1415476-90-2

Basic information

• Product Name: 1-(((4-(diphenylamino)phenyl)imino)methyl)naphthalen-2-ol
• Synonyms: 1-(((4-(diphenylamino)phenyl)imino)methyl)naphthalen-2-ol
• CAS NO: 1415476-90-2
• Molecular Weight: 414.506
• Mol File: 1415476-90-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-(((4-(diphenylamino)phenyl)imino)methyl)naphthalen-2-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(((4-(diphenylamino)phenyl)imino)methyl)naphthalen-2-ol(1415476-90-2)
• EPA Substance Registry System: 1-(((4-(diphenylamino)phenyl)imino)methyl)naphthalen-2-ol(1415476-90-2)

Safety Data

• Hazardous Substances Data: 1415476-90-2(Hazardous Substances Data)

Upstream product

• 2350-01-8 4-aminotriphenylamine 
• 708-06-5 2-hydroxynaphthalene-1-carbaldehyde 

Downstream Products

• 1415476-86-6 C₅₈H₄₂N₄O₂Zn 

Relevant articles and documents

A novel class of Zn(II) Schiff base complexes with aggregation-induced emission enhancement (AIEE) properties: Synthesis, characterization and photophysical/electrochemical properties

A series of novel Zn(II) Schiff base complexes with diphenylamino and carbazole groups that exhibited aggregation-induced emission enhancement were designed and synthesized. The properties of four complexes were investigated by UV-Vis absorption and fluorescence emission spectroscopy, cyclic voltammetry and density functional theory calculations. The fluorescence intensities of the four dyes are weak in tetrahydrofuran, but become strong in a mixture of water/tetrahydrofuran (v/v = 9/1). This work constitutes the first observation of this phenomenon for Zn(II) Schiff base complexes. A simple model complex, without the possibility of intramolecular rotational motion, was prepared in order to determine the mechanism of the AIEE. The present aggregation-induced emission enhancement was attributed to restricted intramolecular rotational motions in the solid by carefully analyzing the difference in molecular structure and photophysical properties amongst the new complexes.