382137-78-2

Usage

Uses

Used in Organic Chemistry Research:
5'-(4-cyanophenyl)-[1,1':3',1''-terphenyl]-4,4''-dicarbonitrile is used as a research compound for studying its unique structural properties and potential applications in the field of organic chemistry. Its symmetrical and rigid structure provides insights into molecular interactions and reactions.
Used in Material Science:
In the field of material science, 5'-(4-cyanophenyl)-[1,1':3',1''-terphenyl]-4,4''-dicarbonitrile is used as a building block for the synthesis of novel organic materials. Its structural characteristics make it a promising candidate for the development of advanced materials with specific properties.
Used in Pharmaceutical Research:
5'-(4-cyanophenyl)-[1,1':3',1''-terphenyl]-4,4''-dicarbonitrile is utilized as a starting material or intermediate in the synthesis of new drugs. Its unique structure and functional groups offer potential for the development of pharmaceutical agents with novel therapeutic properties.
Used in Molecular Electronics:
5'-(4-cyanophenyl)-[1,1':3',1''-terphenyl]-4,4''-dicarbonitrile is employed as a component in the study of molecular electronics. Its rigid and symmetrical structure allows for the exploration of its electronic properties and potential use in molecular-scale electronic devices.

Upstream product

• 7511-49-1 1,3,5-tris(4-bromophenyl)benzene 
• 99-90-1 para-bromoacetophenone 
• 151417-38-8 1,3,5-tris(4-iodophenyl)benzene 
• 626-39-1 1,3,5-trisbromobenzene 
• 126747-14-6 4-cyanophenylboronic acid 

Downstream Products

• 227099-60-7 1,3,5-tris(4-benzoylphenyl)benzene 

Relevant academic research and scientific papers

A rod-packing microporous hydrogen-bonded organic framework for highly selective separation of C2H2/CO2at room temperature

Self-assembly of a trigonal building subunit with diaminotriazines (DAT) functional groups leads to a unique rod-packing 3D microporous hydrogen-bonded organic framework (HOF-3). This material shows permanent porosity and demonstrates highly selective sep

Electrical and electrochemical properties of lithium solvated electron solutions derived from 1,3,5-triphenylbenzenes

A series of 1,3,5-triphenylbenzenes (TPBs) bearing various substituents have been made and their ability to form lithium solvated electron solutions (LiSESs) in tetrahydrofuran (THF) solution have been studied. It was found that the TPBs bearing electron

Intermolecular coupling and intramolecular cyclization of aryl nitriles on Au(111)

The on-surface dimerization reaction of an organic nitrile on Au(111) is reported. The formation of the product, which contains five newly formed σ-bonds and a diazapyrene core structure, was investigated and characterized by scanning tunneling microscopy. Experimental and computational studies of reference compounds support our findings.

Microporous, tetraarylethylene-based polymer networks generated in a reductive polyolefination process

Microporous Polymer Networks (MPNs) that contain aggregate-induced emission (AIE) active tetraphenylethylene (TPE) or other tetraarylethylene units have been generated in a reductive polyolefination process starting from four different tris(α,α-dichlorobenzyl)arene derivatives with dicobalt octacarbonyl or chromium(ii)acetate as reductive olefination agents. Microporosity with moderately high BET surface areas up to 500 m2 g-1 could be combined with high solid state photoluminescence quantum yields up to 25.3% for polymer network P4. This unique combination should be promising for applications as optical solid state sensors, especially for MPNs with electron-deficient triazine core units.