar and the like.
Copying by the electrophotographic element of the present invention can be effected by developing after charging and exposing the photosensitive layer surface and, if necessary, transferring the developed image to paper and the like.
As clearly seen from the above description and the following Examples, the electrophotographic element of the present invention using disazo pigment having the dibenzylidenecyclohexanone structure as a charge generating material can be more easily produced and has a photosensitive wavelength zone in the range of a shorter wavelength range (about 450-600 nm) in comparison with the conventional electrophotographic elements. In addition to these advantages, performances of the electrophotographic element of the present invention are stable even if it is repeatedly used a great number of times.
The present invention is further illustrated by the following Examples, but the present invention should not be limited thereto.
EXAMPLE 1
76 parts by weight of disazo pigment No. 1, 1260 parts by weight of tetrahydrofuran solution (solid content=2%) of polyester resin ("Byron 200" manufactured by Toyo Boseki Ltd.), and 3700 parts by weight of tetrahydrofuran are powdered and mixed in a ball mill. The dispersion thus obtained was coated on an aluminum surface of an aluminum-deposited polyester base (electroconductive substrate) by a doctor blade, and the coated film was allowed to stand for drying, thereby forming a charge generating layer having a thickness of about 1 .mu.m.
On this charge generating layer, was coated a solution prepared by dissolving and mixing 2 parts by weight of 9-ethylcarbazole-3-aldehyde 1-methyl-1-phenylhydrazone, 2 parts by weight of polycarbonate resin ("Panlight K-1300" manufactured by Teijin Co., Ltd.) and 16 parts by weight of tetrahydrofuran by a doctor blade, and the coated film was dried at 80.degree. C. for 2 minutes and 105.degree. C. for 5 minutes, thereby forming a charge transfer layer having a thickness of about 20 .mu.m. The laminated type electrophotographic element No. 1 thus prepared is shown in FIG. 17.
EXAMPLE 2 TO 10
Electrophotographic elements Nos. 2 to 10 were prepared in the same manner as in Example 1, except that disazo pigments as shown in the following Table 4 were used in place of disazo pigment No. 1 used in Example 1.
EXAMPLES 11 TO 15
Electrophotographic elements Nos. 11 to 15 were prepared in the same manner as in Example 1, except that 1-phenyl-3-(4-diethylaminostyryl)-5-(4-diethylaminophenyl)pyrazoline was used as a charge transfer material and disazo pigments as shown in the following Table 5 were used.
EXAMPLES 16 TO 24
Electrophotographic elements Nos. 16 to 24 were prepared in the same manner as in Example 1, except that 4'-diphenylamino-.alpha.-phenylstilbene was used as a charge transfer material and disazo pigments as shown in the following Table 6 were used.
EXAMPLES 25
Electrophotographic element No. 25 was prepared in the same manner as in Example 1, except that 1,1-bis(4-dibenzylaminophenyl)propane was used as a charge transfer material and a disazo pigment as shown in the following Table 7 was used.
The thus prepared electrophotographic elements Nos. 1 to 25 were subjected to -6 KV corona discharge for 20 seconds by an electrostatic copying paper tester (SP428 Type produced by Kawaguchi Denki Works), and were charged negatively. Thereafter, these elements were left to stand in the dark for 20 seconds to measure the surface potential Vpo (V) at that time, and were exposed to radiation of a tungsten lamp so that the intensity of surface illumination may become 4.5 Lux. Then, the time (sec.) required until the surface potential was reduced to 1/2 of Vpo was measured, and the exposure amount E1/2 (Lux-sec) was calculated. The results thus obtained are shown in Tables 4 to 7.
TABLE 4______________________________________Photosensitive Disazo Vpo E1/2Material No. Compound No. (volt) (Lux .multidot. sec)______________________________________1 1 -798 9.12 29 -1120 7.23 17 -1176 5.44 18 -1332 9.35 2 -1206 10.86 3 -918 4.07 4 -1198 5.88 12 -938 9.39 164 -1282 10.210 71 -684 2.2______________________________________
TABLE 5______________________________________Photosensitive Disazo Vpo E1/2Material No. Compound No. (volt) (Lux .multidot. sec)______________________________________11 1 -746 5.812 29 -696 6.813 2 -886 6.414 121 -446 5.215 164 -666 10.5______________________________________
TABLE 6______________________________________Photosensitive Disazo Vpo E1/2Material No. Compound No. (volt) (Lux .multidot. sec)______________________________________16 1 -890 9.717 29 -1194 8.118 17 -1182 4.619 18 -1320 10.420 2 -1206 13.921 3 -806 4.622 4 -1234 3.123 164 -1430 11.524 71 -812 3.6______________________________________
TABLE 7______________________________________Photosensitive Disazo Vpo E1/2Material No. Compound No. (volt) (Lux .multidot. sec)______________________________________25 71 -1136 9.3______________________________________
In order to make comparison, a comparative photosensitive material was prepared in quite the same manner as in the above photosensitive materials of the present invention, except that a stilbene type disazo compound, i.e. 4,4'-bis(2-hydroxy-3-phenylcarbamoyl-1-naphthylazo)stilbene was used in place of the disazo compounds of the present invention.
The comparative photosensitive material thus obtained and the photosensitive material No. 10 of the present invention were then subjected to the electrostatic copying paper tester in the same manner as above, thus measuring Vdo, Vpo, E.sub.1/2, E.sub.1/5, and E.sub.1/10. The results are shown in the following Table 8.
TABLE 8__________________________________________________________________________Photosensitive Vdo Vpo E1/2 E1/5 E1/10Material (V) (V) Vpo/Vdo (Lux .multidot. sec) (Lux .multidot. sec) (Lux .multidot. sec)__________________________________________________________________________Photosensitive -1076 -684 0.636 2.2 3.0 4.5Material No. 10of thisinventionComparative -1817 -1501 0.826 19.3 51.0 75.0PhotosensitiveMaterial__________________________________________________________________________
As proved by data in the above Tables 4 to 8, the photosensitive material of the present invention has a higher sensitivity.
The photosensitive materials Nos. 6 and 21 of the present invention were set in an electrophotographic copying machine (Ricopy-P-500 Type produced by RICOH K.K.), and the image-formation was repeated 10,000 times. As these results, each photosensitive material was found to form a clear-cut image regardless of the numerous repetition of image-formation. It should be understood from these results that the photosensitive materials of the present invention are excellent also in durability.

Number	Date	Country	Kind
59-124572	Jun 1984	JPX
60-56676	Mar 1985	JPX

Number	Name	Date
3687673	Yoshida et al.	Aug 1972
4390611	Ishikawa et al.	Jun 1983
4500619	Ishikawa et al.	Feb 1985
4533613	Kawamura et al.	Aug 1985

Number	Date	Country
57-46246	Mar 1982	JPX
57-47357	Mar 1982	JPX
58-129060	Aug 1983	JPX

Photosensitive material containing disazo compound for use in electrophotography

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Kamoshida et al., Chemical Abstracts, vol. 98, #170382s (1983).
Roemer, Chemical Abstracts, vol. 95, #186873b (1981).