937372-45-7

Basic information

• Product Name: 4-(10-bromoanthracen-9-yl)benzonitrile
• Synonyms: 4-(10-bromoanthracen-9-yl)benzonitrile
• CAS NO: 937372-45-7
• Molecular Formula: C21H12BrN
• Molecular Weight: 358.23068
• Mol File: 937372-45-7.mol
• Article Data: 14

Chemical Properties

• Melting Point: 202 °C
• Appearance: /
• CAS DataBase Reference: 4-(10-bromoanthracen-9-yl)benzonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(10-bromoanthracen-9-yl)benzonitrile(937372-45-7)
• EPA Substance Registry System: 4-(10-bromoanthracen-9-yl)benzonitrile(937372-45-7)

Safety Data

• Hazardous Substances Data: 937372-45-7(Hazardous Substances Data)

Usage

Description

4-(10-Bromoanthracen-9-yl)benzonitrile is a chemical compound with the molecular formula C25H15BrN. It is a derivative of anthracene and benzonitrile, and is often used in the field of organic chemistry. This solid crystalline substance is known for its photophysical and electrochemical properties, making it a versatile compound with various applications in the field of chemistry and materials science.

Uses

Used in Organic Electronic Materials:
4-(10-Bromoanthracen-9-yl)benzonitrile is used as a key component in the development of organic electronic materials for its photophysical and electrochemical properties. It contributes to the advancement of technologies such as organic light-emitting diodes (OLEDs), solar cells, and organic field-effect transistors.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 4-(10-Bromoanthracen-9-yl)benzonitrile is used for its interesting biological activities. Its unique properties make it a promising candidate for the development of new pharmaceutical compounds and therapeutic agents.

Upstream product

• 523-27-3 9,10-Dibromoanthracene 
• 126747-14-6 4-cyanophenylboronic acid 
• 171364-82-2 4-cyanophenylboronic acid pinacol ester 
• 1564-64-3 9-Bromoanthracene 
• 56164-85-3 4-(anthracene-9-yl)benzonitrile 
• 623-00-7 4-bromobenzenecarbonitrile 

Relevant articles and documents

Tuning the excited-state energy of the organic chromophore in bichromophoric systems based on the RuII complexes of tridentate ligands

A series of new heteroleptic and homoleptic RuII complexes containing variously substituted bis(pyridyl)triazine ligands has been prepared and their absorption spectra, redox behaviour and luminescence properties (both in fluid solution at room

Highly efficient deep-blue fluorescence OLEDs with excellent charge balance based on phenanthro[9,10-: D] oxazole-anthracene derivatives

Two blue fluorescent materials, m-PO-ABN and p-PO-ABN, are newly synthesized by controlling the conjugation length based on different linkages of the meta or para position between the phenanthro[9,10-d]oxazole (PO) moiety and anthracene substituted with a cyano group. The two materials emit deep-blue light with a high photoluminescence quantum yield (PLQY) in solution state. Non-doped devices fabricated using m-PO-ABN and p-PO-ABN show the EL peaks at 448 and 460 nm corresponding to the Commission Internationale de L'Eclairage (CIE) coordinates of (0.148, 0.099) and (0.150, 0.164), respectively. The external quantum efficiency (EQE) values of the devices are 5.9% and 5.3% for m-PO-ABN and p-PO-ABN, respectively. Transient EL measurements and optical calculation results reveal that both materials exhibit good charge balance and triplet-triplet annihilation in the devices, which may originate from enhanced bipolar characteristics due to the insertion of PO and cyano moieties.

Blue light organic small molecule based on triplet state-triplet state annihilation mechanism and application thereof

The invention belongs to the field of luminescent materials, and discloses a blue light organic small molecule based on a triplet state-triplet state annihilation mechanism and application thereof. The structural formula of the blue light organic small molecule is shown as P1n, P2n, P3n or P4n. The blue light organic small molecules can still keep high device efficiency under high brightness as alight-emitting layer, can be used for non-doped devices, is beneficial to simplifying the device structure and reducing the device manufacturing cost, and overcomes the problem of serious efficiency roll-off of a metal complex phosphorescent material under high brightness. In addition, the introduction of cyano groups can enhance the interaction between molecules, and is beneficial to improving the efficiency of TTA, thereby further improving the performance of the device.