GB1396838A - Glutamic ester polymers and electro-photographic materials comprising them - Google Patents
Glutamic ester polymers and electro-photographic materials comprising themInfo
- Publication number
- GB1396838A GB1396838A GB891673A GB891673A GB1396838A GB 1396838 A GB1396838 A GB 1396838A GB 891673 A GB891673 A GB 891673A GB 891673 A GB891673 A GB 891673A GB 1396838 A GB1396838 A GB 1396838A
- Authority
- GB
- United Kingdom
- Prior art keywords
- electro
- photographic
- sensitizer
- anhydrides
- tetra
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/02—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
- C08G69/08—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from amino-carboxylic acids
- C08G69/10—Alpha-amino-carboxylic acids
-
- 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
- G03G5/07—Polymeric photoconductive materials
- G03G5/075—Polymeric photoconductive materials obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyamides (AREA)
- Photoreceptors In Electrophotography (AREA)
Abstract
1396838 Electro-photographic elements RICOH KK 23 Feb 1973 [23 Feb 1972] 8916/73 Heading G2C [Also in Division C3] Photo-conductive Homo-or-w-polymers contain the unit:- where n is 1 or 2 and R is a heterocyclic group or a polynuclear aromatic group which can contain N 1 O or S atoms. They may be obtained by polymerizing one or more N-carboxy-anhydrides of the appropriate glutamic acid esters e.g. in dioxan as solvent using a primary amine as catalyst. Examples of R are carbozyl, acrydinyl, indolyl, naphthyl, anthryl, phenanthryl and pyrene groups. They have good film-forming ability but poor adhesion and for use in electro-photographic materials are therefore usually compounded with 10 to 50 wt per cent of a resin binder e.g. polymethyl methacrylate, polycarbonates, polyethylene terephthalate, poly-ethylene-butylene or styrene, polyvinyl cinnamate, vinyl chloride/ acetate copolymers or cyclised rubber. Electro-photographic elementscomprise a layer of the polymer/binder blend, desirably containing 20 to 30% of a plasticizer, 0À1 to 5% of a sensitizer and 10 to 150 mol per cent (of the polymer unit) of a pro-sensitizer on a conductive support such as metal, e.g. zinc, cellulose, e.g. paper, or suitably treated plastics, e.g. polyester or PVC, sheets. Suitable plasticizers are dimethyl or dioctyl phthalate or triphenyl phosphate. Numerous dyestuffs suitable as sensitizers are specified. Speci- fied prosensitizers are tetra-cyanoethylene; tetracyanoquinodimethane; phthalic 2, 7-dinitrophetalic and naphthalic acids and anhydrides; naphtho-and anthra-quinone; 2,4,7-tri and 2,4,5, 7-tetra-nitrofluorenone; mononitroazafluorenone; trichlorobenzene and bromal.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US05/376,747 US3933492A (en) | 1972-02-23 | 1973-07-05 | Novel photoconductive substances and their application |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1926072A JPS4888940A (en) | 1972-02-23 | 1972-02-23 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1396838A true GB1396838A (en) | 1975-06-04 |
Family
ID=11994451
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB891673A Expired GB1396838A (en) | 1972-02-23 | 1973-02-23 | Glutamic ester polymers and electro-photographic materials comprising them |
Country Status (4)
Country | Link |
---|---|
JP (1) | JPS4888940A (en) |
CA (1) | CA1009794A (en) |
DE (1) | DE2308332C3 (en) |
GB (1) | GB1396838A (en) |
-
1972
- 1972-02-23 JP JP1926072A patent/JPS4888940A/ja active Pending
-
1973
- 1973-02-20 DE DE19732308332 patent/DE2308332C3/en not_active Expired
- 1973-02-22 CA CA164,355A patent/CA1009794A/en not_active Expired
- 1973-02-23 GB GB891673A patent/GB1396838A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
DE2308332A1 (en) | 1973-09-06 |
DE2308332B2 (en) | 1977-11-24 |
DE2365400B2 (en) | 1977-06-02 |
JPS4888940A (en) | 1973-11-21 |
DE2308332C3 (en) | 1978-07-27 |
DE2365400A1 (en) | 1974-10-03 |
CA1009794A (en) | 1977-05-03 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PCNP | Patent ceased through non-payment of renewal fee |