79839-38-6

Upstream product

• 603-37-2 p-(diphenylmethyl)toluene 
• 5440-76-6 (4-methylphenyl)diphenylmethanol 
• 106-38-7 para-bromotoluene 
• 119-61-9 benzophenone 
• 108-86-1 bromobenzene 
• 134-84-9 4-Methylbenzophenone 

Downstream Products

• 126062-13-3 Tetra-n-butylammonium 4-methyltetradecachlorotriphenylmethide 
• 329897-50-9 Diethyl 4-[bis(2,3,4,5,6-pentachlorophenyl)methyl]-2,3,5,6-tetrachlorobenzyl phosphonate 
• 101980-97-6 αH-4-(2-acetamido-2,2-bis(ethoxycarbonyl)ethyl)tetradecachlorotriphenylmethane 
• 101981-10-6 4-(2-(alaninocarbonyl)ethyl)tetradecachlorotriphenylmethyl radical ethyl ester 
• 101981-03-7 αH-4-(2-(alaninocarbonyl)ethyl)tetradecachlorotriphenylmethane ethyl ester 
• 101980-96-5 αH-tetradecachloro-4-(2,2-bis(ethoxycarbonyl)ethyl)triphenylmethane 
• 101980-93-2 2,3,5,6-tetrachloro-4-(bis(pentachlorophenyl)methyl)-α-(tosyloxy)toluene 
• 101981-05-9 4-(2-carboxyethyl)tetradecachlorotriphenylmethyl radical 
• 101981-09-3 tetradecachloro-4-(2-(chlorocarbonyl)ethyl)triphenylmethyl radical 
• 101981-01-5 αH-4-(2-carboxyethyl)tetradecachlorotriphenylmethane 
• 101980-92-1 αH-4-(acetoxymethyl)tetradecachlorotriphenylmethane 
• 101981-00-4 αH-4-(carboxymethyl)tetradecachlorotriphenylmethane 
• 101980-99-8 αH-tetradecachloro-4-formyltriphenylmethane 
• 101980-95-4 αH-tetradecachloro-4-(cyanomethyl)triphenylmethane 

Relevant academic research and scientific papers

Electrochemical and Spectroscopic Studies on Triarylamine-Polychlorotriphenylmethyl Dyads with Particularly Strong Triarylamine Donors

We present two new donor-acceptor dyads composed of a polychlorotriphenylmethyl radical (PTM.) as the acceptor (A) and bis(4-dimethylaminophenyl)(phenyl)amine (TPAN) or 2,2’:6’,2’’:6’’,6-trioxytriphenylamine (TOTA) as particularly electron-rich triarylamine (TAA) donors (D). We assessed their electrochemical properties and electronic structures by cyclic voltammetry, UV/vis/NIR spectroscopy, EPR spectroscopy and quantum chemical calculations. By establishing the spectroscopic fingerprints of the oxidized and reduced forms, we probe for the possible coexistence of a zwitterionic TAA+-PTM? valence tautomer (VT), besides neutral TAA-PTM.. UV/vis/NIR and EPR spectroscopic studies at variable temperature and in various solvents however provide no indication for such equilibria. Quantitative spin counting experiments by EPR spectroscopy and quantum chemical calculations indicate that the one-electron oxidized forms of these dyads possess an open-shell singlet ground state which is energetically slightly below the triplet state.

Redox-Active PTM Radical Dendrimers as Promising Multifunctional Molecular Switches

Nowadays there is a great interest in using individual molecules as nanometer-scale switches and logic devices, with the aim of reaching higher power and smaller size. Demonstrating that one molecular switch can be turned on and off at room temperature si

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