1415476-89-9

Basic information

• Product Name: 2-(((4-(diphenylamino)phenyl)imino)methyl)phenol
• Synonyms: 2-(((4-(diphenylamino)phenyl)imino)methyl)phenol
• CAS NO: 1415476-89-9
• Molecular Weight: 364.447
• Mol File: 1415476-89-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-(((4-(diphenylamino)phenyl)imino)methyl)phenol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(((4-(diphenylamino)phenyl)imino)methyl)phenol(1415476-89-9)
• EPA Substance Registry System: 2-(((4-(diphenylamino)phenyl)imino)methyl)phenol(1415476-89-9)

Safety Data

• Hazardous Substances Data: 1415476-89-9(Hazardous Substances Data)

Upstream product

• 2350-01-8 4-aminotriphenylamine 
• 90-02-8 salicylaldehyde 

Downstream Products

• 1415476-85-5 C₅₀H₃₈N₄O₂Zn 

Relevant articles and documents

Mechanofluorochromic behaviors of triphenylamine functionalized salicylaldimine difluoroboron complexes

Triphenylamine functionalized salicylaldimine difluoroboron complexes bearing different substituents have been synthesized. The photophysical results showed that these complexes exhibited intramolecular charge transfer (ICT) emission and solvatochromism.

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.