1138331-98-2

Usage

Chemical class

Organic compounds known as triphenylenes

Molecular structure

Polycyclic aromatic hydrocarbon with two flourene units and a benzene ring

Primary use

Building block in the synthesis of functional materials

Applications

Organic semiconductors, light-emitting diodes, organic electronics, optoelectronic devices, molecular scaffold for advanced materials

Additional potential applications

Organic photovoltaics, organic light-emitting transistors

Stability

High thermal and chemical stability

Electron-rich nature

Contributes to its potential in various applications

Upstream product

• 106-37-6 1.4-dibromobenzene 
• 789-24-2 9-Phenylfluorene 

Relevant academic research and scientific papers

Pure aromatic hydrocarbons with rigid and bulky substituents as bipolar hosts for blue phosphorescent OLEDs

Four pure hydrocarbon molecules of 1,3,5-tris(9-phenyl-9H-fluoren-9-yl)benzene (mTPFB), 4,4′-bis(9-phenyl-9H-fluoren-9-yl)biphenyl (pDPFBP), 1,4-bis(9-phenyl-9H-fluoren-9-yl)benzene (pDPFB) and 1,3-bis(9-phenyl-9H-fluoren-9-yl)benzene (mDPFB), with differ

Palladium-catalyzed direct arylation of C-H bond to construct quaternary carbon centers: The synthesis of diarylfluorene

A novel Pd-catalyzed C-H functionalization reaction was developed to construct a quaternary carbon center with high yield. This reaction provides an efficient method for the synthesis of 9,9′-diarylfluorenes by direct arylation of monoarylfluorene.