625854-02-6

Basic information

• Product Name: 9-(4-broMophenyl)-10-phenylanthracene
• Synonyms: 9-(4-broMophenyl)-10-phenylanthracene
• CAS NO: 625854-02-6
• Molecular Formula: C₂₆H₁₇Br
• Molecular Weight: 409.31718
• Mol File: 625854-02-6.mol
• Article Data: 28

Chemical Properties

• Melting Point: 225.0 to 229.0 °C
• Boiling Point: 505.4±19.0 °C(Predicted)
• Appearance: /
• Density: 1.344±0.06 g/cm3 (20 ºC 760 Torr)
• Storage Temp.: Sealed in dry,Room Temperature
• Solubility: slightly sol. in Toluene
• CAS DataBase Reference: 9-(4-broMophenyl)-10-phenylanthracene(CAS DataBase Reference)
• NIST Chemistry Reference: 9-(4-broMophenyl)-10-phenylanthracene(625854-02-6)
• EPA Substance Registry System: 9-(4-broMophenyl)-10-phenylanthracene(625854-02-6)

Safety Data

• Hazardous Substances Data: 625854-02-6(Hazardous Substances Data)

Usage

Uses

9-(4-Bromophenyl)-10-phenylanthracene (cas# 625854-02-6) is a useful research chemical.

Upstream product

• 460347-59-5 4,4,5,5-tetramethyl-2-(10-phenylanthracen-9-yl)-1,3,2-dioxaborolane 
• 589-87-7 1,4-bromoiodobenzene 
• 334658-75-2 10-phenylanthracene-9-boronic acid 
• 23674-20-6 9-bromo-10-phenylanthracene 
• 602-55-1 9-phenylanthracene 
• 1564-64-3 9-Bromoanthracene 
• 98-80-6 phenylboronic acid 
• 106-37-6 1.4-dibromobenzene 
• 5467-74-3 4-Bromophenylboronic acid 
• 150712-74-6 9-iodo-10-phenylanthracene 

Downstream Products

• 1165951-96-1 9-phenyl-3-[4-(10-phenylanthracen-9-yl)phenyl]-9H-carbazole 
• 952604-36-3 1-(4-bromonaphthalen-1-yl)-4-(9-phenylanthracen-10-yl)benzene 
• 1062555-45-6 C₆₅H₄₄ 
• 1062555-46-7 C₇₀H₅₀ 
• 1062555-49-0 C₆₅H₄₄ 

Relevant articles and documents

Universal electron transporting layers via mixing two homostructure molecules with different polarities for organic light-emitting diodes

In general, electron transport layer (ETL) in organic light-emtting diodes (OLEDs) consists of single component of electron transporting material (ETM) or a mixture with n-dopant such as 8-hydroxyquinolinolato-lithium (Liq). However, there exists a limit to controlling a wide range of carrier density in OLEDs according to the required characteristics of the devices due to electrically insulating property of Liq. Here, we suggest a universal strategy to construct an efficient ETL. We synthesized two ETMs, diphenyl-[4-(10-phenyl-anthracene-9-yl)-phenyl]-amine (An-Ph) and phneyl-[4-(10-phenyl-anthracene-9-yl)-phenyl]-pyridin-3-yl-amine (An-Py) that have the same core structures with different polarities in functional groups. The electrical characteristics of electron-only-devices (EODs) were investigated by space charge limited current (SCLC) modeling and impedance spectroscopy analysis. Interestingly, the homostructure type ETL composed of An-Ph and An-Py showed not only superior electron transporting capability, but also the possibility of controlling electron injection and transporting in a wide range compared to the heterostructure type ETL of An-Ph and Liq. Compared to the An-Ph-only EOD, the electron mobility in 75% An-Py-mixed homostructure EOD increased by almost 4 orders of magnitude. Such dramatic variation of electron mobility was achieved thanks to the molecular design strategy to separate charge injection and charge transport regions within a molecule, which consequently induced the giant surface potential (GSP) effect between the ETL/cathode interface. As a result, the external quantum efficiency (EQE) of blue fluorescent and phosphorescent OLEDs with the homostructure ETLs was enhanced by 28.6% and 34%, respectively, compared to that of each control device without manipulating outcoupling effects.

ANTHRACENE MATERIALS, ORGANIC LIGHT EMITTING DIODES, AND METHOD FOR MANUFACTURING ANTHRACENE MATERIALS

An anthracene material, an organic light emitting diode using the same, and a method for manufacturing the same, are provided. The organic light emitting diode includes a substrate, a first conducting layer, a hole transport layer, a light emitting layer, an electron transport layer, and a second conducting layer. The first conducting layer is disposed on the substrate. The hole transport layer is disposed on the first conducting layer. The light emitting layer having the anthracene material is disposed on the hole transport layer. The electron transport layer is disposed on the light emitting layer. The second conducting layer is disposed on the electron transport layer.

Novel anthracene derivatives and organic light-emitting diode therewith

The present invention relates to an anthracene derivative represented by chemical formula A, and an organic light-emitting device including the same. In the chemical formula A, R_1- R_10, L, M, and n are the same as defined in the present specification. According to the present invention, the organic light-emitting device including the compound in light-emitting layers exhibits long lifespan and high efficiency compared to existing organic light-emitting devices.COPYRIGHT KIPO 2018