99372-95-9

Upstream product

• 113705-11-6 9,10-diiodoanthracene 
• 244205-40-1 (2-bromophenyl)boronic acid 
• 1062586-08-6 9,10-bis(2-bromophenyl)-9,10-dihydroanthracene-9,10-diol 
• 583-53-9 2,3-dibromobenzene 
• 120-12-7 anthracene 

Downstream Products

• 872965-11-2 9,10-bis[2-(trimethylsilyl)phenyl]anthracene 
• 1163157-71-8 9,10-bis{2-[(pentafluorophenyl)dimethylsilyl]phenyl}anthracene 
• 1163157-72-9 9,10-bis[2-(dimethylphenylsilyl)phenyl]anthracene 
• 914306-84-6 9,10-bis(phenyl-2-boronic acid pinacol ester)anthracene 

Relevant academic research and scientific papers

ORGANIC ELECTROLUMINESCENT DEVICE AND BORIC ACID AND BORINIC ACID DERIVATIVES USED THEREIN

The present invention relates to the use of aromatic boronic acid or borinic acid derivatives in organic electronic devices, in particular electroluminescent devices.

THIAZOLE SYSTEM ORGANIC ELECTROLUMINESCENT COMPOUNDS AND ORGANIC LIGHT EMITTING DIODE USING THE SAME

The present invention relates to novel thiazole system organic electroluminescent compounds and organic light emitting diodes comprising the same. Since the thiazole system organic electroluminescent compounds according to the invention have good luminous efficiency and life property, OLED's having very good operation lifetime can be produced.

Intense solid-state blue emission with a small Stokes' shift: π-stacking protection of the diphenylanthracene skeleton

Intense blue emissions with a small Stokes' shift both in solution and in the solid state were attained by introducing (pentafluorophenyl)dimethylsilyl groups to a 9,10-diphenylanthracene skeleton as the π-stacking tethers. The Royal Society of Chemistry

Novel Materials For Organic Electroluminescent Devices

The present invention relates to novel materials which can be used in organic electronic devices, in particular electroluminescent devices, and are derivatives of fused aromatic systems.

PHOTOCHEMICAL VS. ELECTROCHEMICAL ELECTRON-TRANSFER REACTIONS. ONE-ELECTRON REDUCTION OF ARYL HALIDES BY PHOTOEXCITED ANION RADICALS.

Electrochemical reduction of aryl halides generally leads to expulsion of halide ion.The product aryl radical is unavoidably further reduced.In contrast, reduction of aryl halides by photoexcited anion radicals may be stopped at the aryl radical stage owing to the bimolecular nature of electron-transfer reactions.We have tested this hypothesis by photoinducing electron-transfer from anthraquinone anion radical to several aryl halides.For each halide it was possible to trap the corresponding radical by anthracene forming substituted 9-phenylanthracenes.