64005-84-1

Basic information

• Product Name: Benzo[lmn][3,8]phenanthroline-1,3,6,8(2H,7H)-tetrone,2,7-bis(4-methoxyphenyl)-
• CAS NO: 64005-84-1
• Molecular Formula: C₂₈H₁₈N₂O₆
• Molecular Weight: 478.46
• Mol File: 64005-84-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzo[lmn][3,8]phenanthroline-1,3,6,8(2H,7H)-tetrone,2,7-bis(4-methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzo[lmn][3,8]phenanthroline-1,3,6,8(2H,7H)-tetrone,2,7-bis(4-methoxyphenyl)-(64005-84-1)
• EPA Substance Registry System: Benzo[lmn][3,8]phenanthroline-1,3,6,8(2H,7H)-tetrone,2,7-bis(4-methoxyphenyl)-(64005-84-1)

Safety Data

• Hazard Codes: A poison.:
• Safety Statements: x." target="_blank">A poison by intraperitoneal route. When heated to decomposition it emits toxic vapors of NOx.:
• Hazardous Substances Data: 64005-84-1(Hazardous Substances Data)

Upstream product

• 81-30-1 1,4,5,8-naphthalenetetracarboxylic dianhydride 
• 104-94-9 4-methoxy-aniline 

Relevant articles and documents

Pure organic room-temperature phosphorescent material, preparation method thereof and application thereof

The invention provides a pure organic room-temperature phosphorescent material with a structure as shown in formula (I) or formula (II), and also provides a preparation method for the pure organic room-temperature phosphorescent material with the structure as shown in formula (I) or formula (II). The invention discloses a series of pure organic room-temperature phosphorescent materials based on a naphthalimide derivative. The pure organic room-temperature phosphorescent materials are characterized in that pure organic electron-donating groups are introduced into molecules, so that the molecules are excited by an outside light source to generate a charge transfer state (ICT) in the molecules, and ICT can promote intersystem crossing, so that generation of room-temperature phosphorescence is facilitated. The pure organic phosphorescent material provided by the invention has the advantages of being simple and convenient to synthesize, low in cost, easy to chemically modify, low in toxicity, environmentally friendly and the like.

Electronically regulated thermally and light-gated electron transfer from anions to naphthalenediimides

Anion-induced electron transfer (ET) to π-electron-deficient naphthalenediimides (NDIs) can be channeled through two distinct pathways by adjusting the Lewis basicity of the anion and the π-acidity of the NDI: (1) When the anion and NDI are a strong elect