4070-01-3

Usage

Uses

1. Used as a spin probe to study other molecules, including polymers:
PerchlorotriphenylMethyl Radical is utilized as a stable perchlorinated arylmethyl radical in the field of molecular and polymer research. Its unique structure allows it to interact with a wide range of molecules, providing valuable insights into their properties and behavior.
2. Used in Chemical Analysis:
In the chemical analysis industry, PerchlorotriphenylMethyl Radical serves as a valuable tool for studying the structure and properties of various compounds. Its reactivity and stability make it an ideal candidate for probing the characteristics of other molecules, leading to a better understanding of their chemical behavior.
3. Used in Material Science:
In the field of material science, PerchlorotriphenylMethyl Radical can be employed to investigate the properties of polymers and other materials. Its interaction with these substances can help researchers develop new materials with improved characteristics, such as enhanced stability, reactivity, or mechanical properties.
4. Used in Pharmaceutical Research:
PerchlorotriphenylMethyl Radical can also be used in the pharmaceutical industry for studying the interactions between drugs and their target molecules. This can lead to the development of more effective drugs with fewer side effects, ultimately benefiting patients and the healthcare industry as a whole.

Upstream product

• 33240-61-8 αH-Pentadecachlorotriphenylmethane 
• 79855-16-6 4-Bromotetradecachlorotriphenylmethyl Radical 
• 71947-01-8 tetradecachloro-4-methoxytriphenylmethyl radical 
• 126062-01-9 Tetra-n-butylammonium perchlorotriphenylmethide 
• 79855-17-7 4-iodotetradecachlorotriphenylmethyl radical 
• 122898-71-9 perchloro(diphenylmethylene)cyclohexa-1,4-diene 
• 78227-02-8 αH-(Heptadecachloro-4-methyltriphenyl)methane 
• 79839-41-1 4-[bis(2,3,4,5,6-pentachlorophenyl)methyl]-2,3,5,6-tetrachlorobenzoic acid 
• 30482-37-2 perchlorotriphenylcarbenium hexachloroantimonate 
• 79855-13-3 4-H-tetradecachlorotriphenylmethyl radical 

Downstream Products

• 126062-01-9 Tetra-n-butylammonium perchlorotriphenylmethide 
• 79855-13-3 4-H-tetradecachlorotriphenylmethyl radical 
• 71947-01-8 tetradecachloro-4-methoxytriphenylmethyl radical 
• 32390-14-0 Perchloro-9-phenylfluorenyl radical 
• 88180-05-6 α-hydroperchloro-9-phenylfluorene 
• 33240-61-8 αH-Pentadecachlorotriphenylmethane 
• 29972-98-3 perchlorofuchsone, perchloro(diphenylmethylene)cyclohexa-2,5-dienone 
• 47741-76-4 perchlorotriphenylmethylcarbanion 
• 122898-71-9 perchloro(diphenylmethylene)cyclohexa-1,4-diene 
• 88180-06-7 perchloro-9-phenylfluorene 
• 67173-39-1 bis(2,3,4,5,6-pentachlorophenyl)(2,3,5,6-tetrachloro-4-hydroxyphenyl)methyl radical 
• 67173-40-4 Tetradecachloro-4-<(ethoxycarbonyl)oxy>triphenylmethyl radical 
• 82891-71-2 4-(bromoacetoxy)tetradecachlorotriphenylmethyl radical 
• 134081-01-9 4-(dimethylamino)tetrachlorotriphenylmethyl radical 

Relevant academic research and scientific papers

Free Radicals as Clathrate Hosts: Crystal and Molecular Structure of 1:1 Perchlorotriphenylmethyl Radical-Benzene

The perchlorotriphenylmethyl radical (2) acts as a clathrate host forbenzene, halogenobenzenes, and 1,4-dioxane giving inclusion compounds with different stabilities; the structure of (2)-C6H6, established by X-ray diffraction, shows the guest molecules l

Chemical Modification toward Long Spin Lifetimes in Organic Conjugated Radicals

Organic semiconductors for spin-based devices require long spin relaxation times. Understanding their spin relaxation mechanisms is critical to organic spintronic devices and applications for quantum information processing. However, reports on the spin re

Oxidation of the perchlorotriphenylmethyl radical to the carbocation, and its unique abrupt reversion

A solution of AlCl3 in CH2Cl2 reacts slowly, at room temperature, with perchlorotriphenylmethyl radical (PTM.), an inert carbon free radical, to give perchlorotriphenylmethyl cation (PTM+) quantitativ

"Spin-Charge Exchange" in Allodial Radical Ions, a Novel Intramolecular Single Electron Transfer Equilibrium

The intramolecular single-electron transfer in radical anions and radical cations, constituted by two identical triphenylmethyl moieties, has been studied.The preparation of the radical ions has been effected by mixing the corresponding stable diions (tet

Unique Single-Electron Transfers between Chemically Inert Triphenylmethyl Radicals and Triphenylmethyl Anions

A number of SET reactions between inert 4-X-tetradecachlorotriphenylmethyl radicals (X-PTM.) and stable tetra-n-butylammonium (Q+) 4-Y-tetradecachlorotriphenylmethides (Q+ Y-PTM:-; X,Y= H, Me, NH2CO, Me2NCO, Ph2

Inert Carbon Free Radicals. 10. Chlorination of Perchlorotriphenylmethyl (PTM) Radical. Synthesis, Structure, and Reactivity of Perchloro(diphenylmethylene)cyclohexa-1,4-diene

Perchlorotriphenylmethyl radical (PTM-radical) is the paradigm of the chlorine-shielded "inert free radicals" (IFRs), which owe their unique chemical inertia to the colossal overcrowding about their trivalent carbon.However, they are active in single elec

Inert Carbon Free Radicals. 8. Polychlorotriphenylmethyl Radicals. Synthesis, Structure, and Spin-Density Distribution

Some symmetrical Ar3C. and unsymmetrical (C6Cl5)3-xArxC. radicals with different chlorine substitution patterns (X = 1,2; Ar: 2H-C6HCl4, 3H,5H-C6H2Cl4, 4H-C6HCl4, C6H5) are prepared.X-ray crystal structures for

SYNTHESIS AND PROPERTIES OF THE 1/1 COMPLEX OF 1,4,7,10,13,16-HEXAOXACYCLOOCTADECANE WITH POTASSIUM PERCHLOROTRIPHENYLMETHIDE

The 1/1 complex of 1,4,7,10,13,16-hexaoxacyclooctadecane with potassium perchlorotriphenylmethide has been prepared by reaction, in the presence of 18-crown-6, of (C6Cl5)3CH with KOH or reduction of radical (C6Cl5)3 with K metal.Its structure as reveal

Inert Carbon Free Radicals. 2. Monofunctionalized Tetradecachlorotriphenylmethyl Radicals and Related Compounds

Perchlorinated triphenylmethyl radicals, and their nonradical α-H precursors, with hydrogen (2), carboxy (3), carbomethoxy (4), ammonium carboxylate (5), bromo (6), iodo (7), and methyl (8) substituents in the 4-position have been synthesized and their re