142807-63-4

Basic information

• Product Name: Tris(4-(thiophen-2-yl)phenyl)aMine
• Synonyms: Tris(4-(thiophen-2-yl)phenyl)aMine;Tris[4-(2-thienyl)phenyl]amine;4-thiophen-2-yl-N,N-bis(4-thiophen-2-ylphenyl)aniline
• CAS NO: 142807-63-4
• Molecular Formula: C₃₀H₂₁NS₃
• Molecular Weight: 491.68944
• Mol File: 142807-63-4.mol
• Article Data: 21

Chemical Properties

• Melting Point: 139 °C
• Boiling Point: 670.5±55.0 °C(Predicted)
• Appearance: /
• Density: 1.277±0.06 g/cm3(Predicted)
• PKA: -4.47±0.50(Predicted)
• CAS DataBase Reference: Tris(4-(thiophen-2-yl)phenyl)aMine(CAS DataBase Reference)
• NIST Chemistry Reference: Tris(4-(thiophen-2-yl)phenyl)aMine(142807-63-4)
• EPA Substance Registry System: Tris(4-(thiophen-2-yl)phenyl)aMine(142807-63-4)

Safety Data

• Hazardous Substances Data: 142807-63-4(Hazardous Substances Data)

Usage

General Description

Tris(4-(thiophen-2-yl)phenyl)aMine is a chemical compound made up of three molecules of 4-(thiophen-2-yl)phenylamine. It is a trisubstituted amine with a molecular formula of C63H48N2S3. Tris(4-(thiophen-2-yl)phenyl)aMine is commonly used in the field of organic electronics as a hole transporting material in organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). It exhibits good thermal stability and high charge carrier mobility, making it a valuable material for enhancing the performance of electronic devices. Tris(4-(thiophen-2-yl)phenyl)aMine is known for its high efficiency in facilitating the transport of positive charge carriers in organic semiconductor devices.

Upstream product

• 4181-20-8 tris(4-iodophenyl)amine 
• 193978-23-3 2-thiopheneboronic acid pinacol ester 
• 6165-68-0 thiophene boronic acid 
• 4316-58-9 tri(p-bromophenyl)amine 
• 603-34-9 N,N-diphenylaminobenzene 
• 54663-78-4 tributyl(thien-2-yl)stannane 
• 5713-61-1 thiophen-2-yl magnesium bromide 
• 1003-09-4 2-bromothiophene 

Downstream Products

• 572900-60-8 tris-{4-[5-(4-nitro-phenyl)-thiophen-2-yl]-phenyl}-amine 
• 1379804-23-5 tris (4-(5-iodothiophen-2-yl)phenyl)amine 
• 1273594-75-4 tris-[4-[5-[((4,5-bis(methylthio)-1,3-dithiol-2-ylidene)methyl)]2-thienyl]phenyl]amine 
• 1273594-73-2 [4-((4,5-bis(methylthio)-1,3-dithiol-2-ylidene)methyl)thienyl-phenyl]dithienylphenylamine 
• 883236-47-3 5,5',5''-(4,4',4''-nitrilotris(benzene-4,1-diyl))trithiophene-2-carbaldehyde 
• 1189743-36-9 [4-(5-formyl-2-thienyl)phenyl]-bis[4-(2-thienyl)phenyl]amine 
• 1273594-76-5 [bis[4-(2-thienylformyl)phenyl]mono[4-(2-thienyl)phenyl]]amine 
• 339985-35-2 tris(4-(5-(thiophen-2-yl)thiophen-2-yl)phenyl)amine 
• 572900-58-4 C₄₈H₃₆N₄S₃ 
• 883236-54-2 N,N,N-tris[4-[5-(2,2-dicyanoethen-1-yl)-2-thienyl]phenyl]amine 

Relevant articles and documents

Amorphous molecular materials with high carrier mobilities: Thiophene- and selenophene-containing tris(oligoarylenyl)amines

A novel class of amorphous molecular materials, thiophene-and selenophene-containing tris(oligoarylenyl)amines, were developed. They were found to exhibit high hole drift mobilities greater than 10-2 cm 2V-1s-1 at an electric field of 1.0 × 105 Vcm-1 at 293 K in their amorphous glassy states. These values are of the highest level among those reported for organic disordered systems.

Triphenylamine-thienylenevinylene hybrid systems with internal charge transfer as donor materials for heterojunction solar cells

Star-shaped molecules based on a triphenylamine core derivatized with various combinations of thienylenevinylene conjugated branches and electron-withdrawing indanedione or dicyanovinyl groups have been synthesized. UV-vis absorption and fluorescence emis

Electrochromic properties of organic-inorganic composite materials

A new type of electroactive composite material based on tungsten trioxide (WO3) and poly (tri(4-(2′-thienyl)) phenylamine) (P3TPA) was prepared. Using the WO3/P3TPA as electroactive material, the electrochromic device was fabricated,

Di(p-methoxyphenyl)amine end-capped tri(p-thiophenylphenyl)amine based molecular glasses as hole transporting materials for solid-state dye-sensitized solar cells

Three tris(thienylphenyl)amine-based molecular glass hole transporting materials were synthetized, characterized and incorporated in solid state dye-sensitized solar cells. Devices using these compounds as solid hole conductors show relatively high V

Facile one-pot nanocatalysts encapsulation of palladium-NHC complexes for aqueous Suzuki-Miyaura couplings

Organic transformations using water as the solvent have been the focus of intense investigation. We herein present a strategy that uses simple nanoparticle encapsulation to fabricate water-soluble nanocatalysts (NCs) for aqueous cross-coupling reactions. To achieve this goal, three types of N-heterocyclic carbene (NHC)-palladium (Pd) complexes (i.e., 1b, 2b, and 3b) with the chemical formula [PdL(CH3CN)Cl]PF6 (where L is a bidentate pyridine- or pyrimidine-bearing NHC ligand) have been synthesized, and their structures were characterized by NMR spectroscopy and X-ray crystallography. Exploiting a facile one-pot encapsulation process, the water-insoluble Pd-NHC complexes can be integrated into the hydrophobic cores of micelles composed of an amphiphilic copolymer. These water-dispersed nanoparticles exhibited excellent catalytic activity in aqueous Suzuki-Miyaura couplings. Among these NCs, 3b-NC, bearing a mesityl moiety on its NHC ligand, was found to be the most active catalyst under the tested reaction conditions. More impressively, 3b-NC can be reused for at least five cycles without substantial loss of catalytic activity.

Electrochromic properties of polymers/copolymers via electrochemical polymerization based on star-shaped thiophene derivatives with different central cores

Three star-shaped thiophene derivatives, namely TPAT, PHT and TPTT with different central cores of triphenylamine, phenyl and 2,4,6-triphenyl-1,3,5-triazine respectively, were synthesized and characterized. They were further successfully prepared into the