A crystalline radical cation derived from Thiele’s hydrocarbon with redox range beyond 1 V
Organic molecules that can access various redox states have potential applications in electronics, batteries, catalysis, among others. Here the authors report the preparation of an unsymmetrical organoboron analogue of Thiele’s hydrocarbon and study its one- and two-electron oxidation reactions; rem...
Guardado en:
Autores principales: | Ying Kai Loh, Petra Vasko, Caitilín McManus, Andreas Heilmann, William K. Myers, Simon Aldridge |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/8ac58dd707a345c69481b8094024f506 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
SCAVENGING ACTIVITY OF DICLOFENAC: INTERACTION WITH ABTS RADICAL CATION AND PEROXYL RADICALS
por: ROJO,C, et al.
Publicado: (2009) -
EVALUATION OF THE EXTINCTION COEFFICIENT OF THE ABTS DERIVED RADICAL CATION
por: Henriquez,Carola, et al.
Publicado: (2002) -
Phonon-mediated high-T c superconductivity in hole-doped diamond-like crystalline hydrocarbon
por: Chao-Sheng Lian, et al.
Publicado: (2017) -
Molecular mass growth through ring expansion in polycyclic aromatic hydrocarbons via radical–radical reactions
por: Long Zhao, et al.
Publicado: (2019) -
Anion-adaptive crystalline cationic material for 99TcO4 − trapping
por: Lei Mei, et al.
Publicado: (2019)