Cargando…
Edge Decoration of Anthracene Switches Global Diatropic Current That Controls the Acene Reactivity
[Image: see text] The 14π-electron system of anthracene has been merged with the unsaturated Z-1,2-difurylethene to form a macrocycle(s) with the retained local conjugation of all incorporated subunits that were substantially modulated with a redox activation, opening a global delocalization involvi...
Autores principales: | Dutta, Arnab, Stawski, Wojciech, Kijewska, Monika, Pawlicki, Miłosz |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8689655/ https://www.ncbi.nlm.nih.gov/pubmed/34870434 http://dx.doi.org/10.1021/acs.orglett.1c03605 |
Ejemplares similares
-
Substituent effects on paratropicity and diatropicity in π-extended hexapyrrolohexaazacoronene
por: Takase, Masayoshi, et al.
Publicado: (2023) -
Reductive Dimerization of Macrocycles Activated by
BBr(3)
por: Kijewska, Monika, et al.
Publicado: (2021) -
Pushing the Limits of Acene Chemistry: The Recent Surge of Large Acenes
por: Tönshoff, Christina, et al.
Publicado: (2020) -
Strategies for the Synthesis of Higher Acenes
por: Dorel, Ruth, et al.
Publicado: (2016) -
Responding to the pandemic: Nursing education and the ACEN
por: Ard, Nell, et al.
Publicado: (2021)