Cargando…
Diastereoisomers of l-proline-linked trityl-nitroxide biradicals: synthesis and effect of chiral configurations on exchange interactions
The exchange (J) interaction of organic biradicals is a crucial factor controlling their physiochemical properties and potential applications and can be modulated by changing the nature of the linker. In the present work, we for the first time demonstrate the effect of chiral configurations of radic...
Autores principales: | Zhai, Weixiang, Feng, Yalan, Liu, Huiqiang, Rockenbauer, Antal, Mance, Deni, Li, Shaoyong, Song, Yuguang, Baldus, Marc, Liu, Yangping |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5958346/ https://www.ncbi.nlm.nih.gov/pubmed/29896379 http://dx.doi.org/10.1039/c8sc00969d |
Ejemplares similares
-
Highly bioresistant, hydrophilic and rigidly linked trityl-nitroxide biradicals for cellular high-field dynamic nuclear polarization
por: Yao, Ru, et al.
Publicado: (2022) -
In-Cell Trityl–Trityl Distance Measurements
on Proteins
por: Yang, Yin, et al.
Publicado: (2020) -
Mechanism of diastereoisomer-induced chirality of BiOBr
por: Ding, Kun, et al.
Publicado: (2022) -
A Comparative Study of Nitroxide‐Based Biradicals for Dynamic Nuclear Polarization in Cellular Environments
por: Ackermann, Bryce E., et al.
Publicado: (2022) -
PyrroTriPol: a semi-rigid trityl-nitroxide for high field dynamic nuclear polarization
por: Halbritter, Thomas, et al.
Publicado: (2023)