1369779-87-2

Upstream product

• 1172630-54-4 N,N'-2,6-diisopropylphenyl-1,12-dichloroperylene diimide 
• 1369779-85-0 N,N'-di(n-octyl)-2-(tri-n-butylstannyl)naphthalene-1,4,5,8-tetracarboxylic acid diimide 

Relevant academic research and scientific papers

Hybrid rylene arrays via combination of stille coupling and C-H transformation as high-performance electron transport materials

Hybrid rylene arrays have been prepared via a combination of Stille coupling and C-H transformation. The ability to extend the π system along the equatorial axis of rylenes not only leads to broadened light absorption but also increases the electron affinity, which can facilitate electron injection and transport with ambient stability.

REACTION PRODUCTS OF STANNYL DERIVATIVES OF NAPHTHALENE DIIMIDES WITH RYLENE COMPOUNDS

NDI-tin compounds are reacted with rylene compounds to form NDI-rylene compounds. The rylene compounds can be perylene compounds. The NDI-rylene compounds can be used in organic electronic devices including in a field-effect transistor.