339985-36-3

Usage

Uses

Used in Organic Synthesis:
Tris[4-(5-bromothiophen-2-yl)phenyl]amine is used as a building block in various organic synthesis reactions. Its versatile structure allows for the creation of a wide range of organic compounds with different functional groups and properties.
Used in Organic Electronics:
Tris[4-(5-bromothiophen-2-yl)phenyl]amine is used as a component in the development of materials for organic electronics. Its unique structure and properties make it suitable for use in the design of organic semiconductors, which are essential for the fabrication of electronic devices such as organic light-emitting diodes (OLEDs), organic field-effect transistors (OFETs), and organic photovoltaics (OPVs).
Used in Optoelectronics:
Tris[4-(5-bromothiophen-2-yl)phenyl]amine is used as a component in the development of materials for optoelectronic applications. Its unique structure and properties make it suitable for use in the design of organic materials with specific optical and electronic properties, which are essential for the fabrication of optoelectronic devices such as photodetectors, solar cells, and optical sensors.
Used in Research:
Tris[4-(5-bromothiophen-2-yl)phenyl]amine is used as a research compound for studying the properties and behavior of organic materials. Its unique structure and properties make it an interesting subject for research in the fields of organic chemistry, materials science, and nanotechnology.

Upstream product

• 603-34-9 N,N-diphenylaminobenzene 
• 4316-58-9 tri(p-bromophenyl)amine 
• 6165-68-0 thiophene boronic acid 
• 142807-63-4 tris(4-(thiophen-2-yl)phenyl)amine 

Downstream Products

• 339985-35-2 tris(4-(5-(thiophen-2-yl)thiophen-2-yl)phenyl)amine 
• 1447089-15-7 tris(4-(5-(4,4’-dimethoxydiphenylaminyl)-2-thiophenyl)phenyl)amine 

Relevant academic research and scientific papers

Star-shaped Pd(II) and Pt(II) complexes containing C3-symmetric conjugated thiophenes: Synthesis, characterization, and chemical reactions with organic unsaturated molecules

Triple oxidative addition reactions of [M0(styrene)(PMe3)2] (M = Pd/Pt) with C3-symmetric star-shaped molecules containing 1-, 3-, and 5-thiophene-substituted benzene, in 1:0.3 ratio, afforded new Pd(II) and Pt(II) trinuclear complexes in suitable yields. Analogous trinuclear complexes were formed by similar reactions of thiophenyl halide derivatives containing triazine or triphenylamine cores. Alternatively, a trinuclear Pd(II) complex was obtained by oxidative addition of a Pd(0) complex (synthesized from allyl(cyclopentadienyl) palladium(II), [(η5-C5H5)Pd(η3-C3H5)] with PEt3. Sonogashira-type coupling between trinuclear Pt(II) halides (containing C3-symmetric conjugated thiophenes) and alkynes, in the presence of cuprous halide and diethylamine, afforded alkynyl-containing trinuclear Pt(II) complexes with extended π-conjugation. Insertion reactions of organic isocyanides (CN-R) with trinuclear Pd(II) complexes yielded trinuclear Pd(II) imidoyl complexes by insertion of CN-R into Pd-carbon (thiophene) bonds. Reactions of trinuclear Pt(II) halides with Ag(OCOCF3) and NaN3 formed pseudohalogen-containing Pt(II) complexes.

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

Platinum-acetylide polymers with higher dimensionality for organic solar cells

A new series of platinum(II)-acetylide polymers P1-P3 containing thiophene-triarylamine chromophores of different dimensions were synthesized and their electronic band structures, field-effect charge transport, and application in bulk heterojunction solar

New star-shaped molecules derived from thieno[3,2-b]thiophene unit and triphenylamine

A series of new substituted triphenylamine (TPA) derivatives with alkyl thieno[3,2-b]thiophene and thiophene units were synthesized in a combinatorial manner. Suzuki coupling of a dioxaborolane TPA derivative and 2-bromo-3-nonylthieno[3,2-b]thiophene or S

Synthesis and electrochemical properties of oligo- and poly(thienylphenylamine)s

The oxidative polymerization of tris(thienylphenyl)amine derivatives was performed in acetonitrile by electrochemical and chemical methods. Oligomers were synthesized by stepwise coupling using coupling reactions. The polymer prepared using the trifunctio