Eureka AIR delivers breakthrough ideas for toughest innovation challenges, trusted by R&D personnel around the world.

Electrophotographic photosensitive member

An electrophotographic and photoreceptor technology, applied in optics, electrographics, instruments, etc., can solve problems such as difficulty in exerting sensitivity characteristics, and achieve the effect of excellent sensitivity characteristics

Inactive Publication Date: 2015-05-06
KYOCERA DOCUMENT SOLUTIONS INC
View PDF4 Cites 3 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] Here, in general, there is a problem that it is difficult to exhibit sufficient sensitivity characteristics when using an electron transport agent in a material contained in an organic photoreceptor.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Electrophotographic photosensitive member
  • Electrophotographic photosensitive member
  • Electrophotographic photosensitive member

Examples

Experimental program
Comparison scheme
Effect test

Synthetic example 1

[0080] The naphthalene diimide derivative represented by the following general formula (1-2) was synthesize|combined according to the following reaction scheme 3.

[0081] [Electron Transport Agent (ETM-1)]

[0082] [chemical formula 8]

[0083]

[0084] [Reaction Equation 3]

[0085] [chemical formula 9]

[0086]

[0087] In reaction equation 3 (a-2), compound (A-12) 0.875g (1mmol), 2-bromoanisole 0.812g (4mmol), tetrakis (triphenylphosphine) palladium 58mg (0.05mmol) and iodine A toluene solution of 19 mg (0.1 mmol) of cuprous chloride was stirred under reflux for 10 hours under a nitrogen atmosphere at a temperature of 110° C. to obtain a reaction solution.

[0088] The toluene solvent in the obtained reaction solution was distilled off and purified by column chromatography to obtain 0.6 g of compound (A-22) (yield: 85%).

[0089] In the reaction equation 3 (b-2), the solution of compound (A-22) 0.708g (1mmol), acetic acid 10ml and chloroform 10ml is cooled with i...

Synthetic example 2

[0094] The naphthalene diimide derivative represented by the following general formula (1-3) was synthesize|combined according to the following reaction scheme 4.

[0095] [Electron Transport Agent (ETM-2)]

[0096] [chemical formula 10]

[0097]

[0098] [Reaction Equation 4]

[0099] [chemical formula 11]

[0100]

[0101] In reaction equation 4 (a-3), compound (A-13) 0.78g (1mmol), 2-bromoanisole 0.81g (4mmol), tetrakis (triphenylphosphine) palladium 58mg (0.05mmol) and iodine A toluene solution of 19 mg (0.1 mmol) of cuprous chloride was stirred under reflux for 10 hours under a nitrogen atmosphere at a temperature of 110° C. to obtain a reaction solution.

[0102] The toluene solvent in the obtained reaction solution was distilled off and purified by column chromatography to obtain 0.49 g of compound (A-23) (yield: 80%).

[0103] Next, in reaction equation 4 (b-3), the solution of compound (A-23) 0.61g (1mmol), acetic acid 10ml and chloroform 10ml was cooled wit...

Synthetic example 3

[0107] The naphthalene diimide derivative represented by the following general formula (1-4) was synthesize|combined according to the following reaction scheme 5.

[0108] [Electron Transport Agent (ETM-3)]

[0109] [chemical formula 12]

[0110]

[0111] [Reaction Equation 5]

[0112] [chemical formula 13]

[0113]

[0114] In reaction equation 5 (a-4), compound (A-14) 1.17g (1mmol), 2-bromoanisole 1.62g (4mmol), tetrakis (triphenylphosphine) palladium 58mg (0.05mmol) and iodine A toluene solution of 19 mg (0.1 mmol) of cuprous chloride was stirred under reflux for 10 hours under a nitrogen atmosphere at a temperature of 110° C. to obtain a reaction solution.

[0115] The toluene solvent in the obtained reaction solution was distilled off, followed by purification by column chromatography to obtain 0.66 g of compound (A-24) (yield: 80%).

[0116] Then, in the reaction equation 5 (b-4), the solution of compound (A-24) 0.83g, acetic acid 10ml and chloroform 10ml was c...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

An electrophotographic photosensitive member includes a photosensitive layer containing a naphthalenediimide derivative represented by the following formula (1) or (2). In the formula (1) or (2), R 1 represents an alkyl group having 1 to 10 carbon atoms, an aryl group having 6 to 12 carbon atoms and optionally having an alkyl group having 1 to 10 carbon atoms, an aralkyl group having 7 to 12 carbon atoms, a cycloalkyl group having 3 to 10 carbon atoms, or an alkoxy group having 1 to 6 carbon atoms.

Description

technical field [0001] The present invention relates to an electrophotographic photoreceptor. Background technique [0002] As an electrophotographic photoreceptor included in an image forming apparatus or the like, an organic photoreceptor including a binder resin, a charge generating agent, a hole transporting agent as a charge transporting agent, an electron transporting agent, and the like is known. Compared with inorganic photoreceptors using inorganic materials such as amorphous silicon, such an organic photoreceptor is easy to manufacture, and has the advantage of a high degree of freedom in structural design because the choice of photoreceptor materials can be diversified. [0003] Furthermore, in order for an image forming apparatus using an organic photoreceptor to be able to form a high-quality image, materials contained in the organic photoreceptor in the electrophotographic photoreceptor are required to have sufficient sensitivity characteristics. [0004] Here...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(China)
IPC IPC(8): G03G5/04
CPCG03G5/0629G03G5/065G03G5/0651G03G5/0659
Inventor 冈田英树
Owner KYOCERA DOCUMENT SOLUTIONS INC
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Eureka Blog
Learn More
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com