1153-85-1

Usage

Uses

Used in the Manufacturing of OLED Materials:
3-Bromo-9-phenylcarbazole is used as a key component in the production of organic light-emitting diode (OLED) materials. Its electronic and photophysical properties contribute to the efficient performance and emission characteristics of OLED devices, making it an essential material for the development of advanced display and lighting technologies.
Used as an Intermediate in Pharmaceutical Synthesis:
3-Bromo-9-phenylcarbazole also serves as an intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows for further chemical modifications and functionalization, enabling the development of new drugs with potential therapeutic applications in the medical field.

InChI:InChI=1/C18H12BrN/c19-13-10-11-18-16(12-13)15-8-4-5-9-17(15)20(18)14-6-2-1-3-7-14/h1-12H

Upstream product

• 1150-62-5 N-phenylcarbazole 
• 128-08-5 N-Bromosuccinimide 
• 61613-22-7 2-bromodiphenylamine 
• 122-39-4 diphenylamine 
• 1592-95-6 3-bromo-9H-carbazole 
• 100-63-0 phenylhydrazine 
• 3460-18-2 1,4-dibromo-2-nitrobenzene 
• 106-37-6 1.4-dibromobenzene 
• 4630-20-0 3-Methyl-9H-carbazole 
• 591-50-4 iodobenzene 
• 108-86-1 bromobenzene 
• 343864-78-8 4-bromo-2-iodo-1-nitrobenzene 
• 98-80-6 phenylboronic acid 
• 105971-15-1 5-bromo-2-nitro-biphenyl 

Downstream Products

• 894791-43-6 (N-phenyl)-N-(9-phenyl-9H-carbazole-3-yl)amine 
• 854952-58-2 N-phenyl-9H-carbazol-3-boronic acid 
• 1592-95-6 3-bromo-9H-carbazole 
• 1126522-69-7 9-phenyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolane-2-yl)-9H-carbazole 
• 1365452-27-2 3-[4-(naphthalen-1-yl)phenyl]-9-phenyl-9H-carbazole 
• 1060735-14-9 9-phenyl-3,3'-bicarbazole 
• 1028647-93-9 3-(4-bromophenyl)-9-phenyl-9H-carbazole 

Relevant academic research and scientific papers

Pyridyl Pyrrolide Boron Complexes: The Facile Generation of Thermally Activated Delayed Fluorescence and Preparation of Organic Light-Emitting Diodes

The electron positive boron atom usually does not contribute to the frontier orbitals for several lower-lying electronic transitions, and thus is ideal to serve as a hub for the spiro linker of light-emitting molecules, such that the electron donor (HOMO)

Novel bifluorene based conjugated systems: Synthesis and properties

A series of novel bifluorene based systems was synthesised by a convergent approach by means of a Suzuki cross-coupling between 7,7′-bis-(4,4,5,5- tetramethyl-[1,3,2]dioxaborolan-2-yl)-9,9,9′,9′-tetraoctyl-2, 2′-bifluorene and suitable aryl-bromides. All

Efficient thermally activated delayed fluorescence of functional phenylpyridinato boron complexes and high performance organic light-emitting diodes

A new series of functional phenylpyridinato boron complexes possessing thermally activated delayed fluorescence (TADF) has been strategically designed and synthesized. These boron complexes utilize phenylpyridine as the electron acceptor (A) that links to carbazole or triphenyl amine as the electron donor (D) via a core boron atom, forming four-coordinate neutral boron complexes. The selection of boron to spatially separate the donor and acceptor takes advantage of facile functionalization. The TADF properties of the resulting D-A functional materials in various solvents have been investigated via their emission spectra and associated relaxation dynamics. The results show that the operation of TADF is strongly solvent polarity dependent in fluid states, and several underlying mechanisms are discussed. OLEDs fabricated by fppyBTPA and dfppyBTPA show EL efficiencies of up to (20.2%, 63.9 cd A?1, 66.9 lm W?1) and (26.6%, 88.2 cd A?1, 81.5 lm W?1), respectively, in which a nearly 27% EQE for the dfppyBTPA device is among the most efficient TADF OLEDs so far.

Imidazolyl-Phenylcarbazole-Based Host Materials and Their Use for Co-host Designs in Phosphorescent OLEDs

In recent years, owing to the demand for high-efficiency phosphorescent organic light-emitting devices (PhOLEDs), many studies have been conducted on the development of bipolar host materials. A series of imidazolyl-phenylcarbazole-based host materials, i

Method for synthesizing high-purity 3-bromine-N-phenylcarbazole

The invention discloses a method for synthesizing high-purity 3-bromo-N-phenylcarbazole, and belongs to the technical field of chemistry. The method comprises the following steps: dissolving N-phenylcarbazole in a solvent, sequentially adding a brominatin

Amine-based compound and organic light emitting diode comprising the same

Disclosed are an amine-based compound and an organic light emitting device including the same. The amine-based compound is represented by chemical formula 1A.

Preparation method of 3 - bromo - N - phenyl carbazole

The invention relates to a preparation method of 3 -bromo - N -phenyl carbazole, and belongs to the technical field of organic chemistry. To the invention, diphenylamine serves as a starting raw material, and 2 -bromophenylaniline is obtained through bromination reaction. Then, intramolecular cyclization is carried out to obtain carbazole. Then, 3 - bromocarbazole is obtained by bromination reaction. Finally, a substituted 3 - bromo - N -phenyl carbazole is obtained. By controlling the concentration and reaction environment of the reactants, the selectivity of the reaction site is effectively improved, the used raw materials are simple and easy to obtain, the preparation period is relatively short, and the reaction process is simple and easy to control.

Thiophene ethylene malononitrile structural compound and preparation method thereof

The invention discloses a thiophene ethylene malononitrile structural compound and a preparation method thereof. The structural formula is shown in the specification. The thiophene ethylene malononitrile structural compound is obtained through multi-step

Nitrogen-containing compound, electronic element and electronic device

The invention belongs to the technical field of organic materials, and provides a nitrogen-containing compound represented by a chemical formula 1, an electronic element and an electronic device. Thenitrogen-containing compound can improve the performance of an electronic element.

Aromatic compound and organoelectroluminescent device comprising the compound

The present invention relates to an aromatic compound and an organic electroluminescent device including the same. The aromatic compound is represented by chemical formula 1, and the organic electroluminescent device is excellent in driving voltage, luminous efficiency and lifetime characteristics.