150712-74-6

Upstream product

• 23674-20-6 9-bromo-10-phenylanthracene 
• 2232-12-4 1,3-Diiodo-5,5-dimethyl-2,4-imidazolidinedione 
• 602-55-1 9-phenylanthracene 
• 5467-74-3 4-Bromophenylboronic acid 
• 98-80-6 phenylboronic acid 
• 1564-64-3 9-Bromoanthracene 

Downstream Products

• 625854-02-6 9-(4-bromophenyl)-10-phenylanthracene 
• 63018-93-9 9-(naphthalen-1-yl)-10-phenylanthracene 
• 294881-19-9 9-(4'-bromo-[1,1'-biphenyl]-4-yl)-10-phenylanthracene 

Relevant academic research and scientific papers

Radical Cation-Nucleophile Combination Reactions. Displacement of Halogen during Ipso Attack on Haloanthracene Radical Cations

Second-order rate constants for the reactions of radical cations of a number of haloanthracenes with pyridine and 2-substituted pyridines were determined in acetonitrile and dichloromethane using electrochemical techniques.Attack at the ipso positions was

Phenanthridine Derivatives and organic light-emitting diode including the same

PURPOSE: A phenanthridine derivative compound is provided to obatin an organic light emitting diode with excellent light emitting property. CONSTITUTION: A phenanthridine derivative compound is denoted by chemical formula 1 or 2. An organic light emitting diode contains an anode, a cathode, and the phenanthridine derivative compounds inserted between the anode and cathode. The organic light emitting diode further contains a hole injection layer, a hole transport layer, an electron blocking layer, a hole blocking layer, an electron transport layer, or an electron injection layer formed by monomer deposition or solution process.

Org. compd.

To provide a novel anthracene derivative which exhibit blue to blue green light emission, provide a light-emitting element which emits blue to blue green light, provide a light-emitting element which emits blue to blue green light with a long lifetime, and provide a light-emitting element which emits blue to blue green light with high emission efficiency, an anthracene derivative represented by General Formula (G1) is provided. In addition, a light-emitting element which emits blue to blue green light can be obtained by using the anthracene derivatives represented by General Formula (G1). Further, a light-emitting element which emits blue to blue green light with high emission efficiency and/or high reliability can be obtained by using the anthracene derivatives represented by General Formula (G1).

Composition, method for manufacturing thin film, and method for manufacturing light-emitting element

It is an object to provide a composition in which an anthracene derivative is dissolved and a technique in which a thin film that has a favorable film quality is formed by a wet process using the composition. In addition, it is another object to manufacture a highly reliable light-emitting element using the composition at low cost with high productivity. A composition having a solvent and an anthracene derivative having one anthracene structure and one carbazolyl group which is bonded to the anthracene structure directly or through a phenyl group is formed. A thin film with a favorable film quality can be formed by a wet process using the composition. Accordingly, a highly reliable light-emitting element can be manufactured using such a thin film.

Anthracene Derivative, Material for Light-Emitting Element, Light-Emitting Element, Light-Emitting Device, and Electronic Appliance

An anthracene derivative represented by general formula (1) is provided. In the formula, Ar1, Ar3, Ar5, and Ar6 independently represent an aryl group having 6 to 13 carbon atoms, Ar2 and Ar4 independently represent an arylene group having 6 to 13 carbon atoms, and R1 to R8 independently represent hydrogen or an alkyl group having 1 to 4 carbon atoms. Ar1 to Ar6 may independently have a substituent. When Ar1 to Ar6 independently have two or more substituents, the substituents may be bonded to each other to form a ring. When a carbon atom of Ar1 to Ar6 has two substituents, the substituents may be bonded to each other to form a spiro ring.

ORGANIC COMPOUND, ANTHRACENE DERIVATIVE, AND LIGHT-EMITTING ELEMENTS, LIGHT-EMITTING DEVICES, ELECTRONIC DEVICES, AND LIGHTING DEVICES USING THE ANTHRACENE DERIVATIVE

To provide a novel anthracene derivative which exhibit blue to blue green light emission, provide a light-emitting element which emits blue to blue green light, provide a light-emitting element which emits blue to blue green light with a long lifetime, and provide a light-emitting element which emits blue to blue green light with high emission efficiency, an anthracene derivative represented by General Formula (G1) is provided. In addition, a light-emitting element which emits blue to blue green light can be obtained by using the anthracene derivatives represented by General Formula (G1). Further, a light-emitting element which emits blue to blue green light with high emission efficiency and/or high reliability can be obtained by using the anthracene derivatives represented by General Formula (G1).

ANTHRACENE DERIVATIVE AND LIGHT-EMITTING DEVICES, ELECTRONIC DEVICES, AND LIGHTING DEVICE USING THE ANTHRACENE DERIVATIVE

An anthracene derivative is disclosed, and a light-emitting element, a light-emitting device, an electronic device, and a lighting device using the anthracene derivatives are demonstrated. The structure of the anthracene derivative is described in detail in the specification. The use of the anthracene derivative enables the production of a blue emissive light-emitting element having high emission efficiency, excellent purity of emission color, and a long lifetime, which contributes to the production of a high-performance light-emitting device, electronic device, and lighting device.

AROMATIC AMINE COMPOUND, AND LIGHT-EMITTING ELEMENT, LIGHT-EMITTING DEVICE, AND ELECTRONIC APPLIANCE USING THE AROMATIC AMINE COMPOUND

An object of the present invention is to provide a novel aromatic amine compound, and a light-emitting element, a light-emitting device, and an electronic appliance with high luminous efficiency. An aromatic amine compound expressed by General Formula (1) and a light-emitting element, a light-emitting device, and an electronic appliance formed using the aromatic amine compound expressed by General Formula (1) are provided. By the use of the aromatic amine compound expressed by General Formula (1), the light-emitting element, the light-emitting device, and the electronic appliance can have high luminous efficiency.

Method of Synthesizing 9-Aryl-10-Iodoanthracene Derivative and Light-Emitting Material

A method of efficiently synthesizing 9-aryl-10-iodoanthracene from 9-arylanthracene by a simple procedure is provided. By mixing an iodinating agent that is a substance having a structure of an amide group in which nitrogen of the amide group and iodine are directly bonded to each other, an acid, and 9-arylanthracene, iodine is introduced into the 10-position of 9-arylanthracene, whereby 9-aryl-10-iodoanthracene can be synthesized.

ANTHRACENE DERIVATIVE, AND LIGHT-EMITTING MATERIAL, LIGHT-EMITTING ELEMENT, LIGHT-EMITTING DEVICE, AND ELECTRONIC DEVICE USING THE SAME

Novel anthracene derivatives, novel materials capable of blue light emission with high color purity, and a light-emitting element, a light-emitting device, and an electronic device using any of the novel materials. The anthracene derivative represented by general formula (1) is provided. With the anthracene derivative, a light-emitting element with high emission efficiency can be provided. With the anthracene derivative, a light-emitting element emitting blue light with high color purity can be provided. In the formula, A1 represents a substituted or unsubstituted phenyl group, B1 represents any of an alkyl group having 1 to 4 carbon atoms or a substituted or unsubstituted phenyl group, α represents any of a substituted or unsubstituted phenylene group or a substituted or unsubstituted biphenyl-4,4′-diyl group, and R1 to R9 individually represent any of hydrogen, an alkyl group having 1 to 4 carbon atoms, or a substituted or unsubstituted phenyl group.