467238-86-4

Upstream product

• 1202-34-2 di(pyridin-2-yl)amine 
• 106-37-6 1.4-dibromobenzene 
• 589-87-7 1,4-bromoiodobenzene 

Downstream Products

• 467238-88-6 (4-(2,2'-dipyridylamino)phenyl)acetylene 
• 467238-91-1 4,4'-(2,2'-dipyridylamino)diphenylacetylene 
• 497144-91-9 p-(2,2'-dipyridylamino)phenylboronic acid 
• 684243-09-2 p-(2,2'-dipyridylamino)-2-thienylbenzene 
• 792909-36-5 dipyridin-2-yl-(4-trimethylstannylphenyl)amine 
• 1173901-92-2 10-[4-(dipyridyn-2-yl-amino)phenyl]-10-hydroxyanthracen-9-one 
• 1356391-11-1 N-(pyridin-2-yl)-N-(4-(thiophen-3-yl)phenyl)pyridin-2-amine 
• 1373316-49-4 N,N'-(4,4'-(1H,1'H-2,2'-biimidazole-1,1'-diyl)bis(4,1-phenylene))bis(N-(pyridin-2-yl)pyridin-2-amine) 

Relevant academic research and scientific papers

Crystallographic characterization of dipyridylamine derivatives

Dipyridylamine has been coupled with phenyl groups to yield new organic ligands. During the course of one reaction a lithium salt of dipyridylamine was isolated as the product. These new compounds were characterized by single crystal X-ray diffraction, wh

NEW ANTHRACENE DERIVATIVES AND ORGANIC ELECTRONIC DEVICE USING THE SAME

The present invention relates to a novel anthracene derivative and an organic electronic device using the same. The organic electronic device according to the present invention shows excellent characteristics in efficiency, driving voltage, and life time.

Synthesis of new dipyridylphenylaminosiloles for highly emissive organic electroluminescent devices

High-performance organic electroluminescent devices based on two new siloles, 1,1-dimethyl-2,5-bis(p-2,2′-dipyridylaminophenyl)silole (5) and 1,1-dimethyl-2,5-bis(p-2,2′-dipyridylaminophenyl)-3,4-diphenylsilole (8), acting as both electron- and hole-transporting material, are described. The best performance is attained with silole 8, which displays a luminescence of 10 4 Cd m-2 at 10 V for a current density of less than 0.2 A cm-2, which is as efficient as tris(8-hydroxyquinoline)aluminium (Alq3), one of the best candidates for electroluminescent materials under the same conditions.

Syntheses and photophysical properties of rigid-rod conjugated compounds based on N-7-azaindole and 2,2′-dipyridylamine

Rigid-rod conjugated compounds based on N-7-azaindole and 2,2′-dipyridylamine functional groups have been synthesized as potential compounds for molecular electronic devices via Pd-mediated Sonogashira couplings. Their photoluminescent properties have been investigated.