464216-82-8

Upstream product

• 106-41-2 4-bromo-phenol 
• 67900-64-5 3-(4-Bromophenoxy)-1-propanol 
• 1206195-84-7 (3-(4-bromophenoxy)propoxy)(tert-butyl)dimethylsilane 
• 115587-57-0 (dibenzylidene)acetone 
• 104-94-9 4-methoxy-aniline 
• 145073-42-3 3-(4-iodophenoxy)propan-1-ol 
• 540-38-5 p-Iodophenol 
• 464216-79-3 tert-butyl-[3-(4-iodophenoxy)propoxy]-dimethylsilane 

Downstream Products

• 464216-90-8 3-[4-(4-methoxy{4'-[4-methoxy(3-methylphenyl)anilino][1,1'-biphenyl]-4-yl}anilino)phenoxy]propan-1-ol 
• 433716-28-0 3-[4-(4-methoxy{4'-[4-methoxy(3-methylphenyl)anilino][1,1'-biphenyl]-4-yl}anilino)phenoxy]propyl methacrylate 
• 1206195-86-9 N₁-(4-(3-(tert-butyldimethylsilyloxy)propoxy)phenyl)-N₁,N₄,N₄-tris(4-methoxyphenyl)benzene-1,4-diamine 
• 1206195-87-0 3-(4-((4-(bis(4-methoxyphenyl)amino)phenyl)(4-methoxyphenyl)amino)phenoxy)propan-1-ol 
• 1206195-88-1 3-(4-((4-(bis(4-methoxyphenyl)amino)phenyl)(4-methoxyphenyl)amino)phenoxy)propyl methanesulfonate 
• 1206195-89-2 N₁-(4-(3-bromopropoxy)phenyl)-N₁,N₄,N₄-tris(4-methoxyphenyl)benzene-1,4-diamine 
• 1206195-90-5 diethyl 3-(4-((4-(bis(4-methoxyphenyl)amino)phenyl)(4-methoxyphenyl)amino)phenoxy)propylphosphonate 
• 1206195-91-6 3-(4-((4-(bis(4-methoxyphenyl)amino)phenyl)(4-methoxyphenyl)amino)phenoxy)propylphosphonic acid 

Relevant academic research and scientific papers

For organic electronic device, modified stable electrode having a work function and method

A device including an electrode, the electrode having a surface; a molecule bound to the surface of the electrode through a binding group; an organic electronic material in electrical contact with the electrode, wherein the molecule comprises at least one fluorinated aryl group, wherein the electrode contains a transparent conductive metal oxide, a carbon nanotube, or graphene.

Stable electrodes with modified work functions and methods for organic electronic devices

One embodiment is a method, comprising: depositing a molecule on an electrode, wherein the electrode has a surface and the molecule has a binding group (e.g., an anchoring group) that binds to the surface, thereby providing a work function that is stable for at least 100 hours under ambient conditions.

ELECTRONIC DEVICES COMPRISING NOVEL PHOSPHONIC ACID SURFACE MODIFIERS

In some embodiments, the inventions described herein relate to a composition of matter comprising a molecule having the structure: wherein: independently at each occurrence, R1 is a halogen, a alkyl group, a heteroalkyl group, an aryl group, or a heteroaryl group; R2 comprises from 3 to 30 CH2- groups, n = 0-5, m = 0-5, q = 1-3, and R2 comprises at least one ether linkage

Synthesis of photo-crosslinkable hole-transport polymers with tunable oxidation potentials and their use in organic light-emitting diodes

A series of photo-crosslinkable arylamine-based hole-transport copolymers has been synthesized. The synthetic methodology employed allows for the redox potential of the polymer to be tuned by the incorporation of electron-donating or -withdrawing moieties. Upon exposure to ultraviolet radiation, the polymers become insoluble, as evidenced by UV/Vis absorption spectroscopy, a feature that is useful for the fabrication of multilayer organic light-emitting diodes (OLEDs) by solution processing techniques. OLEDs based on these hole-transport polymers have been fabricated and the performance of the devices has been evaluated. The photo-crosslinking process has been optimized so that it no longer adversely impacts device performance.