19112-42-6

Usage

Chemical structure

1,1,2,2-tetraphenylethylbenzene consists of a central benzene ring surrounded by four phenyl groups, each attached to one of the carbon atoms of the benzene ring.

Building block

It is often used as a building block in the synthesis of organic materials and molecules due to its unique structural properties.

Stability

1,1,2,2-tetraphenylethylbenzene is known for its stability, making it useful in various industrial applications.

High melting point

The compound has a high melting point, which contributes to its stability and utility in industrial applications.

Potential use in OLEDs

It has been studied for its potential use in organic light-emitting diodes (OLEDs) due to its ability to emit light.

Electronic device applications

1,1,2,2-tetraphenylethylbenzene has potential applications in other electronic devices, such as conductive materials, due to its ability to conduct electricity.

Academic and industrial interest

The compound has garnered interest in both academic research and industrial applications due to its versatile and useful properties.

Upstream product

• 87655-70-7 pentaphenyl-ethyl 
• 76-83-5 trityl chloride 
• 776-74-9 Bromodiphenylmethane 
• 4303-71-3 triphenylmethyl sodium 
• 90-99-3 diphenylchloromethane 
• 30615-54-4 triphenylmethyl bromide 
• 2051-90-3 Dichlorodiphenylmethane 
• 519-73-3 triphenylmethane 
• 51954-45-1 benzhydryl-trimethyl-ammonium; iodide 
• 2216-49-1 triphenylmethyl radical 
• 71-43-2 benzene 
• 121699-87-4 2-tricarbonylchromium⁽⁰⁾phenyl-1.1.1.2-tetraphenylethane 
• 83576-31-2 1,1,1,3,3-pentaphenylpropan-2-one 

Downstream Products

• 101-81-5 Diphenylmethane 
• 519-73-3 triphenylmethane 
• 2216-49-1 triphenylmethyl radical 
• 596-30-5 ditrityl peroxide 
• 632-51-9 1,1,2,2-tetraphenylethylene 
• 103398-47-6 benzhydryl-trityl peroxide 
• 3178-23-2 dicyclohexylmethane 
• 1610-24-8 tricyclohexylmethane 
• 10060-17-0 (diphenylmethyl)potassium 
• 76-83-5 trityl chloride 
• 108-88-3 toluene 
• 596-43-0 bromo-triphenyl-methane 
• 776-74-9 Bromodiphenylmethane 
• 119-61-9 benzophenone 

Relevant academic research and scientific papers

Transient Kinetics and Quantum Yield Studies of Nanocrystalline α-Phenyl-Substituted Ketones: Sorting Out Reactions from Singlet and Triplet Excited States

Recent work has shown that diarylmethyl radicals generated by pulsed laser excitation in nanocrystalline (NC) suspensions of tetraarylacetones constitute a valuable probe for the detailed mechanistic analysis of the solid-state photodecarbonylation reaction. Using a combination of reaction quantum yields and laser flash photolysis in nanocrystalline suspensions of ketones with different substituents on one of the α-carbons, we are able to suggest with confidence that a significant fraction of the initial α-cleavage reaction takes place from the ketone singlet excited state, that the originally formed diarylmethyl-acyl radical pair loses CO in the crystal with time constants in the sub-nanosecond regime, and that the secondary bis(diarylmethyl) triplet radical pair has a lifetime limited by the rate of intersystem crossing of ca. 70 ns.

Syntheses and X-ray strucutre determinations of the isomeric pentaphwnylethane tricarbonylchromium(0) complexes, 1-tricarbonylchromium(0) phenyl-1,1,2,2-tetraphenylethane and 2-tricarbonylchromium(0) phenyl-1,1,1,2-tetraphenylethane

Two chromium tricarbonyl (CTC) coordinated pentaphenylethanes (PPE) have been synthesized via organometallic coupling reactions.X-Ray structure determinations have shown the ethane carbon-carbon bond distances in C(1) and C(2) CTC complexes of PPE to be 1

Preparation and Characterization of Some Pentaarylethyls

The reaction of triphenylmethylsodium with dichlorodiphenylmethane does not give pentaphenylethyl as previously reported, but when the anion reacts with 9,9-dichlorofluorene, it does form the reported 9-tritylfluorenyl radical which has been characterized by ESR spectroscopy.The radical is better prepared by oxidation of the anion of 9-tritylfluorene.The 9-tritylfluorenyl radical reacts with traces of oxygen to give triphenylmethyl and fluorenone.With light it forms triphenylmethyl and fluorenylidene.The latter was established by photolyzing 9-diazofluorene in the presence of triphenylmethyl with the generation of 9-tritylfluorenyl.Small yields of the persistent pentakis(p-tert-butylphenyl)ethyl radical have been prepared, and it is propable that pentaphenylethyl has also.

SELECTIVE COUPLING OF FREE RADICALS VIA ORGANOCHROMIUM COMPLEXES.

Free radicals can be coupled in high yield to give either symmetric dimers or cross coupling products by reacting chromous chloride in THF with alkyl halides.