Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
  • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
  • C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
  • C07D207/32—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
  • C07D207/323—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to the ring nitrogen atoms
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
  • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
  • C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
  • C07D207/32—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
  • C07D207/325—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms with substituted hydrocarbon radicals directly attached to the ring nitrogen atom
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
  • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
  • C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
  • C07D207/32—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
  • C07D207/33—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms with substituted hydrocarbon radicals, directly attached to ring carbon atoms
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
  • C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
  • C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
  • C07D307/36—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to ring carbon atoms
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
  • C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
  • C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
  • C07D307/38—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
  • C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
  • C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
  • C07D307/38—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
  • C07D307/52—Radicals substituted by nitrogen atoms not forming part of a nitro radical
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
  • C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
  • C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
  • C07D333/06—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
  • C07D333/08—Hydrogen atoms or radicals containing only hydrogen and carbon atoms
• • G—PHYSICS
  • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
  • G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
  • G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
  • G03G5/02—Charge-receiving layers
  • G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
  • G03G5/06—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
  • G03G5/0622—Heterocyclic compounds
  • G03G5/0624—Heterocyclic compounds containing one hetero ring
  • G03G5/0627—Heterocyclic compounds containing one hetero ring being five-membered
  • G03G5/0629—Heterocyclic compounds containing one hetero ring being five-membered containing one hetero atom

Definitions

• Material made light-sensitive in this way can be used for the production of images by electrophotographic means. It is exposed to light beneath a master, so that the electrostatic charge is leaked away in the parts of the layer struck by light.
• the invisible latent electrostatic image thereby produced is made visible (developed) by powdering over with a developer consisting of a mixture of a carrier with a toner.
• the carrier used may be, e.g. tiny glass balls, iron powder or other inorganic substances or even organic substances.
• the toner consists of a resin-carbon black mixture or of pigmented synthetic resin of a grain size of 1-100p, preferably -30
• the image is then made permanent (fixed) by the application of heat to the support.
• Materials known for the preparation of the photoconductive insulating layers required for the above-described process include selenium, sulphur, zinc oride, and also organic substances such as anthracene or anthraquinone. Consideration has also been given to a method of preparation of the photoconductive insulating layers whereby the photoconductive substances in association with binders are dispersed in solvents and the resultant dispersions applied to supports, primarily metal foils, and dried.
• the photoelectrically sensitizable m..- terial thus obtained has not yet satisfied the extensive demands made of modern duplicating material regarding range of use, reliability, simplicity in handling and, not least in importance, light-sensitivity and storageability qualities.
• the compounds to be used in accordance with the invention as photoconductive substances are aryl furans or aryl thiophenes or aryl pyrroles.
• Compounds corresponding to the above formula which contain substituted aryl radicals, e.g. aryl radicals substituted by halogen, amino groups, alkyl or alkoxy groups are also included in the photoconductive substances of the invention.
• the presence of nitro or nitroso groups reduces the suitability of the aryl turans, aryl thiophenes and aryl pyrroles of the invention, or renders them completely unsuitable for the invention.
• aryl furans, aryl thiophenes and aryl pyrroles are advantageous for the aryl furans, aryl thiophenes and aryl pyrroles to be used in solution with organic solvents, e.g., benzene, acetone, methylene chloride, glycol monomethylether, and the like. Mixtures of solvents may also be used. Also, it is possible for the aryl furans, aryl thiophenes and/ or aryl pyrroles to be used in association one with another or with other organic photoconductive substances.
• organic solvents e.g., benzene, acetone, methylene chloride, glycol monomethylether, and the like. Mixtures of solvents may also be used.
• aryl furans, aryl thiophenes and/ or aryl pyrroles may be used in association one with another or with other organic photoconductive substances.
• balsam resins phenol resins modified with colophony and other resins of which colophony constitutes the major part, coumarone resins and indene resins and the substances covered by the collective term synthetic lacquer resins, which according to the Kunststoffstotftaschenbuch (Plastics Pocket Book), published by Saechtling-Zebrowski (11th addition, 1955, page 212 et seq.) include processed natural substances such as cellulose ethers; polymers such as polyvinyl chlorides, polyvinyl acetals, polyvinyl acetates, polyvinyl ethers, polyacrylic and polymethacrylic esters, as also polystyrene and isobutylene; polycoudensates, e.g.
• polesters such as phthalate resins, alkyd resins, maleic acid resins, maleic acid/ colophony/ mixed esters of higher alcohols, phenol-formaldehyde resins, particularly colophonymodified phenol-formaldehyde condensates, urea-formaldehyde resins, melamine-formaldehyde condensates, aldehyde resins, ketone resins, of which particular mention is to be made of those available under the name of AW 2 resins, Xylene formaldehyde resins and polyamides; and polyadducts, such as polyurethanes.
• phthalate resins such as phthalate resins, alkyd resins, maleic acid resins, maleic acid/ colophony/ mixed esters of higher alcohols, phenol-formaldehyde resins, particularly colophonymodified phenol-formaldehyde condensates, urea-formaldehyde
• the proportion of resin to photoconductive substance can vary very greatly, but the content of photoconductive substance should be at least 20%. T he use of mixtures of approximately equal parts of resin and photoconductive substance has been found advantageous; if such mixtures of about equal parts of resin and photoconductive substance are used, the solutions, on drying, generally give transparent colorless layers which physical testing shows to be solid solutions.
• the base materials used may be any that satisfy the requirements of xerography, e.g., metal or glass plates, paper or plates or foils made of electroconductive resins of plastics, such as polyvinyl alcohol, polyamides, and polyurethanes.
• electroconductive supports are suitable for the purposes of the present invention.
• the term electroconductive support comprises materials having a specific conductivity higher than 10- ohm -cm.
• pretreatment of the paper against penetration of the coating solution is advisable, e.g., with methylcellulose in aqueous solution or polyvinyl alcohol in aqueous solution or with a solution in acetone and methylethylketone of a copolymer of acrylic acid methyl ester and acrylonitrile or with solutions of polyamides in aqueous alcohols.
• Aqueous dispersions of substances suitable for the pretreatment of the paper surface may also be used.
• the solutions of the aryl furans, aryl thiophenes and aryl pyrroles to be used in accordance with the invention, with or without the resins, are applied to the supports in the usual manner, for example by spraying, by direct application, by means of rollers and the like, and then dried in a manner such that a homogeneous photoconductive layer is produced on the support.
• the layer can be used, preferably, with long-wave UV. light of 3600-4000 A. for electrophotographic image production. Very short exposure under a master to a high pressure mercury lamp will give good images.
• the amount of sensitizer to be added to the photoconductive substance is generally up to 3% of the photoconductive substance. However, even very small quantities, e.g., less than 0.01%, have con siderable effect.
• dyestuffs in particular are suitable, for the readier identification of which the number is given under which they are listed in Schultz Farbstofit'tabellen (7th edition, 1st vol. 1931). The following are given as examples of effective sensitizers: triarylmethane dyestuffs such as Brilliant Green (No. 760, p. 314-), Victoria Blue B (No.
• quinoline dyestuffs such as Pinacyanol (No. 924, p. 396) and Cryptocyanine (No. 927, p. 397); quinone dyestuffs and ketone dyestuffs such as Alizarin (No. 1141, p. 499), Alizarin Red S (No. 1145, p. 502), and Quinizarine (No. 1148, p. 504); cyanine dyestuffs, e.g. Cyanine (No. 921, p. 394).
• the production or" images by electrophotographic means is carried out as follows: when the photoconductive layer has been charged positively or negatively, by means of for example, a corona discharge with a charging apparatus maintained at 6000 volts, the support, e.g. paper or aluminum foil or plastic foil, with the sensitized coating, is exposed to light under a master or by episcopic or diascopic projection and is then dusted over in known manner with a developer consisting of a mixture of a carrier and a toner.
• the carriers used may be, for example, tiny glass balls, iron powder or other inorganic substances or even organic substances.
• the toner consists of a resin-carbon black mixture or a pigmented resin of a grain size of 1 to 100 preferably 30/.L.
• the finely distributed toner particles adhere to the parts of the coating not struck by light during the exposure, and a positive image becomes visible if the photoconductive layer was negatively charged and the toner carrying a positive polarity is used.
• the image that now becomes visible can easily be wiped off. It therefore has to be fixed; it can, for example, be briefly heated by means of an infrared radiator. The temperature required is less if the heat treatment is carried out in the presence of vapors of solvents such as trichloroethylene, carbon tetrachloride or ethyl alcohol.
• the fixing of the powder image can also be done by steam treatment. Images characterized by good contrast are produced.
• these electrophotographic images can be converted into a printing plate, if a hydrophilic foil, e.g. paper or plastic foil, is used as support and the support and the fixed image are wiped over with a solvent for the photoconductive layer, e.g. alcohol or acetic acid, then wetted with Water and inked up in known manner with greasy ink.
• a solvent for the photoconductive layer e.g. alcohol or acetic acid
• the electrophotographic images can also be used as masters for the production of further copies on any type of light-sensitive sheet.
• the photoconductive compounds of the invention are superior to the substances used hitherto, such as selenium or zinc oxide, inasmuch as the latter give only cloudy layers.
• the image formed by the powdering process may, without dimculty, be transferred in known manner by electrical charging to another support and fixed thereon by heat.
• the transfer material e.g. a sheet of paper
• the transfer material is laid onto the unfixed powder image and charged with a corona discharge having the same polarity as the original charge of the now developed electrostatic image, so that the powder image is attracted by the paper and thereon fixed by heating.
• the photoconductive layers of the invention have another important advantage in that they can be charged positively as well as negatively. This has the advantage, that with the same developer, only by changing the polarity of the corona charging device, it is possible to obtain direct and reversal copies from the same master.
• the photoconductivity of the photoconductors according to the present invention is superior to that of known photoconductive substances, such as anthracene, benzidine, and r rth-raquinone.
• reaction in this last case being at the boiling point.
• 1,2-diphenyl-4-naphthyl- (2 -thiophene, corresponding Formula 27 35 to Formula 6, is obtained if 5 g. of 1,2-diphenyl-4-naphthyl-(2')-butandione-( 1,4) and 2 g. of phosphorus trisulphide are ground together and the mixture heated for a short time to 150 C. and then cooled.
• the reaction mass CH L is recrystalized a number of times from ethanol. Meltm 3 0 3 mg point: 126128 C.
• 2,3-diphenyl-5- (4'-methylphenyl) -pyrrole correspond- Formula 28 ing to Formula 11, is obtained if 5 g. of 1,2-diphenyl- 4(4-methylphenyl)-butandione-(1,4) are boiled under I reflux for 2 /2 hours With 50 ml. of formamide and the re- 3 O action mixture is then cooled.
• the reaction product is a A) separated by suction filtration and recrystallized from H3 methanol. Melting point: 127-l28 C.
• 19 g. of 4-dimethylaminobenzoin, 9 g. of acetyl benzene and 4 g. of finely pulverized potassium hydroxide ing to Formula 31 is 153-154 C.
• Electrophotographic image :production on this coated paper is as described in Example 1.
• Example 3 Melting Potassium Recrystalli- Formula Point, C. Benzom Substitution Second Reactant Hydroxide zation solvent 153-154 4dimethylamin0- tcetylbenzene 31 Ethanol.
• Example 1 A solution containing 2 g. of the compound corresponding to Formula 3 in ml. of benzene is applied to paper, the surface of which has been treated against the penetration of organic solvents, and dried. A direct image is then produced on the coated paper by the electrophotographic process, the paper being provided with a negative electric charge, by means of a corona discharge, exposed under a master to the light of a high pressure mercury vapor lamp and dusted over with a developer consisting of a mixture of tiny glass balls with a toner.
• the toner consists of a resin-carbon black mixture which takes on a positive polarity, or of a pigmented resin, which takes on a negative polarity when the developer is used.
• the particles of the toner have a grain size of 1-10Qu, preferably 5-30 1.
• the finely divided resin adheres to the parts of the coating not struck by light during the exposure and a positive image becomes visible, if the photoconductive layer is negatively charged and a toner carrying a positive polarity is used. With the same toner, only by changing the polarity of the corona discharge, there can be obtained also negatives of the master.
• the images obtained are slightly heated and thereby made permanent (fixed). effect, since the paper is brightened by the substance applied.
• the image produced is suitable as a reproduction master for the preparation of copies by means of any type of light-sensitive sheet.
• Example 2 A solution containing 1 g. of the compound corresponding to Formula 9 and 1 g. of ketone resin, e.g. the Kunststoffharz AP prepared by the condensation of acetophenone with formaldehyde, in 30 ml. of benzene is applied to paper, the surface of which has been treated against the penetration of organic solvents and the solu- They have good contrast 60 means of a corona discharge, the now sensitized paper is exposed under a transparent positive master to the light of Example 4 1 g. of the compound corresponding to Formula 17, 1 g. of ketone resin, e.g. the Kunststoffharz AP mentioned in Example 2, and 0.01 g.
• ketone resin e.g. the Kunststoffharz AP prepared by the condensation of acetophenone with formaldehyde, in 30 ml. of benzene
• Rhodamine B Schotz Farbstofltabellen, 7th edition, 1st vol. (1931) No. 864
• Rhodamine B Schotz Farbstofltabellen, 7th edition, 1st vol. (1931) No. 864
• the solution is applied to paper and dried.
• electrophotographic images can be produced by the process described in Example 1. Images on a blue ground are obtained.
• Example 5 0.5 g. of the compound corresponding to Formula 15, 0.5 g. of 4,5-di-(4'-chlorophenyl)-imidazolone-(2) and 1 g. of ketone resin, e.g. the commercially available Kunststoffharz AP, are dissolved in 30 ml. of a mixture of glycol monomethylether and benzene (1:1). The solution is applied to paper and dried. With the coated paper, electrophotographic images are prepared by the process described in Example 1. Images on pale yellowish ground are obtained.
• Example 6 0.5 g. of the compound corresponding to Formula 13,
• 0.5 g. of 4-phenyl-5 (4'-dimethylamino-phenyl)-imid azolone-(2) and 1 g. of ketone resin, e.g. the commercially available Kunststoffharz EM, are dissolved in 30 ml. of a mixture of glycol monomethyl ether and benzene (12-1). The solution is applied to pretreated paper. The coated 7 paper, after being charged by a corona discharge, is ex- 7 ground is obtained. It is fixed by heating.
• Example 7 1 g. of the compound corresponding to Formula 19 and 1 g. of ketone resin, e.g. the Kunststoffharz SK mentioned in Example 3, are dissolved in 30 ml. of a mixture of glycol monomethyl ether and toluene (1:1). The solution is applied to a superficially roughened aluminum foil and the solvent is evaporated oil. The coating left on the aluminum then adheres firmly to the surface of the foil.
• Example 1 For the preparation of the image, the procedure is as described in Example 1. With a transparent master, a positive image is obtained.
• the aluminum foil with the fixed electrophotographic image can be converted into a positive printing plate if the aluminum foil is wiped over on the image side with a developer liquid consisting of 8 parts by volume of ethanol, 2 parts by volume of glycol monomethyl ether and 1 part by volume of 10% phosphoric acid, and then rinsed down with water and inked up with greasy ink.
• a developer liquid consisting of 8 parts by volume of ethanol, 2 parts by volume of glycol monomethyl ether and 1 part by volume of 10% phosphoric acid
• Example 8 A solution containing 1 g. of the compound corresponding to Formula 19 and 1 g. of chlorinated polyvinyl chloride resin, e.g. the resin marketed under the registered trademark Rhenoflex in 30 ml. of a mixture of methyl-ethyl-ketone and toluene (1:1) is applied to pretreated paper. After the solution has dried, the coated paper is used for the production of an electrophotographic image by the process described in Example 1. With a short exposure, a good image on pale yellowish ground is obtained.
• chlorinated polyvinyl chloride resin e.g. the resin marketed under the registered trademark Rhenoflex in 30 ml. of a mixture of methyl-ethyl-ketone and toluene (1:1) is applied to pretreated paper. After the solution has dried, the coated paper is used for the production of an electrophotographic image by the process described in Example 1. With a short exposure, a good image on pale yellowish ground is obtained.
• Example 9 1. g. of the compound corresponding to Formula 18 and 1 g. of ketone resin, e.g. the Kunststoffharz EM mentioned in Example 6, are dissolved in 30 ml. of a mixture of benzene with glycol monomethyl ether (1:1). The solution is applied to paper and dried. The coated paper is charged, exposed to light under a transparent master and dusted over with developer powder (in the manner described in Example 1) and then a sheet of writing paper is placed on the unfixed electrophotographic image. The coating is again charged, this time through the back of the writing paper. This second charge must have the same polarity as the first; the image is in this Way transferred to the writing paper and is fixed by slight heating.
• An electrophotographic material comprising a conductive support layer and a photoconductive insulating layer, the latter comprising a compound having the formula in which X is selected from the group consisting of O, S, and NR and R R R R and R are selected from the group consisting of hydrogen, alkyl, and aryl groups, at least two of R R R and R being other than hydrogen and alkyl, and a compound selected from the group consisting of a resin and a spectrally sensitizing dyestuff.
• An electrophotographic material comprising a conductive support layer and a photoconductive insulating layer, the latter comprising a compound having the formula 14 in which R R and R are aryl groups, and a compound selected from the group consisting of a resin and a spectrally sensitizing dyestufi".
• An electrophotographic material comprising a conductive support layer and a photoconductive insulating layer, the latter comprising a compound having the formula R2C-C-H Iii-( i ("J-R3 s in which R R and R are aryl groups, and a compound selected from the group consisting of a resin and a spectrally sensitizing dyestuff.
• An electrophotographic material comprising a conductive support layer and a photoconductive insulating layer, the latter comprising a compound having the formula in which R R R and R are aryl groups, and a compound selected from the group consisting of a resin and a spectrally sensitizing dyestuif.
• An electrophotographic material comprising a conductive support layer and a photoconductive insulating layer, the latter comprising a compound having the formula in which R is an alkylamino group and R and R are aryl groups, and a compound selected from the group consisting of a resin and a spectrally sensitizing dyestuif.
• An electrophotographic material comprising a conductive support layer and a photoconductive insulating layer, the latter comprising a compound having the formula R.@ l a...
• R is an alkylamino group and R and R are aryl groups
• An electrophotograpnic material comprising a conductive support layer and a photoconductive insulating layer, the latter comprising a compound having the formula in which R is an alkylamino group and R R and R are aryl groups, and a compound selected from the group consisting of a resin and a spectrally sensitizing dyestutf.
• An electrophotographic material comprising a conductive support layer and a photoconductive insulating layer, the latter comprising a compound having the formula layer, the latter comprising a compound having the formula and a compound selected from the group consisting of a resin and a spectrally sensitizing dyestuff.
• An electrophotographic material comprising a conductive support layer and a photoconductive insulating layer, the latter comprising a compound having the formula Q and a compound selected from the group consisting of a resin and a spectrally sensitizing dyestufi.
• An electrophotograpic material comprising a conductive support layer and a photoconductive insulating layer, the latter comprising a compound having the formula and a compound selected from the group consisting of a resin and a spectrally sensitizing dyestuif.
• An electrophotographic material comprising a conductive support layer and a photoconductive insulating layer, the latter comprising a compound having the formula l5 and a compound selected from the group consisting of a resin and a spectrally sensitizing dyestuff.
• An electrophotographic material comprising a conductive support layer and a photoconductive insulating layer, the latter comprising a compound having the formula and a compound selected from the group consisting of a resin and a spectrally sensitizing dyestufi.
• An electrophotographic material comprising a conductive support layer and a photoconductive insulating layer, the latter comprising a compound having the formula and a compound selected from the group consisting of a resin and a spectrally sensitizing dyestutf.
• a photographic reproduction process which comprises electrostatically charging a supported photocon-' ductive insulating layer, exposing the charged material to a light image, and developing the resulting image with an electroscopic material, the photoconductive layer comprising a compound having the formula Rz-C C-Ra S, NR and R R R R and R are selected from the group consisting of hydrogen, alkyl, and aryl groups,
• R R R and R being other than hydro- 7 gen and alkyl.
• a photographic reproduction process which comprises elcctrostatically charging a supported photoconductive insulating layer, exposing the charged material to a light image, and developing the resulting image with an electroscopic material, the photoconductive layer comprising a compound having the formula 21.
• a photographic reproduction process which comprises electrostatically charging a supported photoconductive insulating layer, exposing the charged material to a light image and developing the resulting image with an electroscopic material, the photocouductive layer comprising a compound having the formula in which R R and R are aryl groups.
• a photographic reproduction process which comprises electrostatically charging a supported photocon- 1 7 ductive insulating layer, exposing the charged material to a light image and developing the resulting image with an electroscopic material, the photoconductive layer comprising a compound having the formula in which R R R and R are aryl groups.
• a photographic reproduction process which comprises electrostatically charging a supported photoconductive insulating layer, exposing the charged material to a light image and developing the resulting image with an electroscopic material, the photoconductive layer comprising a compound having the formula in which R is an alkylamino group and R and R are aryl groups.
• a photographic reproduction process which comprises electrostatically charging a supported photoconductive insulating layer, exposing the charged material to a light image, and developing the resulting image with an electroscopic material, the photoconductive layer comprising a compound having the formula in which R is an alkylamino group and R and R are aryl groups.
• a photographic reproduction process which comprises electrostatically charging a supported photoconductive insulating layer, exposing the charged material to a light image, and developing the resulting image with an electroscopic material, the photoconductive layer comprising a compound having the formula in which R is an alkylarnino group and R R and R are aryl groups.
• a photographic reproduction process which comprises electrostatically charging a supported photoconductive insulating layer, exposing the charged material to a light image and developing the resulting image with an electroscopic material, the photoconductive layer comprising a compound having the formula Q NEG 28.
• a photographic reproduction process which comprises electrostatically charging a supported photocon- 18 ductive insulating layer, exposing the charged material to a light image and developing the resulting image with an electroscopic material, the photoconductive layer comprising a compound having the formula 29.
• a photographic reproduction process which comprises electrostatically charging a supported photoconductive insulating layer, exposing the charged material to a light imageand developing the resulting image with an electroscopic material, the photoconductive layer comprising a compound having the formula 30.
• a photographic reproduction process which comprises electrostatically charging a supported photoconductive insulating layer, exposing the charged material to a light image and developing the resulting image with an electroscopic material, the photoconductive layer comprising a compound having the formula 31.
• a photographic reproduction process which comprises electrostatically charging a supported photoconductive insulating layer, exposing the charged material to a light image and developing the resulting image with an electroscopic material, the photoconductive layer comprising a compound having the formula 3 2.
• a photographic reproduction process which comprises electrostatically charging a supported photoconductive insulating layer, exposing the charged material to a light image and developing the resulting image with an electroscopic material, the photoconductive layer comprising a compound having the formula 33.
• a photographic reproduction process which comprises electrostatically charging a supported photoconductive insulating layer, exposing the charged material to a light image and developing the resulting image with an electroscopic material, the photoconductive layer comprising a compound having the formula i9 20 34.
• a photographic reproduction process which com- 2,768,077 10/56 Neugebauer et a1.
• 96-115 prises electrostatically charging a supported photoconduc- 2,352,503 9/58 Long et a1.

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• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
• Photoreceptors In Electrophotography (AREA)

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• 0
  • LU LU38469D patent/LU38469A1/xx unknown
  • NL NL126228D patent/NL126228C/xx active
  • NL NL250328D patent/NL250328A/xx unknown
• 1959
  • 1959-04-08 DE DEK37423A patent/DE1105714B/de active Pending
• 1960
  • 1960-03-31 GB GB11436/60A patent/GB940573A/en not_active Expired
  • 1960-04-06 US US20283A patent/US3174854A/en not_active Expired - Lifetime

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