1228632-34-5

Basic information

• Product Name: 1-phenyl-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-phenanthro[9,10-d]imidazole
• Synonyms: 1-phenyl-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-phenanthro[9,10-d]imidazole
• CAS NO: 1228632-34-5
• Molecular Weight: 496.416
• Mol File: 1228632-34-5.mol
• Article Data: 26

Chemical Properties

• CAS DataBase Reference: 1-phenyl-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-phenanthro[9,10-d]imidazole(CAS DataBase Reference)
• NIST Chemistry Reference: 1-phenyl-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-phenanthro[9,10-d]imidazole(1228632-34-5)
• EPA Substance Registry System: 1-phenyl-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-phenanthro[9,10-d]imidazole(1228632-34-5)

Safety Data

• Hazardous Substances Data: 1228632-34-5(Hazardous Substances Data)

Usage

Molecular structure

The compound consists of a phenanthroimidazole core with a phenyl and dioxaborolane group attached.

Aromatic and boron-containing functional groups

The compound contains multiple aromatic rings and a boron-containing functional group, which contribute to its unique properties.

Application in materials science

Due to its unique electronic and photophysical properties, as well as high photoluminescence efficiency, the compound has significant potential for use in the development of OLEDs (organic light-emitting diodes) and other electronic devices.

Intricate structure

The compound's complex structure makes it a subject of interest for researchers in the fields of organic chemistry and materials science.

High photoluminescence efficiency

The compound exhibits high photoluminescence efficiency, which is crucial for its potential applications in electronic devices.

Electronic properties

The unique electronic properties of the compound, such as its ability to emit light when an electric current is applied, make it suitable for use in various electronic devices, including OLEDs.

Photophysical properties

The compound's photophysical properties, including its ability to absorb and emit light, contribute to its potential applications in electronic devices and materials science.

Upstream product

• 1147081-43-3 2-(4-bromophenyl)-1-phenyl-1H-phenanthro- [9,10-d]imidazole 
• 73183-34-3 bis(pinacol)diborane 
• 61676-62-8 2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 36951-28-7 2-(4-chloro-phenyl)-1-phenyl-1H-phenanthro[9,10-d]imidazole 
• 104-88-1 4-chlorobenzaldehyde 
• 1122-91-4 4-bromo-benzaldehyde 
• 62-53-3 aniline 
• 84-11-7 9,10-phenanthrenequinone 

Downstream Products

• 1197177-29-9 1-phenyl-2-(4'-(triphenylsilyl)-(1,1'-biphenyl)-4-yl)-1H-phenanthro[9,10-d]imidazole 
• 1579955-06-8 2-(4’-((4-(9H-carbazol-9-yl)phenyl)diphenylsilyl)-(1,1’-biphenyl)-4-yl)-1-phenyl-1H-phenanthro[9,10-d]imidazole 
• 1579955-07-9 2-(4’-((4-(9H-[3,9’-bicarbazol]-9-yl)phenyl)diphenylsilyl)-(1,1’-biphenyl)-4-yl)-1-phenyl-1H-phenanthro[9,10-d]imidazole 
• 1197175-44-2 2-(4-(10-(naphthalen-2-yl)anthracen-9-yl)phenyl)-1-phenyl-1H-phenanthro[9,10-d]imidazole 

Relevant articles and documents

Method for separating halogenated impurities from organic light-emitting material

The invention discloses a method for separating halogenated impurities from an organic light-emitting material. The method comprises the steps: carrying out Suzuki reaction by utilizing halide, coupling with a boric acid ester raw material with an amino-containing side chain, and converting halogenated impurities into a compound containing an amino polar group; and furthermore, ionizing the compound containing the amino polar group by acid, so as to dissolve the compound in strong polar solvents such as alcohol and the like to realize remarkable solubility difference with an organic light-emitting material, and thus obtaining material purification. According to the method, the halogenated impurities in the organic light-emitting material are converted into the compound containing the amino polar groups, efficient separation can be achieved by well utilizing the solubility difference between the compound containing the amino polar groups and the organic light-emitting material, and then the purity of the organic light-emitting material is improved. According to the method, the halogenated impurities are removed in a targeted manner, the negative influence of halogen on an organic light-emitting device can be eliminated, the device efficiency is greatly improved, and the service life is greatly prolonged.

Green light compound based on dibenzophenazine, preparation method and device thereof

The invention belongs to the technical field of photoelectric display devices, and particularly relates to a green light compound based on dibenzophenazine, a preparation method and a device thereof. The invention provides the green light compound based o

Pyridoimidazole derivatives as well as preparation method and application thereof

The invention discloses pyridoimidazole derivatives as well as a preparation method and application thereof. The pyridoimidazole derivatives with two D-pi-A structures are synthesized on the basis that pyridoimidazole serves as an electron acceptor system by means of the electron donating property of phenanthroimidazole/diphenylamine. The pyridoimidazole derivatives can serve as photoinitiators, and the two photoinitiators both have longer conjugated chain lengths, so that the photon absorption cross section is increased, the photoinitiators can initiate polymerization reaction at the wavelength of 365 nm, have higher polymerization efficiency, and can be widely applied to the field of ultraviolet curing.