GB1211595A - Electrophotographic materials - Google Patents
Electrophotographic materialsInfo
- Publication number
- GB1211595A GB1211595A GB31647/68A GB3164768A GB1211595A GB 1211595 A GB1211595 A GB 1211595A GB 31647/68 A GB31647/68 A GB 31647/68A GB 3164768 A GB3164768 A GB 3164768A GB 1211595 A GB1211595 A GB 1211595A
- Authority
- GB
- United Kingdom
- Prior art keywords
- diethylaminophenyl
- bis
- diethyl
- stannane
- dimethyl
- 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
- -1 dimethyl aminophenyl stannane Chemical compound 0.000 abstract 5
- 229910000080 stannane Inorganic materials 0.000 abstract 4
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N N-phenyl amine Natural products NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 abstract 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 3
- KXCAEQNNTZANTK-UHFFFAOYSA-N stannane Chemical compound [SnH4] KXCAEQNNTZANTK-UHFFFAOYSA-N 0.000 abstract 3
- CSTAZLXYCJWOBB-UHFFFAOYSA-N C1=CC(N(CC)CC)=CC=C1P(=O)C1=CC=C(N(CC)CC)C=C1 Chemical compound C1=CC(N(CC)CC)=CC=C1P(=O)C1=CC=C(N(CC)CC)C=C1 CSTAZLXYCJWOBB-UHFFFAOYSA-N 0.000 abstract 2
- GGSUCNLOZRCGPQ-UHFFFAOYSA-N diethylaniline Chemical compound CCN(CC)C1=CC=CC=C1 GGSUCNLOZRCGPQ-UHFFFAOYSA-N 0.000 abstract 2
- 229910000078 germane Inorganic materials 0.000 abstract 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 abstract 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 229910000081 plumbane Inorganic materials 0.000 abstract 2
- JZMNMYXSCROWHQ-UHFFFAOYSA-N 3-ethylaniline Chemical compound [CH2]CC1=CC=CC(N)=C1 JZMNMYXSCROWHQ-UHFFFAOYSA-N 0.000 abstract 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 abstract 1
- 239000007818 Grignard reagent Substances 0.000 abstract 1
- 150000001448 anilines Chemical class 0.000 abstract 1
- 229910052785 arsenic Inorganic materials 0.000 abstract 1
- 235000010290 biphenyl Nutrition 0.000 abstract 1
- 239000004305 biphenyl Substances 0.000 abstract 1
- 125000006267 biphenyl group Chemical group 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 229910052732 germanium Inorganic materials 0.000 abstract 1
- 150000004795 grignard reagents Chemical class 0.000 abstract 1
- 229910052745 lead Inorganic materials 0.000 abstract 1
- 150000002641 lithium Chemical class 0.000 abstract 1
- 229910052751 metal Inorganic materials 0.000 abstract 1
- 239000002184 metal Substances 0.000 abstract 1
- 150000004045 organic chlorine compounds Chemical class 0.000 abstract 1
- 125000002524 organometallic group Chemical group 0.000 abstract 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 abstract 1
- XRCKXJLUPOKIPF-UHFFFAOYSA-N plumbane Chemical compound [PbH4] XRCKXJLUPOKIPF-UHFFFAOYSA-N 0.000 abstract 1
- 125000000382 plumbyl group Chemical group [H][Pb]([H])([H])* 0.000 abstract 1
- 239000011541 reaction mixture Substances 0.000 abstract 1
- 235000011121 sodium hydroxide Nutrition 0.000 abstract 1
- 125000003638 stannyl group Chemical group [H][Sn]([H])([H])* 0.000 abstract 1
- 229910052718 tin Inorganic materials 0.000 abstract 1
- 150000004992 toluidines Chemical class 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
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
- 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, 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Photoreceptors In Electrophotography (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
1,211,595. Bis - (p - diethylaminophenyl) phosphine oxide; organometallic derivatives. EASTMAN KODAK CO. 3 July, 1968 [3 July, 1967], No. 31647/68. Headings C2C and C2J. [Also in Division H1] Bis - (p - diethylaminophenyl) phosphine oxide is prepared by the reaction of PCl 3 and N,N-diethyl aniline on a steam bath. The reaction mixture is poured into water, made alkaline with caustic soda and the compound extracted and crystallized. N,N-Dialkylaminoaryl derivatives of Sn, Pb, As or Ge are prepared by reacting the appropriately substituted aniline or toluidine as a lithium derivative, Grignard reagent or the aniline itself with the chloride or organochloride of the metal. In specific embodiments triphenylp-diethyl or dimethyl aminophenyl stannane, tetrabis-p-diethyl plumbane or germane, tris-pp-dimethyl or diethyl aminophenyl arsine, 2 - methyl - 4 - dimethyl aminophenylarsine oxide, and methyl or phenyl tris-(p-diethylaminophenyl) stannane are prepared. Triphenyl-p-diethylaminophenyl germane or plumbane, diphenyl bis-(p-diethylaminophenyl) stannane,p-diethyl aminophenyl or methyl bis-pdiethylaminophenyl) tris-p-diethylaminophenybismuthine, bis - [phenyl - (p - diethylaminophenyl)] dibismuthine, bis - (p - diethylaminophenyl) thioxotm and tetrabis-[diphenyl-(pdiethylaminophenyl) plumbyl or stannyl] methane or stannane are also mentioned.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US65066467A | 1967-07-03 | 1967-07-03 | |
| US15416371A | 1971-06-17 | 1971-06-17 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1211595A true GB1211595A (en) | 1970-11-11 |
Family
ID=26851210
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB31647/68A Expired GB1211595A (en) | 1967-07-03 | 1968-07-03 | Electrophotographic materials |
Country Status (5)
| Country | Link |
|---|---|
| US (2) | US3647429A (en) |
| BE (1) | BE717265A (en) |
| CH (1) | CH492240A (en) |
| FR (1) | FR1596481A (en) |
| GB (1) | GB1211595A (en) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4123268A (en) * | 1977-06-22 | 1978-10-31 | Addressograph-Multigraph Corporation | Boron chelates as acceptor type sensitizers for photoconductive polymers |
| US4491626A (en) * | 1982-03-31 | 1985-01-01 | Minolta Camera Kabushiki Kaisha | Photosensitive member |
| JPS58189643A (en) * | 1982-03-31 | 1983-11-05 | Minolta Camera Co Ltd | Photoreceptor |
| FR2630442B1 (en) * | 1988-04-20 | 1990-09-07 | Rhone Poulenc Chimie | ORGANOSILICY COMPOUNDS, MATERIALS AND ELECTROOPTIC DEVICES CONTAINING THEM |
| US5151204A (en) * | 1990-02-01 | 1992-09-29 | Exxon Chemical Patents Inc. | Oleaginous compositions containing novel ethylene alpha-olefin polymer viscosity index improver additive |
| US5187310A (en) * | 1990-03-14 | 1993-02-16 | Kao Corporation | Organic silicon compound, method of its production, and photoreceptor for electrophotography incorporating it |
| US5300185A (en) * | 1991-03-29 | 1994-04-05 | Kabushiki Kaisha Toshiba | Method of manufacturing III-V group compound semiconductor |
| US5712360A (en) * | 1995-11-06 | 1998-01-27 | Dow Corning Asia, Ltd. | Method of manufacturing a cohydrolyzed polysiloxane charge transporting material |
| US9885971B2 (en) * | 2015-06-26 | 2018-02-06 | Canon Kabushiki Kaisha | Charging member, process cartridge, and electrophotographic image forming apparatus |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2189417A (en) * | 1937-09-30 | 1940-02-06 | Goodrich Co B F | Antioxidant |
| US2331833A (en) * | 1940-05-21 | 1943-10-12 | Parke Davis & Co | Organic arsenic compounds |
| US2340938A (en) * | 1940-11-30 | 1944-02-08 | Standard Oil Dev Co | Stabilized high molecular weight hydrocarbon polymer |
| US2409291A (en) * | 1942-05-19 | 1946-10-15 | Squibb & Sons Inc | Chemotherapeutic sulfanilamide derivatives |
| US2690435A (en) * | 1949-04-04 | 1954-09-28 | Firestone Tire & Rubber Co | Protection of rubber by stannous complex |
| US2701812A (en) * | 1951-06-26 | 1955-02-08 | Dainippon Pharmaceutical Co | Diarylarsenious acid derivatives and the preparation thereof |
| US2779738A (en) * | 1953-05-06 | 1957-01-29 | Tidewater Oil Company | Oxidation-inhibited mineral oil compositions |
| US2762821A (en) * | 1953-07-06 | 1956-09-11 | Salsbury S Lab Dr | Organotin arsonate derivatives |
| US3079414A (en) * | 1959-09-18 | 1963-02-26 | Tamborski Christ | Method of preparing heterocyclic compounds containing metals or metalloids |
| US3247281A (en) * | 1961-09-27 | 1966-04-19 | Union Carbide Corp | Water repellent compositions containing water soluble aminosilanes and aminosilicones as curing catalysts and process for treating substrates therewith |
| DE1252060B (en) * | 1961-10-23 | |||
| US3344070A (en) * | 1964-03-09 | 1967-09-26 | Dow Corning | High temperature lubricants |
| SE311281B (en) * | 1962-08-01 | 1969-06-02 | Rank Xerox Ltd | |
| US3220878A (en) * | 1962-10-08 | 1965-11-30 | Union Carbide Corp | Wear- and stain-resistant coated articles |
| US3340286A (en) * | 1964-03-09 | 1967-09-05 | Dow Corning | p-diethylaminophenyl silanes |
-
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 GB GB31647/68A patent/GB1211595A/en not_active Expired
- 1968-07-03 CH CH991368A patent/CH492240A/en not_active IP Right Cessation
-
1971
- 1971-06-17 US US00154163A patent/US3719486A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| CH492240A (en) | 1970-06-15 |
| DE1772775B2 (en) | 1972-10-12 |
| US3719486A (en) | 1973-03-06 |
| US3647429A (en) | 1972-03-07 |
| DE1772775A1 (en) | 1970-09-03 |
| FR1596481A (en) | 1970-06-22 |
| BE717265A (en) | 1968-12-27 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| GB1211595A (en) | Electrophotographic materials | |
| ES8105694A1 (en) | Propenylamines, processes for their production, pharmaceutical compositions containing them and their use as pharmaceuticals. | |
| GB1450200A (en) | Development inhibitor-yielding thioethers for silver halide photography | |
| GB935698A (en) | Improvements in colour photographic development | |
| GB1257286A (en) | ||
| GB1347079A (en) | Process for the preparation of a pyrazolone derivative | |
| GB754628A (en) | Photographic silver halide emulsions containing colour couplers | |
| GB1164095A (en) | A Method of Preparing Photographic Light-Sensitive Elements | |
| GB803187A (en) | Production of dye images using 3-ª‡-sulfo acylamino pyrazolone color formers in which the acyl group contains a long aliphatic chain | |
| GB1130685A (en) | Benzaldoxime derivatives | |
| GB1268889A (en) | Photoconductive material for electrophotography | |
| GB1530527A (en) | Method of processing photographic silver dye bleach materials | |
| GB1395779A (en) | Hemioxonal dyes and process for their production | |
| GB635120A (en) | Cyan azo-coupling component for diazotype color process | |
| GB1471399A (en) | Sulphonamides | |
| GB1528308A (en) | Method for preparing tri(beta-substituted phenethyl)tin halides | |
| GB1360939A (en) | Silver dye bleach process | |
| GB1284282A (en) | Photographic element containing a developing agent precursor | |
| GB1227550A (en) | ||
| JPS5323631A (en) | Supplement method of photo developer | |
| GB1184767A (en) | Process for the Preparation of Alkylthionophosphonic Acid Dichlorides | |
| GB861134A (en) | Improvement in the manufacture of antistatic photographic films | |
| GB902266A (en) | Method of incorporating salts of color couplers in photographic emulsions | |
| JPS5565952A (en) | Color image formation method | |
| GB1207530A (en) | Improved photographic silver halide colour emulsion |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| PCNP | Patent ceased through non-payment of renewal fee |