1231948-43-8

Basic information

• Product Name: N-phenyl-4-((trimethylsilyl)ethynyl)-N-(4-((trimethylsilyl)ethynyl)phenyl)aniline
• Synonyms: N-phenyl-4-((trimethylsilyl)ethynyl)-N-(4-((trimethylsilyl)ethynyl)phenyl)aniline
• CAS NO: 1231948-43-8
• Molecular Weight: 437.732
• Mol File: 1231948-43-8.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: N-phenyl-4-((trimethylsilyl)ethynyl)-N-(4-((trimethylsilyl)ethynyl)phenyl)aniline(CAS DataBase Reference)
• NIST Chemistry Reference: N-phenyl-4-((trimethylsilyl)ethynyl)-N-(4-((trimethylsilyl)ethynyl)phenyl)aniline(1231948-43-8)
• EPA Substance Registry System: N-phenyl-4-((trimethylsilyl)ethynyl)-N-(4-((trimethylsilyl)ethynyl)phenyl)aniline(1231948-43-8)

Safety Data

• Hazardous Substances Data: 1231948-43-8(Hazardous Substances Data)

Upstream product

• 81090-53-1 N,N-bis(4-bromophenyl)aniline 
• 1066-54-2 trimethylsilylacetylene 
• 603-34-9 N,N-diphenylaminobenzene 
• 218909-60-5 4-iodo-N-(4-iodophenyl)-N-phenylbenzenamine 

Relevant articles and documents

Aggregation-Induced Emission of Platinum(II) Metallacycles and Their Ability to Detect Nitroaromatics

Two new acceptors containing platinum-carbazole (1) and platinum-triphenylamine (2) backbones with bite angles of 90° and 120°, respectively, have been synthesised and characterised. Reactions of the rigid acceptor 1 with linear dipyridyl-based donors (3 and 4) generated [4+4] self-assembled molecular squares (5 and 6), and similar treatments with acceptor 2 instead of 1 yielded [6+6] self-assembled molecular hexagons (7 and 8). The metallacycles were characterised by multinuclear NMR spectroscopy (1H and 31P) and ESI-MS. The geometries of the metallacycles were optimised by using the PM6 method. When aggregates of the metallacycles were formed by adding hexane solutions in dichloromethane, aggregation-induced emission was observed for metallacycles 5 and 7, and aggregation-caused quenching was observed for metallacycles 6 and 8. The formation of aggregates was verified by dynamic light scattering and TEM analyses. Macrocycles 5 and 7 are white-light emitters in THF. Moreover, their high luminescence in both solution and the solid state was utilised for the recognition of nitroaromatic explosives.

Multistep oxidation of diethynyl oligophenylamine-bridged diruthenium and diiron complexes

Homo-dinuclear nonlinear complexes [{M(dppe)-Cp?}2{μ-(-C=C)2X}] (dppe = 1,2-bis(diphenylphosphino) ethane; Cp? = η5-C5Me5; X = triphenylamine (TPA), M = Ru (1a) and Fe (1b); X =

Synthesis, photophysical, electrochemical, and DSSC application of novel donor-acceptor triazole bridged dendrimers with a triphenylamine core and benzoheterazole as a surface unit

Triazole bridged novel donor-acceptor dendrimers with triphenylamine as the core and benzoheterazole as the surface unit have been synthesized by click chemistry via a convergent approach. All the dendrimers exhibited excellent optical and electrochemical