1311405-84-1

Basic information

• Product Name: 1,7-bis[4-(diphenylamino)phenyl] N,N'-2-ethylhexyl perylene bisimide
• Synonyms: 1,7-bis[4-(diphenylamino)phenyl] N,N'-2-ethylhexyl perylene bisimide
• CAS NO: 1311405-84-1
• Molecular Weight: 1101.4
• Mol File: 1311405-84-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1,7-bis[4-(diphenylamino)phenyl] N,N'-2-ethylhexyl perylene bisimide(CAS DataBase Reference)
• NIST Chemistry Reference: 1,7-bis[4-(diphenylamino)phenyl] N,N'-2-ethylhexyl perylene bisimide(1311405-84-1)
• EPA Substance Registry System: 1,7-bis[4-(diphenylamino)phenyl] N,N'-2-ethylhexyl perylene bisimide(1311405-84-1)

Safety Data

• Hazardous Substances Data: 1311405-84-1(Hazardous Substances Data)

Upstream product

• 267221-88-5 4-(diphenylamino)phenylboronic pinacol ester 
• 851786-15-7 N,N'-di(2-ethylhexyl)-1,7-dibromoperylene-3,4,9,10-bisdicarboximide 
• 118129-60-5 1,7-dibromoperylene-3,4,9,10-tetracarboxylic dianhydride 
• 128-69-8 perylene-3,4,9,10-tetracarboxylic acid 3,4:9,10-dianhydride 
• 201802-67-7 4-(diphenylamino)phenyl boronic acid 

Relevant articles and documents

Air stable electron-transporting and ambipolar bay substituted perylene bisimides

Four new perylene bisimides containing carbazolyl and triphenylamino electron-donor groups in the bay region have been designed, synthesized and characterized. The materials possess high thermal stability and form uniform films. They display a wide absorption window extending to the near infrared region of the spectrum and demonstrate efficient photoinduced intramolecular electron transfer. Ionization potential values of these perylene bisimide derivatives measured by photoelectron spectroscopy range from 5.8 eV to 6 eV. Charge-transporting properties were investigated by the xerographic time of flight (XTOF) technique. Complementary ambipolar charge-transport was observed in differently linked carbazolyl substituted perylene bisimides while the triphenylamino substituted material exhibited competent electron drift mobility (>10-3 cm2 V-1 cm-1) under ambient conditions. Density functional theory (DFT) calculations were performed for carbazolyl bay substituted perylene bisimides in order to understand the complementary ambipolar charge transport as well as the difference in the optical properties.