GB1446966A - Ambipolar photoconductive composition and imaging method - Google Patents
Ambipolar photoconductive composition and imaging methodInfo
- Publication number
- GB1446966A GB1446966A GB776274A GB776274A GB1446966A GB 1446966 A GB1446966 A GB 1446966A GB 776274 A GB776274 A GB 776274A GB 776274 A GB776274 A GB 776274A GB 1446966 A GB1446966 A GB 1446966A
- Authority
- GB
- United Kingdom
- Prior art keywords
- dimethylene
- anthracene
- coated
- compounds
- cyclo
- 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
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L65/00—Compositions of macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain; Compositions of derivatives of such polymers
-
- 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
- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/02—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes
-
- 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
- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/12—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Photoreceptors In Electrophotography (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
Abstract
1446966 Photoconductive polymers XEROX CORP 20 Feb 1974 [20 Feb 1973] 7762/74 Heading C3R [Also in Division G2] Photoconductive material is obtained by polymerizing in situ in a host polymer a cyclic compound of formula where Ar is a polyaromatic radical derived from naphthalene, anthracene, pyrene or carbazole, X and Y are halogen atoms or nitro, amino, alkyl, phenyl, phenoxy, alkoxy, carboxy, hydroxyl or ester radicals, and m and n are 0 or integers. The cyclic compound is mixed with the host polymer and polymerized by heating at above 180 C. Compounds which are electron donors or acceptors may be added to the composition as sensitizers; dyestuff sensitizers also may be included. The material is coated on a conductive substrate which is electrically charged, the coated substrate is exposed to a pattern of light and shadow so that the surface charge is selectively dissipated and the latent image is developed or is transferred to another surface and then developed. In examples cyclobis - (anthracene - 9,10 - dimethylene) is polymerized by heating while mixed with polystyrene, polyethylene, polyvinylchloride, styrene / acrylate copolymer, styrene / butadiene block copolymer and poly-(1-vinylnaphthalene); the photoconductive material so-obtained is coated on aluminium plates, a positive electrical charge is applied and then the plates are exposed to light. Other cyclic compounds mentioned are cyclo - bis - (naphthalene - 1,4 - dimethylene) and cyclo - bis - (anthracene - 9,10- dimethylene) compounds substituted in the 1-position by bromine, chlorine, amino, nitro and methyl.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US333849A US3879198A (en) | 1973-02-20 | 1973-02-20 | Electrophotographic ambipolar photoconductive composition and imaging method |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1446966A true GB1446966A (en) | 1976-08-18 |
Family
ID=23304524
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB776274A Expired GB1446966A (en) | 1973-02-20 | 1974-02-20 | Ambipolar photoconductive composition and imaging method |
Country Status (8)
Country | Link |
---|---|
US (1) | US3879198A (en) |
JP (1) | JPS5230298B2 (en) |
BR (1) | BR7401250D0 (en) |
CA (1) | CA1023189A (en) |
DE (1) | DE2408175C3 (en) |
FR (1) | FR2218583B1 (en) |
GB (1) | GB1446966A (en) |
NL (1) | NL7402352A (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63152462U (en) * | 1987-03-26 | 1988-10-06 | ||
US5494765A (en) * | 1993-01-14 | 1996-02-27 | Mita Industrial Co. Ltd | Electrophotosensitive material using a phenylenediamine derivative |
DE69413367T2 (en) * | 1993-12-27 | 1999-02-04 | Hitachi Chemical Co Ltd | Composition for making a charge transport layer, and electrophotographic element |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3548059A (en) * | 1965-12-16 | 1970-12-15 | Matsushita Electric Ind Co Ltd | 9,10-disubstituted anthracenes for use as photoconductors |
US3684506A (en) * | 1967-01-30 | 1972-08-15 | Anthony J Guarnaccio | Dimeric poly-n-vinyl carbazole organic photoconductor and photoconductive elements embodying same |
US3740218A (en) * | 1971-06-01 | 1973-06-19 | Eastman Kodak Co | Photoconductive elements containing complexes of lewis acids and formaldehyde resins |
-
1973
- 1973-02-20 US US333849A patent/US3879198A/en not_active Expired - Lifetime
-
1974
- 1974-01-11 CA CA189,926A patent/CA1023189A/en not_active Expired
- 1974-01-30 FR FR7403086A patent/FR2218583B1/fr not_active Expired
- 1974-02-13 JP JP49017506A patent/JPS5230298B2/ja not_active Expired
- 1974-02-20 NL NL7402352A patent/NL7402352A/xx unknown
- 1974-02-20 DE DE2408175A patent/DE2408175C3/en not_active Expired
- 1974-02-20 BR BR741250A patent/BR7401250D0/en unknown
- 1974-02-20 GB GB776274A patent/GB1446966A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
NL7402352A (en) | 1974-08-22 |
JPS49115135A (en) | 1974-11-02 |
FR2218583A1 (en) | 1974-09-13 |
JPS5230298B2 (en) | 1977-08-06 |
DE2408175A1 (en) | 1974-08-22 |
BR7401250D0 (en) | 1974-11-19 |
US3879198A (en) | 1975-04-22 |
DE2408175B2 (en) | 1977-10-13 |
FR2218583B1 (en) | 1976-11-26 |
CA1023189A (en) | 1977-12-27 |
DE2408175C3 (en) | 1978-05-24 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed [section 19, patents act 1949] | ||
PCNP | Patent ceased through non-payment of renewal fee |