Classifications

• • 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 or 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
  • G03G5/0601—Acyclic or carbocyclic compounds
  • G03G5/062—Acyclic or carbocyclic compounds containing non-metal elements other than hydrogen, halogen, oxygen or nitrogen
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
  • C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
  • C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
  • C07F7/02—Silicon compounds
  • C07F7/08—Compounds having one or more C—Si linkages
  • C07F7/0803—Compounds with Si-C or Si-Si linkages
  • C07F7/081—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
  • C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
  • C07F7/22—Tin compounds
  • C07F7/2208—Compounds having tin linked only to carbon, hydrogen and/or halogen
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
  • C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
  • C07F7/24—Lead compounds
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
  • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
  • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
  • C07F9/66—Arsenic compounds
  • C07F9/70—Organo-arsenic compounds
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
  • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
  • C07F9/94—Bismuth compounds
• • 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 or 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
  • G03G5/0662—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic containing metal elements

Definitions

• ABSTRACT Photoconductive compositions and electrophotographic elements containing as photoconductors organometallic compounds having at least one aminoaryl group attached to a Group No or Group Va metal atom through an aryl moiety.
• the process of xerography employs an electrophotographic element comprising a support material bearing a coating of a normally insulating material whose electrical resistance varies with the amount of incident actinic radiation it receives during an imagewise exposure.
• the element commonly termed a photoconductive element, is first given a uniform surface charge, generally in the dark after a suitable period of dark adaptation. It is then exposed to a pattern of actinic radiation which has the effect of differentially reducing the potential of this surface charge in accordance with the relative energy contained in various parts of the radiation pattern.
• the differential surface charge or electrostatic latent image remaining on the electrophotographic element is then made visible by contacting the surface with a suitable electroscopic marking material.
• marking material or toner whether contained in an insulating liquid or on a dry carrier, can be deposited on the exposed surface in accordance with either the charge pattern or in the absence of charge pattern as desired. Deposited marking material can then be either permanently fixed to the surface of the sensitive element by known means such as heat, pressure, solvent vapor, or the like, or transferred to a second element to which it can similarly be fixed. Likewise, the electrostatic latent image can be transferred to a second element and developed there.
• Various photoconductive insulating materials have been employed in the manufacture of electrophotographic elements. For example, vapors of selenium and vapors of selenium alloys deposited on a suitable support and particles of photoconductive zinc oxide held in a resinous, film-forming binder have found wide application in the present day document copying applications.
• Typical of these organic photoconductors are the triphenylamines and the triarylmethane leuco bases.
• Optically clear photoconductor-containing elements having desirable electrophotographic properties can be especially useful in electrophotography. Such electrophotographic elements can be exposed through a transparent base if desired, thereby providing unusual flexibility in equipment design.
• Such compositions when coated as a film or layer on a suitable support, also yield an element which is reusable; that is, it can be used to form subsequent images after residual toner from prior images has been removed by transfer and/or cleaning.
• the selection of various compounds for incorporation into photoconductive compositions to form electrophotographic layers has proceeded on a compound-by-compound basis. None as yet has been discovered from the large number of different photoconductive substances tested which permits effective prediction, and therefore selection of the particular compounds exhibiting the desired electrophotographic properties.
• electrophotographic elements having coated thereon photoconductive compositions containing as photoconductors organometallic compounds having at least one amino-aryl substituent attached to a Group lVa or Group Va metal atom.
• the metallic substituents of these organometallic photoconductors are Group [Va or Group Va metals in accordance with the Periodic Table of the Elements (Handbook of Chemistry and Physics, 38th edition, pp. 394-) and include silicon, germanium, tin and lead from Group Na and phosphorus, arsenic, antimony and bismuth from Group Va.
• the organometallic photoconductors of this invention can be substituted in the metallo nucleus with a wide variety of substituents but at least one of the substituents must be an aminoaryl radical.
• the amino radical can be positioned anywhere on the aromatic nucleus, but best results are obtained if the aryl moiety is a phenyl radical having the amino group in the 4 or para position.
• Typical substituents attached to the metal nucleus include the following:
• an aryl radical including unsubstituted as well as substituted aryl radicals such as aminoaryl, alkylaryl and haloaryl,
• an oxygen-containing radical such as an alkoxy or aryloxy radical
• amino radical including unsubstituted and substituted amino radicals such as monoand diarylamines and monoand dialkylamines,
• a heterocyclic radical f. a heterocyclic radical and g. a Group IVa or Va organometallic radical.
• E, G, L and Q can be a. a hydrogen atom
• an aryl radical including unsubstituted as well as substituted aryl radicals such as a phenyl radical, a naphthyl radical, a dialkylaminophenyl radical, or a dialkylaminonaphthyl radical,
• R an amino radical having the formula wherein R, and R can be hydrogen atoms oralkyl radicals having one to eight carbon atoms, or
• a heterocyclic radical having live to six atoms in the hetero nucleus including at least one nitrogen atom such as a triazolyl, a pyridyl radical, etc.
• T is an amino radical such as an alkylamino radical having one to eight carbon atoms or an arylamino radical such as a phenylamino radical
• Ar is an aromatic radical such as phenyl or naphthyl
• M, and M g are the same or different Group lVa metals
• M is a Group Va metal
• D can be any of the substituents set forth above for E, G, L and Q and in addition can be a Group lVa organometallic radical or when taken with E,
• .I can be any of the substituents set forth above for E, G, L and Q and in addition can be,
• organornetallic photoconductors of this invention include triphenyl-p-diethylaminophenylsilane methyl-diphenyl-p-diethylaminophenylsilane triphenyl-p-diethylaminophenylgermane triphenyl-p-dimethylaminophenylstannane triphenyl-p-diethylaminophenylstannane diphenyl-di-(p-diethylaminophenyl)stannane triphenyl-p-diethylaminophenylplumbane tetra-p-diethylaminophenylplumbane phenyl-di-(p-diethylaminophenyl)phosphine bis(p-diethylaminophenyl)phosphine oxide tri-p-dimethylaminophenylarsine tri-p-diethylaminophenylars
• amino-aryl lead and tin compounds can be prepared in accordance with J.A.C.S. 54, 3726-9 (1932) or J. Org. Chem. 15, 994 (1950).
• the amino-aryl germanium compounds are made by the method set forth in CA 60, p. 39511.
• a method for making the amino-aryl bismuthines has been described by Gilman and Yablunky (J.A.C.S. 63, 207-211, 1941).
• Aminoaryl derivatives of arsenic are prepared in accordance with the J. Indian Chemical Soc. 16, 515-518 (1939).
• Phosphorus and antimony compounds containing amino-aryl moieties may-be prepared by methods described in GA. 28, 3392 and GA. 40, 4689 respectively.
• Electrophotographic elements of the invention can be prepared with the photoconducting compounds of the invention in the usual manner, i.e., by blending a dispersion or solution of a photoconductive compound together with a binder, when necessary or desirable, and coating or forming a selfsupporting layer with the photoconductor-containing material. Mixtures of the photoconductors described herein can "be employed. Likewise, other photoconductors known in the art can be combined with the present photoconductors; ln-addition, supplemental materials useful for changing the spectral stansensitivity or electrophotosensitivity of the element can be added to the composition of the element when it is desirable to produce the characteristic effect of such materials.
• Sensitizing compounds useful with the photoconductive compounds of the present invention can include a wide variety of substances such as pyrylium, thiapyrylium, and selenapyrylium salts of U.S. Pat. No. 3,250,615, issued May 10, 1966; fluorenes, such as 7,12-dioxo-l3-dibenzo(a,h)fluorene, 5,10- dioxo-4a1 l-diazabenzo(b)fluorene, 3,13-dioxo-7-oxadibenzo(b,g)-fluorene, trinitrofluorenone, tetranitrofluorenone and the like; aromatic nitro compounds of U.S. Pat. No.
• 2,732,301 mineral acids
• carboxylic acids such as maleic-acid, dichloroacetic acid, and salicylic acid
• sulfonic and phosphoric acids such as triphenylmethane, diarylmethane, thiazine, azine, oxazine, xanthene, phthalein, acridine, azo, anthraquinone dyes and many other suitable sensitizing dyes.
• the preferred sensitizers for use with the compounds of this invention are pyrylium and thiapyrylium salts, fluorenes, carboxylic acids, and triphenylmethane dyes.
• sensitizing compound is to be used within a photoconductive layer as disclosed herein it is conventional practice to mix a suitable amount of the sensitizing compounds with the coating composition so that, after thorough mixing, the sensitizing compound is uniformly distributed throughout the desired layer of the coated element. in preparing the photoconducting layers, no sensitizing compound is needed for the layer to exhibit photoconductivity
• relatively minor amounts of sensitizing compound give substantial improvement in the electrophotographic speed of such layers, the use of some sensitizer is preferred.
• the amount of sensitizer that can be added to a photoconductor-incorporating layer to give effective increases in speed can vary widely.
• any given case will vary with the specific photoconductor. and sensitizing compound used. In general, substantial speed gains can be obtained .
• an appropriate. sensitizer is added in a concentration range from about 0.0001 to about 30 percent by weight based on the weight of the filmforming coating composition. Normally, a sensitizeris added to the coating composition in an amount by weight from about 0.005 to about 5.0 percent by weight of the total coating composition.
• Preferred binders for use in preparing the present photoconductive layers are film-forming polymeric binders having fairly high dielectric strength which are good electrically insulating film-forming vehicles.
• Materials of this type comprise styrene-butadiene copolymers; silicone resins; styrene-alkyd resins; silicone alkyd resins; soya-alkyd resins; poly (vinyl chloride); poly(vinylidene chloride); vinylidene chloride-acrylonitrile"copolymers; poly(vinyl acetate); vinyl acetate-vinyl chloride copolymers; poly(vinyl a'cetals), such as poly (vinyl butyral); polyacrylic and methacrylic esters, such as poly v (methylmethacrylate), poly(nbutylmethacrylate), poly(isobutyl methacrylate), etc.; polystyrene; nitrated polystyrene; polymethylstyren
• styrene-alkyd resins can be prepared according to the method described in U.S. Pats. No. 2,361,019 and No. 2,258,423.
• Suitable resins of the type contemplated for use in the photoconductive layers of the invention are sold under such tradenames as Vitel PE-lOl, Cymac, Piccopale Saran R220 and Lexan '105.
• Other types of binders which can be used in the photoconductive layers of the invention include such materials as paraffin, mineral waxes, etc.
• Solvents of choice for preparing coating compositions of the present invention can include a number of solvents such as benzene, toluene, acetone, Z-butanone, chlorinated hydrocarbons, e.g., methylene chloride, ethylene chloride, etc., ethers, e.g., tetrahydrofuran, or mixtures of these solvents, etc.
• solvents such as benzene, toluene, acetone, Z-butanone, chlorinated hydrocarbons, e.g., methylene chloride, ethylene chloride, etc., ethers, e.g., tetrahydrofuran, or mixtures of these solvents, etc.
• the photoconductor substance is present in an amount equal to at least l weight percent of the coating composition.
• the upper limit in the amount of photoconductor substance present can be widely varied in accordance with usual practice. In those cases where a binder is employed, it is normally required that the photoconductor substance be present in an amount from about 1 weight percent of the coating composition to about 99 weight percent of the coating composition.
• a preferred weight range for the photoconductor substance in the coating composition is from about weight percent to about 60 weight percent.
• Coating thicknesses of the photoconductive composition on a support can vary widely. Normally, a coating in the range of about 0.001 inch to about 0.01 inch before drying is useful for the practice of this invention. The preferred range of coating thickness was found to be in the range from about 0.002 inch to about 0.006 inch before drying although useful results can be obtained outside of this range.
• Suitable supporting materials for coating the photoconductive layers of the present invention can include any of a wide variety of electrically conducting supports, for example, paper (at a relative humidity above percent); aluminum-paper laminates; metal foils such as aluminum foil, zinc foil, etc.; metal plates, such as aluminum, copper, zinc, brass, and galvanized plates; vapor deposited metal layers such as silver or aluminum and the like.
• An especially useful conducting support can be prepared by coating a support material such as polyethylene terephthalate with a layer containing a semiconductor dispersed in a resin. Such conducting layers both with and without insulating barrier layers are described in U.S. Pat. No. 3,245,833.
• a suitable conducting coating can be prepared from the sodium salt of a carboxyester lactone of maleic anhydride and a vinyl acetate polymer.
• Such kinds of conducting layers and methods for their optimum preparation and use are disclosed in U.S. Pats. No. 3,007,901 and No. 3,267,807.
• the elements of the present invention can be employed in any of the well-known electrophotographic processes which require photoconductive layers.
• One such process is the aforementioned xerographic process.
• a process of this type of electrophotographic element is given a blanket electrostatic charge by placing the same under a corona discharge which serves to give a uniform charge to the surface of the photoconductive layer. This charge is retained by the layer owing to the substantial insulating property of the layer, i.e., the low conductivity of the layer in the dark.
• the electrostatic charge formed on the surface of the photoconducting layer is then selectively dissipated from the surface of the layer by exposure to light through an image-bearing transparency by a conventional exposure operation such as, for example, by contact-printing technique, or by lens projection of an image, etc., to form a latent image in the photoconducting layer.
• a charged pattern is created by virtue of the fact that light causes the charge to be conducted away in proportion to the intensity of the illumination in a particular area.
• the charge pattern remaining after exposure is then developed, i.e., rendered visible, by treatment with a medium comprising electrostatically attractable particles having optical density.
• the developing electrostatically attractable particles can be in the form of a dust, e.g., powder, pigment in a resinous carrier, i.e., toner, or a liquid developer may be used in which the developing particles are carried in an electrically insulating liquid carrier.
• a dust e.g., powder
• a resinous carrier i.e., toner
• a liquid developer may be used in which the developing particles are carried in an electrically insulating liquid carrier.
• the present invention is not limited to any particular mode of use of the new electrophotographic materials, and the exposure technique, the charging method, the transfer (if any), the developing method, and the fixing method as well as the materials used in these methods can be selected and adapted to the requirements of any particular technique.
• Electrophotographic materials according to the present invention can be applied to reproduction techniques wherein different kinds of radiations, i.e., electromagnetic radiations as well as nuclear radiations, can be used. For this reason, it is pointed out herein that although materials according to the invention are mainly intended for use in connection with methods comprising an exposure, the term electrophotography" wherever appearing in the description and the claims, is to be interpreted broadly and understood to comprise both xerography and xeroradiography.
• Example 1 PREPARATION OF TRlPHENYL-p- DlMETHYLAMlNOPHENYL STANNANE A rapidly stirred mixture of 1.96 grams (0.28 g. atoms) of lithium wire and 400 ml. of Mallinckrodt dry diethyl ether are kept under nitrogen and are treated (during 10 minutes) with a solution of 26 g. (0.13 moles) of p-bromo-N,N- dimethylaniline in ml. of dry ether. The resulting mixture is heated on a steam bath for 15 minutes. Approximately one gram of lithium dispersion is added and the mixture is heated to reflux temperature. The mixture is concentrated on a steam bath to 6 the original volume.
• Example 2 PREPARATION OF TRIPHENYL-p- DlETHYLAMINOPHENYLSTANNANE A stirred mixture of 1.44 g. (0.06 moles) of magnesium turnings, 30 ml. of distilled tetrahydrofuran and 4.6 g. (0.02 moles) of distilled p-bromo-N,N-diethylaniline is kept under nitrogen and is heated at reflux temperature for 15 minutes. The volume is reduced by a water aspirator to about it the original volume and then the mixture is kept at reflux temperature for one hour. The temperature is lowered to just below reflux and the mixture is treated rapidly with a solution of 7.7 g. (0.02 moles) of triphenyl tin chloride in 50 ml.
• Example 3 PREPARATlON OF TETRA-p- DlETl-lLAMlNOPl-IENYLPLUMBANE A stirred mixture of 6.5 g. (0.27 moles) of magnesium, 20.5 g. (0.09 moles) of distilled p-bromo-N,N-diethylaniline and 90 ml. of distilled tetrahydrofuran is heated under reflux for 45 minutes and then is treated with a mixture of 11.1 g. (0.04 moles) of lead dichloride and 60 m1. of distilled tetrahydrofuran. The resulting dark brown reaction mixture is heated under reflux for eight hours. The result is filtered (after standing overnight) and the filtrate affords white crystals on standing -20 minutes.
• Example 4 PREPARATION OF TRl-p- DIMETHYLAMINOPHENYLARSINE A mixture of 26.8 g. (0.222 moles) of N,N-dimethyl-aniline and 50 g. (0.276 moles) of arsenic trichloride is heated on a steam bath for two hours and then poured, into 800 ml. of stirred water. The mixture is filtered and the filtrate is made alkaline with about 350 ml. of 10 percent sodium hydroxide. The gummy solid which precipitates is washed with P1628 Ligroin, dissolved in 200 ml. of methylene chloride, dried over anhydrous sodium sulfate and the solvent is removed by a Roto-Vac.
• Example 5 PREPARATION OF TRI-p- DIETHYLAMINOPHENYLARSINE A stirred mixture of 8.64 g. (0.36 moles) of magnesium, 27.6 g. (0.12 moles) of distilled p-bromo-N,N-diethylaniline and 120 ml. of distilled tetrahydrofuran is heated under reflux for one hour. The resulting brown mixture is treated dropwise (during 10 minutes) with a solution of 7.3 g. (0.04 moles) of arsenic trichloride in 70 ml. of distilled tetrahydrofuran at such a rate as to maintain reflux.
• Example 6 PREPARATION OF 2-METHYL-4- DIMETHYLAMINOPHENYLARSINE OXIDE A mixture of 20.3 g. (0.15 moles) of N,N-dimethyl-mtoluidine and 27.0 g. (0.15 moles) of arsenic trichloride are heated on a steam bath for 20 minutes and then poured into one liter of stirred water. The resulting solution is made al- Example 7.
• Example 8 Organometallic photoconductors of the type described herein are separately incorporated into a coating dope having the following composition:
• compositions are handcoated at a wet thickness of 0.004 inch on a conducting layer comprising the sodium salt of a carboxyester lactone, such as described in US. Pat. No. 3,120,028, which in turn is coated on a cellulose acetate film base.
• the coating blocks are maintained at a temperature of F.
• These electrophotographic elements are charged under a positive or negative corona source until the surface potentials, as measured by an electromcter probe, reach about 600 volts. They are then subjected to exposure from behind a stepped density gray scale to a 3,000 K. tungsten source.
• the exposure causes reduction of the surface potentials'of the elements under each step of the gray scale from their initial potential, V,, to some lower potential, V whose exact value depends on' the actual amount of exposure in meter-candleseconds received by the areas.
• the results of the measurements are plotted on a graph of surface potential V vs. log exposure for each step.
• the shoulder speed is the numerical expression 0f 10" multiplied by the reciprocal of the exposure in meter-candle-seconds required to reduce the 600 volt charged surface potentials by volts;
• the toe speed is the numerical expression of 10 multiplied by the reciprocal of the exposure in meter-candle-seconds required to reduce the 600 volt charged surface potentials to 100 volts.
• the speeds of the various organometallic photoconductive compositions are shown in Table 1 below.
• the sensitizers referred to in the Table are as follows:
• a no sensitizer added B 2,6-bis(4-ethylphenyl)-4-(4-amyloxyphenyl)thia-pyrylium perchlorate 2,4-bis(4-ethylphenyl)-6-(4-styrylstyryl)pyrylium perchlorate
• the binder is' [4,4-isopropylidene bis-(phenyloxyethyl)- coethylene terephthalate] sold commercially under the tradename Vitel 101.
• Photoconductor-0.97 l' moles for each gram of solids in the final coating composition Sensitizer--2 percent of the final weight of the coating composition Binder-6.0 g.
• the sensitizer is 4-(4-bis(2-chloroethyl)aminophenyl)-2,6- diphenylthiapyrylium perchlorate.
• the binder is Lexan-lOS, a polycarbonate resin by the General Electric Co. prepared by reacting phosgene and a dihydroxydiarylalkane or from the ester exchange between diphenyl carbonate and 2,2-bis-4- hydroxyphenylpropane. The speeds are set forth in Table II 35 below.
• Example 8 Tri-p-diethylaminophenylarsine
• Example 8 and 9 Tri-p-diethylaminophenylarsine
• the coating dopes of Example 8 and 9 are again coated in the manner described in Example 8.
• the surface of each of the photoconductive layers so prepared is charged to a potential of about +600 volts under a corona charger.
• the layer is then covered with a transparent sheet bearing a pattern of opaque and light transmitting areas and exposed to the radiation from an incandescent lamp with an illumination intensity of about 75 meter-candles for 12 seconds.
• the resulting electrostatic latent image is developed in the usual manner by cascading over the surface of the layer a mixture of negatively charged black thermoplastic toner particles and glass beads. A good reproduction of the pattern results in each instance.
• An electrophotographic element comprising an electrically conducting support having coated thereon a photoconductive composition comprising an electrically insulating, film-forming polymeric binder containing at least one percent by weight of a Group lVa organometallic photoconductive compound having at least one aminoaryl group attached through an aryl moiety to a Group [Va metal atom.
• An electrophotographic element comprising an electrically conducting support having coated thereon a photoconductive composition
• a photoconductive composition comprising an electrically insulating, film-forming polymeric binder containing at least one percent by weight of a photoconductor which is a Group lVa organometallic compound having attached to a Group lVa metal atom (l) at least one aminoaryl group which is attached to the metal atom through an aryl moiety and (2) the remaining substituents being selected from the group consisting of a hydrogen atom, an alkyl radical and an aryl radical.
• An electrophotographic element comprising an electrically conducting support having thereon a photoconductive composition comprising an electrically insulating, film-forming polymeric binder containing at least one percent by weight of a photoconductor represented by the formula:
• T is an amino radical
• Ar is an aryl radical
• M is a Group IVa metal and E, D, and G are each selected from the group consisting of a hydrogen atom, an alkyl radical and an aryl radical.
• An electrophotographic element comprising an electrically conducting support having coated thereon a photoconductive composition comprising an electrically insulating, film-forming polymeric binder containing at least one percent by weight of a photoconductor represented by the formula:
• R, and R are alkyl radicals having one to eight carbon atoms
• E, G and D are each selected from the group consisting of an alkyl radical having one to eight carbon atoms and a phenyl radical;
• M is a Group lVa metal.
• the element of claim 4 wherein the photoconductor is sensitized with from about 0.001 to about 30 percent by weight of a compound selected from the group consisting of pyrylium, thiapyrylium and selenapyrylium salts.
• a photoconductive element for use in electrophotog raphy comprising a electrically conductive support having coated thereon a photoconductive composition comprising a photoconductor and an electrically insulating, film-forming polymeric binder for said photoconductor, said photoconductor being an organometallic compound present in an amount of at least one percent by weight of said composition, said compound being selected from the group consisting of triphenyl-p-diethylaminophenylsilane,
• a photoconductive element comprising a conductive support having coated thereon a layer of a photoconductive composition
• said layer comprises an electrically insulating, film-forming polymeric binder having therein at least one percent by weight of a Group lVa organometallic photoconductive compound having at least one aminoaryl group attached through an aryl moiety to a Group lVa metal atom.
• a photoconductive composition for use in electrophotography comprising an electrically insulating, film-forming polymeric binder containing at least one percent by weight of a photoconductor which is a Group IVa organometallic compound having attached to a Group lVa metal atom (l) at least i one aminoaryl group which is attached to the metal atom through an aryl moiety and (2) the remaining substituents being selected from the group consisting of a hydrogen atom, an alkyl radical and an aryl radical, and a sensitizer for said photoconductor selected from the group consisting of pyryli- LII

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

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• 1967
  • 1967-07-03 US US650664A patent/US3647429A/en not_active Expired - Lifetime
• 1968
  • 1968-06-27 BE BE717265D patent/BE717265A/xx unknown
  • 1968-07-02 FR FR1596481D patent/FR1596481A/fr not_active Expired
  • 1968-07-03 CH CH991368A patent/CH492240A/fr not_active IP Right Cessation
  • 1968-07-03 GB GB31647/68A patent/GB1211595A/en not_active Expired
• 1971
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