1351272-41-7

Basic information

• Product Name: (2–(4–vinylphenyl)ethene–1,1,2–triyl)tribenzene
• Synonyms: (2–(4–vinylphenyl)ethene–1,1,2–triyl)tribenzene
• CAS NO: 1351272-41-7
• Molecular Weight: 358.483
• Mol File: 1351272-41-7.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 460.4±45.0 °C(Predicted)
• Density: 1.081±0.06 g/cm3(Predicted)
• CAS DataBase Reference: (2–(4–vinylphenyl)ethene–1,1,2–triyl)tribenzene(CAS DataBase Reference)
• NIST Chemistry Reference: (2–(4–vinylphenyl)ethene–1,1,2–triyl)tribenzene(1351272-41-7)
• EPA Substance Registry System: (2–(4–vinylphenyl)ethene–1,1,2–triyl)tribenzene(1351272-41-7)

Safety Data

• Hazardous Substances Data: 1351272-41-7(Hazardous Substances Data)

Usage

Description

(2–(4–vinylphenyl)ethene–1,1,2–triyl)tribenzene, also known as tris(p-vinylphenyl)benzene, is a conjugated polyaromatic hydrocarbon consisting of three benzene rings connected by a central vinylene unit. This molecule is known for its unique electronic and photophysical properties, including efficient charge transport and light emission capabilities.

Uses

Used in Optoelectronic Devices:
(2–(4–vinylphenyl)ethene–1,1,2–triyl)tribenzene is used as a key component in organic light-emitting diodes (OLEDs) and other optoelectronic devices due to its ability to efficiently transport charge and emit light. Its conjugated structure allows for electron delocalization, making it a promising material for various electronic and photonic applications.
Used in Electronic Devices:
(2–(4–vinylphenyl)ethene–1,1,2–triyl)tribenzene is used as a material in electronic devices for its efficient charge transport properties, which are essential for the performance of these devices.
Used in Photonic Applications:
(2–(4–vinylphenyl)ethene–1,1,2–triyl)tribenzene is used in photonic applications due to its unique photophysical properties, which enable it to interact with light in various ways, such as light emission and absorption.

Upstream product

• 1607-57-4 Triphenylvinyl bromide 
• 2156-04-9 4-Vinylphenylboronic acid 
• 108-05-4 vinyl acetate 
• 34699-28-0 1-(4-bromophenyl)triphenylethene 
• 119-61-9 benzophenone 
• 3139-85-3 4-vinylbenzophenone 
• 100-42-5 styrene 
• 65-85-0 benzoic acid 
• 87199-17-5 4-formylphenylboronic acid, 
• 1289218-74-1 [1-(4-carbaldehydephenyl)-1,2,2-triphenyl]ethylene 
• 2065-66-9 methyl-triphenylphosphonium iodide 
• 101-81-5 Diphenylmethane 
• 881-42-5 diphenylmethyllithium 
• 90-90-4 (4-bromophenyl)(phenyl)methanone 

Relevant articles and documents

Vinyl Groups Containing Tetraphenylethylene Derivatives as Fluorescent Probes Specific for Palladium and the Quenching Mechanism?

We previously reported that a series of tetraphenylethylene (TPE)-containing all-hydrocarbon conjugated polymers exhibited a specific fluorescence quenching by palladium ions (Pd2+). To understand the quenching mechanism, herein we investigate

Preparation of biocompatible aggregation-induced emission homopolymeric nanoparticles for cell imaging

A series of new homopolymers with various degrees of polymerization derived from vinyl tetraphenylethene, that is, poly[2-(4-vinylphenyl)ethene-1,1,2- triyl)tribenzene] homopolymers, is synthesized by reversible addition-fragmentation chain transfer (RAFT) polymerization. The homopolymers exhibit a significant aggregation-induced emission (AIE) effect and an ability to assemble themselves into AIE polymer nanoparticles (NPs) during precipitation in a water/tetrahydrofuran (THF) mixture. The NPs also exhibit good dispersibility, stability, and biocompatibility. The AIE polymer NPs are used in imaging studies of HeLa cells. A series of poly[(2-(4-vinylphenyl)ethene-1,1,2- triyl) tribenzene] homopolymers are successfully synthesized by RAFT polymerization. The homopolymers exhibit a significant AIE effect with 100-fold increase in emission intensity from solution to nanosuspension. The homopolymers can assemble themselves to AIE nanoparticles by quickly charging tetrahydrofuran solution into deionized water. The AIE nanoparticles are used for imaging studies of HeLa cells.

Synthesis and application of reversible fluorescent photochromic molecules based on tetraphenylethylene and photochromic groups

Tetraphenylethylene-naphthopyran (TPE-NP) and tetraphenylethylene-spirooxazine (TPE-SO) with conjugated photochromic groups and fluorophores were designed and synthesized. Both of them exhibit the comprehensive effects of aggregation-induced emission (AIE

Nickel-Catalyzed Reductive Cross-Coupling of Aryl Bromides with Vinyl Acetate in Dimethyl Isosorbide as a Sustainable Solvent

A nickel-catalyzed reductive cross-coupling has been achieved using (hetero)aryl bromides and vinyl acetate as the coupling partners. This mild, applicable method provides a reliable access to a variety of vinyl arenes, heteroarenes, and benzoheterocycles, which should expand the chemical space of precursors to fine chemicals and polymers. Importantly, a sustainable solvent, dimethyl isosorbide, is used, making this protocol more attractive from the point of view of green chemistry.