GB1416603A - Electrophotographic recording material and processes for its manufacture - Google Patents
Electrophotographic recording material and processes for its manufactureInfo
- Publication number
- GB1416603A GB1416603A GB1929873A GB1929873A GB1416603A GB 1416603 A GB1416603 A GB 1416603A GB 1929873 A GB1929873 A GB 1929873A GB 1929873 A GB1929873 A GB 1929873A GB 1416603 A GB1416603 A GB 1416603A
- Authority
- GB
- United Kingdom
- Prior art keywords
- formula
- derivative
- methoxy
- chloro
- coupling
- 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
Links
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, 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
-
- 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
- G03G5/043—Photoconductive layers characterised by having two or more layers or characterised by their composite structure
- G03G5/047—Photoconductive layers characterised by having two or more layers or characterised by their composite structure characterised by the charge-generation layers or charge transport layers
-
- 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
- G03G5/14—Inert intermediate or cover layers for charge-receiving layers
Abstract
1416603 Dyestuffs HOECHST AG 24 April 1973 [26 April 1972 31 July 1972 (4) 14 Aug 1972 (2) 30 Aug 1972 (3) 21 Sept 1972 (3)] 19298/73 Heading C4P [Also in Division G2] The compound of formula (4,5 - dichloronaphthoylene benzimidazole) is made by condensing o-phenylene diamine and 4,5-dichloronaphthalic acid anhydride. A quinonyl diazo naphthylene derivative of formula is made by forming a diazonium salt from 6- amino-4,5,8-trimethyl-2-hydroxy quinoline and. coupling it with 5-(2<SP>1</SP>,3<SP>1</SP>-hydroxynaphthoylamino)benzimidazolone. The compound of formula can be made in an analogous manner. A trisazo derivative of formula is made by forming a diazonium salt of 4,4<SP>1</SP>- diamino - 2,2<SP>1</SP> - dichloro - 5,51 - dimethoxyazobenzene and coupling it with 1-phenyl-3- methyl pyrazolone. Compounds wherein the phenylene nuclei may be substituted by a methyl group or two chloro or methoxy groups may be made in an analogous way. The benzoxanthene derivative of formula is made by the reaction of 10-methoxy benzoxanthene 3,4-dicarboxylic acid anhydride with 3- aminopyrene. A trisazo derivative of formula wherein R 9 and R 10 are methoxy and R 11 and R 12 are chloro, is afforded by coupling the diazonium salt of 4,4<SP>1</SP>-diamino-2,5<SP>1</SP>-dichloro-5,2<SP>1</SP>- dimethoxy azobenzene with acetoacetanilide. The compound wherein R 9 and R 11 are chloro, R 10 is methoxy and R 12 is methyl, can be made in a similar way. A diazomethine of formula is formed by the reaction of 4,41-diaminodiphenyl ether or with dimethylamino benzaldehyde in dimethyformamide. The perylene derivative of formula where R is pyenyl is made in Example 13 by heating perylene-3,4,9,10-tetracarboxylic acid and 3-amino-pyrene in a mixture of quinoline and concentrated sulphuric acid. Dioxatetra-aza-pentacenes of formula wherein R 1 is H are formed in Example 46 from 1,4 - dihydroxy - cyclohexa - ,1,4 - diene - 2,5- dicarboxylic acid ethyl ester and 2-aminopyridine to give tetrahydro compounds of formula which are subsequently boiled under reflux in a mixture of nitrobenzene, glacial acetic acid and piperidine to yield the pentacene.
Applications Claiming Priority (13)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2220408A DE2220408C3 (en) | 1972-04-26 | 1972-04-26 | Electrophotographic recording material and process for its preparation - US Pat |
DE2237680A DE2237680C3 (en) | 1972-07-31 | 1972-07-31 | Electrophotographic recording material |
DE2237539A DE2237539C3 (en) | 1972-07-31 | 1972-07-31 | Electrophotographic recording material |
DE2237679A DE2237679C3 (en) | 1972-07-31 | 1972-07-31 | Electrophotographic recording material |
DE19722237678 DE2237678C3 (en) | 1972-07-31 | 1972-07-31 | Electrophotographic recording material |
DE19722239923 DE2239923C3 (en) | 1972-08-14 | 1972-08-14 | Electrophotographic recording material |
DE2239924A DE2239924C3 (en) | 1972-08-14 | 1972-08-14 | Electrophotographic recording material |
DE2242627A DE2242627C2 (en) | 1972-08-30 | 1972-08-30 | Electrophotographic recording material |
DE19722242596 DE2242596C2 (en) | 1972-08-30 | 1972-08-30 | Electrophotographic recording material |
DE2242595A DE2242595C2 (en) | 1972-08-30 | 1972-08-30 | Electrophotographic recording material |
DE2246254A DE2246254C2 (en) | 1972-09-21 | 1972-09-21 | Electrophotographic recording material |
DE19722246256 DE2246256C2 (en) | 1972-09-21 | 1972-09-21 | Electrophotographic recording material |
DE19722246255 DE2246255C2 (en) | 1972-09-21 | 1972-09-21 | Electrophotographic recording material |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1416603A true GB1416603A (en) | 1975-12-03 |
Family
ID=27583953
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1929873A Expired GB1416603A (en) | 1972-04-26 | 1973-04-24 | Electrophotographic recording material and processes for its manufacture |
Country Status (2)
Country | Link |
---|---|
GB (1) | GB1416603A (en) |
NL (1) | NL180460C (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0078575A1 (en) * | 1981-11-02 | 1983-05-11 | Mita Industrial Co. Ltd. | An electrophotographic photosensitive material |
US4530892A (en) * | 1982-03-23 | 1985-07-23 | Hoechst Aktiengesellschaft | Electrophotographic recording material for printing forms |
US4668600A (en) * | 1984-05-15 | 1987-05-26 | Hoechst Aktiengesellschaft | Electrophotographic recording material containing an n-type conducting pigment |
US4725520A (en) * | 1985-10-08 | 1988-02-16 | Hoechst Aktiengesellschaft | Electrophotographic recording material |
US7655809B2 (en) | 2004-05-18 | 2010-02-02 | University Of Ottawa | Compounds comprising a linear series of five fused carbon rings, and preparation thereof |
US7935836B2 (en) | 2004-05-18 | 2011-05-03 | Alexander Graham Fallis | Compounds comprising a linear series of five fused carbon rings, and preparation thereof |
CN111886318A (en) * | 2018-03-20 | 2020-11-03 | 巴斯夫欧洲公司 | Yellow light emitting device |
-
1973
- 1973-04-16 NL NL7305278A patent/NL180460C/en not_active IP Right Cessation
- 1973-04-24 GB GB1929873A patent/GB1416603A/en not_active Expired
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0078575A1 (en) * | 1981-11-02 | 1983-05-11 | Mita Industrial Co. Ltd. | An electrophotographic photosensitive material |
US4530892A (en) * | 1982-03-23 | 1985-07-23 | Hoechst Aktiengesellschaft | Electrophotographic recording material for printing forms |
US4668600A (en) * | 1984-05-15 | 1987-05-26 | Hoechst Aktiengesellschaft | Electrophotographic recording material containing an n-type conducting pigment |
US4725520A (en) * | 1985-10-08 | 1988-02-16 | Hoechst Aktiengesellschaft | Electrophotographic recording material |
US7655809B2 (en) | 2004-05-18 | 2010-02-02 | University Of Ottawa | Compounds comprising a linear series of five fused carbon rings, and preparation thereof |
US7935836B2 (en) | 2004-05-18 | 2011-05-03 | Alexander Graham Fallis | Compounds comprising a linear series of five fused carbon rings, and preparation thereof |
CN111886318A (en) * | 2018-03-20 | 2020-11-03 | 巴斯夫欧洲公司 | Yellow light emitting device |
Also Published As
Publication number | Publication date |
---|---|
NL7305278A (en) | 1973-10-30 |
NL180460C (en) | 1987-02-16 |
NL180460B (en) | 1986-09-16 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
EER | Erroneous entry in the register of patents: |
Free format text: DOCUMENT WAS IDENTIFIED AS HAVING CEASED WHILE IN FACT IT WAS STILL IN FORCE |
|
EER | Erroneous entry in the register of patents: |
Free format text: DOCUMENT WAS IDENTIFIED AS HAVING CEASED WHILE IN FACT IT WAS STILL IN FORCE |
|
EER | Erroneous entry in the register of patents: |
Free format text: DOCUMENT WAS IDENTIFIED AS HAVING CEASED WHILE IN FACT IT WAS STILL IN FORCE |
|
EER | Erroneous entry in the register of patents: |
Free format text: DOCUMENT WAS IDENTIFIED AS HAVING CEASED WHILE IN FACT IT WAS STILL IN FORCE |
|
PE20 | Patent expired after termination of 20 years |
Effective date: 19930423 |