Cargando…
NMR and EPR Study of Homolysis of Diastereomeric Alkoxyamines
Three alkoxyamines based on imidazoline radicals with a pyridine functional group—potential initiators of nitroxide-mediated, controlled radical polymerization—were synthesized. Electron Paramagnetic Resonance (EPR) measurements reveal biexponential kinetics for the thermolysis for diastereomeric al...
Autores principales: | Cherkasov, Sergey, Parkhomenko, Dmitriy, Genaev, Alexander, Salnikov, Georgii, Edeleva, Mariya, Morozov, Denis, Rybalova, Tatyana, Kirilyuk, Igor, Marque, Sylvain R. A., Bagryanskaya, Elena |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7663419/ https://www.ncbi.nlm.nih.gov/pubmed/33139669 http://dx.doi.org/10.3390/molecules25215080 |
Ejemplares similares
-
How intramolecular coordination bonding (ICB) controls the homolysis of the C–ON bond in alkoxyamines
por: Audran, Gérard, et al.
Publicado: (2019) -
Smart Control of Nitroxide-Mediated Polymerization Initiators’ Reactivity by pH, Complexation with Metals, and Chemical Transformations
por: Edeleva, Mariya, et al.
Publicado: (2019) -
Establishing plasmon contribution to chemical reactions: alkoxyamines as a thermal probe
por: Guselnikova, Olga, et al.
Publicado: (2021) -
Direct observation of reversible bond homolysis by 2D EXSY NMR
por: Takebayashi, Satoshi, et al.
Publicado: (2022) -
Alkoxyamines Designed as Potential Drugs against Plasmodium and Schistosoma Parasites
por: Reyser, Thibaud, et al.
Publicado: (2020)