GB836148A - Improvements in or relating to photographic reproduction - Google Patents

Improvements in or relating to photographic reproduction

Info

Publication number
GB836148A
GB836148A GB20135/57A GB2013557A GB836148A GB 836148 A GB836148 A GB 836148A GB 20135/57 A GB20135/57 A GB 20135/57A GB 2013557 A GB2013557 A GB 2013557A GB 836148 A GB836148 A GB 836148A
Authority
GB
United Kingdom
Prior art keywords
bis
triazole
resins
aminophenyl
formaldehyde
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB20135/57A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kalle GmbH and Co KG
Original Assignee
Kalle GmbH and Co KG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Kalle GmbH and Co KG filed Critical Kalle GmbH and Co KG
Publication of GB836148A publication Critical patent/GB836148A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D249/00Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/081,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03GELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G5/00Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
    • G03G5/02Charge-receiving layers
    • G03G5/04Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
    • G03G5/06Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
    • G03G5/0622Heterocyclic compounds
    • G03G5/0624Heterocyclic compounds containing one hetero ring
    • G03G5/0627Heterocyclic compounds containing one hetero ring being five-membered
    • G03G5/0633Heterocyclic compounds containing one hetero ring being five-membered containing three hetero atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Photoreceptors In Electrophotography (AREA)

Abstract

A composition for use on a support in electrophotography comprises a natural resin (which may be modified) together with a 2:5-bis-(p-aminophenyl)-1:3:4-triazole (which may be substituted in the amino groups and/or the ring N-atom), with or without a sensitizing dyestuff. Specified resins are Manila copal, colophony esterified or modified with formaldehyde, zinc resinate, and polymerized (e.g. dimerized) or hydrated natural resins. Suitable triazoles and sensitizing dyestuffs are listed. In examples glycol monomethyl ether and benzene are used as solvents. Specifications 633,747 and 633,796 are referred to.ALSO:2:5 - Bis - (p - aminophenyl) - 1:3:4 - triazoles of the formula <FORM:0836148/IV (b)/1> or <FORM:0836148/IV (b)/2> where R1 is H, alkyl, cycloalkyl or acetyl, R2 is alkyl or acetyl and R3 is H or alkyl, are prepared from the corresponding oxadiazoles (see Specification 851,218) by heating with formamide, followed if desired by alkylation of the triazole N-atom with a dialkyl sulphate. If the amino groups are primary or secondary the initial product is the N-formyl derivative, and this is subsequently hydrolysed with acid. Specified triazoles made in this way are 2:5bis - (p - aminophenyl), 2:5 - bis - (p - ethylaminophenyl), 2:5 - bis - (p - dimethylaminophenyl), 2:5 - bis - (p - diethylaminophenyl), 2:5 - bis - (p - dipropylaminophenyl), 2:5 - bis(p - ethylpropylaminophenyl), 2:5 - bis - (pisoamylaminophenyl), 2:5 - bis - (p - cyclohexylaminophenyl) and 2 - (p - dimethylaminophenyl) - 5 - (p - diethylaminophenyl). Products made by subsequent alkylation are 1ethyl - 2:5 - bis - (p - dimethylaminophenyl)triazole and 1 - methyl - 2:5 - bis - (p - diethylaminophenyl) - triazole. The N - acetyl compounds are obtained by direct acylation with acetic anhydride, to form e.g. 2:5-bis-(p-acetyl-aminophenyl) - triazole or 2:5 - bis - (p - acetylethylaminophenyl)-triazole.ALSO:A composition for use on a support in electrophotography comprises a synthetic resin together with a photoconductive substance consisting of a 2 : 5-bis-(p-aminophenyl)-1 : 3 : 4-triazole (which may be substituted in the amino groups and/or the ring N-atom), with or without a sensitizing dyestuff. Examples are given of compositions containing the following resins: coumarone, cyclohexanone condensed with methylcyclohexanone, colophony - formaldehyde, resin - modified maleic acid, phenolmodified, ketone, polymerized natural resin and chlorinated polyvinyl chloride. Other types of resins mentioned are indene; phenolic (especially phenol-formaldehyde, which may be modified with colophony); polyvinyl chloride, acetate, acetals, alcohol and ethers; polyacrylic and methacrylic esters; poly-styrene and isobutylene; phthalates; alkyds; maleic acid resins; colophony esters of mixed higher alcohols; urea- and melamine-formaldehyde, xylene-formaldehyde; polyamides and polyurethanes; aldehyde resins. Suitable triazoles and sensitizing dyestuffs are listed. The composition may be applied to the support in the form of a solution in benzene, methylene chloride or glycol monomethyl ether. Specifications 633,747 and 633,796 are referred to.
GB20135/57A 1956-06-27 1957-06-26 Improvements in or relating to photographic reproduction Expired GB836148A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEK29200A DE1060260B (en) 1956-06-27 1956-06-27 Material for electrophotographic reproduction

Publications (1)

Publication Number Publication Date
GB836148A true GB836148A (en) 1960-06-01

Family

ID=7218431

Family Applications (1)

Application Number Title Priority Date Filing Date
GB20135/57A Expired GB836148A (en) 1956-06-27 1957-06-26 Improvements in or relating to photographic reproduction

Country Status (8)

Country Link
US (1) US3112197A (en)
BE (1) BE558630A (en)
CH (1) CH360284A (en)
DE (1) DE1060260B (en)
FR (1) FR1177936A (en)
GB (1) GB836148A (en)
LU (1) LU35237A1 (en)
NL (2) NL218434A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3161505A (en) * 1961-01-28 1964-12-15 Azoplate Corp Material for electrophotographic purposes
US3634080A (en) * 1968-06-06 1972-01-11 Agfa Gevaert Nv Persistent conductivity and positive charging characteristics of a zinc oxide photoconductor

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NL249273A (en) * 1959-03-12
NL250327A (en) * 1959-04-08
LU38469A1 (en) * 1959-04-08
NL250331A (en) * 1959-04-09
NL124075C (en) * 1959-04-09
NL266999A (en) * 1959-08-04
NL132172C (en) * 1959-10-31
BE625683A (en) * 1960-02-19
BE585507A (en) * 1960-03-31
US3148982A (en) * 1960-04-11 1964-09-15 Gevaert Photo Prod Nv Electrophotographic process utilizing organic photoconductors
US3287116A (en) * 1961-07-24 1966-11-22 Azoplate Corp Process for the sensitization of photoconductors
USB373140I5 (en) * 1964-09-24
DE2336094C2 (en) * 1973-07-16 1983-03-03 Hoechst Ag, 6000 Frankfurt Electrophotographic recording material
JPS57150853A (en) * 1981-03-13 1982-09-17 Konishiroku Photo Ind Co Ltd Electrophotographic receptor
DE3210576A1 (en) * 1982-03-23 1983-10-06 Hoechst Ag ELECTROPHOTOGRAPHIC RECORDING MATERIAL
DE3215967A1 (en) * 1982-04-29 1983-11-03 Basf Ag, 6700 Ludwigshafen ELECTROGRAPHIC RECORDING MATERIALS WITH SPECIAL CONNECTORS TRANSPORTING CONNECTIONS
JPS5942352A (en) 1982-09-01 1984-03-08 Fuji Photo Film Co Ltd Disazo compound, photoconductive composition and electrophotographic sensitive material containing the same
DE3409888A1 (en) * 1984-03-17 1985-09-19 Hoechst Ag, 6230 Frankfurt LIGHT-SENSITIVE RECORDING MATERIAL AND USE THEREOF IN A METHOD FOR PRODUCING A PRINTING FORM OR PRINTED CIRCUIT
DE3417951A1 (en) * 1984-05-15 1985-11-21 Hoechst Ag, 6230 Frankfurt ELECTROPHOTOGRAPHIC RECORDING MATERIAL
DE3506436A1 (en) * 1985-02-23 1986-08-28 Hoechst Ag, 6230 Frankfurt NEW STYRENE DERIVATIVES CONTAINING SULPHON, METHOD FOR THE PRODUCTION AND USE THEREOF
DE3509147A1 (en) * 1985-03-14 1986-09-18 Hoechst Ag, 6230 Frankfurt ELECTROPHOTOGRAPHIC RECORDING MATERIAL
DE3513747A1 (en) * 1985-04-17 1986-10-23 Hoechst Ag, 6230 Frankfurt ELECTROPHOTOGRAPHIC RECORDING MATERIAL
DE3740421A1 (en) * 1987-11-28 1989-06-08 Basf Ag MULTILAYERED, ELECTROPHOTOGRAPHIC RECORDING MATERIAL
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US3161505A (en) * 1961-01-28 1964-12-15 Azoplate Corp Material for electrophotographic purposes
US3634080A (en) * 1968-06-06 1972-01-11 Agfa Gevaert Nv Persistent conductivity and positive charging characteristics of a zinc oxide photoconductor

Also Published As

Publication number Publication date
FR1177936A (en) 1959-04-30
US3112197A (en) 1963-11-26
CH360284A (en) 1962-02-15
DE1060260B (en) 1959-06-25
NL218434A (en)
NL100993C (en)
LU35237A1 (en)
BE558630A (en)

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