109745-46-2

Upstream product

• 108-70-3 1,3,5-trichlorobenzene 
• 105633-27-0 tris(2,4,6-trichlorophenyl)methane 

Downstream Products

• 881917-50-6 [4-(N-carbazolyl)-2,6-dichlorophenyl]bis(2,4,6-trichlorophenyl)methane 
• 881917-48-2 (4-(N-carbazolyl)-2,6-dichlorophenyl)bis(2,4,6-trichlorophenyl)methyl radical 
• 955094-70-9 [2,6-dichloro-4-(3,6-diethyl-N-carbazolyl)phenyl]bis(2,4,6-trichlorophenyl)methane 
• 105633-27-0 tris(2,4,6-trichlorophenyl)methane 
• 955094-67-4 [2,6-dichloro-4-(3,6-dimethoxy-N-carbazolyl)phenyl]bis(2,4,6-trichlorophenyl)methane 
• 955094-68-5 [2,6-dichloro-4-(3,6-dibromo-N-carbazolyl)phenyl]bis(2,4,6-trichlorophenyl)methane 
• 955094-69-6 [2,6-dichloro-4-(3,6-dicyano-N-carbazolyl)phenyl]bis(2,4,6-trichlorophenyl)methane 
• 1018803-41-2 bis[4-(N-carbazolyl)-2,6-dichlorophenyl](2,4,6-trichlorophenyl)methane 
• 1018803-45-6 tris[4-(N-carbazolyl)-2,6-dichlorophenyl]methane 
• 1050673-43-2 [4-(N-indolyl)-2,6-dichlorophenyl]bis(2,4,6-trichlorophenyl)methane 
• 1018803-11-6 bis[4-(N-carbazolyl)-2,6-dichlorophenyl](2,4,6-trichlorophenyl)methyl 

Relevant academic research and scientific papers

Chemical Modification toward Long Spin Lifetimes in Organic Conjugated Radicals

Organic semiconductors for spin-based devices require long spin relaxation times. Understanding their spin relaxation mechanisms is critical to organic spintronic devices and applications for quantum information processing. However, reports on the spin re

Solution-processed organic light-emitting diodes with emission from a doublet exciton; using (2,4,6-trichlorophenyl)methyl as emitter

Neutral-π radical based open shell molecules foster new potential in light emitting diodes because of their theoretical near-equity quantum efficiencies. In this study, we report organic light emitting diodes (OLEDs) based on a novel open shell molecule (

A pure red organic light-emitting diode based on a luminescent derivative of tris(2,4,6-trichlorotriphenyl)methyl radical

A novel derivative of Tris(2,4,6-trichlorotriphenyl)methyl radical was synthesized and used as the emitter of an organic light-emitting diode. Stable electroluminescent (EL) spectra at the full-range driving voltages and pure red color were obtained throu

Organic light-emitting diodes using a neutral π radical as emitter: The emission from a doublet

Abstract Triplet harvesting is a main challenge in organic light-emitting devices (OLEDs), because the radiative decay of the triplet is spin-forbidden. Here, we propose a new kind of OLED, in which an organic open-shell molecule, (4-N-carbazolyl-2,6-dich

Inert Carbon Free Radicals. 8. Polychlorotriphenylmethyl Radicals. Synthesis, Structure, and Spin-Density Distribution

Some symmetrical Ar3C. and unsymmetrical (C6Cl5)3-xArxC. radicals with different chlorine substitution patterns (X = 1,2; Ar: 2H-C6HCl4, 3H,5H-C6H2Cl4, 4H-C6HCl4, C6H5) are prepared.X-ray crystal structures for