123560-37-2Relevant academic research and scientific papers
An oxo-verdazyl radical for a symmetrical non-aqueous redox flow battery
Cekic-Laskovic, Isidora,Grünebaum, Mariano,Korshunov, Aleksandr,Milner, Matthew James,Studer, Armido,Winter, Martin
, p. 22280 - 22291 (2020)
Verdazyl free radical compounds are promising candidates for symmetrical all-organic redox flow batteries (RFBs) due to their redox stability, the ease with which their chemical structure can be varied, and their unique bipolar nature. The present work re
Kinetic investigation of thermal and photoinduced homolysis of alkylated verdazyls
Audran, Gérard,Marque, Sylvain R. A.,Petunin, Pavel V.,Postnikov, Pavel S.,Trusova, Marina E.,Votkina, Darya E.
, p. 21881 - 21887 (2020/10/26)
The on-demand generation of stable organic radicals from the precursors can be considered as an essential challenge for the plethora of applications in various fields of science. In this contribution, we prepared a range of N-(methyl)benzyl derivatives of
Effect of the C(3)-Substituent in Verdazyl Radicals on their Profluorescent Behavior
Eusterwiemann, Steffen,Matuschek, David,Stegemann, Linda,Klabunde, Sina,Doerenkamp, Carsten,Daniliuc, Constantin G.,Doltsinis, Nikos L.,Strassert, Cristian A.,Eckert, Hellmut,Studer, Armido
, p. 172 - 176 (2016/05/02)
Methods for the detection of reactive intermediates such as transient radicals are important in organic chemistry, polymer chemistry, biology or medicine. Along these lines we recently reported that 1,5-diphenyl-6- oxo verdazyl radicals can be used as flu
New General Synthesis of Tetrahydro-1,2,4,5-tetrazin-3(2H)-one Derivatives and Stable 3,4-Dihydro-3-oxo-1,2,4,5-tetrazin-1(2H)-yl Radical Derivatives
Milcent, Rene,Barbier, Geo,Capelle, Sylvie,Catteau, Jean-Pierre
, p. 319 - 324 (2007/10/02)
Reactions of 2-chloroformylhydrazones of aromatic aldehydes or ketones 2 with various hydrazines were converted to monocarbonohydrazone derivatives 3 or 5 and/or tetrahydro-1,2,4,5-tetrazin-3(2H)-one derivatives 6,7.By oxidation with lead dioxide, compounds 6 were transformed into stable 3,4-dihydro-3-oxo-1,2,4,5-tetrazin-1(2H)-yl radical derivatives 8.
