1228778-59-3

Usage

Uses

Used in Organic Synthesis:
2-Iodotriphenylene is used as a building block in organic synthesis for the preparation of functionalized triphenylene derivatives. Its unique structure allows for the creation of various compounds with specific properties, making it valuable in the development of new materials and chemical products.
Used in Organic Electronic Devices:
In the field of organic electronics, 2-Iodotriphenylene is utilized in the development of organic light-emitting diodes (OLEDs) and organic photovoltaics. Its properties contribute to the performance and efficiency of these devices, making it an important component in the advancement of organic electronic technology.
Used in Materials Science:
2-Iodotriphenylene's potential application in materials science stems from its unique structure and properties. Researchers are interested in exploring its use in creating new materials with specific characteristics, which could have a wide range of applications in various industries.
Overall, 2-Iodotriphenylene is a versatile chemical compound with a broad range of applications in organic synthesis, organic electronic devices, and materials science, making it a valuable asset in the field of chemistry and materials development.

Upstream product

• 217-59-4 triphenylene 
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• 1073353-89-5 2-(2-fluoro-4-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 583-55-1 1-Bromo-2-iodobenzene 
• 1993-03-9 o-fluorophenylboronic acid 
• 185331-69-5 1-bromo-2-fluoro-4-nitrobenzene 
• 2052-07-5 2-Bromobiphenyl 

Downstream Products

• 1228778-60-6 2-(5-tert-butyl-2-formylphenylethynyl)triphenylene 

Relevant academic research and scientific papers

Intramolecular aryl-aryl coupling: Via C-F bond activation tolerant towards C-I functionality

Herein we report a transition-metal free activation of a particularly stable aromatic carbon-fluorine bond allowing intramolecular aryl-aryl coupling which is orthogonal to carbon-iodine functionality.

NOVEL COMPOUND FOR ORGANIC ELECTROLUMINESCENT DEVICE AND ORGANIC ELECTROLUMINESCENT DEVICE COMPRISING THE SAME

Disclosed are: an organic electroluminescent element compound represented by structural formula 1 or 2 below; and an organic electroluminescent element comprising same. In this way, it is possible to provide an organic electroluminescent element compound which can be used as a host, hole-transport material and electron-transport material that has outstanding electrical stability and electron- and hole-transporting ability, a high level of triplet state energy and is able to improve the light-emitting efficiency of phosphorescent light-emitting materials, and an organic electroluminescent element.

Unusual fluorescene emission from ethynyltriphenylene-substituted diacetylenic molecular hinge. Formation of intramolecular excimer

A diacetylenic molecular hinge bearing two ethynyltriphenylene units (1) has been synthesized. Evidence from 1H NMR and variable temperature NMR (VT-NMR) of 1 in comparison to model compounds bearing only one triphenylene unit suggests that there is an equilibrium between the open conformer and the intramolecularly π-π interacting closed conformer in solution (equilibrium constant K = 6.5 at 298 K in CDCl3) arising from the rotation of the diacetylenic hinge. Unusual fluorescence emission observed from 1 has been assigned to excimer formation arising from intramolecularly π-π interacting triphenylene units in the excited state. Steady state and picosecond time resolved fluorescence spectra of 1 were nearly identical and corresponded to intramolecular excimer emission.

Donor-acceptor substituted phenylethynyltriphenylenes - Excited state intramolecular charge transfer, solvatochromic absorption and fluorescence emission

Several 2-(phenylethynyl)triphenylene derivatives bearing electron donor and acceptor substituents on the phenyl rings have been synthesized. The absorption and fluorescence emission properties of these molecules have been studied in solvents of different